(Q35958046)

11 August 2017

Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene (English)

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11 August 2017

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oculocutaneous albinism

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S Rosemblat

1

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11 August 2017

D Durham-Pierre

2

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11 August 2017

J M Gardner

3

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11 August 2017

Y Nakatsu

4

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11 August 2017

M H Brilliant

5

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11 August 2017

S J Orlow

6

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11 August 2017

language of work or name

English

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publication date

1 December 1994

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Proceedings of the National Academy of Sciences of the United States of America

11 August 2017

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11 August 2017

91

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11 August 2017

25

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11 August 2017

12071-12075

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A Quantitative Histological Study of the Pigment Found in the Coat-Color Mutants of the House Mouse. IV. the Nature of the Effects of Genic Substitution in Five Major Allelic Series

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Effect of genic substitution on the incorporation of tyrosine into the melanin of mouse skin

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

High-molecular-weight forms of tyrosinase and the tyrosinase-related proteins: evidence for a melanogenic complex

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Phase separation of integral membrane proteins in Triton X-114 solution

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Improved tools for biological sequence comparison

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Uptake of radioactive DOPA by Mycobacterium leprae in vitro

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Assay of diphenoloxidase--difficulties and how to avoid them.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Membrane glycoproteins common to vesicles and melanosomes in mouse melanoma cells

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Postnatal ocular expression of tyrosinase and related proteins: disruption by the pink-eyed unstable (p(un)) mutation.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Levels of tyrosinase and its mRNA in coat-color mutants of C57BL/10J congenic mice: effects of genic substitution at the agouti, brown, albino, dilute, and pink-eyed dilution loci

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=45378

Human melanocytes cultured from nevi and melanomas

24 September 2018

1 reference

12 December 2020

Direct Molecular Identification of the Mouse Pink-Eyed Unstable Mutation by Genome Scanning

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12 December 2020

Genetic variations in the fine structure and ontogeny of mouse melanin granules

1 reference

12 December 2020

Pink-eyed dilution (p) gene in rodents: Increased pigmentation in tissue culture

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12 December 2020

Biosynthesis, glycosylation, movement through the Golgi system, and transport to lysosomes by an N-linked carbohydrate-independent mechanism of three lysosomal integral membrane proteins

1 reference

12 December 2020

Ophthalmologic, biochemical, platelet, and ultrastructural defects in the various types of oculocutaneous albinism

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12 December 2020

Subcellular localization of melanin biosynthesis

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12 December 2020

Selective aberration and pigment loss in melanosomes of malignant melanoma cells in vitro by glycosylation inhibitors: premelanosomes as glycoprotein

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.91.25.12071

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11 August 2017

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1 reference

11 August 2017

PubMed publication ID

7991586

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