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P Froguel

Showing results (61-70 of 225) with videos related to

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Biotechniques|May 22, 2002
Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencingB Neve, P Froguel, L Corset, et al.
Diabetologia|January 25, 2007
A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese populationM Horikoshi, K Hara, C Ito, et al.
Diabetes|July 1, 1997
Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2qE H Hani, J Hager, A Philippi, et al.
The Journal of Clinical Investigation|July 21, 2000
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesityC Vaisse, K Clement, E Durand, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1994
Phenotyping is an accurate means of analysing the principal apolipoprotein E isoformsR W James, J Ruiz, H Blanché, et al.
Diabetes & Metabolism|March 1, 1997
Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?A Ktorza, C Bernard, V Parent, et al.
Biotechniques|May 1, 1994
Nonradioactive screening of glucokinase mutations in maturity onset diabetes of the youngH Blanché, J Hager, F Sun, et al.
The Journal of Biological Chemistry|December 10, 1999
Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutationsM Vaxillaire, A Abderrahmani, P Boutin, et al.
Diabetologia|December 29, 2000
An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohortA Meirhaeghe, P Amouyel, N Helbecque, et al.
Diabetes|May 20, 1998
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French CaucasiansJ C Chèvre, E H Hani, D A Stoffers, et al.
Pageof 23

Showing results (61-70 of 225) with videos related to

Sort By:
Pageof 23
Biotechniques|May 22, 2002
Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencingB Neve, P Froguel, L Corset, et al.
Diabetologia|January 25, 2007
A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese populationM Horikoshi, K Hara, C Ito, et al.
Diabetes|July 1, 1997
Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2qE H Hani, J Hager, A Philippi, et al.
The Journal of Clinical Investigation|July 21, 2000
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesityC Vaisse, K Clement, E Durand, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1994
Phenotyping is an accurate means of analysing the principal apolipoprotein E isoformsR W James, J Ruiz, H Blanché, et al.
Diabetes & Metabolism|March 1, 1997
Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?A Ktorza, C Bernard, V Parent, et al.
Biotechniques|May 1, 1994
Nonradioactive screening of glucokinase mutations in maturity onset diabetes of the youngH Blanché, J Hager, F Sun, et al.
The Journal of Biological Chemistry|December 10, 1999
Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutationsM Vaxillaire, A Abderrahmani, P Boutin, et al.
Diabetologia|December 29, 2000
An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohortA Meirhaeghe, P Amouyel, N Helbecque, et al.
Diabetes|May 20, 1998
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French CaucasiansJ C Chèvre, E H Hani, D A Stoffers, et al.
Pageof 23