Literature DB >> 7860080

Detection of a Tsp509I polymorphism in the 3' UTR of the human tyrosinase related protein-1 (TYRP) gene.

S C Wildenberg1, R A King, W S Oetting.   

Abstract

We have identified a Tsp509I polymorphism in the 3' UTR of the human tyrosinase related protein-1 gene (TYRP). TYRP is one of several genes involved in melanin pigment production.

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Year:  1995        PMID： 7860080     DOI： 10.1007/bf00209417

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  2 in total

1.  Nucleotide sequence of the cDNA encoding human tyrosinase-related protein.

Authors:  T Cohen; R M Muller; Y Tomita; S Shibahara
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

2.  Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization.

Authors:  V V Murty; B Bouchard; S Mathew; S Vijayasaradhi; A N Houghton
Journal:  Genomics       Date:  1992-05       Impact factor: 5.736
  2 in total
  2 in total

1.  Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

Authors:  P Manga; J G Kromberg; N F Box; R A Sturm; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

2.  Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1.

Authors:  N F Box; J R Wyeth; C J Mayne; L E O'Gorman; N G Martin; R A Sturm
Journal:  Mamm Genome       Date:  1998-01       Impact factor: 2.957
  2 in total

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