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Unraveling the melanocyte.
scientific article published in January 1993
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
editorial
0 references
title
Unraveling the melanocyte
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
author name string
Hearing VJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
language of work or name
English
0 references
publication date
1 January 1993
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
volume
52
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
page(s)
1-7
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
cites work
A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Human tyrosinase gene, mapped to chromosome 11 (q14----q21), defines second region of homology with mouse chromosome 7.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
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25 May 2018
A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
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25 May 2018
Cloning and expression of cDNA encoding mouse tyrosinase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Nucleotide sequence of the cDNA encoding human tyrosinase-related protein
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
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25 May 2018
Novel myosin heavy chain encoded by murine dilute coat colour locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Structural organization of the pigment cell-specific gene located at the brown locus in mouse. Its promoter activity and alternatively spliced transcript.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Mapping the human CAS2 gene, the homologue of the mouse brown (b) locus, to human chromosome 9p22-pter
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
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25 May 2018
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Molecular characterization of a region of DNA associated with mutations at the agouti locus in the mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Enzymatic control of pigmentation in mammals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The kit ligand: A cell surface molecule altered in steel mutant fibroblasts
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
A second tyrosinase-related protein, TRP-2, is a melanogenic enzyme termed DOPAchrome tautomerase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
5,6-Dihydroxyindole-2-carboxylic acid is incorporated in mammalian melanin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Molecular cloning and expression of the human melanocyte stimulating hormone receptor cDNA.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The cloning of a family of genes that encode the melanocortin receptors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
25 May 2018
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
15 August 2018
Light is a dominant mouse mutation resulting in premature cell death
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682135
retrieved
1 December 2018
A melanocyte-specific complementary DNA clone whose expression is inducible by melanotropin and isobutylmethyl xanthine
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8434579
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Isolation, Chromosomal Mapping, and Expression of the Mouse Tyrosinase Gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8434579
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Molecular basis of tyrosinase-negative oculocutaneous albinism. A single base mutation in the tyrosinase gene causing arginine to glutamine substitution at position 59
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8434579
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Direct Molecular Identification of the Mouse Pink-Eyed Unstable Mutation by Genome Scanning
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8434579
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Molecular Analysis of an Extended Family with Type IA (Tyrosinase-Negative) Oculocutaneous Albinism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8434579
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1682135
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PubMed ID
8434579
1 reference
stated in
Europe PubMed Central
PMCID
1682135
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434579%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
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