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Francis Vasseur

Showing results (11-20 of 40) with videos related to

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Human Mutation|June 29, 2004
A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetesFrédéric Leprêtre, Francis Vasseur, Martine Vaxillaire, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 2, 2016
Growth Pattern in Paediatric Crohn Disease Is Related to Inflammatory StatusDelphine Ley, Alain Duhamel, Hélène Behal, et al.
Biochemical and Biophysical Research Communications|August 22, 2006
Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese womenKarin Séron, Laetitia Corset, Francis Vasseur, et al.
Cancer Management and Research|October 2, 2019
Spatial heterogeneity of <i>KRAS</i> mutations in colorectal cancers in northern FranceAnthony Turpin, Michael Genin, Mohamed Hebbar, et al.
Diabetes|April 30, 2002
Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetesMouna Barat-Houari, Karine Clément, Vincent Vatin, et al.
Journal of Human Genetics|February 27, 2010
Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French populationFrancis Vasseur, Thomas Caeyseele, Mouna Barat-Houari, et al.
Diabetes Care|June 28, 2006
Hypoadiponectinemia is associated with progression toward type 2 diabetes and genetic variation in the ADIPOQ gene promoterPeter E H Schwarz, Gordon W Towers, Sabine Fischer, et al.
BMC Medical Genetics|March 20, 2013
The CARD8 p.C10X mutation associates with a low anti-glycans antibody response in patients with Crohn's diseaseFrancis Vasseur, Boualem Sendid, Franck Broly, et al.
Scientific Reports|July 13, 2016
Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease PatientsLaura Choteau, Francis Vasseur, Frederic Lepretre, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 31, 2012
Epidemiology of inflammatory bowel diseases: new insights from a French population-based registry (EPIMAD)Corinne Gower-Rousseau, Francis Vasseur, Mathurin Fumery, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Human Mutation|June 29, 2004
A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetesFrédéric Leprêtre, Francis Vasseur, Martine Vaxillaire, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 2, 2016
Growth Pattern in Paediatric Crohn Disease Is Related to Inflammatory StatusDelphine Ley, Alain Duhamel, Hélène Behal, et al.
Biochemical and Biophysical Research Communications|August 22, 2006
Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese womenKarin Séron, Laetitia Corset, Francis Vasseur, et al.
Cancer Management and Research|October 2, 2019
Spatial heterogeneity of <i>KRAS</i> mutations in colorectal cancers in northern FranceAnthony Turpin, Michael Genin, Mohamed Hebbar, et al.
Diabetes|April 30, 2002
Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetesMouna Barat-Houari, Karine Clément, Vincent Vatin, et al.
Journal of Human Genetics|February 27, 2010
Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French populationFrancis Vasseur, Thomas Caeyseele, Mouna Barat-Houari, et al.
Diabetes Care|June 28, 2006
Hypoadiponectinemia is associated with progression toward type 2 diabetes and genetic variation in the ADIPOQ gene promoterPeter E H Schwarz, Gordon W Towers, Sabine Fischer, et al.
BMC Medical Genetics|March 20, 2013
The CARD8 p.C10X mutation associates with a low anti-glycans antibody response in patients with Crohn's diseaseFrancis Vasseur, Boualem Sendid, Franck Broly, et al.
Scientific Reports|July 13, 2016
Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease PatientsLaura Choteau, Francis Vasseur, Frederic Lepretre, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 31, 2012
Epidemiology of inflammatory bowel diseases: new insights from a French population-based registry (EPIMAD)Corinne Gower-Rousseau, Francis Vasseur, Mathurin Fumery, et al.
Pageof 4