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 *

121 related articles for article (PubMed ID: 8428754)

  • 1. Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism.
    Colman MA; Stevens G; Ramsay M; Kwon B; Jenkins T
    Hum Genet; 1993 Jan; 90(5):556-60. PubMed ID: 8428754
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.
    Kedda MA; Stevens G; Manga P; Viljoen C; Jenkins T; Ramsay M
    Am J Hum Genet; 1994 Jun; 54(6):1078-84. PubMed ID: 8198130
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In quest of the tyrosinase-positive oculocutaneous albinism gene.
    Jenkins T; Heim RA; Dunn DS; Zwane E; Colman MA; Ramsay M; Kromberg JG
    Ophthalmic Paediatr Genet; 1990 Dec; 11(4):251-4. PubMed ID: 1982896
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.
    Oetting WS; King RA
    Hum Mutat; 1993; 2(1):1-6. PubMed ID: 8477259
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The tyrosinase-positive oculocutaneous albinism locus is not linked to the beta-globin locus in man.
    Heim RA; Dunn DS; Candy SE; Zwane E; Kromberg JG; Jenkins T
    Hum Genet; 1988 May; 79(1):89. PubMed ID: 3130302
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparative genetics of albinism.
    Searle AG
    Ophthalmic Paediatr Genet; 1990 Sep; 11(3):159-64. PubMed ID: 2126367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic mapping of the dominant albino locus in rainbow trout (Oncorhynchus mykiss).
    Nakamura K; Ozaki A; Akutsu T; Iwai K; Sakamoto T; Yoshizaki G; Okamoto N
    Mol Genet Genomics; 2001 Jun; 265(4):687-93. PubMed ID: 11459189
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pigmented skin lesions in tyrosinase-positive oculocutaneous albinos: a study in black South Africans.
    Bothwell JE
    Int J Dermatol; 1997 Nov; 36(11):831-6. PubMed ID: 9427075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.
    Tripathi RK; Strunk KM; Giebel LB; Weleber RG; Spritz RA
    Am J Med Genet; 1992 Jul; 43(5):865-71. PubMed ID: 1642278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetics of oculocutaneous albinism].
    Zühlke C; Stell A; Käsmann-Kellner B
    Ophthalmologe; 2007 Aug; 104(8):674-80. PubMed ID: 17646993
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion.
    Coupry I; Taine L; Goizet C; Soriano C; Mortemousque B; Arveiler B; Lacombe D
    J Med Genet; 2001 Jan; 38(1):35-8. PubMed ID: 11134238
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The molecular basis of type I (tyrosinase-deficient) human oculocutaneous albinism.
    Giebel LB; Spritz RA
    Pigment Cell Res; 1992; Suppl 2():101-6. PubMed ID: 1409411
    [No Abstract]   [Full Text] [Related]  

  • 15. A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.
    Giebel LB; Tripathi RK; King RA; Spritz RA
    J Clin Invest; 1991 Mar; 87(3):1119-22. PubMed ID: 1900309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene.
    Sundaresan P; Sil AK; Philp AR; Randolph MA; Natchiar G; Namperumalsamy P
    Mol Vis; 2004 Dec; 10():1005-10. PubMed ID: 15635296
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Human oculocutaneous albinism. From clinical observation to molecular biology].
    Aquaron R
    Bull Soc Pathol Exot; 1993; 86(5):313-26. PubMed ID: 8124097
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sequence analysis of tyrosinase gene in ocular and oculocutaneous albinism patients: introducing three novel mutations.
    Khordadpoor-Deilamani F; Akbari MT; Karimipoor M; Javadi G
    Mol Vis; 2015; 21():730-5. PubMed ID: 26167114
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Might the refractive state in oculocutaneous albino patients be a clue for distinguishing between tyrosinase-positive and tyrosinase-negative forms of oculocutaneous albinism?
    Käsmann B; Ruprecht KW
    Ger J Ophthalmol; 1996 Nov; 5(6):422-7. PubMed ID: 9479530
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.