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 *

180 related articles for article (PubMed ID: 21174522)

  • 1. Genetic linkage analyses and Cx50 mutation detection in a large multiplex Chinese family with hereditary nuclear cataract.
    He W; Li X; Chen J; Xu L; Zhang F; Dai Q; Cui H; Wang DM; Yu J; Hu S; Lu S
    Ophthalmic Genet; 2011 Mar; 32(1):48-53. PubMed ID: 21174522
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Gao X; Cheng J; Lu C; Li X; Li F; Liu C; Zhang M; Zhu S; Ma X
    Curr Eye Res; 2010 Jul; 35(7):597-604. PubMed ID: 20597646
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A heterozygous transversion of connexin 50 in a family with congenital nuclear cataract in the northeast of China].
    Zheng JQ; Ma ZW; Sun HM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):76-8. PubMed ID: 15696487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Yang G; Xing B; Liu G; Lu X; Jia X; Lu X; Wang X; Yu H; Fu Y; Zhao J
    Mol Vis; 2011 Apr; 17():1070-3. PubMed ID: 21552498
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. An autosomal dominant progressive congenital zonular nuclear cataract linked to chromosome 20p12.2-p11.23.
    Li N; Yang Y; Bu J; Zhao C; Lu S; Zhao J; Yan L; Cui L; Zheng R; Li J; Tang J; Zhao K
    Mol Vis; 2006 Dec; 12():1506-10. PubMed ID: 17167408
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family.
    Zhang X; Wang L; Wang J; Dong B; Li Y
    Mol Vis; 2012; 18():203-10. PubMed ID: 22312188
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in GJA3 associated with congenital Coppock-like cataract in a large Chinese family.
    Zhang L; Qu X; Su S; Guan L; Liu P
    Mol Vis; 2012; 18():2114-8. PubMed ID: 22876138
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract.
    Wang L; Luo Y; Wen W; Zhang S; Lu Y
    Mol Vis; 2011; 17():2380-5. PubMed ID: 21921990
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of a p.R76H mutation in Cx50 identified in a Chinese family with congenital nuclear cataract.
    Wang KJ; Da Wang J; Chen DD; Wang MY; Yun B; Zhu SQ
    J Formos Med Assoc; 2020 Jan; 119(1 Pt 1):144-149. PubMed ID: 30928190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
    Li Y; Wang J; Dong B; Man H
    Mol Vis; 2004 Sep; 10():668-71. PubMed ID: 15448617
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract.
    Yan M; Xiong C; Ye SQ; Chen Y; Ke M; Zheng F; Zhou X
    Mol Vis; 2008 Mar; 14():418-24. PubMed ID: 18334966
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract.
    Arora A; Minogue PJ; Liu X; Reddy MA; Ainsworth JR; Bhattacharya SS; Webster AR; Hunt DM; Ebihara L; Moore AT; Beyer EC; Berthoud VM
    J Med Genet; 2006 Jan; 43(1):e2. PubMed ID: 16397066
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.
    Liu M; Ke T; Wang Z; Yang Q; Chang W; Jiang F; Tang Z; Li H; Ren X; Wang X; Wang T; Li Q; Yang J; Liu J; Wang QK
    Invest Ophthalmol Vis Sci; 2006 Aug; 47(8):3461-6. PubMed ID: 16877416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.