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原发性先天性青光眼的遗传学与生物化学

Genetics and biochemistry of primary congenital glaucoma.

作者信息

Sarfarazi Mansoor, Stoilov Ivaylo, Schenkman John B

机构信息

Molecular Ophthalmic Genetics Laboratory, University of Connecticut Health Center, Farmington 06030, USA.

出版信息

Ophthalmol Clin North Am. 2003 Dec;16(4):543-54, vi. doi: 10.1016/s0896-1549(03)00062-2.

Abstract

Several observations noted by early investigators supported the supposition that in most cases, congenital glaucoma is determined by genetic factors. The genetic heterogeneity of PCG was confirmed by genetic linkage studies conducted in the 1990s when the authors determined that CYP1B1 is the congenital glaucoma gene at the GLC3A locus. The coding sequence of CYP1B1 has been subjected to extensive screening in familial and sporadic cases of glaucoma from numerous countries and from a large number of ethnic groups. These studies have provided evidence for extensive allelic heterogeneity at the GLC3A locus. This article also discusses the molecular evidence for reduced penetrance in congenital glaucoma and the phenotypic heterogeneity of CYP1B1 mutations, mouse models of CYP1B1, and the biochemistry of CYP1B1.

摘要

早期研究者注意到的一些观察结果支持了这样一种假设,即在大多数情况下,先天性青光眼是由遗传因素决定的。20世纪90年代进行的遗传连锁研究证实了原发性先天性青光眼的遗传异质性,当时作者确定CYP1B1是位于GLC3A位点的先天性青光眼基因。CYP1B1的编码序列已在来自众多国家和大量种族的青光眼家族性和散发性病例中进行了广泛筛查。这些研究为GLC3A位点广泛的等位基因异质性提供了证据。本文还讨论了先天性青光眼基因外显率降低的分子证据、CYP1B1突变的表型异质性、CYP1B1的小鼠模型以及CYP1B1的生物化学。

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