178 related articles for article (PubMed ID: 10704279)
1. 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]
2. 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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.
Gill D; Klose R; Munier FL; McFadden M; Priston M; Billingsley G; Ducrey N; Schorderet DF; Héon E
Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):159-65. PubMed ID: 10634616
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse.
Graw J; Neuhäuser-Klaus A; Klopp N; Selby PB; Löster J; Favor J
Invest Ophthalmol Vis Sci; 2004 Apr; 45(4):1202-13. PubMed ID: 15037589
[TBL] [Abstract][Full Text] [Related]
18. 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]
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. A frameshift mutation in the gamma E-crystallin gene of the Elo mouse.
Cartier M; Breitman ML; Tsui LC
Nat Genet; 1992 Sep; 2(1):42-5. PubMed ID: 1303247
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
