BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 12202521)

  • 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. A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
    Bennett TM; Mackay DS; Knopf HL; Shiels A
    Mol Vis; 2004 Jun; 10():376-82. PubMed ID: 15208569
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
    Puk O; Esposito I; Söker T; Löster J; Budde B; Nürnberg P; Michel-Soewarto D; Fuchs H; Wolf E; Hrabé de Angelis M; Graw J
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4311-8. PubMed ID: 19407009
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
    Jiang H; Jin Y; Bu L; Zhang W; Liu J; Cui B; Kong X; Hu L
    Mol Vis; 2003 Oct; 9():579-83. PubMed ID: 14627959
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice.
    Sidjanin DJ; Parker-Wilson DM; Neuhäuser-Klaus A; Pretsch W; Favor J; Deen PM; Ohtaka-Maruyama C; Lu Y; Bragin A; Skach WR; Chepelinsky AB; Grimes PA; Stambolian DE
    Genomics; 2001 Jun; 74(3):313-9. PubMed ID: 11414759
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Characteristics of ethylnitrosourea-induced cataracts.
    Lee MJ; Kim JY; Kim YJ; Cho JW; Cho KH; Song CW; Jung HS
    Curr Eye Res; 2009 May; 34(5):360-8. PubMed ID: 19401879
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
    Puk O; Löster J; Dalke C; Soewarto D; Fuchs H; Budde B; Nürnberg P; Wolf E; de Angelis MH; Graw J
    Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1525-32. PubMed ID: 18385072
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.
    Smaoui N; Beltaief O; BenHamed S; M'Rad R; Maazoul F; Ouertani A; Chaabouni H; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2716-21. PubMed ID: 15277496
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The ldis1 lens mutation in RIIIS/J mice maps to chromosome 8 near cadherin 1.
    Jablonski MM; Lu L; Wang X; Chesler EJ; Carps E; Qi S; Gu J; Williams RW
    Mol Vis; 2004 Aug; 10():577-87. PubMed ID: 15343150
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel allele of crybb2 in the mouse and its expression in the brain.
    Ganguly K; Favor J; Neuhäuser-Klaus A; Sandulache R; Puk O; Beckers J; Horsch M; Schädler S; Vogt Weisenhorn D; Wurst W; Graw J
    Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1533-41. PubMed ID: 18385073
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
    Ma X; Li FF; Wang SZ; Gao C; Zhang M; Zhu SQ
    Mol Vis; 2008; 14():1906-11. PubMed ID: 18958306
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Cataract mutations and lens development.
    Graw J
    Prog Retin Eye Res; 1999 Mar; 18(2):235-67. PubMed ID: 9932285
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract.
    Steele EC; Lyon MF; Favor J; Guillot PV; Boyd Y; Church RL
    Curr Eye Res; 1998 Sep; 17(9):883-9. PubMed ID: 9746435
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family.
    Riazuddin SA; Yasmeen A; Zhang Q; Yao W; Sabar MF; Ahmed Z; Riazuddin S; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):623-6. PubMed ID: 15671291
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.