[甲状腺超微结构与激素生成的生化紊乱] - Suppr | 超能文献

[Thyroid ultrastructure and biochemical disturbances of hormonogenesis].

作者信息

Michel-Bechet M, Gotte G, Codaccioni J L, Athouël-Haon A M

出版信息

Acta Anat (Basel). 1969;73(3):389-409.

Abstract

摘要

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引用本文的文献

1

A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases.甲状腺球蛋白乙酰胆碱酯酶样结构域中的单个氨基酸变化导致cog/cog小鼠出现先天性甲状腺肿并伴有甲状腺功能减退：一种人类内质网储存疾病的模型

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9909-13. doi: 10.1073/pnas.95.17.9909.

2

Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones.伴有甲状腺球蛋白缺乏的先天性甲状腺功能减退性甲状腺肿。一种内质网贮积病的鉴定及分子伴侣的诱导。

J Clin Invest. 1996 Dec 15;98(12):2838-44. doi: 10.1172/JCI119112.

3

An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism.一种导致先天性甲状腺肿伴甲状腺功能减退的内质网贮积病。

J Cell Biol. 1996 May;133(3):517-27. doi: 10.1083/jcb.133.3.517.