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 *

254 related articles for article (PubMed ID: 20300939)

  • 21. A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
    Li CR; Li M; Ma HJ; Luo D; Yang LJ; Wang DG; Zhu XH; Yue XZ; Chen WQ; Zhu WY
    J Dermatol Sci; 2005 Feb; 37(2):95-9. PubMed ID: 15659327
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Four novel mutations of
    Hu W; Shi X; Li H; Chen L; Wang T; Dong Y; Zhang Y; Hu M; Liu X; Zhang C; Liu D; Deng Y
    Indian J Dermatol Venereol Leprol; 2019; 85(1):69-73. PubMed ID: 29536976
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of two novel splice mutations of the ADAR1 gene in two Chinese families with dyschromatosis symmetrica hereditaria.
    Liu H; Fu XA; Yu YX; Yu GQ; Yan XX; Liu HX; Tian HQ; Zhang FR
    Clin Exp Dermatol; 2011 Oct; 36(7):797-9. PubMed ID: 21933234
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update.
    Kono M; Akiyama M
    J Dermatol Sci; 2019 Feb; 93(2):75-81. PubMed ID: 30692041
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Six novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria.
    Zhang F; Liu H; Jiang D; Tian H; Wang C; Yu L
    J Dermatol Sci; 2008 May; 50(2):109-14. PubMed ID: 18243666
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.
    Miyamura Y; Suzuki T; Kono M; Inagaki K; Ito S; Suzuki N; Tomita Y
    Am J Hum Genet; 2003 Sep; 73(3):693-9. PubMed ID: 12916015
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Dyschromatosis symmetrica hereditaria: A clue to early diagnosis of Aicardi-Goutières syndrome.
    Ahmed F; Do N; Vanderver AL; Treat JR
    Pediatr Dermatol; 2024; 41(1):156-157. PubMed ID: 37770123
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.
    Murata I; Hozumi Y; Kawaguchi M; Katagiri Y; Yasumoto S; Kubo Y; Fujimoto W; Horikawa T; Kondo T; Kono M; Tomita Y; Suzuki T
    J Dermatol Sci; 2009 Jan; 53(1):76-7. PubMed ID: 18799292
    [No Abstract]   [Full Text] [Related]  

  • 30. [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]  

  • 31. Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria.
    Liu Q; Wang Z; Wu Y; Cao L; Tang Q; Xing X; Ma H; Zhang S; Luo Y
    BMC Med Genet; 2014 Jun; 15():69. PubMed ID: 24950769
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria.
    Tang ZL; Wang S; Tu C; Wang T; Ma CW; Liu Y; Xiao SX; Wang XP
    Genet Test Mol Biomarkers; 2018 Feb; 22(2):104-108. PubMed ID: 29185800
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a novel DSRAD gene mutation in a Chinese family with dyschromatosis symmetrica hereditaria.
    Li M; Yang LJ; Zhu XH
    Clin Exp Dermatol; 2008 Aug; 33(5):644-6. PubMed ID: 18627385
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.
    Wang P; Yu S; Liu J; Zhang D; Kang X
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00905. PubMed ID: 31423758
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of five novel variants of
    Ma Q; Che L; Chen Y; Gu Z
    Front Pediatr; 2023; 11():1161502. PubMed ID: 37476031
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria.
    Suzuki N; Suzuki T; Inagaki K; Ito S; Kono M; Horikawa T; Fujiwara S; Ishiko A; Matsunaga K; Aoyama Y; Tosaki-Ichikawa H; Tomita Y
    J Invest Dermatol; 2007 Feb; 127(2):309-11. PubMed ID: 16917490
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of two novel DSRAD mutations in two Chinese families with dyschromatosis symmetrica hereditaria.
    Lu J; Liao Z; Chen J; Xiang Y; Wu Z; Zuo C; Jiang X; Huang J
    Arch Dermatol Res; 2006 Dec; 298(7):357-60. PubMed ID: 17021765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathogenesis of a variant in the 5' untranslated region of ADAR1 in dyschromatosis symmetrica hereditaria.
    Suganuma M; Kono M; Yamanaka M; Akiyama M
    Pigment Cell Melanoma Res; 2020 Jul; 33(4):591-600. PubMed ID: 31926050
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a novel ADAR mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).
    Xing Q; Wang M; Chen X; Qian X; Qin W; Gao J; Wu S; Gao R; Feng G; He L
    Arch Dermatol Res; 2005 Sep; 297(3):139-42. PubMed ID: 16133458
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Two novel mutations in the DSRAD gene in two Chinese pedigrees with dyschromatosis symmetrica hereditaria.
    Zhang S; Jiang M; Zhao J
    Eur J Dermatol; 2013; 23(6):782-5. PubMed ID: 24446047
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.