Incontinentia pigmenti: the first single gene disorder due to disrupted NF-kappa B function

Ernst Schering Res Found Workshop. 2002:(36):95-107. doi: 10.1007/978-3-662-04667-8_6.
No abstract available

MeSH terms

  • Alleles
  • Animals
  • Ectodermal Dysplasia / genetics
  • Female
  • Humans
  • I-kappa B Kinase
  • Incontinentia Pigmenti / genetics*
  • Male
  • Mice
  • Models, Biological
  • Models, Genetic
  • Mutation
  • NF-kappa B / genetics*
  • NF-kappa B / physiology
  • Phenotype
  • Protein Serine-Threonine Kinases / metabolism
  • X Chromosome / genetics

Substances

  • NF-kappa B
  • Protein Serine-Threonine Kinases
  • CHUK protein, human
  • Chuk protein, mouse
  • I-kappa B Kinase
  • IKBKB protein, human
  • IKBKE protein, human
  • Ikbkb protein, mouse
  • Ikbke protein, mouse