Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.

Documenti analoghi

• Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships.
  di: Gidh-Jain, M, et al.
  Pubblicazione: (1993)
• Insulin secretory defects in polycystic ovary syndrome. Relationship to insulin sensitivity and family history of non-insulin-dependent diabetes mellitus.
  di: Ehrmann, D A, et al.
  Pubblicazione: (1995)
• Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.
  di: Stoffel, M, et al.
  Pubblicazione: (1992)
• Association with Nitric Oxide Synthase on Insulin Secretory Granules Regulates Glucokinase Protein Levels
  di: Markwardt, Michele L., et al.
  Pubblicazione: (2012)
• Antenatal Diagnosis of Fetal Genotype Determines if Maternal Hyperglycemia Due to a Glucokinase Mutation Requires Treatment
  di: Chakera, Ali J., et al.
  Pubblicazione: (2012)