Pelloux V - Search Results

1

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.

Otabe S, Clement K, Dina C, Pelloux V, Guy-Grand B, Froguel P, Vasseur F. Otabe S, et al. Among authors: pelloux v. Diabetologia. 2000 Feb;43(2):245-9. doi: 10.1007/s001250050037. Diabetologia. 2000. PMID: 10753049

2

Chronic intermittent hypoxia triggers cardiac fibrosis: Role of epididymal white adipose tissue senescent remodeling?

Naushad S, Gaucher J, Mezdari Z, Détrait M, Belaidi E, Zhang Y, Vial G, Bouyon S, Czibik G, Pini M, Aldekwer S, Liang H, Pelloux V, Aron-Wisnewsky J, Tamisier R, Pépin JL, Derumeaux G, Sawaki D, Arnaud C. Naushad S, et al. Among authors: pelloux v. Acta Physiol (Oxf). 2024 Nov;240(11):e14231. doi: 10.1111/apha.14231. Epub 2024 Sep 12. Acta Physiol (Oxf). 2024. PMID: 39263916

3

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

Clément K, Vaisse C, Lahlou N, Cabrol S, Pelloux V, Cassuto D, Gourmelen M, Dina C, Chambaz J, Lacorte JM, Basdevant A, Bougnères P, Lebouc Y, Froguel P, Guy-Grand B. Clément K, et al. Among authors: pelloux v. Nature. 1998 Mar 26;392(6674):398-401. doi: 10.1038/32911. Nature. 1998. PMID: 9537324

4

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

Hager J, Clement K, Francke S, Dina C, Raison J, Lahlou N, Rich N, Pelloux V, Basdevant A, Guy-Grand B, North M, Froguel P. Hager J, et al. Among authors: pelloux v. Int J Obes Relat Metab Disord. 1998 Mar;22(3):200-5. doi: 10.1038/sj.ijo.0800567. Int J Obes Relat Metab Disord. 1998. PMID: 9539186

5

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

Otabe S, Clement K, Dubois S, Lepretre F, Pelloux V, Leibel R, Chung W, Boutin P, Guy-Grand B, Froguel P, Vasseur F. Otabe S, et al. Among authors: pelloux v. Diabetes. 1999 Jan;48(1):206-8. Diabetes. 1999. PMID: 9892245 No abstract available.

6

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.

Clément K, Dina C, Basdevant A, Chastang N, Pelloux V, Lahlou N, Berlan M, Langin D, Guy-Grand B, Froguel P. Clément K, et al. Among authors: pelloux v. Diabetes. 1999 Feb;48(2):398-402. doi: 10.2337/diabetes.48.2.398. Diabetes. 1999. PMID: 10334320

7

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

Dubern B, Clément K, Pelloux V, Froguel P, Girardet JP, Guy-Grand B, Tounian P. Dubern B, et al. Among authors: pelloux v. J Pediatr. 2001 Aug;139(2):204-9. doi: 10.1067/mpd.2001.116284. J Pediatr. 2001. PMID: 11487744

8

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

Clément K, Vega N, Laville M, Pelloux V, Guy-Grand B, Basdevant A, Vidal H. Clément K, et al. Among authors: pelloux v. Int J Obes Relat Metab Disord. 2002 Dec;26(12):1533-8. doi: 10.1038/sj.ijo.0802180. Int J Obes Relat Metab Disord. 2002. PMID: 12461669

9

Adiponectin gene expression in subcutaneous adipose tissue of obese women in response to short-term very low calorie diet and refeeding.

Liu YM, Lacorte JM, Viguerie N, Poitou C, Pelloux V, Guy-Grand B, Coussieu C, Langin D, Basdevant A, Clément K. Liu YM, et al. Among authors: pelloux v. J Clin Endocrinol Metab. 2003 Dec;88(12):5881-6. doi: 10.1210/jc.2003-030886. J Clin Endocrinol Metab. 2003. PMID: 14671185

10

Association between CST3 rs2424577 polymorphism and corpulence related phenotypes during lifetime in populations of European ancestry.

Hooton H, Dubern B, Henegar C, Paternoster L, Nohr EA, Alili R, Rousseau F, Pelloux V, Galan P, Hercberg S, Arner P, Sørensen TI, Clément K. Hooton H, et al. Among authors: pelloux v. Obes Facts. 2011;4(2):131-44. doi: 10.1159/000327797. Epub 2011 Apr 15. Obes Facts. 2011. PMID: 21577020 Free PMC article.

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