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Author Correction: Genomic and epigenomic mapping of leptin-responsive neuronal populations involved in body weight regulation. Nat Metab. 2024 Mar; 6(3):598.
Inoue F, Eckalbar WL, Wang Y, Murphy KK, Matharu N, Vaisse C, Ahituv N. PMID: 38429391.
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PubMed Mentions: Fields:
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Postnatal Dynamic Ciliary ARL13B and ADCY3 Localization in the Mouse Brain. Cells. 2024 Jan 30; 13(3).
Brewer KK, Brewer KM, Terry TT, Caspary T, Vaisse C, Berbari NF. PMID: 38334651; PMCID: PMC10854790.
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PubMed Mentions: Fields:
Translation:
Animals
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Identification of AgRP cells in the murine hindbrain that drive feeding. Mol Metab. 2024 Feb; 80:101886.
Bachor TP, Hwang E, Yulyaningsih E, Attal K, Mifsud F, Pham V, Vagena E, Huarcaya R, Valdearcos M, Vaisse C, Williams KW, Emmerson PJ, Xu AW. PMID: 38246589; PMCID: PMC10844855.
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PubMed Mentions:
1 Fields:
Translation:
Animals
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Ciliary ARL13B prevents obesity in mice. bioRxiv. 2023 Aug 04.
Terry TT, Gigante ED, Alexandre CM, Brewer KM, Engle SE, Yue X, Berbari NF, Vaisse C, Caspary T. PMID: 37577625; PMCID: PMC10418222.
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1522-P: Identification of AgRP Cells in the Murine Hindbrain That Drive Feeding. Diabetes. 2023 Jun 20; 72(Supplement_1).
BACHOR BT, ATTAL AK, VAGENA VE, MIFSUD MF, PHAM PV, VALDEARCOS-CONTRERAS VM, VAISSE VC, XU XA. .
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Physiological Condition-Dependent Changes in Ciliary GPCR Localization in the Brain. eNeuro. 2023 03; 10(3).
Brewer KM, Engle SE, Bansal R, Brewer KK, Jasso KR, McIntyre JC, Vaisse C, Reiter JF, Berbari NF. PMID: 36849261; PMCID: PMC10012409.
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PubMed Mentions:
4 Fields:
Translation:
AnimalsCells
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MRAP2 regulates energy homeostasis by promoting primary cilia localization of MC4R. JCI Insight. 2023 01 24; 8(2).
Bernard A, Ojeda Naharros I, Yue X, Mifsud F, Blake A, Bourgain-Guglielmetti F, Ciprin J, Zhang S, McDaid E, Kim K, Nachury MV, Reiter JF, Vaisse C. PMID: 36692018; PMCID: PMC9977312.
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PubMed Mentions:
5 Fields:
Translation:
HumansCells
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KLF15 cistromes reveal a hepatocyte pathway governing plasma corticosteroid transport and systemic inflammation. Sci Adv. 2022 Mar 11; 8(10):eabj2917.
Jiang Z, Elsarrag SZ, Duan Q, LaGory EL, Wang Z, Alexanian M, McMahon S, Rulifson IC, Winchester S, Wang Y, Vaisse C, Brown JD, Quattrocelli M, Lin CY, Haldar SM. PMID: 35263131; PMCID: PMC8906731.
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PubMed Mentions:
4 Fields:
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Melanocortin 4 receptor signals at the neuronal primary cilium to control food intake and body weight. J Clin Invest. 2021 05 03; 131(9).
Wang Y, Bernard A, Comblain F, Yue X, Paillart C, Zhang S, Reiter JF, Vaisse C. PMID: 33938449; PMCID: PMC8087202.
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PubMed Mentions:
31 Fields:
Translation:
AnimalsCells
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OR04-01 MRAP2 Regulates Energy Homeostasis by Promoting Primary Cilia Localization of MC4R. Journal of the Endocrine Society. 2020 May 8; 4(Supplement_1):or04-01-.
