Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti

By Sebban-Benin Hlne   Pescatore Alessandra   Fusco Francesca   Pascuale Valrie   Gautheron Jrmie   Yamaoka Shoji   Moncla Anne   Ursini Matilde Valeria   Courtois Gilles  

Human Molecular Genetics, Vol. 17, Iss. 4, 2008-02 ,pp. : 639-639

Oxford University Press

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Identification of a new NEMO/TRAF6 interface affected in incontinentia pigmenti pathology

By Gautheron Jrmie   Pescatore Alessandra   Fusco Francesca   Esposito Elio   Yamaoka Shoji   Agou Fabrice   Ursini Matilde Valeria   Courtois Gilles  

Human Molecular Genetics, Vol. 19, Iss. 16, 2010-08 ,pp. : 3138-3149

Oxford University Press

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Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling

By Nenci Arianna   Huth Marion   Funteh Alfred   Schmidt-Supprian Marc   Bloch Wilhelm   Metzger Daniel   Chambon Pierre   Rajewsky Klaus   Krieg Thomas   Haase Ingo   Pasparakis Manolis  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 531-542

Oxford University Press

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A recurrent deletion in the ubiquitously expressed NEMO ( IKK- γ) gene accounts for the vast majority of incontinentia pigmenti mutations

By D’Urso M.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2171-2179

Oxford University Press

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Somatic mosaicism of a novel IKBKG mutation in a male patient with incontinentia pigmenti

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1601-1604

John Wiley & Sons Inc

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