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ectodermal dysplasia, hypohidrotic, with immune deficiency
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IKBKG
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations
A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
I����B-���� controls the constitutive NF-����B target gene network and survival of ABC DLBCL
Selective inhibition of NF-kappaB activation by a peptide that blocks the interaction of NEMO with the IkappaB kinase complex
Use of cell permeable NBD peptides for suppression of inflammation
The future of peptide-based drugs
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