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

147 related items for PubMed ID: 11179026

  • 1. In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.
    Manga P, Kromberg J, Turner A, Jenkins T, Ramsay M.
    Am J Hum Genet; 2001 Mar; 68(3):782-7. PubMed ID: 11179026
    [Abstract] [Full Text] [Related]

  • 2. Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.
    Manga P, Kromberg JG, Box NF, Sturm RA, Jenkins T, Ramsay M.
    Am J Hum Genet; 1997 Nov; 61(5):1095-101. PubMed ID: 9345097
    [Abstract] [Full Text] [Related]

  • 3. Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.
    Kerr R, Stevens G, Manga P, Salm S, John P, Haw T, Ramsay M.
    Hum Mutat; 2000 Nov; 15(2):166-72. PubMed ID: 10649493
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.
    Wang Y, Wang Z, Chen M, Fan N, Yang J, Liu L, Wang Y, Liu X.
    PLoS One; 2015 Nov; 10(4):e0125651. PubMed ID: 25919014
    [Abstract] [Full Text] [Related]

  • 8. The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
    Ramsay M, Colman MA, Stevens G, Zwane E, Kromberg J, Farrall M, Jenkins T.
    Am J Hum Genet; 1992 Oct; 51(4):879-84. PubMed ID: 1415228
    [Abstract] [Full Text] [Related]

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

  • 10. The pink-eyed dilution gene and the molecular pathogenesis of tyrosinase-positive albinism (OCA2).
    Manga P, Orlow SJ.
    J Dermatol; 1999 Nov; 26(11):738-47. PubMed ID: 10635616
    [No Abstract] [Full Text] [Related]

  • 11. Molecular basis of oculocutaneous albinism.
    Oetting WS, King RA.
    J Invest Dermatol; 1994 Nov; 103(5 Suppl):131S-136S. PubMed ID: 7963676
    [Abstract] [Full Text] [Related]

  • 12. Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2).
    Lee ST, Nicholls RD, Schnur RE, Guida LC, Lu-Kuo J, Spinner NB, Zackai EH, Spritz RA.
    Hum Mol Genet; 1994 Nov; 3(11):2047-51. PubMed ID: 7874125
    [Abstract] [Full Text] [Related]

  • 13. Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.
    Forshew T, Khaliq S, Tee L, Smith U, Johnson CA, Mehdi SQ, Maher ER.
    Clin Genet; 2005 Aug; 68(2):182-4. PubMed ID: 15996218
    [No Abstract] [Full Text] [Related]

  • 14. Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism.
    Preising MN, Forster H, Gonser M, Lorenz B.
    Mol Vis; 2011 Apr 15; 17():939-48. PubMed ID: 21541274
    [Abstract] [Full Text] [Related]

  • 15. Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".
    Boissy RE, Zhao H, Oetting WS, Austin LM, Wildenberg SC, Boissy YL, Zhao Y, Sturm RA, Hearing VJ, King RA, Nordlund JJ.
    Am J Hum Genet; 1996 Jun 15; 58(6):1145-56. PubMed ID: 8651291
    [Abstract] [Full Text] [Related]

  • 16. Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.
    Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA.
    N Engl J Med; 1994 Feb 24; 330(8):529-34. PubMed ID: 8302318
    [Abstract] [Full Text] [Related]

  • 17. The etiology of oculocutaneous albinism (OCA) type II: the pink protein modulates the processing and transport of tyrosinase.
    Toyofuku K, Valencia JC, Kushimoto T, Costin GE, Virador VM, Vieira WD, Ferrans VJ, Hearing VJ.
    Pigment Cell Res; 2002 Jun 24; 15(3):217-24. PubMed ID: 12028586
    [Abstract] [Full Text] [Related]

  • 18. Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.
    Stevens G, Ramsay M, Jenkins T.
    Hum Genet; 1997 Apr 24; 99(4):523-7. PubMed ID: 9099845
    [Abstract] [Full Text] [Related]

  • 19. A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
    Rinchik EM, Bultman SJ, Horsthemke B, Lee ST, Strunk KM, Spritz RA, Avidano KM, Jong MT, Nicholls RD.
    Nature; 1993 Jan 07; 361(6407):72-6. PubMed ID: 8421497
    [Abstract] [Full Text] [Related]

  • 20. Ancestral origins of TYR and OCA2 gene mutations in oculocutaneous albinism from two admixed populations in Colombia.
    Cárdenas WA, Conley AB, Nagar SD, Núñez-Ríos DL, Jordan IK, Lattig MC.
    PLoS One; 2024 Jan 07; 19(11):e0313777. PubMed ID: 39556609
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.