AbstractInositol trisphosphate, when added to permeabilized rat fat cells, led to a several-fold increase of pyruvate dehydrogenase activity due to conversion of the inactive phospho form (PDHb) to the active, dephospho form (PDHa). It is suggested that inositol trisphosphate, probably through intracellular Ca2+-mobilisation, acts as a physiological mediator of insulin for activation of the mitochondrial PDH-complex
Phosphatidylinositide (PI) 3-kinase binds to tyrosyl-phosphorylated insulin receptor substrate-1 (IR...
AbstractPemeabilised, dimethyl sulphoxide-differentiated HL-60 human myelomonocytic leukemia cells a...
In isolated rat adipocytes, the insulin stimulation of pyruvate dehydrogenase can be partially inhib...
AbstractInositol trisphosphate, when added to permeabilized rat fat cells, led to a several-fold inc...
Abstractα1-Adrenergic activation of isolated brown adipocytes causes a rapid mobilization of intrace...
AbstractGlucose-induced insulin secretion from pancreatic β-cells depends on mitochondrial activatio...
In L6 skeletal muscle cells and immortalized hepatocytes, insulin induced a 2-fold increase in the a...
Factors underlying the transience of inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] accumulation follow...
Glucose-induced insulin secretion from pancreatic β-cells depends on mitochondrial activation. In th...
Inositides are key cellular regulators, but their role in physiology has often lagged behind our und...
We have previously shown that inositol-1,4,5-trisphosphate (IP3) releases Ca2+ from an intracellular...
In L6 skeletal muscle cells and immortalized hepatocytes, insulin induced a 2-fold increase in the a...
In the present study we identify inosine-5' monophosphate dehydrogenase (IMPDH), a key enzyme in de ...
AbstractWe studied the effects of insulin on the incorporation of 32Pi into phospholipids in rat fat...
AbstractEffects of membrane potential and cytosolic free Ca2+ concentrations ([Ca2+]i) on acetycholi...
Phosphatidylinositide (PI) 3-kinase binds to tyrosyl-phosphorylated insulin receptor substrate-1 (IR...
AbstractPemeabilised, dimethyl sulphoxide-differentiated HL-60 human myelomonocytic leukemia cells a...
In isolated rat adipocytes, the insulin stimulation of pyruvate dehydrogenase can be partially inhib...
AbstractInositol trisphosphate, when added to permeabilized rat fat cells, led to a several-fold inc...
Abstractα1-Adrenergic activation of isolated brown adipocytes causes a rapid mobilization of intrace...
AbstractGlucose-induced insulin secretion from pancreatic β-cells depends on mitochondrial activatio...
In L6 skeletal muscle cells and immortalized hepatocytes, insulin induced a 2-fold increase in the a...
Factors underlying the transience of inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] accumulation follow...
Glucose-induced insulin secretion from pancreatic β-cells depends on mitochondrial activation. In th...
Inositides are key cellular regulators, but their role in physiology has often lagged behind our und...
We have previously shown that inositol-1,4,5-trisphosphate (IP3) releases Ca2+ from an intracellular...
In L6 skeletal muscle cells and immortalized hepatocytes, insulin induced a 2-fold increase in the a...
In the present study we identify inosine-5' monophosphate dehydrogenase (IMPDH), a key enzyme in de ...
AbstractWe studied the effects of insulin on the incorporation of 32Pi into phospholipids in rat fat...
AbstractEffects of membrane potential and cytosolic free Ca2+ concentrations ([Ca2+]i) on acetycholi...
Phosphatidylinositide (PI) 3-kinase binds to tyrosyl-phosphorylated insulin receptor substrate-1 (IR...
AbstractPemeabilised, dimethyl sulphoxide-differentiated HL-60 human myelomonocytic leukemia cells a...
In isolated rat adipocytes, the insulin stimulation of pyruvate dehydrogenase can be partially inhib...