BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 16817193)

  • 1. Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation.
    Tojo K; Sekijima Y; Suzuki T; Suzuki N; Tomita Y; Yoshida K; Hashimoto T; Ikeda S
    Mov Disord; 2006 Sep; 21(9):1510-3. PubMed ID: 16817193
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dyschromatosis symmetrica hereditaria associated with neurological disorders.
    Kondo T; Suzuki T; Ito S; Kono M; Negoro T; Tomita Y
    J Dermatol; 2008 Oct; 35(10):662-6. PubMed ID: 19017046
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dyschromatosis symmetrica hereditaria.
    Hayashi M; Suzuki T
    J Dermatol; 2013 May; 40(5):336-43. PubMed ID: 22974014
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes.
    Kondo T; Suzuki T; Mitsuhashi Y; Ito S; Kono M; Komine M; Akita H; Tomita Y
    J Dermatol; 2008 Jul; 35(7):395-406. PubMed ID: 18705826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.
    Zhang GL; Shi HJ; Shao MH; Li M; Mu HJ; Gu Y; Du XF; Xie P
    Genet Mol Res; 2013 Jan; 12(3):2794-9. PubMed ID: 23315877
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis].
    Tojyo K; Hattori T; Sekijima Y; Yoshida K; Ikeda S
    Rinsho Shinkeigaku; 2001 Jun; 41(6):299-305. PubMed ID: 11771159
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.
    Murata I; Hayashi M; Hozumi Y; Fujii K; Mitsuhashi Y; Oiso N; Fukai K; Kuroki N; Mori Y; Utani A; Tomita Y; Fujita Y; Suzuki T
    J Dermatol Sci; 2010 Jun; 58(3):218-20. PubMed ID: 20439151
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria.
    Zhu CY; Zhu KJ; Zhou Y; Fan YM
    Genet Mol Res; 2013 Aug; 12(3):2858-62. PubMed ID: 24065641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
    Suzuki N; Suzuki T; Inagaki K; Ito S; Kono M; Fukai K; Takama H; Sato K; Ishikawa O; Abe M; Shimizu H; Kawai M; Horikawa T; Yoshida K; Matsumoto K; Terui T; Tsujioka K; Tomita Y
    J Invest Dermatol; 2005 Jun; 124(6):1186-92. PubMed ID: 15955093
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.
    Liu Y; Xiao S; Peng Z; Chu Y; Wang J; Li X; Zhou S
    Dermatology; 2006; 213(3):200-3. PubMed ID: 17033168
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The double-RNA-specific adenosine deaminase (DSRAD) gene in dyschromatosis symmetrica hereditaria patients: two novel mutations and one previously described.
    Sun XK; Xu AE; Chen JF; Tang X
    Br J Dermatol; 2005 Aug; 153(2):342-5. PubMed ID: 16086746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression.
    Kono M; Suganuma M; Dutta A; Ghosh SK; Takeichi T; Muro Y; Akiyama M
    Br J Dermatol; 2018 Aug; 179(2):509-511. PubMed ID: 29603717
    [No Abstract]   [Full Text] [Related]  

  • 13. A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
    Li M; Jiang YX; Liu JB; Yang S; He PP; Gao M; Wei SC; Yan KL; Huang W; Zhang XJ
    Clin Exp Dermatol; 2004 Sep; 29(5):533-5. PubMed ID: 15347341
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria.
    Li M; Yang L; Li C; Jin C; Lai M; Zhang G; Hu Y; Ji J; Yao Z
    Arch Dermatol Res; 2010 Aug; 302(6):469-76. PubMed ID: 20186421
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two new mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.
    Li CR; Xu XL; Sun XJ; Zong WK; Sheng N; Bu J; Li M; Cui PG
    Arch Dermatol Res; 2010 Aug; 302(6):477-80. PubMed ID: 20300939
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The c.3463C>T mutation of the ADAR1 gene in patients with dyschromatosis symmetrical hereditaria].
    Song J; Zhou H; Lu RQ; Zhang LP; Sun H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):576-8. PubMed ID: 20931541
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.
    Li M; Li C; Hua H; Zhu W; Lu Y; Yang L
    Arch Dermatol Res; 2005 Nov; 297(5):196-200. PubMed ID: 16215765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria.
    Hou Y; Chen J; Gao M; Zhou F; Du W; Shen Y; Yang S; Zhang XJ
    Acta Derm Venereol; 2007; 87(1):18-21. PubMed ID: 17225010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria.
    Chao SC; Lee JY; Sheu HM; Yang MH
    Br J Dermatol; 2005 Nov; 153(5):1064-6. PubMed ID: 16225627
    [No Abstract]   [Full Text] [Related]  

  • 20. Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria.
    Liu Q; Jiang L; Liu WL; Kang XJ; Ao Y; Sun M; Luo Y; Song Y; Lo WH; Zhang X
    Br J Dermatol; 2006 Apr; 154(4):636-42. PubMed ID: 16536805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.