242 related articles for article (PubMed ID: 12226711)
21. Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.
Chang B; Hawes NL; Roderick TH; Smith RS; Heckenlively JR; Horwitz J; Davisson MT
Mol Vis; 1999 Sep; 5():21. PubMed ID: 10493778
[TBL] [Abstract][Full Text] [Related]
22. First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts.
Puk O; Ahmad N; Wagner S; Hrabé de Angelis M; Graw J
Invest Ophthalmol Vis Sci; 2011 Apr; 52(5):2571-6. PubMed ID: 21212184
[TBL] [Abstract][Full Text] [Related]
23. Special fasciculiform cataract caused by a mutation in the gammaD-crystallin gene.
Shentu X; Yao K; Xu W; Zheng S; Hu S; Gong X
Mol Vis; 2004 Mar; 10():233-9. PubMed ID: 15064679
[TBL] [Abstract][Full Text] [Related]
24. Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract.
Reddy MA; Bateman OA; Chakarova C; Ferris J; Berry V; Lomas E; Sarra R; Smith MA; Moore AT; Bhattacharya SS; Slingsby C
Hum Mol Genet; 2004 May; 13(9):945-53. PubMed ID: 15016766
[TBL] [Abstract][Full Text] [Related]
25. Towards a molecular understanding of phase separation in the lens: a comparison of the X-ray structures of two high Tc gamma-crystallins, gammaE and gammaF, with two low Tc gamma-crystallins, gammaB and gammaD.
Norledge BV; Hay RE; Bateman OA; Slingsby C; Driessen HP
Exp Eye Res; 1997 Nov; 65(5):609-30. PubMed ID: 9367641
[TBL] [Abstract][Full Text] [Related]
26. A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family.
Gu F; Luo W; Li X; Wang Z; Lu S; Zhang M; Zhao B; Zhu S; Feng S; Yan YB; Huang S; Ma X
Hum Mutat; 2008 May; 29(5):769. PubMed ID: 18407550
[TBL] [Abstract][Full Text] [Related]
27. AlphaA-crystallin expression prevents gamma-crystallin insolubility and cataract formation in the zebrafish cloche mutant lens.
Goishi K; Shimizu A; Najarro G; Watanabe S; Rogers R; Zon LI; Klagsbrun M
Development; 2006 Jul; 133(13):2585-93. PubMed ID: 16728471
[TBL] [Abstract][Full Text] [Related]
28. Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1.
Löster J; Pretsch W; Sandulache R; Schmitt-John T; Lyon MF; Graw J
Genomics; 1994 Sep; 23(1):240-2. PubMed ID: 7829079
[TBL] [Abstract][Full Text] [Related]
29. Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.
Santhiya ST; Manisastry SM; Rawlley D; Malathi R; Anishetty S; Gopinath PM; Vijayalakshmi P; Namperumalsamy P; Adamski J; Graw J
Invest Ophthalmol Vis Sci; 2004 Oct; 45(10):3599-607. PubMed ID: 15452067
[TBL] [Abstract][Full Text] [Related]
30. Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract.
Graw J; Neuhäuser-Klaus A; Löster J; Klopp N; Favor J
Genetics; 2002 Aug; 161(4):1633-40. PubMed ID: 12196406
[TBL] [Abstract][Full Text] [Related]
31. Chromosomal localization of a new mouse lens opacity gene (lop18).
Chang B; Hawes NL; Smith RS; Heckenlively JR; Davisson MT; Roderick TH
Genomics; 1996 Aug; 36(1):171-3. PubMed ID: 8812430
[TBL] [Abstract][Full Text] [Related]
32. 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; 13():2096-104. PubMed ID: 18079686
[TBL] [Abstract][Full Text] [Related]
33. [Autosomal dominant congenital nuclear cataract caused by a deletion mutation in the beta A1-crystallin gene].
Qi YH; Jia HY; Huang SZ; Lin H; Gu JZ; Su H; Zhang TY; Gao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):486-9. PubMed ID: 14669215
[TBL] [Abstract][Full Text] [Related]
34. A comprehensive analysis of the expression of crystallins in mouse retina.
Xi J; Farjo R; Yoshida S; Kern TS; Swaroop A; Andley UP
Mol Vis; 2003 Aug; 9():410-9. PubMed ID: 12949468
[TBL] [Abstract][Full Text] [Related]
35. Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families.
Riazuddin SA; Yasmeen A; Yao W; Sergeev YV; Zhang Q; Zulfiqar F; Riaz A; Riazuddin S; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):2100-6. PubMed ID: 15914629
[TBL] [Abstract][Full Text] [Related]
36. [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. PubMed ID: 14767902
[TBL] [Abstract][Full Text] [Related]
37. Mapping of six dominant cataract genes in the mouse.
Everett CA; Glenister PH; Taylor DM; Lyon MF; Kratochvilova-Loester J; Favor J
Genomics; 1994 Apr; 20(3):429-34. PubMed ID: 8034315
[TBL] [Abstract][Full Text] [Related]
38. Visualization of in situ intracellular aggregation of two cataract-associated human gamma-crystallin mutants: lose a tail, lose transparency.
Talla V; Srinivasan N; Balasubramanian D
Invest Ophthalmol Vis Sci; 2008 Aug; 49(8):3483-90. PubMed ID: 18421082
[TBL] [Abstract][Full Text] [Related]
39. The P23T cataract mutation causes loss of solubility of folded gammaD-crystallin.
Evans P; Wyatt K; Wistow GJ; Bateman OA; Wallace BA; Slingsby C
J Mol Biol; 2004 Oct; 343(2):435-44. PubMed ID: 15451671
[TBL] [Abstract][Full Text] [Related]
40. 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. PubMed ID: 19390652
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]