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Literature DB >> 17296892

Genetic origins of cataract.

Alan Shiels¹, J Fielding Hejtmancik.

Abstract

Entities: Disease

Mesh：

Year: 2007 PMID： 17296892 DOI： 10.1001/archopht.125.2.165

Source DB: PubMed Journal: Arch Ophthalmol ISSN： 0003-9950

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Cited

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85 in total

Review 1. Molecular Genetics of Cataract.

Authors: Alan Shiels; J Fielding Hejtmancik
Journal: Prog Mol Biol Transl Sci Date: 2015-06-12 Impact factor: 3.622

2. Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2.

Authors: Vasudha Kemmanu; Subramanya K Giliyar; Harsha L Rao; Bhujanga K Shetty; Govindasamy Kumaramanickavel; Catherine A McCarty
Journal: J Community Genet Date: 2018-12-01

3. An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.

Authors: Li-Yun Zhang; Gary Hin-Fai Yam; Pancy Oi-Sin Tam; Ricky Yiu-Kwong Lai; Dennis Shun-Chiu Lam; Chi-Pui Pang; Dorothy Shu-Ping Fan
Journal: Mol Vis Date: 2009-06-04 Impact factor: 2.367

4. A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.

Authors: Li-Yun Zhang; Bo Gong; Jian-Ping Tong; Dorothy Shu-Ping Fan; Sylvia Wai-Yee Chiang; Dinghua Lou; Dennis Shun-Chiu Lam; Gary Hin-Fai Yam; Chi-Pui Pang
Journal: Mol Vis Date: 2009-08-06 Impact factor: 2.367

10. AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice.

Authors: Usha P Andley
Journal: BMC Ophthalmol Date: 2009-07-20 Impact factor: 2.209

Genetic origins of cataract.

Review 1. Molecular Genetics of Cataract.

2. Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2.

3. An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.

4. A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.

5. Association of G>A transition in exon-1 of alpha crystallin gene in age-related cataracts.

6. A novel human CRYGD mutation in a juvenile autosomal dominant cataract.

Review 7. Cat-Map: putting cataract on the map.

8. Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family.

9. The membrane proteome of the mouse lens fiber cell.

10. AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice.