NEMO/IKKγ: linking NF-κB to human disease
- 1 October 2001
- journal article
- review article
- Published by Elsevier in Trends in Molecular Medicine
- Vol. 7 (10) , 427-430
- https://doi.org/10.1016/s1471-4914(01)02154-2
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Mutations Leading to X-linked Hypohidrotic Ectodermal Dysplasia Affect Three Major Functional Domains in the Tumor Necrosis Factor Family Member Ectodysplasin-AJournal of Biological Chemistry, 2001
- The Ectodermal Dysplasia Receptor Activates the Nuclear Factor-κB, JNK, and Cell Death Pathways and Binds to Ectodysplasin AJournal of Biological Chemistry, 2001
- Two-Amino Acid Molecular Switch in an Epithelial Morphogen That Regulates Binding to Two Distinct ReceptorsScience, 2000
- NEMO/IKKγ-Deficient Mice Model Incontinentia PigmentiMolecular Cell, 2000
- The IKK complex: an integrator of all signals that activate NF-κB?Trends in Cell Biology, 2000
- Phosphorylation Meets Ubiquitination: The Control of NF-κB ActivityAnnual Review of Immunology, 2000
- Complementation Cloning of NEMO, a Component of the IκB Kinase Complex Essential for NF-κB ActivationCell, 1998
- Requirement for NF-κB in osteoclast and B-cell developmentGenes & Development, 1997
- X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinNature Genetics, 1996
- Ectodermal dysplasias: A clinical classification and a causal reviewAmerican Journal of Medical Genetics, 1994