Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Froguel

Showing results (181-190 of 225) with videos related to

Pageof 23
Sort By:
American Journal of Human Genetics|January 1, 1997
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6M Delépine, F Pociot, C Habita, et al.
Diabetes & Metabolism|January 27, 2005
Genetic study of the CD36 gene in a French diabetic populationF Leprêtre, K J Linton, C Lacquemant, et al.
International Journal of Obesity (2005)|October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French populationS Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Biochimica Et Biophysica Acta|July 2, 2014
Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetesP Perimenis, T Bouckenooghe, J Delplanque, et al.
Diabetes|April 1, 1996
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutationG Velho, M M Byrne, K Clément, et al.
Diabetes & Metabolism|April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous familyA Bonnefond, E Vaillant, J Philippe, et al.
Nature Genetics|March 4, 2000
The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetesG Waeber, J Delplanque, C Bonny, et al.
Diabetes & Metabolism|April 3, 2012
European genetic variants associated with type 2 diabetes in North African ArabsS Cauchi, I Ezzidi, Y El Achhab, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Diabetologia|July 19, 2012
GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetesA Bonnefond, O Sand, B Guerin, et al.
Pageof 23

Showing results (181-190 of 225) with videos related to

Sort By:
Pageof 23
American Journal of Human Genetics|January 1, 1997
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6M Delépine, F Pociot, C Habita, et al.
Diabetes & Metabolism|January 27, 2005
Genetic study of the CD36 gene in a French diabetic populationF Leprêtre, K J Linton, C Lacquemant, et al.
International Journal of Obesity (2005)|October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French populationS Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Biochimica Et Biophysica Acta|July 2, 2014
Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetesP Perimenis, T Bouckenooghe, J Delplanque, et al.
Diabetes|April 1, 1996
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutationG Velho, M M Byrne, K Clément, et al.
Diabetes & Metabolism|April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous familyA Bonnefond, E Vaillant, J Philippe, et al.
Nature Genetics|March 4, 2000
The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetesG Waeber, J Delplanque, C Bonny, et al.
Diabetes & Metabolism|April 3, 2012
European genetic variants associated with type 2 diabetes in North African ArabsS Cauchi, I Ezzidi, Y El Achhab, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Diabetologia|July 19, 2012
GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetesA Bonnefond, O Sand, B Guerin, et al.
Pageof 23