Bernard BA, Naharros NI, Guglielmetti GF, Yue YX, Vaisse VC. .
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Detailed 3-dimensional body shape features predict body composition, blood metabolites, and functional strength: the Shape Up! studies. Am J Clin Nutr. 2019 12 01; 110(6):1316-1326.
Ng BK, Sommer MJ, Wong MC, Pagano I, Nie Y, Fan B, Kennedy S, Bourgeois B, Kelly N, Liu YE, Hwaung P, Garber AK, Chow D, Vaisse C, Curless B, Heymsfield SB, Shepherd JA. PMID: 31553429; PMCID: PMC6885475.
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PubMed Mentions:
47 Fields:
Translation:
Humans
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CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiency. . 2019 Sep 12.
N NM, S SR, S ST, L LM, Y YW, A AB, A AH, WL WE, C CV, N NA. .
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Genomic and epigenomic mapping of leptin-responsive neuronal populations involved in body weight regulation. Nat Metab. 2019 04; 1(4):475-484.
Inoue F, Eckalbar WL, Wang Y, Murphy KK, Matharu N, Vaisse C, Ahituv N. PMID: 31535083; PMCID: PMC6750255.
View in:
PubMed Mentions:
9 Fields:
Translation:
HumansAnimalsCells
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CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiency. Science. 2019 01 18; 363(6424).
Matharu N, Rattanasopha S, Tamura S, Maliskova L, Wang Y, Bernard A, Hardin A, Eckalbar WL, Vaisse C, Ahituv N. PMID: 30545847; PMCID: PMC6570489.
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PubMed Mentions:
133 Fields:
Translation:
AnimalsCells
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Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesity. Nat Genet. 2018 02; 50(2):180-185.
Siljee JE, Wang Y, Bernard AA, Ersoy BA, Zhang S, Marley A, Von Zastrow M, Reiter JF, Vaisse C. PMID: 29311635; PMCID: PMC5805646.
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PubMed Mentions:
113 Fields:
Translation:
HumansAnimalsCells
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Cilia and Obesity. Cold Spring Harb Perspect Biol. 2017 Jul 05; 9(7).
Vaisse C, Reiter JF, Berbari NF. PMID: 28096262; PMCID: PMC5495057.
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PubMed Mentions:
55 Fields:
Translation:
HumansAnimalsCells
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Acute Lesioning and Rapid Repair of Hypothalamic Neurons outside the Blood-Brain Barrier. Cell Rep. 2017 06 13; 19(11):2257-2271.
Yulyaningsih E, Rudenko IA, Valdearcos M, Dahlén E, Vagena E, Chan A, Alvarez-Buylla A, Vaisse C, Koliwad SK, Xu AW. PMID: 28614713; PMCID: PMC5651178.
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PubMed Mentions:
25 Fields:
Translation:
AnimalsCells
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The Association of Serum Leptin with Mortality in Older Adults. PLoS One. 2015; 10(10):e0140763.
Mishra S, Harris TB, Hsueh WC, Hue T, Leak TS, Li R, Mehta M, Vaisse C, Sahyoun NR. PMID: 26473487; PMCID: PMC4608587.
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PubMed Mentions:
10 Fields:
Translation:
HumansCTClinical Trials
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Genetic association study of adiposity and melanocortin-4 receptor (MC4R) common variants: replication and functional characterization of non-coding regions. PLoS One. 2014; 9(5):e96805.
Evans DS, Calton MA, Kim MJ, Kwok PY, Miljkovic I, Harris T, Koster A, Liu Y, Tranah GJ, Ahituv N, Hsueh WC, Vaisse C. PMID: 24820477; PMCID: PMC4018404.
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PubMed Mentions:
15 Fields:
Translation:
HumansAnimals
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Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia. Obesity (Silver Spring). 2014 Feb; 22 Suppl 1:S1-S17.
Heymsfield SB, Avena NM, Baier L, Brantley P, Bray GA, Burnett LC, Butler MG, Driscoll DJ, Egli D, Elmquist J, Forster JL, Goldstone AP, Gourash LM, Greenway FL, Han JC, Kane JG, Leibel RL, Loos RJ, Scheimann AO, Roth CL, Seeley RJ, Sheffield V, Tauber M, Vaisse C, Wang L, Waterland RA, Wevrick R, Yanovski JA, Zinn AR. PMID: 24574081; PMCID: PMC4159941.
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PubMed Mentions:
40 Fields:
Translation:
Humans
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Functional characterization of SIM1-associated enhancers. Hum Mol Genet. 2014 Apr 01; 23(7):1700-8.
Kim MJ, Oksenberg N, Hoffmann TJ, Vaisse C, Ahituv N. PMID: 24203700; PMCID: PMC3943516.
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PubMed Mentions:
8 Fields:
Translation:
HumansAnimalsCells
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The melanocortin system and insulin resistance in humans: insights from a patient with complete POMC deficiency and type 1 diabetes mellitus. Int J Obes (Lond). 2014 Jan; 38(1):148-51.
Aslan IR, Ranadive SA, Valle I, Kollipara S, Noble JA, Vaisse C. PMID: 23649472; PMCID: PMC4648369.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Mechanism of N-terminal modulation of activity at the melanocortin-4 receptor GPCR. Nat Chem Biol. 2012 Aug; 8(8):725-30.
Ersoy BA, Pardo L, Zhang S, Thompson DA, Millhauser G, Govaerts C, Vaisse C. PMID: 22729149; PMCID: PMC3657613.
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PubMed Mentions:
27 Fields:
Translation:
HumansCells
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Weight loss after Roux-en-Y gastric bypass in obese patients heterozygous for MC4R mutations. Obes Surg. 2011 Jul; 21(7):930-4.
Aslan IR, Campos GM, Calton MA, Evans DS, Merriman RB, Vaisse C. PMID: 20957447; PMCID: PMC3119798.
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PubMed Mentions:
36 Fields:
Translation:
Humans
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Replication and extension of association between common genetic variants in SIM1 and human adiposity. Obesity (Silver Spring). 2011 Dec; 19(12):2394-2403.
Swarbrick MM, Evans DS, Valle MI, Favre H, Wu SH, Njajou OT, Li R, Zmuda JM, Miljkovic I, Harris TB, Kwok PY, Vaisse C, Hsueh WC. PMID: 21512513; PMCID: PMC4646950.
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PubMed Mentions:
14 Fields:
Translation:
HumansCells
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Monogenic Disorders Within the Energy Balance Pathway. Obesity Before Birth. 2011 Jan 1; 30:53-69.
Aslan AI, Ranadive RS, Vaisse VC. .
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Changes in cortical bone response to high-fat diet from adolescence to adulthood in mice. Osteoporos Int. 2011 Aug; 22(8):2283-93.
Ionova-Martin SS, Wade JM, Tang S, Shahnazari M, Ager JW, Lane NE, Yao W, Alliston T, Vaisse C, Ritchie RO. PMID: 20941479; PMCID: PMC3132390.
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PubMed Mentions:
42 Fields:
Translation:
Animals
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Systematic examination of the SIM1 gene region: Replication and extension of association between common genetic variants and adiposity. Obesity Research & Clinical Practice. 2010 Oct 1; 4:s10-s11.
Swarbrick SM, Evans ED, Ascencio AM, Favre FH, Wu WS, Njajou NO, Li LR, Zmuda ZJ, Miljkovic MI, Harris HT, Kwok KP, Vaisse VC, Hsueh HW. .
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Bariatric surgery in a patient with complete MC4R deficiency. Int J Obes (Lond). 2011 Mar; 35(3):457-61.
Aslan IR, Ranadive SA, Ersoy BA, Rogers SJ, Lustig RH, Vaisse C. PMID: 20733581; PMCID: PMC4648366.
