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<title cf:type="text"><![CDATA[Progress in Biochemistry and Biophysics -->Mini-review]]></title>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[MAR Library and Its Application in Eukaryotic Genome Mapping]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980601]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Matrix association region (MAR) is not only a kind of <i>cis</i>-acting element for regulation of eukaryotic gene expression and chromosome dynamics, but also a type of fixed and specific DNA marker on the eukaryotic chromosomes. MAR library can be constructed by <i>in vitro</i> or <i>in vivo</i> association of DNA fragments with the nuclear matrix. <i>In vitro</i> MARs can be used in construction of chromosome's physical map, and <i>in vivo</i> MARs can be applied in studying the expression, regulation and chromosomal organization of known genes, and analyzing the newly discovered genes.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHOU Cong-Zhao,QIAN Xin-Guo and LI Zhen-Gang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHOU Cong-Zhao,QIAN Xin-Guo and LI Zhen-Gang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980601]]></guid><cfi:id>65</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Advances in the Study of Chemokines]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980602]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Chemokines family is divided into four subfamilies(CXC、CC、C&CX3C)，it has been estimated that there may be as many as 40 to 50 human chemokines. Structure,gene location and function of chemokines and their receptors have gradually been eluciated. They play important roles in normal and disordered physiological states.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[HUANG Shi-He]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HUANG Shi-He</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980602]]></guid><cfi:id>64</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Non-coding mRNA]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980501]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Non-coding mRNA is a kind of newly discovered mRNA. Though spliced and tailed,it does not have any typical ORF. Up to date, several such genes have been cloned: <i>H</i>19 gene, <i>XIST</i> gene, <i>XLSIRT</i> gene, <i>His</i>-1 gene, <i>bic</i> gene, <i>rox</i>1 and <i>rox</i>2 genes. Non-coding mRNA play important roles in the development of embryos, in the inactivation of X chromosome and in the tumorigenesis.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LUO Wen-qin,YUAN Jian-gang and QIANG Bo-qin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LUO Wen-qin,YUAN Jian-gang and QIANG Bo-qin</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980501]]></guid><cfi:id>63</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress of Chromosome Microdissection and Microcloning Technology]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980502]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Progress of chromosome microdissection and microcloning technology were reviewed. Some main technology problems such as chromosome identification, microdissection and microcloning were disscussed. Some progress in plants was reviewed about chromosome microdissection and microcloning.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[TIAN Chai,LU Yi-fan,DENG Ji-xian and LIU Guang-tian]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>TIAN Chai,LU Yi-fan,DENG Ji-xian and LIU Guang-tian</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980502]]></guid><cfi:id>62</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[TRAIL: A New Member of Tumor Necrosis Factor Superfamily]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980503]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Tumor necrosis factor related apoptosis-inducing ligand (TRAIL), which called also Apo-2L, is a new member of the tumor necrosis factor superfamily. TRAIL cDNA was isolated via searching homology to Fas/Apo-1 ligand and TNF in an expressed sequenced tag (EST) data base. It consists of 281 amino acids with a calculated molecular mass of 32.5 ku. Transfected TRAIL is expressed at the cell  surface with its C-terminus exposed, indicating a type Ⅱ transmembrane protein topology. Like Fas/Apo-1 ligand and TNF, its C-terminal exhibits a homotrimeric subunit structure. Soluble TRAIL induces extensive apoptosis in most tumor cell lines, but the effect of TRAIL is not inhibited by soluble Fas/Apo-1 and TNF receptors. So far, three receptors of TRAIL have been identified, i.e. DR4, DR5 and TRID. These discoveries suggest that the mechanism of TRAIL is different from TNF and FasL. TRAIL may likely be elaborated as a new anti-cancer drug.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WANG Liang-hua and JIAO Bing-hua]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Liang-hua and JIAO Bing-hua</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980503]]></guid><cfi:id>61</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Research Progress of Raf-1 Protein Kinase in Signal Transduction]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980401]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Raf-1 protein kinase has been known as an important component of Ras/Raf-1/MAPK signaling pathway related to cell proliferation. It also may be a cross-talk point among different signal transduction pathways. This is a review about the characteristics of Raf-1 molecule, its activation and relationship with other proteins.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LI Biao and LI Xiao-mei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Biao and LI Xiao-mei</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980401]]></guid><cfi:id>60</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Expression of Foreign Gene in Chloroplast]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980402]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The characterizations of chloroplast expressing system were described, and research progressing was also summerized, then put forward some questions about foreign gene expression in chloroplast, and give some ideas to resolve them.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[FAN Guo-chang,ZHANG Zhong-lin,QIAN Kai-xian and SHEN Gui-fang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>FAN Guo-chang,ZHANG Zhong-lin,QIAN Kai-xian and SHEN Gui-fang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980402]]></guid><cfi:id>59</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Cardiotrophin-1, the New Member of the Interleukin-6 Cytokine Family]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980403]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Cardiotrophin-1 is a novel member of the interleukin-6 cytokine family. Mouse CT-1 mRNA is about 1.4 kb in length, and the encoded protein contains a 203-aa open reading frame. It utilizes gp130 and LIFR as the signal transducing receptor components. As a multifunctional cytokine, it induces cardiac myocyte hypertrophy and promote cardiac myocyte survival. It can induce a phenotypic switch in rat sympathetic neurons and promote the survival of dopaminergic neurons, ciliary neurons and motoneurons. It can also inhibit the growth of the mouse myeloid leukemia cell M1, and induce liver acute phase response. The chronic administration of CT-1 to mouse increases platelet counts, red blood cell counts and haemoglobin concentration.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[HUA Ping and GE Zhong-liang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HUA Ping and GE Zhong-liang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980403]]></guid><cfi:id>58</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[3′-Untranslated Region of Eukaryotic mRNA in Gene Regulation]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980301]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The 3′untranslated region (3′-UTR) of eukaryotic mRNA plays an important role in the eukaryotic gene regulation. It controls not only the stability and degradation of eukaryotic mRNA, but the translation as well.