(Q34394973)

1 August 2017

title

Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation (English)

1 reference

single-nucleotide polymorphism

1 August 2017

main subject

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Justin Graf

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1 August 2017

Richard Hodgson

series ordinal

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1 August 2017

Angela van Daal

series ordinal

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1 August 2017

language of work or name

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1 March 2005

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1 August 2017

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

278-284

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Characterization of Melanocyte Stimulating Hormone Receptor Variant Alleles in Twins with Red Hair

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Identification of Aim-1 as the underwhite mouse mutant and its transcriptional regulation by MITF

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Regulation of the catalytic activity of preexisting tyrosinase in black and Caucasian human melanocyte cell cultures

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Evidence for variable selective pressures at MC1R

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

A polymorphism in the agouti signaling protein gene is associated with human pigmentation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Organization and sequence of the human P gene and identification of a new family of transport proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

The underwhite (uw) locus acts autonomously and reduces the production of melanin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

A mutation in the MATP gene causes the cream coat colour in the horse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Distinctive distribution of AIM1 polymorphism among major human populations with different skin color

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Genetics of Hair and Skin Color

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Apportionment of global human genetic diversity based on craniometrics and skin color

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

A new allelic series for the underwhite gene on mouse chromosome 15.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

A polymorphism study of the human Agouti gene and its association with MC1R.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Population Differences in the Frequency of the Agouti Signaling Protein g.8818A > G Polymorphism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20143

7 January 2021

Identifiers

DOI

10.1002/HUMU.20143

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1 August 2017

1 reference