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A phosphoproteomic analysis of the ErbB2 receptor tyrosine kinase signaling pathways.表皮生长因子受体2(ErbB2)受体酪氨酸激酶信号通路的磷酸化蛋白质组学分析
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Functional and quantitative proteomics using SILAC.使用稳定同位素标记氨基酸法进行功能和定量蛋白质组学研究。
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Presenilin-dependent ErbB4 nuclear signaling regulates the timing of astrogenesis in the developing brain.早老素依赖的ErbB4核信号传导调节发育中大脑星形胶质细胞生成的时间。
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Quantitative analysis of the activation mechanism of the multicomponent growth-factor receptor Ret.多组分生长因子受体Ret激活机制的定量分析
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7
Crystal structure of the agrin-responsive immunoglobulin-like domains 1 and 2 of the receptor tyrosine kinase MuSK.受体酪氨酸激酶MuSK的聚集蛋白反应性免疫球蛋白样结构域1和2的晶体结构
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Structure of the insulin receptor ectodomain reveals a folded-over conformation.胰岛素受体胞外域的结构显示出一种折叠构象。
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Single-molecule analysis of epidermal growth factor binding on the surface of living cells.活细胞表面表皮生长因子结合的单分子分析。
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Quantitative multiplexed profiling of cellular signaling networks using phosphotyrosine-specific DNA-tagged SH2 domains.使用磷酸酪氨酸特异性DNA标记的SH2结构域对细胞信号网络进行定量多重分析。
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受体酪氨酸激酶:激活与信号传导机制

Receptor tyrosine kinases: mechanisms of activation and signaling.

作者信息

Hubbard Stevan R, Miller W Todd

机构信息

Skirball Institute of Biomolecular Medicine and Department of Pharmacology, New York University School of Medicine, New York, NY 10016, USA.

出版信息

Curr Opin Cell Biol. 2007 Apr;19(2):117-23. doi: 10.1016/j.ceb.2007.02.010. Epub 2007 Feb 16.

DOI:10.1016/j.ceb.2007.02.010
PMID:17306972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2536775/
Abstract

Receptor tyrosine kinases (RTKs) are essential components of signal transduction pathways that mediate cell-to-cell communication. These single-pass transmembrane receptors, which bind polypeptide ligands - mainly growth factors - play key roles in processes such as cellular growth, differentiation, metabolism and motility. Recent progress has been achieved towards an understanding of the precise (and varied) mechanisms by which RTKs are activated by ligand binding and by which signals are propagated from the activated receptors to downstream targets in the cell.

摘要

受体酪氨酸激酶(RTKs)是介导细胞间通讯的信号转导通路的重要组成部分。这些单次跨膜受体可结合多肽配体——主要是生长因子——在细胞生长、分化、代谢和运动等过程中发挥关键作用。在理解RTKs通过配体结合被激活以及信号从激活的受体传递到细胞内下游靶点的精确(且多样)机制方面,已取得了最新进展。