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English
Combing the genome for the root cause of baldness
scientific article published on 01 November 2008
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
title
Combing the genome for the root cause of baldness
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
author
Irwin McLean
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
author name string
W H Irwin McLean
series ordinal
1
0 references
language of work or name
English
0 references
publication date
1 November 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
volume
40
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
issue
11
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
page(s)
1270-1271
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
cites work
Susceptibility variants for male-pattern baldness on chromosome 20p11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male-pattern baldness susceptibility locus at 20p11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hair follicle-specific keratins and their diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alopecia universalis associated with a mutation in the human hairless gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in hairless dogs implicates FOXI3 in ectodermal development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1108-1270
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1108-1270
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
PubMed publication ID
18957981
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18957981
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18957981%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 December 2019
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