BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 28755661)

  • 1. Association of alpha A-crystallin polymorphisms with susceptibility to nuclear age-related cataract in a Han Chinese population.
    Zhao Z; Fan Q; Zhou P; Ye H; Cai L; Lu Y
    BMC Ophthalmol; 2017 Jul; 17(1):133. PubMed ID: 28755661
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polymorphism rs7278468 is associated with Age-related cataract through decreasing transcriptional activity of the CRYAA promoter.
    Ma X; Jiao X; Ma Z; Hejtmancik JF
    Sci Rep; 2016 Mar; 6():23206. PubMed ID: 26984531
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Correlations of single nucleotide polymorphisms of CRYAA and CRYAB genes with the risk and clinicopathological features of children suffering from congenital cataract.
    Cui XJ; Lv FY; Li FH; Zeng K
    Medicine (Baltimore); 2017 Jun; 96(25):e7158. PubMed ID: 28640093
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphisms in
    Yu H; Liu K; Lu P
    Semin Ophthalmol; 2021 Aug; 36(5-6):429-436. PubMed ID: 34010109
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A silent mutation in human alpha-A crystallin gene in patients with age-related nuclear or cortical cataract.
    Mynampati BK; Muthukumarappa T; Ghosh S; Ram J
    Bosn J Basic Med Sci; 2017 May; 17(2):114-119. PubMed ID: 28146420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Down-regulation and CpG island hypermethylation of CRYAA in age-related nuclear cataract.
    Zhou P; Luo Y; Liu X; Fan L; Lu Y
    FASEB J; 2012 Dec; 26(12):4897-902. PubMed ID: 22889833
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association between single nucleotide polymorphisms in exon 3 of the
    Zhao Z; Chen J; Yuan W; Jiang Y; Lu Y
    Ophthalmic Genet; 2023 Apr; 44(2):127-132. PubMed ID: 36380611
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CpG site methylation in CRYAA promoter affect transcription factor Sp1 binding in human lens epithelial cells.
    Liu X; Zhou P; Fan F; Li D; Wu J; Lu Y; Luo Y
    BMC Ophthalmol; 2016 Aug; 16():141. PubMed ID: 27507241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population.
    Tan W; Hou S; Jiang Z; Hu Z; Yang P; Ye J
    Mol Vis; 2011; 17():1553-8. PubMed ID: 21686326
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract.
    Nair V; Sankaranarayanan R; Vasavada AR
    Indian J Ophthalmol; 2021 Aug; 69(8):2064-2070. PubMed ID: 34304179
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese.
    Zhou Z; Wang B; Luo Y; Zhou G; Hu S; Zhang H; Ma X; Qi Y
    Mol Vis; 2011; 17():2292-6. PubMed ID: 21921980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.
    Zhang LY; Yam GH; Tam PO; Lai RY; Lam DS; Pang CP; Fan DS
    Mol Vis; 2009 Jun; 15():1127-38. PubMed ID: 19503744
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
    Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M
    Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2909-15. PubMed ID: 11687536
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of Interleukin-1 Gene Single Nucleotide Polymorphisms with Keratoconus in Chinese Han Population.
    Wang Y; Wei W; Zhang C; Zhang X; Liu M; Zhu X; Xu K
    Curr Eye Res; 2016 May; 41(5):630-5. PubMed ID: 26200829
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Polymorphism rs2968 of
    Zou X; Wang H; Zhou D; Liu Z; Wang Y; Deng G; Guan H
    DNA Cell Biol; 2020 Nov; 39(11):1970-1975. PubMed ID: 32877255
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A variant in a microRNA binding site in NEIL2 3'UTR confers susceptibility to age-related cataracts.
    Kang L; Zou X; Zhang G; Xiang J; Wang Y; Yang M; Chen X; Wu J; Guan H
    FASEB J; 2019 Sep; 33(9):10469-10476. PubMed ID: 31253066
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Probing the changes in gene expression due to α-crystallin mutations in mouse models of hereditary human cataract.
    Andley UP; Tycksen E; McGlasson-Naumann BN; Hamilton PD
    PLoS One; 2018; 13(1):e0190817. PubMed ID: 29338044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Protective association of A-T-T haplotype of DMT1 gene against risk of human age-related nuclear cataract.
    Sankaranarayanan R; Vidya NG; Vasavada AR
    Ophthalmic Genet; 2019 Apr; 40(2):99-109. PubMed ID: 30870050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family.
    Song Z; Si N; Xiao W
    BMC Med Genet; 2018 Oct; 19(1):190. PubMed ID: 30340470
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.