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[SHI Tong-dong,WU Yu-zhang and ZHU Xi-hua]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>SHI Tong-dong,WU Yu-zhang and ZHU Xi-hua</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980301]]></guid><cfi:id>57</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Overexpression and Suppression of <i>neu</i> Gene in Human Cancers]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980201]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The <i>neu</i> gene is known to encode a PTK-activity-bearing phosphoprotein which is one of the homologous proteins of epidermal growth factor receptor (EGFR). Amplification and (or) overexpression of <i>neu</i> gene have been found in various human cancers recently. Some protein factors and chemical agents can suppress <i>neu</i> gene transcription or reduce the PTK activity of p185<sup>neu</sup>, resulting in the inhibition of metastasis and proliferation of cancer cells with <i>neu</i> overexpression.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[GONG Hai-biao,ZHANG Wei-jie and XU Jin-lin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GONG Hai-biao,ZHANG Wei-jie and XU Jin-lin</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980201]]></guid><cfi:id>56</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Hypoxia-inducible Factor 1]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980202]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Hypoxia-inducible factor 1(HIF<sub>1</sub>) is a nuclear factor whose production and DNA binding activity is induced by hypoxia in a variety of cell types, which is composed of two different subunits: 120 ku HIF<sub>1α</sub> and 91～94 ku HIF<sub>1β</sub>. HIF<sub>1</sub>, as a hypoxia inducible transcription factor, promotes the expression of erythropoietin gene and glycolytic enzymes gene etc. in response to hypoxia which maintain the oxygen homeostasis.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHANG Ji-feng,CHEN Guang-hui and TANG Jian]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Ji-feng,CHEN Guang-hui and TANG Jian</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980202]]></guid><cfi:id>55</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress on the Studies of Insulin-like Growth Factor Binding Proteins]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980203]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The insulin-like growth factor binding proteins(IGFBPs)are a family of soluble proteins that bind the insulin-like growth factors(IGFs) with high affinity.These proteins not merely carry the IGFs and prolong the half-life of IGFs,but have influences on both the bioactivity and distribution of IGFs in the extracellular environment.Under the different experiment conditions, IGFBPs can either inhibit or augment IGFs actions. In addition, IGFBPs appear to have intrinsic biological activity independent on IGFs. Research on molecular structure,gene expression, post-translational modifications, and bioactivity of IGFBPs were summarized.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[DU Qing-you and WANG Hui-xin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DU Qing-you and WANG Hui-xin</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980203]]></guid><cfi:id>54</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[抗原呈递分子三维结构与功能研究进展]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980101]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[曾宗浩]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>曾宗浩</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980101]]></guid><cfi:id>53</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[蛋白质的豆蔻酰化]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980102]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[许正平,李伯良]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>许正平,李伯良</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980102]]></guid><cfi:id>52</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[核基质与瘤基因、抑瘤基因]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980103]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[钟叔平]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>钟叔平</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19980103]]></guid><cfi:id>51</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Synuclein Family]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990601]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Synucleins, as a family of small proteins enriched in presynaptic element in CNS, share a secondary structure feature of periodicity of amphipathic α-helix with 11 amino acid  residues throughout the N-terminus. The physiological function of synucleins is unknown, but large quantities of research suggest that synucleins may be implicated in synaptic genesis and plasticity. Also, the relations of synuleins to many neurodegenerative diseases such as Alzheimer's and Parkinson's as well as to the invasion of breast cancer have been gaining attention of researchers.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[YANG Nuo,ZHANG Lin and SHEN Li]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YANG Nuo,ZHANG Lin and SHEN Li</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990601]]></guid><cfi:id>50</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[RRM RNA Binding Protein: Structure and Function]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990401]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[RRM RNA binding protein is a kind of RNA binding protein which contains one or more RNA recognition motifs and some affiliated motifs. It participates in genes' post-transcriptional regulations including splicing of pre-mRNA, cellular localization and stability maintenance of RNA. Conservative amino acids in the RRM motif are essential for RNA binding, but the specific binding depends on other factors. Some RRM RNA binding proteins are related to genetic diseases and tumors.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[DU Guang-Wei,ZHOU Yan,YUAN Jian-Gang and QIANG Bo-Qin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DU Guang-Wei,ZHOU Yan,YUAN Jian-Gang and QIANG Bo-Qin</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990401]]></guid><cfi:id>49</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Integrins and Blastocyst Implantation]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990402]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Integrins are cell adhesive molecules (CAMs) comprised of α and β subunits. These CAMs usually contain a large domain, a transmembrane segment and a short cytoplasmic domain. They can interact with the extracellular matrix components, such as collagen, fibronectin, or vitronectin, to regulate the cell adhesion and trafficking. As a bidirectional transducer, integrins are involved in cell signaling by way of inside-outside signaling and outside-inside signaling. Successful implantation depends on the intimate interaction between the penetrative blastocyst and the receptive endometrium, which contains many cellular or molecular events. More recently, accumulating evidences have shown that expression of integrins during the “implantation window” stage plays an important role in “maternal-fetal dialogue” and becomes a potential marker of the receptive uterine endometrium.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[CAI Li-Quan and DUAN En-Kui]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CAI Li-Quan and DUAN En-Kui</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990402]]></guid><cfi:id>48</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Function and Structure of Peptide α-Amidating Monooxygenase]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990301]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Carboxy-terminal amidation is an essential posttranslational modification for numerous neuronal and endocrine peptides.It is catalyzed by peptide α-amidating monooxygenase (PAM),in a two-step reaction. Peptidylglycine α-hydroxylating monooxygenase(PHM) and peptidyl-hydroxyglycine -α-amidating lyase(PAL) act in one of the two step.PHM catalytic core is composed of two nine-stranded β-sandwich domains similar in three-dimessional structure.Each domain contains an activity center with a copper coordinated by three conserved His or two His and a Met residues.In the reaction cycle of producing peptidyl α-hydroxyglycine,the two coppers are reduced independently by ascorbate,and they transfer one electron each to molecular oxygen.