Search Results - "Pelloux, V"
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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children
Published in The Journal of pediatrics (01-08-2001)“…Objective: To search for mutations in melanocortin pathway elements, that is, the melanocortin-4 receptor (MC4R ), agouti-related protein (AGRP ), and…”
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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
Published in Diabetologia (01-02-2000)“…In obese French Caucasian subjects we previously described a silent UCP3 Tyr99Tyr mutation, associated with body mass index. We hypothesised that an unknown…”
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PO37 Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity
Published in Diabetes & metabolism (01-03-2012)“…Introduction Obesity has become a global epidemic and is one the most significant public health challenges of the 21st century. In recent years, more and more…”
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A polymorphism in the 5' untranslated region of the human ob gene is associated with low leptin levels
Published in International Journal of Obesity (01-03-1998)“…To search the human ob gene for mutations and evaluate their role in massive obesity. Direct mutation screening of the gene and case-control association study…”
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Microarray profiling of human white adipose tissue after exogenous leptin injection
Published in European journal of clinical investigation (01-03-2006)“…Background Leptin is a secreted adipocyte hormone that plays a key role in the regulation of body weight homeostasis. The leptin effect on human white adipose…”
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Adipose tissue gene expression in patients with a loss of function mutation in the leptin receptor
Published in International Journal of Obesity (01-12-2002)“…BACKGROUND: In order to maintain body weight regulation, leptin directly or indirectly signals nutritional changes to key organs, but little is known about its…”
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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
Published in Diabetes (New York, N.Y.) (01-02-1999)“…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. K Clément ,…”
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Acyl-CoA-Binding Protein Is a Lipogenic Factor that Triggers Food Intake and Obesity
Published in Cell metabolism (01-10-2019)“…Autophagy facilitates the adaptation to nutritional stress. Here, we show that short-term starvation of cultured cells or mice caused the autophagy-dependent…”
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SMRT-GPS2 corepressor pathway dysregulation coincides with obesity-linked adipocyte inflammation
Published in The Journal of clinical investigation (01-01-2013)“…Low-grade chronic inflammation is a major characteristic of obesity and results from deregulated white adipose tissue function. Consequently, there is interest…”
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Cathepsin S inhibition lowers blood glucose levels in mice
Published in Diabetologia (01-08-2014)“…Aims/hypothesis Cathepsin S (CatS) belongs to a family of proteases that have been implicated in several disease processes. We previously identified CatS as a…”
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Needle and surgical biopsy techniques differentially affect adipose tissue gene expression profiles
Published in The American journal of clinical nutrition (01-01-2009)“…Adipose tissue gene expression analysis in humans now provides a tremendous means to discover the physiopathologic gene targets critical for our understanding…”
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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
Published in Nature (London) (26-03-1998)“…The adipocyte-specific hormone leptin, the product of the obese (ob) gene,regulates adipose-tissue mass through hypothalamic effects on satiety and energy…”
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Adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders
Published in Pharmacy practice : official journal of the GRIPP (Global Research Institute of Pharmacy Practice) (19-12-2007)“…The ability to identify obese individuals who will successfully lose weight in response to dietary intervention will revolutionize disease management…”
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Gene expression profiling of human skeletal muscle in response to stabilized weight loss
Published in The American journal of clinical nutrition (01-07-2008)“…BACKGROUND:Diet-induced weight reduction promotes a decrease in resting energy expenditure that could partly explain the difficulty in maintaining reduced body…”
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Fréquence des mutations des gènes de la voie leptine/mélanocortines dans l’obésité sévère
Published in Nutrition clinique et métabolisme (01-03-2019)“…Clinique. La voie leptine/mélanocortines joue un rôle critique dans le contrôle hypothalamique de la prise alimentaire. Des mutations sur les gènes de cette…”
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Identification de gènes candidats par séquençage d’exome dans l’obésité syndromique
Published in Nutrition clinique et métabolisme (01-09-2016)“…Les obésités syndromiques sont des modèles d’obésité sévère à début précoce, associée à une atteinte multiviscérale (retard mental, dysmorphie, atteintes…”
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Dysregulation of SMRT/GPS2 Corepressor Complex Is Associated with Adipose Tissue Inflammation in Human Obesity
Published in DIABETES & METABOLISM (2012)Get full text
Conference Proceeding -
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SFP CO-69 - Inflammation systémique et tissulaire dans le syndrome de Prader-Willi
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-05-2014)“…Le syndrome de Prader-Willi (SPW) représente un modèle de développement extrême et précoce du tissu adipeux (TA). Le but de ce travail était d’étudier les…”
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Subeutaneous adipose gene expression prior to weight loss can differentiate and weakly predict dietary responders
Published in International Journal of Obesity (01-05-2008)Get full text
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Association between CST3 rs2424577 Polymorphism and Corpulence Related Phenotypes during Lifetime in Populations of European Ancestry
Published in Obesity facts (2011)“…Objective: Cystatin C, a protein coded by CST3 gene, is implicated in adipose tissue biology. Our hypothesis is that common variants in CST3 gene could play a…”
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