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Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
title
Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
author
Joanne Voisey
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
author name string
Justin Graf
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Ian Hughes
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Angela van Daal
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
language of work or name
English
0 references
publication date
1 July 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
volume
28
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
page(s)
710-717
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
issue
7
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
cites work
The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage disequilibrium analysis identifies an FGFR1 haplotype-tag SNP associated with normal variation in craniofacial shape
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LDA—a java-based linkage disequilibrium analyzer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of Aim-1 as the underwhite mouse mutant and its transcriptional regulation by MITF
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism in the agouti signaling protein gene is associated with human pigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the MATP gene causes the cream coat colour in the horse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinctive distribution of AIM1 polymorphism among major human populations with different skin color
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for recent positive selection at the human AIM1 locus in a European population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic association and cellular function of MC1R variant alleles in human pigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new allelic series for the underwhite gene on mouse chromosome 15.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism study of the human Agouti gene and its association with MC1R.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism in the agouti signalling protein (ASIP) is associated with decreased levels of mRNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MATP polymorphisms in Germans and Japanese: the L374F mutation as a population marker for Caucasoids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20504
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/HUMU.20504
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
Fatcat ID
release_gy4tfrf6gbcutfrqgomdkupreu
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/gy4tfrf6gbcutfrqgomdkupreu
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed ID
17358008
1 reference
stated in
Europe PubMed Central
PubMed ID
17358008
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17358008%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 December 2019
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