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LIU Shen-Ji and CHEN Song-Sen]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Shen-Ji and CHEN Song-Sen</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990301]]></guid><cfi:id>47</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Neural Cell Adhesion Molecules and Memory]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990302]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Synaptic plasticity is involved in the process of memory formation. It's proved that neural cell adhesion molecules play an important role both in promoting synaptic plasticity and keeping the synaptic stability. Many evidences have been showed that neural cell adhesion molecules can regulate some process in association with learning and memory.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[HU Jia-Fen,SUI Nan,KUANG Pei-Zi and GUAN Lin-Chu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HU Jia-Fen,SUI Nan,KUANG Pei-Zi and GUAN Lin-Chu</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990302]]></guid><cfi:id>46</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Regulation of Retinal Homeobox Gene Concerned with the Development of Visual System]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990303]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Rx (retinal homeobox) is a new gene family, which is closely correlated to the development of visual system. The expression of these genes is related to the development of eye primordia, optic vesicle, retina, forebrain and some regions of middle brain. The research of Rx genes will throw light on the regulation mechanism of development of visual system.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[HUA Qian]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>HUA Qian</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990303]]></guid><cfi:id>45</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Immunotherapy of Tumor]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990201]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Tumor antigen is the substance which gives tumor cell antigenicity and make it to be recognized by the immune system. The discovery of tumor antigen is the basis of the development of tumor vaccine. Until now, there is great progress in tumor antigen. Meantime, along with the new understanding of tumor antigen, the development of tumor vaccine has got into a new stage.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WAN Qian,ZHANG Chao-Liang and ZHAI Chao-Yang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WAN Qian,ZHANG Chao-Liang and ZHAI Chao-Yang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990201]]></guid><cfi:id>44</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Interleukin-17 Receptor]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990202]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Interleukin-17 receptor (IL-17R) has been recently identified, which exhibits no homology to any known family of receptors. Studies show that soluble mouse IL-17R (smIL-17R) can not only inhibit T-cell activation, but also suppress the response to alloantigen in established allograft transplant models.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHOU Li-Mei and WANG Jia-Xi]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHOU Li-Mei and WANG Jia-Xi</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990202]]></guid><cfi:id>43</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress in the Studies of Foreign Gene Silencing in Transgenic Plants]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990203]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Gene silencing is one of the important factors of transgene inactivation. The main mechanisms, including postion effects, transcriptional silencing and post-transcriptional silencing was presented, the means of stabilizing gene expression in transgeneic plants was discussed.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHU Li,ZHANG Chun-Yi and FAN Yun-Liu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHU Li,ZHANG Chun-Yi and FAN Yun-Liu</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990203]]></guid><cfi:id>42</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Pitx2: a left-right Asymmetric Signalling Molecule]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990101]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Pitx</i>2 is asymmetrically expressed in the left lateral plate mesoderm and derived organs such as heart and gut during chick, mouse and <i>Xenopus</i> development. Pitx2 appears to be downstream effector of Shh and Nodal. Misexpression of <i>Pitx</i>2 is sufficient to produce reversed organs of body rotation. Defect of <i>Pitx</i>2 in human may cause Rieger syndrome. Pitx2 seems to be a key conserved signalling molecules that mediates left-right asymmetry in vertebrate.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LIU Ji-Long and TAN Yan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Ji-Long and TAN Yan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990101]]></guid><cfi:id>41</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Vitrification of Proteins]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990102]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The glassified proteinaceous bioactive substances are  extremely stabilized at room temperature by the presence of the specific carbohydrates as a glass-forming carrier and chaperonins／dehydrins as a protector. There are indications that the natural vitrification of bioactive substances in seed of plant lead the seeds into the dormant phase.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[FAN Pei-Chang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>FAN Pei-Chang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990102]]></guid><cfi:id>40</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Myostatin(Mstn) Gene and Its Potential Utilization in Meat Production]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990103]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Myostatin(Mstn) gene is a new member of the TGF-β superfamily, which is expressed specifically in skeletal muscle and functions as a negative regulator of skeletal muscle growth. Myostatin gene may represent an ideal target for manipulating muscle mass because it is a single gene, the absence of which results in increased muscle mass, and a natural knockout is already present in the existing double-muscled cattle population, suggesting that manipulation of this gene should not interfere with other growth systems and result in abnormal pathology.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LIANG Xu-Fang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIANG Xu-Fang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/19990103]]></guid><cfi:id>39</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Interleukin 18]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000602]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Interleukin 18 (IL-18) is a recently identified cytokine, originally called interferon gamma inducing factor. Due to its capacity to induce interferon gamma production in Th1 type cells. It has pleiotropic biological functions. IL-18 belongs structurally to the IL-1 cytokine family and shares biological properties with IL-12. Consequently, IL-18 is a potential regulator of antitumor immune response. IL-18 plays an important role in autoimmune disease and endotoxin-induced injury. So, future work will focus on its application as an immunotherapeutic agent for a variety of diseases.