Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans. (Q34117142)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

review article

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title

Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans (English)

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7 December 2019

1

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7 December 2019

author name string

Frank McKeon

series ordinal

2

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7 December 2019

publication date

1 March 2002

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Trends in Molecular Medicine

7 December 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

volume

8

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7 December 2019

issue

3

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7 December 2019

page(s)

133-139

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7 December 2019

cites work

Surfing the p53 network

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7 January 2021

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

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7 January 2021

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

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7 January 2021

Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours

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7 January 2021

Monoallelically Expressed Gene Related to p53 at 1p36, a Region Frequently Deleted in Neuroblastoma and Other Human Cancers

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7 January 2021

p73 is a simian [correction of human] p53-related protein that can induce apoptosis

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7 January 2021

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities

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7 January 2021

A novel protein with strong homology to the tumor suppressor p53.

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7 January 2021

Cloning and functional analysis of human p51, which structurally and functionally resembles p53

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7 January 2021

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7 January 2021

A new human p53 homologue

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7 January 2021

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

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7 January 2021

p63 is a p53 homologue required for limb and epidermal morphogenesis

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7 January 2021

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27

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7 January 2021

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

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7 January 2021

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

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7 January 2021

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

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7 January 2021

Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome

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7 January 2021

p53 mutations in human cancers

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7 January 2021

Preferential formation of benzo[a]pyrene adducts at lung cancer mutational hotspots in P53.

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7 January 2021

Slow repair of pyrimidine dimers at p53 mutation hotspots in skin cancer

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7 January 2021

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

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7 January 2021

The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition

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7 January 2021

The Van der Woude syndrome (dominantly inherited lip pits and clefts).

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7 January 2021

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

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7 January 2021

ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia

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7 January 2021

ADULT syndrome allelic to limb mammary syndrome (LMS)?

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7 January 2021

TP63 gene mutation in ADULT syndrome

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7 January 2021

Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

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7 January 2021

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

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7 January 2021

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

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7 January 2021

A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.

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7 January 2021

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2

7 January 2021

Serrate2 is disrupted in the mouse limb-development mutant syndactylism

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7 January 2021

p63 identifies keratinocyte stem cells

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7 January 2021

Vertebrate limb development--the early stages in chick and mouse

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7 January 2021

Stem cell fate and patterning in mammalian epidermis

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7 January 2021

Signalling networks regulating dental development

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7 January 2021

Genetics of craniofacial development and malformation

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7 January 2021

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2

7 January 2021

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2

7 January 2021

Mutations in GJB6 cause hidrotic ectodermal dysplasia

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902260-2

7 January 2021

AIS is an oncogene amplified in squamous cell carcinoma

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7 January 2021

10.1016/S1471-4914(01)02260-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11879774%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference