Master regulatory role of p63 in epidermal development and disease.
Soares, Eduardo; Zhou, Huiqing.
Cell Mol Life Sci
; 75(7): 1179-1190, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29103147
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Ectodermal dysplasias: the p63 tail.
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling.
Etiology and pathogenesis of ectodermal dysplasias.
WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
Aplasia cutis congenita : mise au point et prise en charge.
Ectodermal dysplasias: a clinical and molecular review.
ORAI1 mutations abolishing store-operated Ca<sup>2+</sup> entry cause anhidrotic ectodermal dysplasia with immunodeficiency.
Using implants for prosthodontic rehabilitation of a 4-year-old with ectodermal dysplasia.
Implant-supported Oral Rehabilitation in Child with Ectodermal Dysplasia - 4-year Follow-up.