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. 16, Iss. 23, 2007-12 ,pp. : 2805-2815

Oxford University Press

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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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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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