242 related articles for article (PubMed ID: 12226711)
1. V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice.
Graw J; Löster J; Soewarto D; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Mamm Genome; 2002 Aug; 13(8):452-5. PubMed ID: 12226711
[TBL] [Abstract][Full Text] [Related]
2. Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2909-15. PubMed ID: 11687536
[TBL] [Abstract][Full Text] [Related]
3. Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
Graw J; Löster J; Soewarto D; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1574-80. PubMed ID: 11381063
[TBL] [Abstract][Full Text] [Related]
4. Characterization of a 1-bp deletion in the gammaE-crystallin gene leading to a nuclear and zonular cataract in the mouse.
Klopp N; Löster J; Graw J
Invest Ophthalmol Vis Sci; 2001 Jan; 42(1):183-7. PubMed ID: 11133865
[TBL] [Abstract][Full Text] [Related]
5. Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.
Graw J; Jung M; Löster J; Klopp N; Soewarto D; Fella C; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Genomics; 1999 Nov; 62(1):67-73. PubMed ID: 10585769
[TBL] [Abstract][Full Text] [Related]
6. A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse.
Graw J; Neuhäuser-Klaus A; Löster J; Favor J
Invest Ophthalmol Vis Sci; 2002 Jan; 43(1):236-40. PubMed ID: 11773036
[TBL] [Abstract][Full Text] [Related]
7. GammaD-crystallin associated protein aggregation and lens fiber cell denucleation.
Wang K; Cheng C; Li L; Liu H; Huang Q; Xia CH; Yao K; Sun P; Horwitz J; Gong X
Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3719-28. PubMed ID: 17652744
[TBL] [Abstract][Full Text] [Related]
8. Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.
Smith RS; Hawes NL; Chang B; Roderick TH; Akeson EC; Heckenlively JR; Gong X; Wang X; Davisson MT
Genomics; 2000 Feb; 63(3):314-20. PubMed ID: 10704279
[TBL] [Abstract][Full Text] [Related]
9. Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity.
Graw J; Klopp N; Neuhäuser-Klaus A; Favor J; Löster J
Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2998-3002. PubMed ID: 12202521
[TBL] [Abstract][Full Text] [Related]
10. Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.
Li L; Chang B; Cheng C; Chang D; Hawes NL; Xia CH; Gong X
Invest Ophthalmol Vis Sci; 2008 Jan; 49(1):304-9. PubMed ID: 18172107
[TBL] [Abstract][Full Text] [Related]
11. Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.
Klopp N; Favor J; Löster J; Lutz RB; Neuhäuser-Klaus A; Prescott A; Pretsch W; Quinlan RA; Sandilands A; Vrensen GF; Graw J
Genomics; 1998 Sep; 52(2):152-8. PubMed ID: 9782080
[TBL] [Abstract][Full Text] [Related]
12. A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese family.
Gu F; Li R; Ma XX; Shi LS; Huang SZ; Ma X
Mol Vis; 2006 Jan; 12():26-31. PubMed ID: 16446699
[TBL] [Abstract][Full Text] [Related]
13. A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
Mackay DS; Andley UP; Shiels A
Mol Vis; 2004 Mar; 10():155-62. PubMed ID: 15041957
[TBL] [Abstract][Full Text] [Related]
14. Genetics of crystallins: cataract and beyond.
Graw J
Exp Eye Res; 2009 Feb; 88(2):173-89. PubMed ID: 19007775
[TBL] [Abstract][Full Text] [Related]
15. Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.
Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Exp Eye Res; 2001 Dec; 73(6):867-76. PubMed ID: 11846517
[TBL] [Abstract][Full Text] [Related]
16. Arginine 54 and Tyrosine 118 residues of {alpha}A-crystallin are crucial for lens formation and transparency.
Xia CH; Liu H; Chang B; Cheng C; Cheung D; Wang M; Huang Q; Horwitz J; Gong X
Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3004-10. PubMed ID: 16799046
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.
Xu WZ; Zheng S; Xu SJ; Huang W; Yao K; Zhang SZ
Chin Med J (Engl); 2004 May; 117(5):727-32. PubMed ID: 15161542
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 17724170
[TBL] [Abstract][Full Text] [Related]
19. CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract.
Zenteno JC; Morales ME; Moran-Barroso V; Sanchez-Navarro A
Mol Vis; 2005 Jun; 11():438-42. PubMed ID: 16030500
[TBL] [Abstract][Full Text] [Related]
20. Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.
Pauli S; Söker T; Klopp N; Illig T; Engel W; Graw J
Mol Vis; 2007 Jun; 13():962-7. PubMed ID: 17653036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]