BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 17214724)

  • 1. Novel mutations in two families with Darier's disease.
    Amichai B; Karpati M; Goldman B; Peleg L
    Int J Dermatol; 2007 Jan; 46(1):64-7. PubMed ID: 17214724
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations of the ATP2A2 gene in two families with Darier's disease.
    Shi BJ; Feng J; Ma CC; Yan XN; Li WB; Wei YP; Hu G; Wang XL
    Arch Dermatol Res; 2009 Jan; 301(1):27-30. PubMed ID: 18979109
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis of the ATP2A2 gene in Taiwanese patients with Darier's disease.
    Chao SC; Yang MH; Lee JY
    Br J Dermatol; 2002 Jun; 146(6):958-63. PubMed ID: 12072062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification a novel missense mutation p.R761L in Chinese patients with Darier's disease.
    Song J; Li M; Yang LJ; Zhang GL
    Arch Dermatol Res; 2010 May; 302(4):311-4. PubMed ID: 20204653
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical case of acral hemorrhagic Darier's disease is not caused by mutations in exon 15 of the ATP2A2 gene.
    Pećina-Slaus N; Milavec-Puretić V; Kubat M; Furac I; Karija M; Fischer-Zigmund M; Lipozencić J
    Coll Antropol; 2003 Jun; 27(1):125-33. PubMed ID: 12974140
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
    Sakuntabhai A; Ruiz-Perez V; Carter S; Jacobsen N; Burge S; Monk S; Smith M; Munro CS; O'Donovan M; Craddock N; Kucherlapati R; Rees JL; Owen M; Lathrop GM; Monaco AP; Strachan T; Hovnanian A
    Nat Genet; 1999 Mar; 21(3):271-7. PubMed ID: 10080178
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel missense mutation of the ATP2A2 gene in a Chinese family with Darier's disease.
    Yang S; Sun LD; Liu HS; Wang JY; He PP; Li M; Gao M; Liu JB; Yang J; Wang ZX; Zhu YY; Lin D; Zhang XJ
    Arch Dermatol Res; 2004 Jun; 296(1):21-4. PubMed ID: 15095095
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of two novel Darier disease‑associated mutations in the ATP2A2 gene.
    Zheng L; Jiang H; Mei Q; Chen B
    Mol Med Rep; 2015 Aug; 12(2):1845-9. PubMed ID: 25872913
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two novel missense mutations of ATP2A2 in two Chinese patients with sporadic Darier disease.
    Liang YH; Zhang QG; Liu QX
    Clin Exp Dermatol; 2015 Mar; 40(2):201-3. PubMed ID: 25283811
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New mutations of Darier disease in Tunisian patients.
    Bchetnia M; Benmously R; Ben Brick AS; Charfeddine C; Ben Ameur Y; Fajraoui M; Debbiche A; Ben Ayed M; Mokni M; Fenniche S; Mokhtar I; Abdelhak S
    Arch Dermatol Res; 2009 Sep; 301(8):615-9. PubMed ID: 19488774
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's disease.
    Klausegger A; Nischler E; Wagner RN; Pletschacher F; Hintner H; Bauer JW
    Arch Dermatol Res; 2011 Jul; 303(5):371-4. PubMed ID: 21519848
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey.
    Nakamura T; Kazuno AA; Nakajima K; Kusumi I; Tsuboi T; Kato T
    Psychiatry Clin Neurosci; 2016 Aug; 70(8):342-50. PubMed ID: 27106560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Darier disease: a guide to the physician.
    Godic A
    J Med; 2004; 35(1-6):5-17. PubMed ID: 18084860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of mutations in the ATP2A2 gene in patients with Darier's disease from Hungary.
    Rácz E; Csikós M; Kornsée Z; Horváth A; Kárpáti S
    Exp Dermatol; 2004 Jun; 13(6):396-9. PubMed ID: 15186327
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and mutational heterogeneity of Darier disease in Tunisian families.
    Bchetnia M; Charfeddine C; Kassar S; Zribi H; Guettiti HT; Ellouze F; Cheour M; Boubaker S; Osman AD; Abdelhak S; Mokni M
    Arch Dermatol; 2009 Jun; 145(6):654-6. PubMed ID: 19528419
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
    Ruiz-Perez VL; Carter SA; Healy E; Todd C; Rees JL; Steijlen PM; Carmichael AJ; Lewis HM; Hohl D; Itin P; Vahlquist A; Gobello T; Mazzanti C; Reggazini R; Nagy G; Munro CS; Strachan T
    Hum Mol Genet; 1999 Sep; 8(9):1621-30. PubMed ID: 10441324
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The ATP2A2 gene in patients with Darier's disease: one novel splicing mutation.
    Shi BJ; Xue M; Zhong GS; Jiang Y; Chen DY; Feng J; Hao J; Diao QC
    Int J Dermatol; 2012 Sep; 51(9):1074-7. PubMed ID: 22909361
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of novel ATP2A2 mutations in patients with Darier's disease.
    Sakuntabhai A; Burge S; Monk S; Hovnanian A
    Hum Mol Genet; 1999 Sep; 8(9):1611-9. PubMed ID: 10441323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel splice-site mutation of ATP2A2 gene in a Chinese family with Darier disease.
    Huo J; Liu Y; Ma J; Xiao S
    Arch Dermatol Res; 2010 Dec; 302(10):769-72. PubMed ID: 20857128
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.