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PubMed Mentions:
28 Fields:
Translation:
Humans
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Reduced size-independent mechanical properties of cortical bone in high-fat diet-induced obesity. Bone. 2010 Jan; 46(1):217-25.
Ionova-Martin SS, Do SH, Barth HD, Szadkowska M, Porter AE, Ager JW, Ager JW, Alliston T, Vaisse C, Ritchie RO. PMID: 19853069; PMCID: PMC4501030.
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PubMed Mentions:
46 Fields:
Translation:
Animals
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In silico mutagenesis: a case study of the melanocortin 4 receptor. FASEB J. 2009 Sep; 23(9):3059-69.
Bromberg Y, Overton J, Vaisse C, Leibel RL, Rost B. PMID: 19417090; PMCID: PMC2735358.
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PubMed Mentions:
22 Fields:
Translation:
HumansAnimalsCells
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Narrowing down the role of common variants in the genetic predisposition to obesity. Genome Med. 2009 Mar 11; 1(3):31.
Calton MA, Vaisse C. PMID: 19341502; PMCID: PMC2664942.
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PubMed Mentions:
4 Fields:
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Identification, characterization and rescue of a novel vasopressin-2 receptor mutation causing nephrogenic diabetes insipidus. Clin Endocrinol (Oxf). 2009 Sep; 71(3):388-93.
Ranadive SA, Ersoy B, Favre H, Cheung CC, Rosenthal SM, Miller WL, Vaisse C. PMID: 19170711; PMCID: PMC5881569.
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PubMed Mentions:
15 Fields:
Translation:
HumansCells
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Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case-control study. Hum Mol Genet. 2009 Mar 15; 18(6):1140-7.
Calton MA, Ersoy BA, Zhang S, Kane JP, Malloy MJ, Pullinger CR, Bromberg Y, Pennacchio LA, Dent R, McPherson R, Ahituv N, Vaisse C. PMID: 19091795; PMCID: PMC2649015.
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PubMed Mentions:
55 Fields:
Translation:
HumansCells
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Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene. J Clin Endocrinol Metab. 2008 Dec; 93(12):4955-62.
Clément K, Dubern B, Mencarelli M, Czernichow P, Ito S, Wakamatsu K, Barsh GS, Vaisse C, Leger J. PMID: 18765507; PMCID: PMC2729235.
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PubMed Mentions:
23 Fields:
Translation:
Humans
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Lessons from extreme human obesity: monogenic disorders. Endocrinol Metab Clin North Am. 2008 Sep; 37(3):733-51, x.
Ranadive SA, Vaisse C. PMID: 18775361; PMCID: PMC5877402.
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PubMed Mentions:
52 Fields:
Translation:
Humans
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Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain. Pediatr Res. 2008 Feb; 63(2):211-6.
Dubern B, Lubrano-Berthelier C, Mencarelli M, Ersoy B, Frelut ML, Bouglé D, Costes B, Simon C, Tounian P, Vaisse C, Clement K. PMID: 18091355.
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PubMed Mentions:
23 Fields:
Translation:
HumansCells
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Gender and neurogenin3 influence the pathogenesis of ketosis-prone diabetes. Diabetes Obes Metab. 2008 Sep; 10(10):912-20.
Louet JF, Smith SB, Gautier JF, Molokhia M, Virally ML, Kevorkian JP, Guillausseau PJ, Vexiau P, Charpentier G, German MS, Vaisse C, Urbanek M, Mauvais-Jarvis F. PMID: 18093211.
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PubMed Mentions:
15 Fields:
Translation:
HumansCells
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Engineering the melanocortin-4 receptor to control constitutive and ligand-mediated G(S) signaling in vivo. PLoS One. 2007 Aug 01; 2(7):e668.
Srinivasan S, Santiago P, Lubrano C, Vaisse C, Conklin BR. PMID: 17668051; PMCID: PMC1930153.
