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Diabetes|July 2, 1998
Chronic central leptin infusion enhances insulin-stimulated glucose metabolism and favors the expression of uncoupling proteinsI Cusin, K E Zakrzewska, O Boss, et al.
Circulation|January 29, 2003
Protective role of uncoupling protein 2 in atherosclerosisJ Blanc, M C Alves-Guerra, B Esposito, et al.
Prenatal Diagnosis|December 2, 2009
Gestational age-related reference values for amniotic fluid organic acidsC Ottolenghi, N Abermil, A Lescoat, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|August 1, 1994
DNA polymorphism in the uncoupling protein (UCP) gene and human body fatJ M Oppert, M C Vohl, M Chagnon, et al.
Magnesium Research|September 1, 1991
Magnesium and thermoregulation. I. Newborn and infant. Is sudden infant death syndrome a magnesium-dependent disease of the transition from chemical to physical thermoregulation?J Durlach, V Durlach, Y Rayssiguier, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|October 2, 1998
Analysis of the uncoupling protein-1 (UCP1) gene in obese and lean subjects: identification of four amino acid variantsA Hamann, J Tafel, B Büsing, et al.
Biochemical and Biophysical Research Communications|June 27, 1997
Kupffer cells are a dominant site of uncoupling protein 2 expression in rat liverD Larrouy, P Laharrague, G Carrera, et al.
FEBS Letters|January 1, 1999
Increased uncoupling protein-2 and -3 gene expressions in skeletal muscle of STZ-induced diabetic ratsH Kageyama, A Suga, M Kashiba, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 31, 2002
Changes in FAT/CD36, UCP2, UCP3 and GLUT4 gene expression during lipid infusion in rat skeletal and heart muscleR Vettor, R Fabris, R Serra, et al.
Clinical Pharmacology and Therapeutics|May 28, 2010
Long-term follow-up of bezafibrate treatment in patients with the myopathic form of carnitine palmitoyltransferase 2 deficiencyJ P Bonnefont, J Bastin, P Laforêt, et al.
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