|
|
Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing
Philippe Froguel
Biotechniques, 2002, 35, pp.1138-1142
Journal articles
hal-00093655v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Identification of two missense mutations in glucokinase linked to early-onset non-insulin-dependent diabetes mellitus
M. Stoffel
,
Ph. Froguel
,
J. Takeda
,
H. Zouali
,
N. Vionnet
et al.
Proceedings of the National Academy of Sciences of the United States of America, 1992, 89, pp.7698-7702
Journal articles
hal-00094195v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Common Polymorphisms In The Adiponectin Gene Acdc Are Not Associated Withdiabetes In Pima Indians.
De Courten Bv
,
Hanson Rl
,
T. Funahashi
,
Lindsay Rs
,
Y. Matsuzawa
et al.
Diabetes, 2005, 54, pp.284-289
Journal articles
hal-00094168v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Lack of association between the Pro(12)Ala polymorphism of the PPAR-gamma2 gene and type 2 diabetes mellitus in the Qatari consanguineous population.
Ramin Badii
,
Abdulbari Bener
,
Mahmoud Zirie
,
Ammar Al-Rikabi
,
Mehmet Simsek
et al.
Journal articles
hal-00172941v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.
Benjamin G Challis
,
Lynn E Pritchard
,
John W M Creemers
,
Jerome Delplanque
,
Julia M Keogh
et al.
Human Molecular Genetics, 2002, 11 (17), pp.1997-2004
Journal articles
hal-00174706v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Expanding the cardiac spectrum of Noonan syndrome with RIT1 variant: Left main coronary artery atresia causing sudden death
Francis Ramond
,
Sébastien Duband
,
Pierre Croisille
,
Hélène Cavé
,
Georges Teyssier
et al.
Journal articles
hal-02071037v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes.
F. Lepretre
,
F. Vasseur
,
M. Vaxillaire
,
Scherer Pe
,
S. Ali
et al.
Human Mutation, 2004, 24, pp.104
Journal articles
hal-00094124v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
In vivo calibration of a subcutaneous sensor for determination of subcutaneous glucose kinetics
G. Velho
,
P. Froguel
,
Daniel R. Thevenot
,
G. Reach
Diab., Nutr. Metab, 1988, 1, pp.227-233
Journal articles
hal-00094172v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France
Samuel Dupont
,
N. Vionnet
,
C. Chèvre
,
Sophie Gallina
,
C. Dina
et al.
Journal articles
hal-01655342v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Le récepteur 4 aux mélanocortines, un paradigme de la génétique de l'obésité
Fanny Stutzmann
Sciences du Vivant [q-bio]. Université du Droit et de la Santé - Lille II, 2009. Français. ⟨NNT : ⟩
Theses
tel-00422165v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Preadipocyte response and impairment of differentiation in an inflammatory environment.
Odile Poulain-Godefroy
,
Philippe Froguel
Journal articles
istex
hal-00173683v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Adiponectin gene polymorphisms and adiponectin levels are independently associated with the development of hyperglycemia during a 3-year period: the epidemiologic data on the insulin resistance syndrome prospective study.
Frédéric Fumeron
,
Roberte Aubert
,
Afshan Siddiq
,
Dina Betoulle
,
Frank Péan
et al.
Journal articles
hal-00174545v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene.
Fanny Stutzmann
,
Vincent Vatin
,
Stéphane Cauchi
,
Anita Morandi
,
Béatrice Jouret
et al.
Journal articles
hal-00172976v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses.
Tetsuo Tsuchiya
,
Schwarz Pe
,
Bosque-Plata Ld
,
Geoffrey Hayes M
,
C. Dina
et al.
Mol Genet Metab, 2006, 89, pp.174-84
Journal articles
hal-00093643v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.
Nabila Bouatia-Naji
,
Vincent Vatin
,
Cécile Lecoeur
,
Barbara Heude
,
Christine Proença
et al.
Journal articles
hal-00173645v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians.
Fernando Gibson
,
Serge Hercberg
,
Philippe Froguel
Diabetes, 2005, 54 (10), pp.3040-2
Journal articles
hal-00174470v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
[ENPP1, the first example of common genetic link between childhood and adult obesity and type 2 diabetes]
David Meyre
,
Philippe Froguel
médecine/sciences, 2006, 22 (3), pp.308-12
Journal articles
hal-00174458v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.
M. Vaxillaire
,
C. Samson
,
H. Cavé
,
C. Metz
,
P. Froguel
et al.
Journal articles
hal-00174747v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in caucasian families.
J. Delplanque
,
M. Barat-Houari
,
C. Dina
,
P. Gallina
,
K. Clément
et al.
Diabetologia, 2000, 43 (12), pp.1554-7
Journal articles
hal-00174921v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects.
A. Siddiq
,
M. Gueorguiev
,
C. Samson
,
S. Hercberg
,
Barbara Heude
et al.
Journal articles
hal-00173827v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects.
S. Cauchi
,
M. Vaxillaire
,
H. Choquet
,
E. Durand
,
A. Duval
et al.
Journal articles
hal-00126948v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Role of the DGAT gene C79T single-nucleotide polymorphism in French obese subjects.
Sylvie Kipfer Coudreau
,
Patrick Tounian
,
Geneviève Bonhomme
,
Philippe Froguel
,
Jean-Philippe Girardet
et al.
Obesity Research, 2003, 11 (10), pp.1163-7
Journal articles
hal-00174573v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Understanding the rising incidence of type 2 diabetes in adolescence.
J. Weill
,
S. Vanderbecken
,
P. Froguel
Archives of Disease in Childhood, 2004, 89 (6), pp.502-4
Journal articles
hal-00174531v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Hypoadiponectinaemia and high risk of type 2 diabetes are associated with adiponectin-encoding (ACDC) gene promoter variants in morbid obesity: evidence for a role of ACDC in diabesity.
F. Vasseur
,
N. Helbecque
,
S. Lobbens
,
V. Vasseur-Delannoy
,
C. Dina
et al.
Journal articles
hal-00174484v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Unexpected genetic associations with human longevity at the Apo E and ACE loci
F. Schachter
,
L. Faure-Delanef
,
H. Rouger
,
F. Guenot
,
Ph. Froguel
et al.
Nature Genetics, 1994, 6, pp.29-32
Journal articles
hal-00094419v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population
Philippe Froguel
Diabetes, 2002, 51, pp.536-540
Journal articles
hal-00093667v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians
Philippe Froguel
Journal of Clinical Endocrinology and Metabolism, 2002, 87, pp.867-869
Journal articles
hal-00093661v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
Two Taq 1 RFLPs at the Glut-2 locus in French Caucasian population
Ph. Froguel
,
N. Vionnet
,
S. Lesage
,
D. Cohen
Nucleic Acids Research, 1991, 19, pp.5799
Journal articles
hal-00094186v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
EIF4A2 Is a Positional Candidate Gene at the 3q27 Locus Linked to Type 2 Diabetes in French Families
C. Cheyssac
,
C. Dina
,
F. Lepretre
,
V. Vasseur-Delannoy
,
A. Dechaume
et al.
Diabetes, 2006, 55, pp.1171-6
Journal articles
hal-00093807v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|
|
|
A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children
Philippe Froguel
Journal of Clinical Endocrinology and Metabolism, 2002, 87, pp.4005-4008
Journal articles
hal-00093604v1
|
Share
Gmail
Facebook
Twitter
LinkedIn
More
|