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PubMed Mentions:
8 Fields:
Translation:
HumansCells
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Medical sequencing at the extremes of human body mass. Am J Hum Genet. 2007 Apr; 80(4):779-91.
Ahituv N, Kavaslar N, Schackwitz W, Ustaszewska A, Martin J, Hebert S, Doelle H, Ersoy B, Kryukov G, Schmidt S, Yosef N, Ruppin E, Sharan R, Vaisse C, Sunyaev S, Dent R, Cohen J, McPherson R, Pennacchio LA. PMID: 17357083; PMCID: PMC1852707.
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PubMed Mentions:
133 Fields:
Translation:
Humans
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MUTATIONAL ANALYSIS OF THE PROOPIOMELANOCORTIN GENE IN OBESE CHILDREN. Journal of Pediatric Gastroenterology and Nutrition. 2006 May 1; 42(5):e81-e81.
Dubern DB, Lubrano-berthelier LC, Bouglé BD, Frelut FM, Simon SC, Vaisse VC, Clément CK, Tounian TP. .
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Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eating. J Clin Endocrinol Metab. 2006 May; 91(5):1811-8.
Lubrano-Berthelier C, Dubern B, Lacorte JM, Picard F, Shapiro A, Zhang S, Bertrais S, Hercberg S, Basdevant A, Clement K, Vaisse C. PMID: 16507637.
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PubMed Mentions:
76 Fields:
Translation:
HumansCells
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Obesity-associated mutations in the melanocortin 4 receptor provide novel insights into its function. Peptides. 2005 Oct; 26(10):1909-19.
Govaerts C, Srinivasan S, Shapiro A, Zhang S, Picard F, Clement K, Lubrano-Berthelier C, Vaisse C. PMID: 16083993.
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PubMed Mentions:
26 Fields:
Translation:
HumansAnimals
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Lack of support for the association between GAD2 polymorphisms and severe human obesity. PLoS Biol. 2005 Sep; 3(9):e315.
Swarbrick MM, Waldenmaier B, Pennacchio LA, Lind DL, Cavazos MM, Geller F, Merriman R, Ustaszewska A, Malloy M, Scherag A, Hsueh WC, Rief W, Mauvais-Jarvis F, Pullinger CR, Kane JP, Dent R, McPherson R, Kwok PY, Hinney A, Hebebrand J, Vaisse C. PMID: 16122350; PMCID: PMC1193520.
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PubMed Mentions:
17 Fields:
Translation:
HumansCells
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High prevalence of glucose-6-phosphate dehydrogenase deficiency without gene mutation suggests a novel genetic mechanism predisposing to ketosis-prone diabetes. J Clin Endocrinol Metab. 2005 Aug; 90(8):4446-51.
Sobngwi E, Gautier JF, Kevorkian JP, Villette JM, Riveline JP, Zhang S, Vexiau P, Leal SM, Vaisse C, Mauvais-Jarvis F. PMID: 15914531; PMCID: PMC6143174.
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PubMed Mentions:
23 Fields:
Translation:
HumansCells
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Leptin regulation of bone resorption by the sympathetic nervous system and CART. Nature. 2005 Mar 24; 434(7032):514-20.
Elefteriou F, Ahn JD, Takeda S, Starbuck M, Yang X, Liu X, Kondo H, Richards WG, Bannon TW, Noda M, Clement K, Vaisse C, Karsenty G. PMID: 15724149.
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PubMed Mentions:
449 Fields:
Translation:
HumansAnimalsCells
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A statistical approach for array CGH data analysis. BMC Bioinformatics. 2005 Feb 11; 6:27.
Picard F, Robin S, Lavielle M, Vaisse C, Daudin JJ. PMID: 15705208; PMCID: PMC549559.
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PubMed Mentions:
103 Fields:
Translation:
HumansCells
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PAX4 gene variations predispose to ketosis-prone diabetes. Hum Mol Genet. 2004 Dec 15; 13(24):3151-9.
