X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
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Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
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Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors
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TAB 2, TRAF6 and TAK1 are involved in NF-kappaB activation induced by the TNF-receptor, EDAR and its adaptator EDARADD
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A rare case of hypohidrotic ectodermal dysplasia caused by compound heterozygous mutations in the EDAR gene
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Characterization of human keratin-associated protein 2 (KRTAP2) gene family
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Mutational analysis of TRAF6 reveals a conserved functional role of the RING dimerization interface and a potentially necessary but insufficient role of RING-dependent TRAF6 polyubiquitination towards NF-jB activation
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