A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.

Παρόμοια τεκμήρια

• Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.
  ανά: Rittig, S., κ.ά.
  Έκδοση: (1996)
• Structural organization of the rat gene for the arginine vasopressin-neurophysin precursor.
  ανά: Schmale, H, κ.ά.
  Έκδοση: (1983)
• Molecular basis of autosomal dominant neurohypophyseal diabetes insipidus. Cellular toxicity caused by the accumulation of mutant vasopressin precursors within the endoplasmic reticulum.
  ανά: Ito, M, κ.ά.
  Έκδοση: (1997)
• A murine model of autosomal dominant neurohypophyseal diabetes insipidus reveals progressive loss of vasopressin-producing neurons
  ανά: Russell, Theron A., κ.ά.
  Έκδοση: (2003)
• Immunological identification of a common precursor to arginine vasopressin and neurophysin II synthesized by in vitro translation of bovine hypothalamic mRNA.
  ανά: Schmale, H, κ.ά.
  Έκδοση: (1981)