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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

140 related items for PubMed ID: 8875953

  • 1. Mutations in the ligand-binding domain of the kit receptor: an uncommon site in human piebaldism.
    Fleischman RA, Gallardo T, Mi X.
    J Invest Dermatol; 1996 Nov; 107(5):703-6. PubMed ID: 8875953
    [Abstract] [Full Text] [Related]

  • 2. Human piebald trait resulting from a dominant negative mutant allele of the c-kit membrane receptor gene.
    Fleischman RA.
    J Clin Invest; 1992 Jun; 89(6):1713-7. PubMed ID: 1376329
    [Abstract] [Full Text] [Related]

  • 3. Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.
    Spritz RA, Giebel LB, Holmes SA.
    Am J Hum Genet; 1992 Feb; 50(2):261-9. PubMed ID: 1370874
    [Abstract] [Full Text] [Related]

  • 4. Human piebaldism: six novel mutations of the proto-oncogene KIT.
    Syrris P, Heathcote K, Carrozzo R, Devriendt K, Elçioglu N, Garrett C, McEntagart M, Carter ND.
    Hum Mutat; 2002 Sep; 20(3):234. PubMed ID: 12204004
    [Abstract] [Full Text] [Related]

  • 5. Novel mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.
    Spritz RA, Holmes SA, Itin P, Küster W.
    J Invest Dermatol; 1993 Jul; 101(1):22-5. PubMed ID: 7687267
    [Abstract] [Full Text] [Related]

  • 6. Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.
    Spritz RA, Holmes SA, Ramesar R, Greenberg J, Curtis D, Beighton P.
    Am J Hum Genet; 1992 Nov; 51(5):1058-65. PubMed ID: 1384325
    [Abstract] [Full Text] [Related]

  • 7. A novel KIT missense mutation in one Chinese family with piebaldism.
    Yin XY, Ren YQ, Yang S, Xu SX, Zhou FS, Du WH, Lin D, Wang PG, Zhang SM, Zhang XJ.
    Arch Dermatol Res; 2009 Jun; 301(5):387-9. PubMed ID: 19430803
    [Abstract] [Full Text] [Related]

  • 8. A novel KIT mutation results in piebaldism with progressive depigmentation.
    Richards KA, Fukai K, Oiso N, Paller AS.
    J Am Acad Dermatol; 2001 Feb; 44(2):288-92. PubMed ID: 11174389
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Mice transgenic for Kit(V620A): recapitulation of piebaldism but not progressive depigmentation seen in humans with this mutation.
    Tosaki H, Kunisada T, Motohashi T, Aoki H, Yoshida H, Kitajima Y.
    J Invest Dermatol; 2006 May; 126(5):1111-8. PubMed ID: 16456533
    [Abstract] [Full Text] [Related]

  • 14. [Identification of a novel KIT mutation in a Chinese family affected with piebaldism].
    Wang R, Shu S, Zhang Y, Luo W, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):637-40. PubMed ID: 27577211
    [Abstract] [Full Text] [Related]

  • 15. Three novel mutations of the proto-oncogene KIT cause human piebaldism.
    Syrris P, Malik NM, Murday VA, Patton MA, Carter ND, Hughes HE, Metcalfe K.
    Am J Med Genet; 2000 Nov 06; 95(1):79-81. PubMed ID: 11074500
    [No Abstract] [Full Text] [Related]

  • 16. KIT-related piebaldism in a Chinese girl.
    Zhu L, Yang C, Zhong W, Huang YQ, Zhang Q, Xu WC, Chen YF.
    Am J Med Genet A; 2020 Jun 06; 182(6):1321-1328. PubMed ID: 32220041
    [Abstract] [Full Text] [Related]

  • 17. Molecular basis of human piebaldism.
    Spritz RA.
    J Invest Dermatol; 1994 Nov 06; 103(5 Suppl):137S-140S. PubMed ID: 7525736
    [Abstract] [Full Text] [Related]

  • 18. New KIT mutations in patients with piebaldism.
    Murakami T, Fukai K, Oiso N, Hosomi N, Kato A, Garganta C, Barnicoat A, Poppelaars F, Aquaron R, Paller AS, Ishii M.
    J Dermatol Sci; 2004 Jun 06; 35(1):29-33. PubMed ID: 15194144
    [Abstract] [Full Text] [Related]

  • 19. Piebaldism with café-au-lait macules resulting from a novel mutation of KIT gene in a three-generation Chinese family.
    Li X, Xing X, Liang X, Song C, Yang J, Ren D, Zhou Y.
    Skin Res Technol; 2023 Jun 06; 29(6):e13352. PubMed ID: 37357653
    [Abstract] [Full Text] [Related]

  • 20. A novel mutation of the KIT gene in a Chinese family with piebaldism.
    Wen GD, Zhou C, Yu C, DU J, Xu QX, Liu ZY, Zhang JZ.
    Chin Med J (Engl); 2013 Jun 06; 126(12):2325-8. PubMed ID: 23786947
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.