Literature DB >> 18035564

Congenital cataracts and their molecular genetics.

J Fielding Hejtmancik1.   

Abstract

Cataract can be defined as any opacity of the crystalline lens. Congenital cataract is particularly serious because it has the potential for inhibiting visual development, resulting in permanent blindness. Inherited cataracts represent a major contribution to congenital cataracts, especially in developed countries. While cataract represents a common end stage of mutations in a potentially large number of genes acting through varied mechanisms in practice most inherited cataracts have been associated with a subgroup of genes encoding proteins of particular importance for the maintenance of lens transparency and homeostasis. The increasing availability of more detailed information about these proteins and their functions and is making it possible to understand the pathophysiology of cataracts and the biology of the lens in general.

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Year:  2007        PMID: 18035564      PMCID: PMC2288487          DOI: 10.1016/j.semcdb.2007.10.003

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  163 in total

1.  A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.

Authors:  Yang Li; Jun Wang; Bing Dong; Hong Man
Journal:  Mol Vis       Date:  2004-09-14       Impact factor: 2.367

2.  A locus for autosomal dominant anterior polar cataract on chromosome 17p.

Authors:  V Berry; A C Ionides; A T Moore; C Plant; S S Bhattacharya; A Shiels
Journal:  Hum Mol Genet       Date:  1996-03       Impact factor: 6.150

Review 3.  Lens crystallins: the evolution and expression of proteins for a highly specialized tissue.

Authors:  G J Wistow; J Piatigorsky
Journal:  Annu Rev Biochem       Date:  1988       Impact factor: 23.643

4.  AlphaB-crystallin in lens development and muscle integrity: a gene knockout approach.

Authors:  J P Brady; D L Garland; D E Green; E R Tamm; F J Giblin; E F Wawrousek
Journal:  Invest Ophthalmol Vis Sci       Date:  2001-11       Impact factor: 4.799

5.  An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12.

Authors:  K Yamada; H Tomita; K Yoshiura; S Kondo; K Wakui; Y Fukushima; S Ikegawa; Y Nakamura; T Amemiya; N Niikawa
Journal:  Eur J Hum Genet       Date:  2000-07       Impact factor: 4.246

6.  The expanding small heat-shock protein family, and structure predictions of the conserved "alpha-crystallin domain".

Authors:  G J Caspers; J A Leunissen; W W de Jong
Journal:  J Mol Evol       Date:  1995-03       Impact factor: 2.395

7.  A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene.

Authors:  V Sarhadi; A Reis; M Jung; D Singh; K Sperling; J R Singh; J Bürger
Journal:  J Med Genet       Date:  2001-06       Impact factor: 6.318

8.  Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.

Authors:  V Berry; D Mackay; S Khaliq; P J Francis; A Hameed; K Anwar; S Q Mehdi; R J Newbold; A Ionides; A Shiels; T Moore; S S Bhattacharya
Journal:  Hum Genet       Date:  1999 Jul-Aug       Impact factor: 4.132

9.  A progressive early onset cataract gene maps to human chromosome 17q24.

Authors:  M M Armitage; J D Kivlin; R E Ferrell
Journal:  Nat Genet       Date:  1995-01       Impact factor: 38.330

10.  Identification of the gene for Nance-Horan syndrome (NHS).

Authors:  S P Brooks; N D Ebenezer; S Poopalasundaram; O J Lehmann; A T Moore; A J Hardcastle
Journal:  J Med Genet       Date:  2004-10       Impact factor: 6.318

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  181 in total

1.  Mutations in FYCO1 cause autosomal-recessive congenital cataracts.

Authors:  Jianjun Chen; Zhiwei Ma; Xiaodong Jiao; Robert Fariss; Wanda Lee Kantorow; Marc Kantorow; Eran Pras; Moshe Frydman; Elon Pras; Sheikh Riazuddin; S Amer Riazuddin; J Fielding Hejtmancik
Journal:  Am J Hum Genet       Date:  2011-06-10       Impact factor: 11.025

Review 2.  Molecular Genetics of Cataract.

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

3.  Ultrasound diagnosis of bilateral cataracts in a fetus with possible cerebro-ocular congential muscular dystrophy during the routine second trimester anomaly scan.

Authors:  Alexandra Drought; Ruwan Wimalasundera; Susan Holder
Journal:  Ultrasound       Date:  2015-03-27

4.  The effect of hyperglycinemic treatment in captive-bred Vervet monkeys (Chlorocebus aethiops).

Authors:  Zandisiwe E Magwebu; Mikateko Mazinu; Sahar Abdul-Rasool; Chesa G Chauke
Journal:  Metab Brain Dis       Date:  2019-06-22       Impact factor: 3.584

5.  Racemization of two proteins over our lifespan: deamidation of asparagine 76 in γS crystallin is greater in cataract than in normal lenses across the age range.

Authors:  Michelle Yu Sung Hooi; Mark J Raftery; Roger John Willis Truscott
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-06-14       Impact factor: 4.799

6.  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

7.  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

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

Authors:  Jin Jiang; Chongfei Jin; Wei Wang; Xiajing Tang; Xingchao Shentu; Renyi Wu; Yao Wang; Kun Xia; Ke Yao
Journal:  Mol Vis       Date:  2009-01-12       Impact factor: 2.367

9.  The zebrafish lens proteome during development and aging.

Authors:  Teri M S Greiling; Scott A Houck; John I Clark
Journal:  Mol Vis       Date:  2009-11-13       Impact factor: 2.367

10.  Mutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2.

Authors:  Maneo Emily Mothobi; Shuren Guo; Yuanyuan Liu; Qiang Chen; Ali Said Yussuf; Xinli Zhu; Zheng Fang
Journal:  Mol Vis       Date:  2009-07-30       Impact factor: 2.367

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