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[PEI Dong-Sheng and ZHAO Hui-Ren]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>PEI Dong-Sheng and ZHAO Hui-Ren</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000602]]></guid><cfi:id>38</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Early Morphogenesis of Visual System Is Related to Vax Family]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000403]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Development and morphogenesis of visual system is a complicated procedure, and the gene regulation is widely paid attentions by neurodevelopmental biologists. Vax (ventral anterior homeobox) family was found in 1998, which is related to development of forebrain, optic vesicle, eye-predium, optic stalk and neuroretina. Vax-1 is involved in differentiation of pigmented epithelium and optic stalk, while Vax-2 could function in the establishment of the dorso-ventral axis of the retina and visual system. Investigation of Vax genes will be helpful to understand the mechanism of molecular events, which happened during the early development of the visual system.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LIU Yang and HE Rong-Qiao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Yang and HE Rong-Qiao</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000403]]></guid><cfi:id>37</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Milestone for Ribosome Structure Studies]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000302]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Ribosome is a molecular machine based on RNA,which provides the workshop and tools to synthesize all of the proteins in cells.Its sophisticated structure enables crystallographers regarding it as the Mount Everest for a long time.Recently ,the breakthrough has made for ribosome structure studies.For the first time,several proteins of known three-dimensional structure,and many regions of double-stranded rRNA,have been located in highly complex electron-density maps of ribosomal subunits. And the delicate structure of subunit interface and complicated tRNA,mRNA and ribosome interactions have been revealed.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[MING Zhen-Huan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MING Zhen-Huan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000302]]></guid><cfi:id>36</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Isthmo-optic Nucleus：a New Model to Study the Development and Apoptosis of Central Nervous System]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000202]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In recent years, the isthmo-optic nucleus (ION) in the avian centrifugal system became a new model to study the apoptosis and the development of central nervous system (CNS). During its development, together with the formation, folding and laminating of the nucleus, there exist some temporal pathways linked to the nucleus. More than half of its neurons befall apoptosis in this period. Researches show that proper efferent and afferent projections are essential to the survival of neurons. The molecular mechanism indicates that apoptosis is related to a series of neurotrophins and their receptors. Apoptosis plays an important role in the development of CNS.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[XIAO Quan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIAO Quan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000202]]></guid><cfi:id>35</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Brain Marrow:a Region of Survival Neuropoietic Stem Cells in Adult Brain]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000203]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Recently lot of research indicated that pluripotent neural stem cells with self-renewal and multilineage potential are present in the adult mammalian forebrain. The forebrain tissue containing persistent neural stem cells is referred to as “brain marrow”, since it has much in common with hematopoietic bone marrow. Neuropoiesis are very important field in neuroscience. A thorough investigation of neuropoiesis in the brain marrow should facilitate utilizing of migrating neurons in the adult human forebrain and transplanting human ES cells to treat neurodegeneraton diseases.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[CHEN Yan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>CHEN Yan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000203]]></guid><cfi:id>34</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[New Advances in Animal Transgenic Technology]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000204]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The technique of pronuclear microinjcetion is the most reliable and popular method for transgenic livestock production to date. However, pronuclear microinjection has been proven to be inefficient in producing transgenics and in inserting a piece of DNA into a specific site in the host genome. In the past 20 years, some new approaches have been used. These include sperm-mediated DNA transfer, retroviral mediated DNA transfer into oocytes, somatic cell carrying exogenous genes nuclear transfer, the use of embryonic stem(ES) cell. But these ways can not solve existing problems thoroughly. In recent papers, the existing techniques have been improved and significant progress has been made in developing transgenic techniques.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LI Jin-Song,ZHUANG Da-Zhong,SUN Qing-Yuan and CHEN Da-Yuan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Jin-Song,ZHUANG Da-Zhong,SUN Qing-Yuan and CHEN Da-Yuan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20000204]]></guid><cfi:id>33</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress on Immunization with Amyloid-β in a Mouse Model of Alzheimer's Disease]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010603]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[β-amyloid(Aβ) is a predominant component of senile plaques, one central pathological hallmark of Alzheimer's disease. Immunization with Aβ causes a marked reduction of Aβ burden and its associated pathologies in brain. A clearance of the preexisting plaques has been observed in transgenic mice, with an inhibition of lesion of cognitive functions. No signs of an immune-mediated response could be detected to endogenous Aβ peptide of mice. The chronic inflammatory response resulted from the immunization itself has not obviously impaired functions of central nerve system.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHANG Wei,HUA Qian,ZHANG Dai and HE Rong-Qiao]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHANG Wei,HUA Qian,ZHANG Dai and HE Rong-Qiao</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010603]]></guid><cfi:id>32</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Structure and Function of Membrane-associated Guanylate Kinase Family Proteins]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010501]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Membrane-associated guanylate kinase family proteins mediate the clustering and aggregation of ion channels,receptors and cell adhesion molecules via their PDZ、SH<sub>3</sub>、GK domains,respectively. MAGUKs construct the cytoskeleton, take part in the signal transduction and modulate the cell cycle process,as well as the neural development. The characters of MAGUKs'structure ,their functions and some members of the family were explicated.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHU Ke-Yi,WAN Yong-Qi and XIE Wei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHU Ke-Yi,WAN Yong-Qi and XIE Wei</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010501]]></guid><cfi:id>31</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Paired Helical Filament of tau and Neural Cell Death]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010401]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Neurofibrillary tangle (NFT), paired helical filament (PHF) as the major component, is an important pathological character of Alzheimer's disease. Further evidence suggests that PHF plays an important role in neural cell death, including necrotic and apoptotic death. Induction of reactive oxygen species (ROS) by PHF production may be an important mechanism of neural cell death.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[Nie Chun-Lai]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Nie Chun-Lai</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010401]]></guid><cfi:id>30</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Adenylate Kinase and Cellular Apoptosis]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010402]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[As an important kinase in the organism, adenylate kinase (AK) not only plays a crucial role in keeping the energy balance, but also takes part in the procedure of apoptosis. In apoptotic cells the release of AK2 from mitochondrial intermembrane to the cytosol is very common, but its function is still not clear. The latest research of AK in apoptosis and the possible role of AK during apoptosis are reviewed.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LAI Qiu-An,HU Jian-Jun and SUN Jiu-Rong]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LAI Qiu-An,HU Jian-Jun and SUN Jiu-Rong</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010402]]></guid><cfi:id>29</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Molecular Mechanism for Proton Translocation of Bacteriorhodopsin]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010302]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Bacteriorhodopsin (bR) is the sole protein in the purple membrane of <i>Halobacterium salinarium</i>, which functions as proton pump, charge separation and photochromism. The chromophore retinal is covalently attached to Lys 216 via a protonated Schiff base. Upon illumination, the all-<i>trans</i> to 13-<i>cis</i> isomerization of the retinal results in deprotonation of the Schiff base followed by alterations in protonatable groups within bacteriorhodopsin. The changed force field induces changes, even in the tertiary structure, which facilitate and warrant the vectorial proton translocation.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WANG Li-Ping,LI Bao-Fang and JIANG Long]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Li-Ping,LI Bao-Fang and JIANG Long</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010302]]></guid><cfi:id>28</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Retinal Mosaics Related to Eye Development and Formation]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010202]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Different types of neurons are regularly dispersed on retina. For finding the mechanism of eye and retina formation, it is important to know how this regular pattern is formed during embryonic stage. It was claimed that multiple genes regulate the development of eye and retina. These genes regulate the development of tissues and differentiation of cells in different parts of the visual system during embryo development. Also, it was found that different tissues and differentiated cells cohere with each other both temporally and spatially to form the eye.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[YAN Wing-Yi and HUA Qian]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YAN Wing-Yi and HUA Qian</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20010202]]></guid><cfi:id>27</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The 22nd Amino Acid and The Redefinition of Nonsense Coden]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020601]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Universality as one of the fundarmental features for genetic codes has been known since its proposal. But some extraodinary conditions have been discovered recently. Mitochondria use one set of genetic codes for different meaning and some nonsense codes which should have the meaning to stop translation may redefined. UGA may be redefined as selenocysteine. Results of recent research showed that some amber codens are translated as a sense coden for the 22nd natural amino acid, pyrrolysine.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[MING Zhen-Huan and ZHONG Li-Ren]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MING Zhen-Huan and ZHONG Li-Ren</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020601]]></guid><cfi:id>26</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Nogo and Nogo Receptor]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020602]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>nogo</i> is a recently discovered gene. It mainly encodes three proteins: Nogo-A, Nogo-B and Nogo-C. To date, it has been proved to be associated with axonal outgrowth inhibition in mature central nervous system(CNS) and apoptosis-inducing. Nogo receptor is a glycosylphosphatidylinositol(GPI)-anchored protein. To investigate the Nogo and Nogo receptor is important for understanding of neurite outgrowth inhibition following CNS injury and cancer.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WU Lan-Xiang,SUN Chang-Kai and FAN Ming]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WU Lan-Xiang,SUN Chang-Kai and FAN Ming</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020602]]></guid><cfi:id>25</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress in Nonribosomal Peptide Synthetases]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020501]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Some important peptides of bacterial or fungal origin are synthesized via a template-directed, nucleic-acid-independent nonribosomal mechanism. Recent studies revealed that there is a special kind of macroenzymes, nonribosomal peptide synthetases, which plays a key role in the alternative system. Nonribosomal peptide synthetases are composed of modules, the sequences of which contain the message for peptide synthesis. The understanding of the structure and function of nonribosomal peptide synthetases enables scientists believe that some new peptides can be produced by modifying or recombining these special enzymes.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[MING Zhen-Huan,PAN Jian-Wei and ZHU Mu-Yuan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MING Zhen-Huan,PAN Jian-Wei and ZHU Mu-Yuan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020501]]></guid><cfi:id>24</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress in Functional Characterization of F-box Protein Family]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020401]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[F-box protein is an expanding family of eukaryotic protein characterized by an F-box motif which has specificity of substrate recognition in the ubiquitin-mediated proteolysis. These proteins have been shown to be critical for many physiological process, such as cell-cycle transition, signal transduction, development, and so on.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WU Jing,PENG Xiao-Zhong,YUAN Jian-Gang and QIANG Bo-Qin]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WU Jing,PENG Xiao-Zhong,YUAN Jian-Gang and QIANG Bo-Qin</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020401]]></guid><cfi:id>23</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Roles of Ribosome S6 Protein Kinase p90<sup>rsk</sup> in Oocyte Meiosis]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020402]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Mitogen-activated protein kinase (MAPK) signaling pathway plays important roles in the meiosis of oocytes. p90<sup>rsk</sup> is the best known target of MAPK, which mediates multiple functions of MAPK during oocyte meiotic maturation, including the resumption of meiosis, the MⅠ/MⅡ transition and the sustain of MⅡ arrest. The phosphorylation of p90<sup>rsk</sup> is the result of MAPK activation, and the dephosphorylation of p90<sup>rsk</sup> is following the inactivation of MAPK at the end of meiosis. The progress of p90<sup>rsk</sup> in oocytes is introduced.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[FAN Heng-Yu,TONG Chao and SUN Qing-Yuan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>FAN Heng-Yu,TONG Chao and SUN Qing-Yuan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020402]]></guid><cfi:id>22</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Recent Advances in a Novel Anti-apoptosis Factor: Survivin]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020301]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Survivin is a recently identified member of the inhibitor of apoptosis protein (IAP)family, which inhibits processing of downstream effector caspase-3 and caspase-7 in cell receiving apoptotic stimulus. Unlike other IAP protein, found during embryonic and fetal development, survivin was completely down-regulated and undetectable in normal adult tissues, and became prominently reexpressed in all of the most common cancers. Survivin plays important pole in regulation of cell cycle. Its expression in tumors has been associated with increased aggressiveness, recurrence and decreased patient survival. Survivin may be a new target for cancer therapy.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[MIN Ling and ZHOU Ke-Yuan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>MIN Ling and ZHOU Ke-Yuan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020301]]></guid><cfi:id>21</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Vocal Learning and Memory in Songbird are Related to Immediate Early Genes]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020202]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[On the basis of the recent reports, immediate early gene (IEG) can be rapidly induced and expressed when a songbird is either stimulated by bird-song or in its vocal-behavior. The expression area and level in brain of IEG, such as <i>zenk</i>, <i>c-fos</i> and <i>c-jun</i>, are corresponding to where the neurons are related, as a songbird is stimulated, suggesting that IEG plays an important role in vocal learning and memory.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHAO Jing and LI Dong-Feng]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHAO Jing and LI Dong-Feng</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020202]]></guid><cfi:id>20</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[AIF is One of the Critical Mitochondrial Proteins to Mediate Nuclear Apoptosis]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020203]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Apoptosis-inducing factor(AIF), whose gene lies in X-chromosome, is likely an apoptogenic effector protein to mediates nuclear apoptosis directly. Once synthesized in the cytoplasm, the mouse AIF-precursor preprotein can be effectively imported into the mitochondrial intermembrane space through its N-terminal mitochondrial localization sequence (MLS). Then the MLS is cut off at position Gly 102 of the full-length preprotein, and the remains is refolded and bound with FAD group to produce the apoptogenic mature AIF, with a relative molecular mass of 57 ku. When death stimuli present, AIF is released from mitochondria to the cytoplasm and then to the nucleus, inducing peripheral chromatin condensation and large-scale fragmentation of DNA (～50 kb). These effects cannot be prevented either by the presence of wide-spectrum caspase inhibitor z-VAD.fmkor by the overexpression of Bcl-2. The evidences of gene knockout experiments indicate that AIF is essential for the cavitation of embryoid bodies during mouse morphogenesis, and the cavitation can be caused by AIF itself, independent on caspase-3 activity. Therefore, AIF-mediated cell death maybe constitutes a caspases-independent, more ancient and conserved apoptosis pathway.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[YU Cui-Juan,MENG Yan-Ling,WANG Cheng-Ji and YANG An-Gang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YU Cui-Juan,MENG Yan-Ling,WANG Cheng-Ji and YANG An-Gang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020203]]></guid><cfi:id>19</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Formation of an Early Three-dimensional Embryonic Pattern is Dependent upon Gene Transcriptional Regulation]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020204]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[In the view of molecular biology on morphogeny of a three-dimensinal embryo, morphogenesis and development are dependent upon activation of transcription of involving genes followed by the inactivation in a specific part of embryo at a certain time. It has been demonstrated that <i>cis</i>-acting elements of genes can act to provide sharply defined patterns. Simultaneously, it is accepted as an important mechanism that both activation and repression of transcription factors are closely related to cell differentiation and morphogenesis.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[XU Ya-Jie]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XU Ya-Jie</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020204]]></guid><cfi:id>18</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Eukaryotic Initiation Factor 5]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020101]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Eukaryotic initiation factor 5 (eIF-5) is an important factor in translation initiation. It acts as a GTPase activating factor to mediate the hydrolysis of GTP binding to eIF-2 which is essential for the composition of functional 80S complex. Besides,eIF-5 binds eIF-2 and eIF-3 at the same time, so induces the construction of translation initiation factors complex.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WAN Yong-Qi,ZHU Ke-Yi,WANG Shan-Zhi and XIE Wei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WAN Yong-Qi,ZHU Ke-Yi,WANG Shan-Zhi and XIE Wei</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020101]]></guid><cfi:id>17</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Ankyrin Repeat Mediated Protein-protein Interaction]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020102]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Ankyrin repeat (ANK) is a widely used sequence motif in organisms. An individual ankyrin repeat has an L-shaped structure consisting of a β hairpin followed by two α helices, namely β<sub>2</sub>α<sub>2</sub> pattern. These ANK repeats form a compact domain stabilized through hydrogen-bonding interaction and hydrophobic stacking. Massive of structurally similar but functionally diverse proteins containing ANK repeats can be formed by virtue of assembly of the tandem array motifs. The central role of ANK repeat is to mediate protein-protein interaction, so that proteins can make sophisticated functions by interacting with a variety of ligands. This review focuses on structure, function and related diseases of the ANK repeats and their complexes from several members of the ANK family.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[DU Hai-Ning and HU Hong-Yu]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>DU Hai-Ning and HU Hong-Yu</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020102]]></guid><cfi:id>16</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Advance on Exosome]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020103]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The exosome is a conserved complex which identified in <i>Saccharomyces cerevisiae</i> and has 3′ exoribonuclease activity <i>in vitro</i>. The exosome contains ten core subunits, and all except Csl4p/Ski4p are 3′ exoribonucleases <i>in vitro</i>. The exosome acts important role in several pathways of RNA metabolism. The exosome is a universal complex in eukaryote and is related to expression of eukaryotic genes.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WANG Shu-Qi and WANG Jin-Fa]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Shu-Qi and WANG Jin-Fa</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20020103]]></guid><cfi:id>15</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress in The <i>Neuronatin</i> Gene]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20030101]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[<i>Neuronatin(Nnat)</i> is a recently cloned brain-specific gene that is selectively expressed during brain development. Human <i>Nnat</i> gene spans 3 973 bases and contains three exons and two introns. <i>Nnat</i> mRNA has two different splice isoforms, α and β, the former encoding a protein of 81 amino acids and the latter 54 amino acids. These two isoforms share the same open reading frame, but the α-form contained an additional 81 bp sequence inserted in the middle of the coding region. The human <i>Nnat</i> is a single copy gene located at chromosome 20q11.2～12, while the rat gene is located on the distal region of chromosome 2, 2H1. <i>Nnat</i> is an imprinted gene and expressed from the paternal allele, while the maternal allele is methylated and silenced. As <i>Nnat</i> is highly expressed in the central nervous system from mid-gestation through early postnatal development and down-regulated in adulthood and senescence, <i>Nnat</i> may be involved in brain development and differentiation. The expression is also detected in the adult brain stem, suggesting roles in neuroplasticity. The deduced protein sequence contains a hydrophobic N-terminal and a hydrophilic C-terminal, and appears to code for a transmembrane protein. The biological function of <i>Nnat</i> remains to be elucidated.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[YU Li-Hong,ZHOU Ren-Ping and ZHANG Cheng-Gang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>YU Li-Hong,ZHOU Ren-Ping and ZHANG Cheng-Gang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20030101]]></guid><cfi:id>14</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Annotation for The Functions of Junk DNA]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20040601]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The prevailing sequences in the massive genome sequences, which do not code for proteins or RNAs, have been named junk DNA. It is unreasonable for organisms，in which there is the principle of maximum economy，to accumulate nonfunctional garbage in vital living cells during their long-term evolution. Recent researches have demonstrated that so-called junk DNA possesses important functions and it is believed that more and more junk DNA will be proved to be not garbage but the treasures of the genome.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LI Ming-Zhen,ZHANG Ming and MING Zhen-Huan]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Ming-Zhen,ZHANG Ming and MING Zhen-Huan</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20040601]]></guid><cfi:id>13</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Water Channels on The Move: a New Focus on Mechanisms of Cell Migration and Related Biological Processes]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/2005-0504]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Cell migration plays a pivotal role in many physiological and pathophysiological processes including embryogenesis, angiogenesis, immune defense, wound healing, or the formation of tumor metastases. Evidence is accumulating that ion channels and transporters is also required for optimal cell migration and a model is proposed that combines ion transport with cytoskeletal mechanisms of cell migration. However, the role of water transport in cell migration is underinvestigated. In the April 7, 2005 issue of Nature, Saadoun et al. discovered the importance of aquaporin-mediated transmembrane water flux in cell migration, angiogenesis and tumor growth, provided a new molecular mechanism of cell migration and opened a new field of aquaporin gene function and therapeutic application.]]></description>
<pubDate></pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LIU Jun,SHI Lin-Lin,YANG Hong and MA Tong-Hui]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LIU Jun,SHI Lin-Lin,YANG Hong and MA Tong-Hui</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/2005-0504]]></guid><cfi:id>12</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Molecular Basis of Activation and Replenishment on Satellite Cell Shed Light on Myopathy]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060192]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Satellite cells, as the major stem cells, are responsible for postnatal skeletal muscle growth, regeneration and maintenance. As a result, satellite cells have great potential as therapeutic agents. Activation of satellite cells <i>in vivo</i> is a key link in the muscle regeneration processes. And their replenishment is necessary to keep the capacity of skeletal muscle to regenerate after recurrence of muscle damage.  Cellular and molecular regulation of activation and replenishment for satellite cells issues were reviewed. Hoping through the points of nitric oxide-hepatocyte growth factor (NO-HGF), myostatin and Notch signaling and the niche of satellite cells to overcome the recent obstruction in cell therapy in clinic myopathy, such as Duchenne muscle destrophy.]]></description>
<pubDate>2006/9/15 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[PAN Ling-Mei,WANG Tian and SHI Fang-Xiong]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>PAN Ling-Mei,WANG Tian and SHI Fang-Xiong</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060192]]></guid><cfi:id>11</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[An Anti-apoptotic Protein Expressed Specifically and Highly in The Cardiac Tissue: ARC]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060253]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Many apoptosis-related heart diseases such as myocardial infarction, cardiomyopathies, and heart failure severely impair human's health and life. Currently, a key focus for the medical researchers is to find out effective ways to prevent or treat these heart diseases. ARC (apoptosis repressor with caspase recruitment domain) is the first anti-apoptotic protein so far identified to be highly and specifically expressed in the cardiac tissue. ARC could be structurally phosphorylated and involved in various signaling pathways during apoptosis.]]></description>
<pubDate>2006/9/15 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LI Yu-Zhen]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Yu-Zhen</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060253]]></guid><cfi:id>10</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[24p3-24p3 Receptor System: A New Pathway of Iron Transport]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060939]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The 24p3 of mouse is a member of lipocalin family and it has been implicated in iron transport and apoptosis due to interleukin-3(IL-3) deprivation. Devireddy and colleagues cloned the receptor of 24p3 and further confirmed that the pathway of 24p3-24p3R is a new iron transport approach in Dec 2005. A link between iron internalization mediated by 24p3R and regulation of apoptosis was suggested.]]></description>
<pubDate>2007/5/11 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHAO Song-Min,SHI Zhen-Hua,DUAN Xiang-Lin and CHANG Yan-Zhong]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHAO Song-Min,SHI Zhen-Hua,DUAN Xiang-Lin and CHANG Yan-Zhong</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060939]]></guid><cfi:id>9</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Progress of Caveolin and Its Role in Brain]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060899]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Caveolins are a family of plasmalemmal vesicles caveolae-associated integral membrane proteins and a marker protein of caveolae involved in the formation and localization that associated with vesicular transport, cellular cholesterol homeostasis and signal transduction. Recent years, strong experimental evidences indicated that caveolins play a pivotal role in the brain function such as neural development, synaptic plasticity and neurodegenerative diseases. Recent progress on studies of the structure and functions of caveolins was simply summarized. The regulatory role of caveolins in the brain functions has been reviewed and expected.]]></description>
<pubDate>2007/4/10 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WANG Lu,JI Zhi-Hong,CHEN Dong-Dong,WANG Hong-Xia and ZOU Wei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WANG Lu,JI Zhi-Hong,CHEN Dong-Dong,WANG Hong-Xia and ZOU Wei</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060899]]></guid><cfi:id>8</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Transient Outward Potassium Current in Hippocampal Neurons]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060847]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Transient outward potassium current (I<sub>A</sub>), highly expressing in hippocampal dendrites, has characteristics of rapid activation and inactivation following appropriate voltage depolarization. I<sub>A</sub> is the predominant outward potassium current at the subthreshold range of the action potential and during early phase of repolarization. IA current plays an important role in modulating synaptic input and affecting action potential back-propagation by reducing the speed of depolarization and delaying the action-potential initiation, suggesting its important roles in regulating the electric signal integration and synaptic plasticity. I<sub>A</sub> currents have been associated with many diseases, such as seizure.]]></description>
