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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

The Journal of pediatrics, 2001-08, Vol.139 (2), p.204-209

2001

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A genetic variation in the 5 'flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity

Diabetologia, 2000-02, Vol.43 (2), p.245-249

2000

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PO37 Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity

Diabetes & metabolism, 2012-03, Vol.38, p.A30-A31

2012

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A polymorphism in the 5' untranslated region of the human ob gene is associated with low leptin levels

International Journal of Obesity, 1998-03, Vol.22 (3), p.200-205

1998

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SMRT-GPS2 corepressor pathway dysregulation coincides with obesity-linked adipocyte inflammation

The Journal of clinical investigation, 2013-01, Vol.123 (1), p.362-379

2013

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Cathepsin S inhibition lowers blood glucose levels in mice

Diabetologia, 2014-08, Vol.57 (8), p.1674-1683

2014

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Microarray profiling of human white adipose tissue after exogenous leptin injection

European journal of clinical investigation, 2006-03, Vol.36 (3), p.153-163

2006

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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Nature (London), 1998-03, Vol.392 (6674), p.398-401

1998

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Needle and surgical biopsy techniques differentially affect adipose tissue gene expression profiles

The American journal of clinical nutrition, 2009-01, Vol.89 (1), p.51-57

2009

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A sib-pair analysis study of 15 candidate genes in French families with morbid obesity: indication for linkage with islet 1 locus on chromosome 5q

Diabetes (New York, N.Y.), 1999-02, Vol.48 (2), p.398-402

1999

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Adipose tissue gene expression in patients with a loss of function mutation in the leptin receptor

International Journal of Obesity, 2002-12, Vol.26 (12), p.1533-1538

2002

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Adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders

Pharmacy practice : official journal of the GRIPP (Global Research Institute of Pharmacy Practice), 2007-12, Vol.2 (12), p.e1344-e1344

2007

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Fréquence des mutations des gènes de la voie leptine/mélanocortines dans l’obésité sévère

Nutrition clinique et métabolisme, 2019-03, Vol.33 (1), p.19-20

2019

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Gene expression profiling of human skeletal muscle in response to stabilized weight loss

The American journal of clinical nutrition, 2008-07, Vol.88 (1), p.125-132

2008

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Identification de gènes candidats par séquençage d’exome dans l’obésité syndromique

Nutrition clinique et métabolisme, 2016-09, Vol.30 (3), p.260-260

2016

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SFP CO-69 - Inflammation systémique et tissulaire dans le syndrome de Prader-Willi

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2014-05, Vol.21 (5), p.647-647

2014

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O01 Étude du profil inflammatoire systémique et du tissu adipeux de patients ayant une obésité syndromique : exemple du syndrome de Prader-Willi

Nutrition clinique et métabolisme, 2013-12, Vol.27, p.S23-S23

2013

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O01 Étude du profil inflammatoire systémique et du tissu adipeux de patients ayant une obésité syndromique : exemple du syndrome de Prader-Willi

Cahiers de nutrition et de diététique, 2013-12, Vol.48, p.S23-S23

2013

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L’hypoxie chronique intermittente induit les voies physiopathologiques de la NAFLD et modifie le tissu adipeux chez la souris de corpulence normale

Médecine du sommeil, 2015-01, Vol.12 (1), p.11

2015

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Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry

Obesity facts, 2011, Vol.4 (2), p.131-144

2011

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Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity

DIABETES & METABOLISM, 2012, Vol.38, p.A30

2012

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Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients

Diabetes (New York, N.Y.), 1999-01, Vol.48 (1), p.206-208

1999

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Subeutaneous adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders

International Journal of Obesity, 2008-05, Vol.32 (S1-2), p.S19

2008

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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

A genetic variation in the 5 'flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity

Acyl-CoA-Binding Protein Is a Lipogenic Factor that Triggers Food Intake and Obesity

PO37 Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity

A polymorphism in the 5' untranslated region of the human ob gene is associated with low leptin levels

SMRT-GPS2 corepressor pathway dysregulation coincides with obesity-linked adipocyte inflammation

Cathepsin S inhibition lowers blood glucose levels in mice

Microarray profiling of human white adipose tissue after exogenous leptin injection

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Needle and surgical biopsy techniques differentially affect adipose tissue gene expression profiles

A sib-pair analysis study of 15 candidate genes in French families with morbid obesity: indication for linkage with islet 1 locus on chromosome 5q

Adipose tissue gene expression in patients with a loss of function mutation in the leptin receptor

Adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders

Fréquence des mutations des gènes de la voie leptine/mélanocortines dans l’obésité sévère

Gene expression profiling of human skeletal muscle in response to stabilized weight loss

Identification de gènes candidats par séquençage d’exome dans l’obésité syndromique

SFP CO-69 - Inflammation systémique et tissulaire dans le syndrome de Prader-Willi

O01 Étude du profil inflammatoire systémique et du tissu adipeux de patients ayant une obésité syndromique : exemple du syndrome de Prader-Willi

O01 Étude du profil inflammatoire systémique et du tissu adipeux de patients ayant une obésité syndromique : exemple du syndrome de Prader-Willi

L’hypoxie chronique intermittente induit les voies physiopathologiques de la NAFLD et modifie le tissu adipeux chez la souris de corpulence normale

Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry

Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity

Mutation screening and association studies of the human uncoupling protein 3 gene in normoglycemic and diabetic morbidly obese patients

Subeutaneous adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders

Toxoplasmosis in Transplant Recipients, Europe, 2010-2014

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