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: 16186368)

  • 1. Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations.
    Lee KY; Koh AH; Aung T; Yong VH; Yeung K; Ang CL; Vithana EN
    Invest Ophthalmol Vis Sci; 2005 Oct; 46(10):3812-6. PubMed ID: 16186368
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy.
    Shan M; Dong B; Zhao X; Wang J; Li G; Yang Y; Li Y
    Mol Vis; 2005 Sep; 11():738-43. PubMed ID: 16179904
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: report on a novel mutation.
    Haddad NM; Waked N; Bejjani R; Khoueir Z; Chouery E; Corbani S; Mégarbané A
    Mol Vis; 2012; 18():1182-8. PubMed ID: 22605929
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype phenotype analysis of Bietti's crystalline dystrophy in patients with CYP4V2 mutations.
    Lai TY; Ng TK; Tam PO; Yam GH; Ngai JW; Chan WM; Liu DT; Lam DS; Pang CP
    Invest Ophthalmol Vis Sci; 2007 Nov; 48(11):5212-20. PubMed ID: 17962476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy.
    Lin J; Nishiguchi KM; Nakamura M; Dryja TP; Berson EL; Miyake Y
    J Med Genet; 2005 Jun; 42(6):e38. PubMed ID: 15937078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in
    Lockhart CM; Smith TB; Yang P; Naidu M; Rettie AE; Nath A; Weleber R; Kelly EJ
    Br J Ophthalmol; 2018 Feb; 102(2):187-194. PubMed ID: 28698241
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of novel CYP4V2 genotypes associated with Bietti crystalline dystrophy and atypical anterior segment phenotypes in Spanish patients.
    García-García GP; Martínez-Rubio M; Moya-Moya MA; Pérez-Santonja JJ; Escribano J
    Acta Ophthalmol; 2018 Nov; 96(7):e865-e873. PubMed ID: 29691984
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy.
    Halford S; Liew G; Mackay DS; Sergouniotis PI; Holt R; Broadgate S; Volpi EV; Ocaka L; Robson AG; Holder GE; Moore AT; Michaelides M; Webster AR
    Ophthalmology; 2014 Jun; 121(6):1174-84. PubMed ID: 24480711
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization.
    Mamatha G; Umashankar V; Kasinathan N; Krishnan T; Sathyabaarathi R; Karthiyayini T; Amali J; Rao C; Madhavan J
    Mol Vis; 2011; 17():1970-7. PubMed ID: 21850171
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bietti crystalline corneoretinal dystrophy associated with CYP4V2 gene mutations.
    Nakamura M; Lin J; Nishiguchi K; Kondo M; Sugita J; Miyake Y
    Adv Exp Med Biol; 2006; 572():49-53. PubMed ID: 17249554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy.
    Yin H; Jin C; Fang X; Miao Q; Zhao Y; Chen Z; Su Z; Ye P; Wang Y; Yin J
    PLoS One; 2014; 9(4):e94960. PubMed ID: 24739949
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype-phenotype analysis of Bietti crystalline dystrophy in a family with the CYP4V2 Ile111Thr mutation.
    García-García GP; López-Garrido MP; Martínez-Rubio M; Moya-Moya MA; Belmonte-Martínez J; Escribano J
    Cornea; 2013 Jul; 32(7):1002-8. PubMed ID: 23538635
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy.
    Yin X; Yang L; Chen N; Cui H; Zhao L; Feng L; Li A; Zhang H; Ma Z; Li G
    Exp Eye Res; 2016 May; 146():154-162. PubMed ID: 26971461
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CYP4V2 mutations in two Japanese patients with Bietti's crystalline dystrophy.
    Gekka T; Hayashi T; Takeuchi T; Goto-Omoto S; Kitahara K
    Ophthalmic Res; 2005; 37(5):262-9. PubMed ID: 16088246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Crystal deposits on the lens capsules in Bietti crystalline corneoretinal dystrophy associated with a mutation in the CYP4V2 gene.
    Yokoi Y; Nakazawa M; Mizukoshi S; Sato K; Usui T; Takeuchi K
    Acta Ophthalmol; 2010 Aug; 88(5):607-9. PubMed ID: 19508456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comprehensive screening of
    Zhang X; Xu K; Dong B; Peng X; Li Q; Jiang F; Xie Y; Tian L; Li Y
    Mol Vis; 2018; 24():700-711. PubMed ID: 30429639
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy.
    Xiao X; Mai G; Li S; Guo X; Zhang Q
    Biochem Biophys Res Commun; 2011 Jun; 409(2):181-6. PubMed ID: 21565171
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
    Li A; Jiao X; Munier FL; Schorderet DF; Yao W; Iwata F; Hayakawa M; Kanai A; Shy Chen M; Alan Lewis R; Heckenlively J; Weleber RG; Traboulsi EI; Zhang Q; Xiao X; Kaiser-Kupfer M; Sergeev YV; Hejtmancik JF
    Am J Hum Genet; 2004 May; 74(5):817-26. PubMed ID: 15042513
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti's crystalline corneoretinal dystrophy.
    Meng XH; Guo H; Xu HW; Li QY; Jin X; Bai Y; Li SY; Yin ZQ
    Mol Vis; 2014; 20():1806-14. PubMed ID: 25593508
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Alterations in serum fatty acid concentrations and desaturase activities in Bietti crystalline dystrophy unaffected by CYP4V2 genotypes.
    Lai TY; Chu KO; Chan KP; Ng TK; Yam GH; Lam DS; Pang CP
    Invest Ophthalmol Vis Sci; 2010 Feb; 51(2):1092-7. PubMed ID: 19797200
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.