(Q40783379)

23 September 2017

1 reference

title

From gene to protein: determination of melanin synthesis (English)

1 reference

23 September 2017

K Urabe

1

1 reference

23 September 2017

P Aroca

series ordinal

2

1 reference

23 September 2017

V J Hearing

series ordinal

3

1 reference

23 September 2017

language of work or name

1 reference

1 August 1993

1 reference

Pigment Cell & Melanoma Research

23 September 2017

published in

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23 September 2017

volume

6

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23 September 2017

issue

4 Pt 1

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23 September 2017

page(s)

186-192

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Human tyrosinase gene, mapped to chromosome 11 (q14----q21), defines second region of homology with mouse chromosome 7.

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Molecular characterization of the mouse agouti locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Characteristic sequences in the upstream region of the human tyrosinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Detection of point mutation in the tyrosinase gene of a Japanese albino patient by a direct sequencing of amplified DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Sequence analysis of mouse tyrosinase cDNA and the effect of melanotropin on its gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Positive and negative elements regulate a melanocyte-specific promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Novel myosin heavy chain encoded by murine dilute coat colour locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Mosaic expression of a tyrosinase fusion gene in albino mice yields a heritable striped coat color pattern in transgenic homozygotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Subcellular distribution of tyrosinase and tyrosinase-related protein-1: implications for melanosomal biogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

A point mutation in the tyrosinase gene of BALB/c albino mouse causing the cysteine----serine substitution at position 85.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Expression of tyrosinase gene in amelanotic mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

The melanoma antigen gp75 is the human homologue of the mouse b (brown) locus gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Structural and functional characterization of full-length heparin-binding growth associated molecule

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Light is a dominant mouse mutation resulting in premature cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

Isolation, Chromosomal Mapping, and Expression of the Mouse Tyrosinase Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0749.1993.TB00601.X

10.1111/J.1600-0749.1993.TB00601.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference