Posttranslational cleavage of proinsulin is blocked by a point mutation in familial hyperproinsulinemia.

Ítems similars

• A novel point mutation in the human insulin gene giving rise to hyperproinsulinemia (proinsulin Kyoto).
  per: Yano, H, et al.
  Publicat: (1992)
• A mutation in the B chain coding region is associated with impaired proinsulin conversion in a family with hyperproinsulinemia.
  per: Chan, S J, et al.
  Publicat: (1987)
• Familial hyperproinsulinemia: partial characterization of circulating proinsulin-like material.
  per: Gabbay, K H, et al.
  Publicat: (1979)
• Familial hyperproinsulinemia. Two cohorts secreting indistinguishable type II intermediates of proinsulin conversion.
  per: Robbins, D C, et al.
  Publicat: (1984)
• Glucocorticoids increase insulin binding and the amount of insulin-receptor mRNA in human cultured lymphocytes.
  per: Shibasaki, Y, et al.
  Publicat: (1988)