The whn transcription factor encoded by the nude locus contains an evolutionarily conserved and functionally indispensable activation domain.

Mutations in the whn gene are associated with the phenotype of congenital athymia - and hairlessness in mouse and rat. The whn gene encodes a presump...

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Detalles Bibliográficos
Autores principales: Kutsche, Kerstin (Autor) , Schorpp-Kistner, Marina (Autor) , Boehm, Thomas (Autor)
Formato: Article (Journal)
Lenguaje:inglés
Publicado: 1996
In: Proceedings of the National Academy of Sciences of the United States of America
Year: 1996, Volumen: 93, Número: 18, Pages: 9661-9664
ISSN:1091-6490
DOI:10.1073/pnas.93.18.9661
Acceso en línea:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1073/pnas.93.18.9661
Verlag, lizenzpflichtig, Volltext: https://www.pnas.org/doi/abs/10.1073/pnas.93.18.9661
Enlace del recurso
Notas de Autor:K. Schüddekopf, M. Schorpp, T. Boehm
Descripción
Sumario:Mutations in the whn gene are associated with the phenotype of congenital athymia - and hairlessness in mouse and rat. The whn gene encodes a presump...
Notas:Gesehen am 23.04.2024
Descripción Física:Online Resource
ISSN:1091-6490
DOI:10.1073/pnas.93.18.9661