BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 1909058)

  • 1. Nucleotide sequence of the putative human tyrosinase pseudogene.
    Takeda A; Matsunaga J; Tomita Y; Tagami H; Shibahara S
    Tohoku J Exp Med; 1991 Apr; 163(4):295-7. PubMed ID: 1909058
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations of the tyrosinase gene in oculocutaneous albinism.
    Shibahara S
    Pigment Cell Res; 1992 Nov; 5(5 Pt 2):279-83. PubMed ID: 1292010
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification.
    Chaki M; Mukhopadhyay A; Ray K
    Hum Mutat; 2005 Jul; 26(1):53-8. PubMed ID: 15895460
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sequence-based diagnosis of tyrosinase-related oculocutaneous albinism: successful sequence analysis of the tyrosinase gene from blood spots dried on filter paper.
    Matsunaga J; Dakeishi-Hara M; Miyamura Y; Nakamura E; Tanita M; Satomura K; Tomita Y
    Dermatology; 1998; 196(2):189-93. PubMed ID: 9568405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.
    Matsunaga J; Takeda A; Tomita Y; Hara M; Shibahara S; Tagami H
    J Dermatol Sci; 1992 May; 3(3):181-5. PubMed ID: 1498098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.
    King RA; Mentink MM; Oetting WS
    Mol Biol Med; 1991 Feb; 8(1):19-29. PubMed ID: 1943686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of the DNA segments cross-hybridizable to the tyrosinase gene in patients affected with oculocutaneous albinism.
    Takeda A; Matsunaga J; Tomita Y; Tagami H; Shibahara S
    Tohoku J Exp Med; 1989 Dec; 159(4):333-40. PubMed ID: 2517365
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment.
    Giebel LB; Strunk KM; Spritz RA
    Genomics; 1991 Mar; 9(3):435-45. PubMed ID: 1903356
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification and functional validation of a 5' upstream regulatory sequence in the human tyrosinase gene homologous to the locus control region of the mouse tyrosinase gene.
    Regales L; Giraldo P; García-Díaz A; Lavado A; Montoliu L
    Pigment Cell Res; 2003 Dec; 16(6):685-92. PubMed ID: 14629727
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The tyrosinase gene in gorillas and the albinism of 'Snowflake'.
    Martínez-Arias R; Comas D; Andrés A; Abelló MT; Domingo-Roura X; Bertranpetit J
    Pigment Cell Res; 2000 Dec; 13(6):467-70. PubMed ID: 11153699
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phylogeny of regulatory regions of vertebrate tyrosinase genes.
    Yamamoto H; Kudo T; Masuko N; Miura H; Sato S; Tanaka M; Tanaka S; Takeuchi S; Shibahara S; Takeuchi T
    Pigment Cell Res; 1992 Nov; 5(5 Pt 2):284-94. PubMed ID: 1292011
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evolution of the tyrosinase related gene (TYRL) in primates.
    Oetting WS; Stine OC; Townsend D; King RA
    Pigment Cell Res; 1993 Jun; 6(3):171-7. PubMed ID: 8234203
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of a partial pseudogene homologous to the Hermansky-Pudlak syndrome gene HPS-1; relevance for mutation detection.
    Huizing M; Anikster Y; Gahl WA
    Hum Genet; 2000 Mar; 106(3):370-3. PubMed ID: 10798370
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Insertion of a novel transposable element in the tyrosinase gene is responsible for an albino mutation in the medaka fish, Oryzias latipes.
    Koga A; Inagaki H; Bessho Y; Hori H
    Mol Gen Genet; 1995 Dec; 249(4):400-5. PubMed ID: 8552044
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of oculocutaneous albinism by analysis of the fetal tyrosinase gene.
    Shimizu H; Niizeki H; Suzumori K; Aozaki R; Kawaguchi R; Hikiji K; Nishikawa T
    J Invest Dermatol; 1994 Jul; 103(1):104-6. PubMed ID: 8027570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.
    Giebel LB; Strunk KM; King RA; Hanifin JM; Spritz RA
    Proc Natl Acad Sci U S A; 1990 May; 87(9):3255-8. PubMed ID: 1970634
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple alternatively spliced transcripts of the mouse tyrosinase-encoding gene.
    Porter S; Mintz B
    Gene; 1991 Jan; 97(2):277-82. PubMed ID: 1900251
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles.
    Budd PS; Jackson IJ
    Genomics; 1995 Sep; 29(1):35-43. PubMed ID: 8530099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic structure and evolutionary conservation of the tyrosinase gene family from Fugu.
    Camacho-Hübner A; Richard C; Beermann F
    Gene; 2002 Feb; 285(1-2):59-68. PubMed ID: 12039032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.