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11. Joint effect of insulin signaling genes on all-cause mortality

15. Early-Onset Diabetes in an Infant with a Novel Frameshift Mutation in LRBA

23. Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia

27. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy

28. Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia.

31. Gain of Function of Malate Dehydrogenase 2 and Familial Hyperglycemia

32. Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus

37. Serum Resistin, Cardiovascular Disease and All-Cause Mortality in Patients with Type 2 Diabetes

38. ENPP1 Affects Insulin Action and Secretion: Evidences from In Vitro Studies

39. ENPP1 Q121 Variant, Increased Pulse Pressure and Reduced Insulin Signaling, and Nitric Oxide Synthase Activity in Endothelial Cells

42. The PPARγ2P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus

44. GALNT2 Expression Is Reduced in Patients with Type 2 Diabetes: Possible Role of Hyperglycemia.

45. Mutations in the APPL1 Gene May Contribute to Familial Diabetes Mellitus

46. Modulation of ENPP1 (PC-1) Gene Expression by Heat Shock Protein 70.

47. Inflammation and prediction of death in type 2 diabetes. Evidence of an intertwined link with tryptophan metabolism.

48. The -318 C>G single-nucleotide polymorphism in GNAI2 gene promoter region impairs transcriptional activity through specific binding of Sp1 transcription factor and is associated with high blood pressure in Caucasians from Italy.

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