<pubDate>2007/3/16 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[GONG Bo,HUANG Mei-Yan,MA Yi-Cai and QI Zhi]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GONG Bo,HUANG Mei-Yan,MA Yi-Cai and QI Zhi</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060847]]></guid><cfi:id>7</cfi:id><cfi:read>true</cfi:read></item>
<item>
<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Novel Noncoding Small RNA: Piwi-interacting RNA(piRNA)]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20060678]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[piRNA is a novel class of small single strand RNA that were recently isolated from testes of the mammals. These RNAs are bigger (26～31 nt) than most previously described small RNAs (21～23 nt) and are associated with Piwi-subfamily members of the Argonaute protein family.]]></description>
<pubDate>2007/2/12 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[Li Pei-Wang,LU Xiang-Yang,LI Chang-Zhu and Tian Yun]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>Li Pei-Wang,LU Xiang-Yang,LI Chang-Zhu and Tian Yun</atom:name>
</atom:author>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Strategies Exploited by Viruses for Evading The RNAi]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20070266]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[RNAi is an efficient antiviral system, and viral gene-specific siRNAs are very promising antiviral inhibitors. However, many viruses have evolved highly sophisticated mechanisms that interfere with both siRNA- and miRNA-guided silencing pathways. Deeper understanding the strategies exploited by viruses provides the basis for the development of effective RNAi-based therapies that prevent viral evading. Therefore, the latest progress on the strategies exploited by viruses for evading the RNAi is reviewed.]]></description>
<pubDate>2007/9/11 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[ZHENG Yu-Shu,ZHAO Pu and LIU Xing-You]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>ZHENG Yu-Shu,ZHAO Pu and LIU Xing-You</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20070266]]></guid><cfi:id>5</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[tRNA Nuclear-cytoplasmic Dynamics and Cell Fate]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20080537]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[The robust nuclear-cytoplasmic transport is vital for eukaryotes’ life cycle. Not only proteins and RNAs are transferred to their destination by this system, the important cellular activities such as mitosis are also regulated by the transport pathways via adjusting the local concentrations of some critical cargoes. tRNA is one of the most important biomacromolecules in the cell, synthesized in nucleus, and taking part in protein synthesis in cytoplasm. It is a long-held belief that tRNA functions only as a key player in protein synthesis, and tRNA nuclear-cytoplasmic transport is a unidirectional movement from nucleus to cytoplasm. However, the recent discoveries are overturning the traditional opinions. Nuclear-born tRNA can be exported out of nucleus, while cytoplasmic-residing tRNA can also be retrogradely transport into nucleus. The new concept tRNA nuclear-cytoplasmic dynamics was coined in 2008 to describe the tRNA communication between nucleus and cytoplasm, which was found able to regulate protein synthesis and cell cycle in <i>S. cerevisiae</i>. The latest results in this field are going to change the landscape of eukaryotic tRNA biology.]]></description>
<pubDate>2008/12/9 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[LI Sheng and ZHANG Jia-Ning]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>LI Sheng and ZHANG Jia-Ning</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20080537]]></guid><cfi:id>4</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Function of PRDM9 on Mammalian Recombination Hotspots]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20100224]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[PRDM9(PR domain containing 9) is one kind of histone trimethylase which catalyzes the H3K4 trimethylation, and possesses the activity of transcription factor. PRDM9 transcripts were only expressed in germ cells entering meiotic prophase in female fetal gonads and in postnatal testis, whose deficiency results in sterility. The zinc finger motif of mammalian PRDM9 rapidly evolves, which is respond to the sequences of recombination hotspots. Several researches indicated that PRDM9 was involved in the binding to recombination hotspots and initiation of recombination. These progresses are important for understanding of species evolution and the mechanism of genetic recombination.]]></description>
<pubDate>2010/8/3 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[GUO Xiao-Qiang]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>GUO Xiao-Qiang</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20100224]]></guid><cfi:id>3</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[Transmenbrance Serine Proteases 6: A Newly Discovered Hepcidin Regulator]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20090584]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[Transmenbrance serine proteases 6(TMPRSS6) is a recently identified transmembrane serine protease, this protein regulates the expression of hepcidin in the process of iron metabolism, thereby affecting the body of the iron steady. The discovery of TMPRSS6 is not only very important to the understanding of mechanism of iron metabolism but also reveals the etiology of iron metabolism-related diseases, it provides a new way of thinking about how to treat these diseases.]]></description>
<pubDate>2009/12/28 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[WU Wen-Shuang,ZHENG Xin,DUAN Xiang-Lin and CHANG Yan-Zhong]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>WU Wen-Shuang,ZHENG Xin,DUAN Xiang-Lin and CHANG Yan-Zhong</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20090584]]></guid><cfi:id>2</cfi:id><cfi:read>true</cfi:read></item>
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<title xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="text"><![CDATA[The Protective Effects of Ubiquitin C-Terminal Hydrolase L1 on Neurons]]></title>
<link><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20100253]]></link>
<description xmlns:cf="http://www.microsoft.com/schemas/rss/core/2005" cf:type="html"><![CDATA[UCH-L1 is abundantly expressed in brain which possesses ubiquitin hydrolase activity, ubiquitin ligase activity and the effect of monomeric ubiquitin stabilizing. UCH-L1 is critical for the normal morphology and function of the synapses, which can rescue the LTP deficit and impaired memory induced by β-amyloid protein (Aβ). In addition, the I93M mutation in UCH-L1 is associated with familial Parkinson's disease (PD) while the S18Y polymorphic variant of UCH-L1 is associated with a specific antioxidant protective function in neurons. By researching the structure, function and the mechanism in the nervous system of UCH-L1, hopes to provide a concept or a method to treat neurodegenerative diseases such as AD and PD.]]></description>
<pubDate>2010/8/3 0:00:00</pubDate>
<category><![CDATA[Mini-review]]></category>
<author><![CDATA[XIE Min,CHEN Qi-Cai and LIAO Xiao-Mei]]></author>
<atom:author xmlns:atom="http://www.w3.org/2005/Atom">
<atom:name>XIE Min,CHEN Qi-Cai and LIAO Xiao-Mei</atom:name>
</atom:author>
<guid><![CDATA[http://www.pibb.ac.cn/pibben/article/abstract/20100253]]></guid><cfi:id>1</cfi:id><cfi:read>true</cfi:read></item>
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