Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1 (Q28259397)

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J R Wyeth

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C J Mayne

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L E O'Gorman

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N G Martin

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R A Sturm

A high-resolution map of the brown (b, Tyrp1) deletion complex of mouse chromosome 4.

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language of work or name

English

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publication date

January 1998

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published in

Mammalian Genome

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volume

9

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page(s)

50-3

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issue

1

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cites work

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Dinucleotide repeat polymorphism at the human TYRP1 locus

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Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair

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Tyrosinase and related proteins in mammalian pigmentation

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RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.

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Molecular and developmental genetics of mouse coat color

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The tyrosinase-related protein-1 gene has a structure and promoter sequence very different from tyrosinase

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Subfamily structure and evolution of the human L1 family of repetitive sequences

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Reconstruction and analysis of human alu genes

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

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A simple salting out procedure for extracting DNA from human nucleated cells

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

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Downstream region of the human tyrosinase-related protein gene enhances its promoter activity

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Expression studies of pigmentation and POU-domain genes in human melanoma cells

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Chromosomal structure of the human TYRP1 and TYRP2 loci and comparison of the tyrosinase-related protein gene family

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Cell number and distribution in human and rat airways

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Fibroblasts co-expressing tyrosinase and the b-protein synthesize both eumelanin and phaeomelanin

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Functional analysis of microphthalmia-associated transcription factor in pigment cell-specific transcription of the human tyrosinase family genes

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Low nucleotide diversity in man

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12 December 2020

The mouse brown (b) locus protein has dopachrome tautomerase activity and is located in lysosomes in transfected fibroblasts

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12 December 2020

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

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12 December 2020

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele

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12 December 2020

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Tyrosinases from two different loci are expressed by normal and by transformed melanocytes.

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Unraveling the melanocyte.

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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"

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Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles

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Contribution of melanogenic proteins to the heterogeneous pigmentation of human melanocytes

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Structural organization of the pigment cell-specific gene located at the brown locus in mouse. Its promoter activity and alternatively spliced transcript.

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The tyrosinase gene family--interactions of melanogenic proteins to regulate melanogenesis

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A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1).

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A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.

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12 December 2020

Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)

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12 December 2020