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肺基质重塑障碍

Disorders of lung matrix remodeling.

作者信息

Chapman Harold A

机构信息

Department of Medicine and Cardiovascular Research Institute, University of California at San Francisco, San Francisco, California 94143-0130, USA.

出版信息

J Clin Invest. 2004 Jan;113(2):148-57. doi: 10.1172/JCI20729.

DOI:10.1172/JCI20729
PMID:14722604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC311438/
Abstract

A set of lung diseases share the tendency for the development of progressive fibrosis ultimately leading to respiratory failure. This review examines the common pathogenetic features of these disorders in light of recent observations in both humans and animal models of disease, which reveal important pathways of lung matrix remodeling.

摘要

一组肺部疾病都有发展为进行性纤维化并最终导致呼吸衰竭的倾向。本综述根据在人类和动物疾病模型中的最新观察结果,探讨了这些疾病的共同发病机制,这些观察揭示了肺基质重塑的重要途径。

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本文引用的文献

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2
Injury and repair in lung and airways.肺与气道的损伤及修复
Crit Care Med. 2003 Aug;31(8 Suppl):S524-31. doi: 10.1097/01.CCM.0000081437.06466.B3.
3
Cross-talk between ERK MAP kinase and Smad signaling pathways enhances TGF-beta-dependent responses in human mesangial cells.ERK丝裂原活化蛋白激酶与Smad信号通路之间的相互作用增强了人肾小球系膜细胞中转化生长因子β依赖性反应。
FASEB J. 2003 Aug;17(11):1576-8. doi: 10.1096/fj.03-0037fje. Epub 2003 Jun 17.
4
Fibronectin requirement in branching morphogenesis.分支形态发生中纤连蛋白的需求
Nature. 2003 Jun 19;423(6942):876-81. doi: 10.1038/nature01712.
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Fas (CD95) induces proinflammatory cytokine responses by human monocytes and monocyte-derived macrophages.Fas(CD95)可诱导人单核细胞和单核细胞衍生的巨噬细胞产生促炎细胞因子反应。
J Immunol. 2003 Jun 15;170(12):6209-16. doi: 10.4049/jimmunol.170.12.6209.
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Fibrotic idiopathic interstitial pneumonia: the prognostic value of longitudinal functional trends.纤维化性特发性间质性肺炎:纵向功能趋势的预后价值
Am J Respir Crit Care Med. 2003 Sep 1;168(5):531-7. doi: 10.1164/rccm.200210-1245OC. Epub 2003 Jun 5.
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