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Items: 1 to 20 of 126

1.

Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.

Plotnikova OV, Kondrashov FA, Vlasov PK, Grigorenko AP, Ginter EK, Rogaev EI.

Am J Hum Genet. 2007 Jul;81(1):32-43. Epub 2007 May 16.

2.

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

Roshan M, Vijaya PH, Lavanya GR, Shama PK, Santhiya ST, Graw J, Gopinath PM, Satyamoorthy K.

Mol Vis. 2010 May 22;16:887-96.

3.

Mutation analysis of CRYAA, CRYGC, and CRYGD associated with autosomal dominant congenital cataract in Brazilian families.

Santana A, Waiswol M, Arcieri ES, Cabral de Vasconcellos JP, Barbosa de Melo M.

Mol Vis. 2009;15:793-800. Epub 2009 Apr 17.

4.

Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.

Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):3937-44.

PMID:
17724170
5.

Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.

Li F, Wang S, Gao C, Liu S, Zhao B, Zhang M, Huang S, Zhu S, Ma X.

Mol Vis. 2008 Mar 4;14:378-86.

6.

Molecular evolution of the betagamma lens crystallin superfamily: evidence for a retained ancestral function in gamma N crystallins?

Weadick CJ, Chang BS.

Mol Biol Evol. 2009 May;26(5):1127-42. doi: 10.1093/molbev/msp028. Epub 2009 Feb 20.

PMID:
19233964
7.

Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.

Vanita V, Singh JR, Singh D, Varon R, Sperling K.

Mol Vis. 2009;15:476-81. Epub 2009 Mar 4.

10.

A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataract.

Zhang LY, Yam GH, Fan DS, Tam PO, Lam DS, Pang CP.

Mol Vis. 2007 Nov 7;13:2096-104.

PMID:
18079686
11.

Mutation screening and genotype phenotype correlation of α-crystallin, γ-crystallin and GJA8 gene in congenital cataract.

Kumar M, Agarwal T, Khokhar S, Kumar M, Kaur P, Roy TS, Dada R.

Mol Vis. 2011 Mar 11;17:693-707.

12.

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

Zhang LY, Gong B, Tong JP, Fan DS, Chiang SW, Lou D, Lam DS, Yam GH, Pang CP.

Mol Vis. 2009 Aug 6;15:1521-9.

13.

Crystallin gene mutations in Indian families with inherited pediatric cataract.

Devi RR, Yao W, Vijayalakshmi P, Sergeev YV, Sundaresan P, Hejtmancik JF.

Mol Vis. 2008 Jun 16;14:1157-70.

14.

Characterization of gammaS-crystallin isoforms from a catfish: evolutionary comparison of various gamma-, gammaS-, and beta-crystallins.

Chiou SH, Pan FM, Peng HW, Chao YK, Chang WC.

Biochem Biophys Res Commun. 1998 Nov 18;252(2):412-9.

PMID:
9826544
15.

[Autosomal dominant congenital golden crystal nuclear cataract caused by a missense mutation in gammaD crystallin gene (CRYGD) in a Chinese family].

Gu JZ, Qi YH, Lin H, Li X, Wang J, Meng WM, Su H.

Zhonghua Yan Ke Za Zhi. 2006 Oct;42(10):913-7. Chinese.

PMID:
17217786
16.

The gamma-crystallins and human cataracts: a puzzle made clearer.

Héon E, Priston M, Schorderet DF, Billingsley GD, Girard PO, Lubsen N, Munier FL.

Am J Hum Genet. 1999 Nov;65(5):1261-7.

17.
18.

A 5-base insertion in the gammaC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract.

Ren Z, Li A, Shastry BS, Padma T, Ayyagari R, Scott MH, Parks MM, Kaiser-Kupfer MI, Hejtmancik JF.

Hum Genet. 2000 May;106(5):531-7.

19.

[Localization and screening of autosomal dominant coralliform cataract associated gene].

Xu WZ, Zheng S, Xu SJ, Huang W, Yao K, Zhang SZ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):19-22. Chinese.

PMID:
14767902
20.

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