DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations-Reference-Cited by-同舟云学术

DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations

Published:2014-02-25 Issue:14 Volume:23 Page:3830-3842
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Restelli Michela,Lopardo Teresa,Lo Iacono Nadia,Garaffo Giulia,Conte Daniele,Rustighi Alessandra,Napoli Marco,Del Sal Giannino,Perez-Morga David,Costanzo Antonio,Merlo Giorgio Roberto,Guerrini Luisa

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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3. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly;J. Orthop. Res.,2004

4. p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation;Am. J. Hum. Genet.,2001

5. p63 is a p53 homologue required for limb and epidermal morphogenesis;Nature,1999

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