Mauvais-Jarvis F, Smith SB, Le May C, Leal SM, Gautier JF, Molokhia M, Riveline JP, Rajan AS, Kevorkian JP, Zhang S, Vexiau P, German MS, Vaisse C. PMID: 15509590; PMCID: PMC6145178.
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PubMed Mentions:
44 Fields:
Translation:
Humans
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Constitutive activity of the melanocortin-4 receptor is maintained by its N-terminal domain and plays a role in energy homeostasis in humans. J Clin Invest. 2004 Oct; 114(8):1158-64.
Srinivasan S, Lubrano-Berthelier C, Govaerts C, Picard F, Santiago P, Conklin BR, Vaisse C. PMID: 15489963; PMCID: PMC522250.
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PubMed Mentions:
80 Fields:
Translation:
HumansAnimalsCells
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A homozygous null mutation delineates the role of the melanocortin-4 receptor in humans. J Clin Endocrinol Metab. 2004 May; 89(5):2028-32.
Lubrano-Berthelier C, Le Stunff C, Bougnères P, Vaisse C. PMID: 15126516.
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PubMed Mentions:
21 Fields:
Translation:
Humans
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Ketosis-prone type 2 diabetes in patients of sub-Saharan African origin: clinical pathophysiology and natural history of beta-cell dysfunction and insulin resistance. Diabetes. 2004 Mar; 53(3):645-53.
Mauvais-Jarvis F, Sobngwi E, Porcher R, Riveline JP, Kevorkian JP, Vaisse C, Charpentier G, Guillausseau PJ, Vexiau P, Gautier JF. PMID: 14988248.
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PubMed Mentions:
105 Fields:
Translation:
Humans
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The human MC4R promoter: characterization and role in obesity. Diabetes. 2003 Dec; 52(12):2996-3000.
Lubrano-Berthelier C, Cavazos M, Le Stunff C, Haas K, Shapiro A, Zhang S, Bougneres P, Vaisse C. PMID: 14633862.
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PubMed Mentions:
18 Fields:
Translation:
HumansAnimalsCells
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Emerging trends in the search for genetic variants predisposing to human obesity. Curr Opin Clin Nutr Metab Care. 2003 Jul; 6(4):369-75.
Swarbrick MM, Vaisse C. PMID: 12806208.
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PubMed Mentions:
11 Fields:
Translation:
Humans
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Molecular genetics of human obesity-associated MC4R mutations. Ann N Y Acad Sci. 2003 Jun; 994:49-57.
Lubrano-Berthelier C, Cavazos M, Dubern B, Shapiro A, Stunff CL, Zhang S, Picart F, Govaerts C, Froguel P, Bougneres P, Clement K, Vaisse C. PMID: 12851297.
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PubMed Mentions:
32 Fields:
Translation:
HumansCells
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Engineering the melanocortin-4 receptor to control G(s) signaling in vivo. Ann N Y Acad Sci. 2003 Jun; 994:225-32.
Srinivasan S, Vaisse C, Conklin BR. PMID: 12851320.
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PubMed Mentions:
15 Fields:
Translation:
HumansAnimalsCells
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Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations. Hum Mol Genet. 2003 Jan 15; 12(2):145-53.
Lubrano-Berthelier C, Durand E, Dubern B, Shapiro A, Dazin P, Weill J, Ferron C, Froguel P, Vaisse C. PMID: 12499395.
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PubMed Mentions:
51 Fields:
Translation:
HumansCells
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Elevated plasma ghrelin levels in Prader Willi syndrome. Nat Med. 2002 Jul; 8(7):643-4.
Cummings DE, Clement K, Purnell JQ, Vaisse C, Foster KE, Frayo RS, Schwartz MW, Basdevant A, Weigle DS. PMID: 12091883.
