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    Results: 1 to 20 of 160

    1.

    Understanding the molecular genetics of congenital cataract may have wider implications for age related cataract.

    Moore AT.

    Br J Ophthalmol. 2004 Jan;88(1):2-3. No abstract available. PMID: 14693758 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

    Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

    Br J Ophthalmol. 2004 Jan;88(1):79-83.PMID: 14693780 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    [The genetics of hereditary cataract]

    Beby F, Morle L, Michon L, M B, Edery P, Burillon C, Denis P.

    J Fr Ophtalmol. 2003 Apr;26(4):400-8. Review. French. PMID: 12843900 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    [Genetics of iron overloads and hereditary hyperferritinemia cataract syndrome]

    García-Erce JA, Salvador Osuna C.

    An Med Interna. 2003 Apr;20(4):213-4. Spanish. No abstract available. PMID: 12768838 [PubMed - indexed for MEDLINE]Related articles

    5.

    The genetics of cataract.

    McCarty CA, Taylor HR.

    Invest Ophthalmol Vis Sci. 2001 Jul;42(8):1677-8. Review. No abstract available. PMID: 11431427 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Molecular genetics of age-related cataract.

    Hejtmancik JF, Kantorow M.

    Exp Eye Res. 2004 Jul;79(1):3-9. Review.PMID: 15183095 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Lens biology: development and human cataractogenesis.

    Francis PJ, Berry V, Moore AT, Bhattacharya S.

    Trends Genet. 1999 May;15(5):191-6. Review.PMID: 10322486 [PubMed - indexed for MEDLINE]Related articles

    9.

    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.PMID: 18407550 [PubMed - indexed for MEDLINE]Related articles

    10.

    Hereditary hyperferritinemia-cataract syndrome.

    Christiansen G, Mohney BG.

    J AAPOS. 2007 Jun;11(3):294-6.PMID: 17572344 [PubMed - indexed for MEDLINE]Related articles

    11.

    Hereditary cataract mouse with lens rupture: disputed priority.

    Hiai H.

    Lab Anim. 1997 Oct;31(4):389-90. No abstract available. PMID: 9350710 [PubMed - indexed for MEDLINE]Related articles

    12.

    CRYBA3/A1 gene mutation associated with suture-sparing autosomal dominant congenital nuclear cataract: a novel phenotype.

    Ferrini W, Schorderet DF, Othenin-Girard P, Uffer S, Héon E, Munier FL.

    Invest Ophthalmol Vis Sci. 2004 May;45(5):1436-41.PMID: 15111599 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Congenital cataracts: gene mapping.

    He W, Li S.

    Hum Genet. 2000 Jan;106(1):1-13. Review.PMID: 10982175 [PubMed - indexed for MEDLINE]Related articles

    14.

    Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.

    Graw J, Klopp N, Illig T, Preising MN, Lorenz B.

    Graefes Arch Clin Exp Ophthalmol. 2006 Aug;244(8):912-9. Epub 2006 Feb 2.PMID: 16453125 [PubMed - indexed for MEDLINE]Related articles

    15.

    2005 Gregg Lecture: Congenital cataract--from rubella to genetics.

    Mackey DA.

    Clin Experiment Ophthalmol. 2006 Apr;34(3):199-207.PMID: 16671898 [PubMed - indexed for MEDLINE]Related articles

    16.

    Zebrafish mutants as models for congenital ocular disorders in humans.

    Gross JM, Perkins BD.

    Mol Reprod Dev. 2008 Mar;75(3):547-55. Review. No abstract available. PMID: 18058918 [PubMed - indexed for MEDLINE]Related articles

    17.

    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 1;13(9):945-53. Epub 2004 Mar 11.PMID: 15016766 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Crystallins and hereditary cataracts: molecular mechanisms and potential for therapy.

    Andley UP.

    Expert Rev Mol Med. 2006 Oct 19;8(25):1-19. Review.PMID: 17049104 [PubMed - indexed for MEDLINE]Related articles

    19.

    Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C).

    Khan AO, Aldahmesh MA, Meyer B.

    Am J Ophthalmol. 2007 Dec;144(6):949-952. Epub 2007 Oct 15.PMID: 17937925 [PubMed - indexed for MEDLINE]Related articles

    20.

    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.PMID: 15914629 [PubMed - indexed for MEDLINE]Related articlesFree article

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