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角蛋白与皮肤疾病。

Keratins and skin disorders.

作者信息

Lane E B, McLean W H I

机构信息

Cancer Research UK Cell Structure Research Group, Division of Cell and Developmental Biology, University of Dundee School of Life Sciences, MSI/WTB Complex, Dow Street, Dundee DD1 5EH, UK.

出版信息

J Pathol. 2004 Nov;204(4):355-66. doi: 10.1002/path.1643.

Abstract

The association of keratin mutations with genetic skin fragility disorders is now one of the best-established examples of cytoskeleton disorders. It has served as a paradigm for many other diseases and has been highly informative for the study of intermediate filaments and their associated components, in helping to understand the functions of this large family of structural proteins. The keratin diseases have shown unequivocally that, at least in the case of the epidermal keratins, a major function of intermediate filaments is to provide physical resilience for epithelial cells. This review article reflects on the variety of phenotypes arising from mutations in keratins and the reasons for this variation.

摘要

角蛋白突变与遗传性皮肤脆性疾病的关联,如今是细胞骨架疾病中最确凿的例子之一。它已成为许多其他疾病的范例,对于研究中间丝及其相关成分极具参考价值,有助于理解这一庞大结构蛋白家族的功能。角蛋白疾病已明确表明,至少就表皮角蛋白而言,中间丝的主要功能是为上皮细胞提供物理弹性。这篇综述文章探讨了由角蛋白突变产生的各种表型及其变异原因。

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