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 *

241 related articles for article (PubMed ID: 21921990)

  • 1. 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]  

  • 2. 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]  

  • 3. A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family.
    Wang L; Chen X; Lu Y; Wu J; Yang B; Sun X
    Mol Vis; 2011 Mar; 17():804-9. PubMed ID: 21527994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A novel GJA8 mutation in a Chinese family with autosomal dominant congenital cataract].
    Lin Y; Liu NN; Lei CT; Fan YC; Liu XQ; Yang Y; Wang JF; Liu B; Yang ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):59-62. PubMed ID: 18247306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree.
    Hu S; Wang B; Zhou Z; Zhou G; Wang J; Ma X; Qi Y
    Mol Vis; 2010 Aug; 16():1585-92. PubMed ID: 20806042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract.
    Wang L; Chen Y; Chen X; Sun X
    Indian J Ophthalmol; 2016 Jul; 64(7):508-12. PubMed ID: 27609163
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A Missense Mutation in GJA8 Encoding Connexin 50 in a Chinese Pedigree with Autosomal Dominant Congenital Cataract.
    Zhang L; Liang Y; Zhou Y; Zeng H; Jia S; Shi J
    Tohoku J Exp Med; 2018 Feb; 244(2):105-111. PubMed ID: 29434075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family.
    Shen C; Wang J; Wu X; Wang F; Liu Y; Guo X; Zhang L; Cao Y; Cao X; Ma H
    BMC Ophthalmol; 2017 May; 17(1):73. PubMed ID: 28526010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel beaded filament structural protein 1 (BFSP1) gene mutation associated with autosomal dominant congenital cataract in a Chinese family.
    Wang H; Zhang T; Wu D; Zhang J
    Mol Vis; 2013; 19():2590-5. PubMed ID: 24379646
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification and preliminary functional analysis of two novel congenital cataract associated mutations of Cx46 and Cx50.
    Ye Y; Wu M; Qiao Y; Xie T; Yu Y; Yao K
    Ophthalmic Genet; 2019 Oct; 40(5):428-435. PubMed ID: 31618082
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Detection of c.139G>A (D47N) mutation in
    Gunda P; Manne M; Adeel SS; Kondareddy RKR; Tirunilai P
    J Genet; 2018 Sep; 97(4):879-885. PubMed ID: 30262699
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Identification and functional analysis of GJA8 mutation in a Chinese family with autosomal dominant perinuclear cataracts.
    Su D; Yang Z; Li Q; Guan L; Zhang H; E D; Zhang L; Zhu S; Ma X
    PLoS One; 2013; 8(3):e59926. PubMed ID: 23555834
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational screening of Indian families with hereditary congenital cataract.
    Ponnam SP; Ramesha K; Matalia J; Tejwani S; Ramamurthy B; Kannabiran C
    Mol Vis; 2013; 19():1141-8. PubMed ID: 23734083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
    Vanita V; Singh JR; Singh D; Varon R; Sperling K
    Mol Vis; 2008 Feb; 14():323-6. PubMed ID: 18334946
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.