(Q55670365)

https://api.crossref.org/works/10.1177%2F154405910308200606

Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

p63 and p73 transactivate differentiation gene promoters in human keratinocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

p63 is a p53 homologue required for limb and epidermal morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Mixed clefting type in Rapp-Hodgkin syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Association of p63 with proliferative potential in normal and neoplastic human keratinocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

p63 identifies keratinocyte stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Rapp-Hodgkin ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Rapp-Hodgkin ectodermal dysplasia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

p53 Family members p63 and p73 are SAM domain-containing proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

Ectodermal dysplasia and multiple defects (Rapp-Hodgkins type).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

p63 and p73 are required for p53-dependent apoptosis in response to DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F154405910308200606

10.1177/154405910308200606

21 January 2018

Identifiers

DOI

0 references

Fatcat ID

release_47dpwru6bzampoy6jmmgft5auy

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/47dpwru6bzampoy6jmmgft5auy