Mutation of the Ectodysplasin-A Gene Results in Bone Defects in Mice

This publication has 20 references indexed in Scilit:

• Three‐dimensional microimaging (MRμI and μCT), finite element modeling, and rapid prototyping provide unique insights into bone architecture in osteoporosis
  The Anatomical Record, 2001
• The Ectodermal Dysplasia Receptor Activates the Nuclear Factor-κB, JNK, and Cell Death Pathways and Binds to Ectodysplasin A
  Journal of Biological Chemistry, 2001
• Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells.
  Human Molecular Genetics, 1999
• Involvement of a novel Tnf receptor homologue in hair follicle induction
  Nature Genetics, 1999
• Direct Three-Dimensional Morphometric Analysis of Human Cancellous Bone: Microstructural Data from Spine, Femur, Iliac Crest, and Calcaneus
  Journal of Bone and Mineral Research, 1999
• Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain
  Human Molecular Genetics, 1997
• X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
  Nature Genetics, 1996
• Anhidrosis and Absence of Sweat Glands in Mice Hemizygous for the Tabby Gene; Supportive Evidence for the Hypothesis of Homology Between Tabby and Human Anhidrotic (Hypohidrotic) Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)
  Journal of Investigative Dermatology, 1986
• Technique for Revealing the Three-Dimensional Architecture of Whole Preserved Spiculated Invertebrates
  Stain Technology, 1984
• Effects of the flexed‐tailed gene on the development of the house mouse
  Journal of Morphology, 1935