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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Bibliographic Details
Main Authors: Kutsche, Kerstin (Author) , Schorpp-Kistner, Marina (Author) , Boehm, Thomas (Author)
Format: Article (Journal)
Language:English
Published: 1996
In: Proceedings of the National Academy of Sciences of the United States of America
Year: 1996, Volume: 93, Issue: 18, Pages: 9661-9664
ISSN:1091-6490
DOI:10.1073/pnas.93.18.9661
Online Access: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
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Author Notes:K. Schüddekopf, M. Schorpp, T. Boehm
Description
Summary: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...
Item Description:Gesehen am 23.04.2024
Physical Description:Online Resource
ISSN:1091-6490
DOI:10.1073/pnas.93.18.9661