A murine model of autosomal dominant neurohypophyseal diabetes insipidus reveals progressive loss of vasopressin-producing neurons

Lignende værker

• Molecular basis of autosomal dominant neurohypophyseal diabetes insipidus. Cellular toxicity caused by the accumulation of mutant vasopressin precursors within the endoplasmic reticulum.
  af: Ito, M, et al.
  Udgivet: (1997)
• A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.
  af: Bahnsen, U, et al.
  Udgivet: (1992)
• Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.
  af: Rittig, S., et al.
  Udgivet: (1996)
• Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family
  af: Kim, Myo-Jing, et al.
  Udgivet: (2014)
• Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP-NPII gene
  af: Yang, Hongbo, et al.
  Udgivet: (2019)