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Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.Blood|April 1, 1994
Putative oncogenic role of the erythropoietin receptor in murine and human erythroleukemia cellsS Chretien, F Moreau-Gachelin, F Apiou, et al.Nature Genetics|March 10, 2001
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signalingR Döffinger, A Smahi, C Bessia, et al.Cell|July 10, 1998
Complementation cloning of NEMO, a component of the IkappaB kinase complex essential for NF-kappaB activationS Yamaoka, G Courtois, C Bessia, et al.Cell Death and Differentiation|October 13, 2007
Inhibition of the NF-kappaB survival pathway via caspase-dependent cleavage of the IKK complex scaffold protein and NF-kappaB essential modulator NEMOC Frelin, V Imbert, V Bottero, et al.Genes, Chromosomes & Cancer|September 1, 1990
The 11q13 amplicon of a mammary carcinoma cell lineM Lafage, C Nguyen, P Szepetowski, et al.Blood|July 15, 1995
Tyrosine phosphorylation of the erythropoietin receptor: role for differentiation and mitogenic signal transductionS Gobert, F Porteu, S Pallu, et al.Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.Human Molecular Genetics|October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutationsS Aradhya, H Woffendin, T Jakins, et al.Pageof 7