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 *

268 related articles for article (PubMed ID: 9497259)

  • 1. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.
    Shiels A; Mackay D; Ionides A; Berry V; Moore A; Bhattacharya S
    Am J Hum Genet; 1998 Mar; 62(3):526-32. PubMed ID: 9497259
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Connexin46 mutations in autosomal dominant congenital cataract.
    Mackay D; Ionides A; Kibar Z; Rouleau G; Berry V; Moore A; Shiels A; Bhattacharya S
    Am J Hum Genet; 1999 May; 64(5):1357-64. PubMed ID: 10205266
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.
    Mackay D; Ionides A; Berry V; Moore A; Bhattacharya S; Shiels A
    Am J Hum Genet; 1997 Jun; 60(6):1474-8. PubMed ID: 9199569
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.
    Berry V; Mackay D; Khaliq S; Francis PJ; Hameed A; Anwar K; Mehdi SQ; Newbold RJ; Ionides A; Shiels A; Moore T; Bhattacharya SS
    Hum Genet; 1999; 105(1-2):168-70. PubMed ID: 10480374
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q.
    Bennett TM; Shiels A
    Mol Vis; 2011; 17():2255-62. PubMed ID: 21897748
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. 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]  

  • 12. Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
    Devi RR; Vijayalakshmi P
    Mol Vis; 2006 Mar; 12():190-5. PubMed ID: 16604058
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Analysis on gene mutations in a Chinese pedigree with autosomal dominant inheritance cataract].
    Yan M; Zhou X; Chen YM; Ma JJ; Xiong CL; Cheng XH
    Zhonghua Yan Ke Za Zhi; 2009 Aug; 45(8):693-8. PubMed ID: 20021880
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
    Addison PK; Berry V; Holden KR; Espinal D; Rivera B; Su H; Srivastava AK; Bhattacharya SS
    Mol Vis; 2006 Jul; 12():791-5. PubMed ID: 16885921
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.
    Li J; Wang Q; Fu Q; Zhu Y; Zhai Y; Yu Y; Zhang K; Yao K
    Mol Vis; 2013; 19():767-74. PubMed ID: 23592913
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A locus for autosomal dominant posterior polar cataract on chromosome 1p.
    Ionides AC; Berry V; Mackay DS; Moore AT; Bhattacharya SS; Shiels A
    Hum Mol Genet; 1997 Jan; 6(1):47-51. PubMed ID: 9002669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.
    Arora A; Minogue PJ; Liu X; Addison PK; Russel-Eggitt I; Webster AR; Hunt DM; Ebihara L; Beyer EC; Berthoud VM; Moore AT
    J Med Genet; 2008 Mar; 45(3):155-60. PubMed ID: 18006672
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
    Chang B; Wang X; Hawes NL; Ojakian R; Davisson MT; Lo WK; Gong X
    Hum Mol Genet; 2002 Mar; 11(5):507-13. PubMed ID: 11875045
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 14.