Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q34117142)
Watch
English
Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author
Hans van Bokhoven
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
Frank McKeon
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 March 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Trends in Molecular Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
133-139
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
Surfing the p53 network
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p73 is a simian [correction of human] p53-related protein that can induce apoptosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel protein with strong homology to the tumor suppressor p53.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and functional analysis of human p51, which structurally and functionally resembles p53
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A second p53-related protein, p73L, with high homology to p73.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new human p53 homologue
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p63 is a p53 homologue required for limb and epidermal morphogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p53 mutations in human cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preferential formation of benzo[a]pyrene adducts at lung cancer mutational hotspots in P53.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Slow repair of pyrimidine dimers at p53 mutation hotspots in skin cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Van der Woude syndrome (dominantly inherited lip pits and clefts).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ADULT syndrome allelic to limb mammary syndrome (LMS)?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TP63 gene mutation in ADULT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serrate2 is disrupted in the mouse limb-development mutant syndactylism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p63 identifies keratinocyte stem cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vertebrate limb development--the early stages in chick and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Stem cell fate and patterning in mammalian epidermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Signalling networks regulating dental development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of craniofacial development and malformation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in GJB6 cause hidrotic ectodermal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
AIS is an oncogene amplified in squamous cell carcinoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1471-4914(01)02260-2
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed ID
11879774
1 reference
stated in
Europe PubMed Central
PubMed ID
11879774
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit