These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 21850180)

  • 1. Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP.
    Xiao X; Li W; Wang P; Li L; Li S; Jia X; Sun W; Guo X; Zhang Q
    Mol Vis; 2011; 17():2049-55. PubMed ID: 21850180
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallin.
    Wang L; Lin H; Gu J; Su H; Huang S; Qi Y
    Ophthalmic Res; 2009; 41(3):148-53. PubMed ID: 19321936
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract.
    Ding X; Zhou N; Lin H; Chen J; Zhao C; Zhou G; Hejtmancik JF; Qi Y
    PLoS One; 2014; 9(7):e102733. PubMed ID: 25033405
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family.
    Lin H; Hejtmancik JF; Qi Y
    Mol Vis; 2007 Sep; 13():1822-7. PubMed ID: 17960133
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese family.
    Gu F; Zhai H; Li D; Zhao L; Li C; Huang S; Ma X
    Mol Vis; 2007 Sep; 13():1651-6. PubMed ID: 17893667
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Yang G; Zhang G; Wu Q; Zhao J
    Mol Vis; 2011; 17():1320-3. PubMed ID: 21647270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
    Vanita V; Singh JR; Singh D; Varon R; Sperling K
    Mol Vis; 2009; 15():476-81. PubMed ID: 19262743
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
    Zhang L; Zhang Y; Liu P; Cao W; Tang X; Su S
    Mol Vis; 2011; 17():2693-7. PubMed ID: 22065922
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.
    Yu Y; Yu Y; Chen P; Li J; Zhu Y; Zhai Y; Yao K
    BMC Med Genet; 2014 Jan; 15():6. PubMed ID: 24405844
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.
    Vanita V; Singh D; Robinson PN; Sperling K; Singh JR
    Am J Med Genet A; 2006 Mar; 140(6):558-66. PubMed ID: 16470690
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family.
    Jiang J; Jin C; Wang W; Tang X; Shentu X; Wu R; Wang Y; Xia K; Yao K
    Mol Vis; 2009; 15():38-44. PubMed ID: 19137077
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
    Vanita V; Hennies HC; Singh D; Nürnberg P; Sperling K; Singh JR
    Mol Vis; 2006 Oct; 12():1217-22. PubMed ID: 17110920
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel human CRYGD mutation in a juvenile autosomal dominant cataract.
    Roshan M; Vijaya PH; Lavanya GR; Shama PK; Santhiya ST; Graw J; Gopinath PM; Satyamoorthy K
    Mol Vis; 2010 May; 16():887-96. PubMed ID: 20508808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).
    VanderVeen DK; Andrews C; Nihalani BR; Engle EC
    Mol Vis; 2011; 17():3333-8. PubMed ID: 22219628
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.
    Wang K; Wang B; Wang J; Zhou S; Yun B; Suo P; Cheng J; Ma X; Zhu S
    Mol Vis; 2009 Dec; 15():2813-20. PubMed ID: 20019893
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.
    Li F; Wang S; Gao C; Liu S; Zhao B; Zhang M; Huang S; Zhu S; Ma X
    Mol Vis; 2008 Mar; 14():378-86. PubMed ID: 18334953
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families.
    Yang G; Xiong C; Li S; Wang Y; Zhao J
    Mol Vis; 2011 Apr; 17():1085-9. PubMed ID: 21552497
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.
    Geyer DD; Spence MA; Johannes M; Flodman P; Clancy KP; Berry R; Sparkes RS; Jonsen MD; Isenberg SJ; Bateman JB
    Am J Ophthalmol; 2006 Apr; 141(4):761-3. PubMed ID: 16564824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
    Guleria K; Sperling K; Singh D; Varon R; Singh JR; Vanita V
    Mol Vis; 2007 Sep; 13():1657-65. PubMed ID: 17893674
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification and Functional Analysis of a Novel MIP Gene Mutation Associated with Congenital Cataract in a Chinese Family.
    Shentu X; Miao Q; Tang X; Yin H; Zhao Y
    PLoS One; 2015; 10(5):e0126679. PubMed ID: 25946197
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.