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Showing results (81-90 of 225) with videos related to

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Diabetes|October 1, 1995
Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptorS Gremlich, A Porret, E H Hani, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|February 9, 2007
Two Caucasian families with the hepatocyte nuclear factor-1alpha mutation Tyr218CysM Hummel, F Vasseur, C Mathieu, et al.
Obesity Research|April 17, 1998
Leptin receptor gene in a large cohort of massively obese subjects: no indication of the fa/fa rat mutation. Detection of an intronic variant with no association with obesityV Rolland, K Clément, I Dugail, et al.
Journal of Neuroendocrinology|June 10, 2000
B219/OB-R 5'-UTR and leptin receptor gene-related protein gene expression in mouse brain and placenta: tissue-specific leptin receptor promoter activityJ G Mercer, K M Moar, N Hoggard, et al.
Diabetes & Metabolism|January 7, 1998
Gender effect of the Trp64Arg mutation in the beta 3 adrenergic receptor gene on weight gain in morbid obesityK Clement, B S Manning, A Basdevant, et al.
Diabetes|September 30, 1998
No association between the Friedreich's ataxia gene and NIDDM in the French populationS Dupont, D Dubois, N Vionnet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French CaucasiansE H Hani, S Dupont, E Durand, et al.
Diabetologia|February 7, 2001
A genetic variation in the 5' flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activityS Otabe, K Clement, C Dina, et al.
Diabetes|June 1, 1996
The Gly40Ser mutation in the human glucagon receptor gene associated with NIDDM results in a receptor with reduced sensitivity to glucagonL H Hansen, N Abrahamsen, J Hager, et al.
The Journal of Clinical Investigation|January 1, 1997
Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetesM C Garin, R W James, P Dussoix, et al.
Pageof 23

Showing results (81-90 of 225) with videos related to

Sort By:
Pageof 23
Diabetes|October 1, 1995
Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptorS Gremlich, A Porret, E H Hani, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|February 9, 2007
Two Caucasian families with the hepatocyte nuclear factor-1alpha mutation Tyr218CysM Hummel, F Vasseur, C Mathieu, et al.
Obesity Research|April 17, 1998
Leptin receptor gene in a large cohort of massively obese subjects: no indication of the fa/fa rat mutation. Detection of an intronic variant with no association with obesityV Rolland, K Clément, I Dugail, et al.
Journal of Neuroendocrinology|June 10, 2000
B219/OB-R 5'-UTR and leptin receptor gene-related protein gene expression in mouse brain and placenta: tissue-specific leptin receptor promoter activityJ G Mercer, K M Moar, N Hoggard, et al.
Diabetes & Metabolism|January 7, 1998
Gender effect of the Trp64Arg mutation in the beta 3 adrenergic receptor gene on weight gain in morbid obesityK Clement, B S Manning, A Basdevant, et al.
Diabetes|September 30, 1998
No association between the Friedreich's ataxia gene and NIDDM in the French populationS Dupont, D Dubois, N Vionnet, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French CaucasiansE H Hani, S Dupont, E Durand, et al.
Diabetologia|February 7, 2001
A genetic variation in the 5' flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activityS Otabe, K Clement, C Dina, et al.
Diabetes|June 1, 1996
The Gly40Ser mutation in the human glucagon receptor gene associated with NIDDM results in a receptor with reduced sensitivity to glucagonL H Hansen, N Abrahamsen, J Hager, et al.
The Journal of Clinical Investigation|January 1, 1997
Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetesM C Garin, R W James, P Dussoix, et al.
Pageof 23