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线粒体ATP合酶亚基c在巴滕病(蜡样脂褐质沉积症)中的溶酶体储存。

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis).

作者信息

Hall N A, Lake B D, Dewji N N, Patrick A D

机构信息

Department of Clinical Biochemistry, Institute of Child Health, London, U.K.

出版信息

Biochem J. 1991 Apr 1;275 ( Pt 1)(Pt 1):269-72. doi: 10.1042/bj2750269.

Abstract

Immunochemical studies demonstrate that subunit c of mitochondrial ATP synthase is stored in the late-infantile, juvenile and adult forms of Batten's disease. It does not accumulate in the infantile form, or in other conditions involving lysosomal hypertrophy. These results suggest that the defective metabolism of subunit c is central to the pathogenesis of these three forms of Batten's disease.

摘要

免疫化学研究表明,线粒体ATP合酶的亚基c存在于晚期婴儿型、青少年型和成人型巴滕病中。它不会在婴儿型中积累,也不会在其他涉及溶酶体肥大的病症中积累。这些结果表明,亚基c的代谢缺陷是这三种形式的巴滕病发病机制的核心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07ac/1150044/f930ade331f6/biochemj00162-0263-a.jpg

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