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PubMed Mentions:
140 Fields:
Translation:
Humans
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The human HNF-3 genes: cloning, partial sequence and mutation screening in patients with impaired glucose homeostasis. Hum Hered. 2000 Nov-Dec; 50(6):370-81.
Navas MA, Vaisse C, Boger S, Heimesaat M, Kollee LA, Stoffel M. PMID: 10899756.
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PubMed Mentions:
11 Fields:
Translation:
HumansCells
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Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass. Diabetes. 2000 Aug; 49(8):1347-52.
Lahlou N, Clement K, Carel JC, Vaisse C, Lotton C, Le Bihan Y, Basdevant A, Lebouc Y, Froguel P, Roger M, Guy-Grand B. PMID: 10923636.
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PubMed Mentions:
19 Fields:
Translation:
Humans
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Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity. J Clin Invest. 2000 Jul; 106(2):253-62.
Vaisse C, Clement K, Durand E, Hercberg S, Guy-Grand B, Froguel P. PMID: 10903341; PMCID: PMC314306.
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PubMed Mentions:
215 Fields:
Translation:
Humans
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The Pro115Gln and Pro12Ala PPAR gamma gene mutations in obesity and type 2 diabetes. Int J Obes Relat Metab Disord. 2000 Mar; 24(3):391-3.
Clement K, Hercberg S, Passinge B, Galan P, Varroud-Vial M, Shuldiner AR, Beamer BA, Charpentier G, Guy-Grand B, Froguel P, Vaisse C. PMID: 10757637.
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PubMed Mentions:
26 Fields:
Translation:
Humans
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Glycodelin: a pane in the implantation window. Semin Reprod Med. 2000; 18(3):289-98.
Mueller MD, Vigne JL, Vaisse C, Taylor RN. PMID: 11299967.
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PubMed Mentions:
4 Fields:
Translation:
HumansCells
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Promegestone (R5020) and mifepristone (RU486) both function as progestational agonists of human glycodelin gene expression in isolated human epithelial cells. J Clin Endocrinol Metab. 1998 Nov; 83(11):4006-12.
Taylor RN, Savouret JF, Vaisse C, Vigne JL, Ryan I, Hornung D, Seppälä M, Milgrom E. PMID: 9814484.
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PubMed Mentions:
18 Fields:
Translation:
HumansCells
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A frameshift mutation in human MC4R is associated with a dominant form of obesity. Nat Genet. 1998 Oct; 20(2):113-4.
Vaisse C, Clement K, Guy-Grand B, Froguel P. PMID: 9771699.
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PubMed Mentions:
309 Fields:
Translation:
HumansCells
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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction. Nature. 1998 Mar 26; 392(6674):398-401.
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. PMID: 9537324.
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PubMed Mentions:
467 Fields:
Translation:
Humans
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La mutation du gène du récepteur de la leptine entraîne chez l'homme une obésité massive associée à des anomalies hypothalamo-hypophysaires. Médecine/sciences. 1998 Jan 1; 14(5):675.
Clément CK, Vaisse VC, Basdevant BA, Guy-Grand GB, Froguel FP. .
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Pancreatic islet expression studies and polymorphic DNA markers in the genes encoding hepatocyte nuclear factor-3alpha, -3beta, -3gamma, -4gamma, and -6. Diabetes. 1997 Aug; 46(8):1364-7.
Vaisse C, Kim J, Espinosa R, Le Beau MM, Stoffel M. PMID: 9231664.
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PubMed Mentions:
5 Fields:
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HumansCells
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Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db mice. Nat Genet. 1996 Sep; 14(1):95-7.
Vaisse C, Halaas JL, Horvath CM, Darnell JE, Stoffel M, Friedman JM. PMID: 8782827.
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301 Fields:
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AnimalsCells
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Gln-Arg192 polymorphism of paraoxonase and coronary heart disease in type 2 diabetes. Lancet. 1995 Sep 30; 346(8979):869-72.
Ruiz J, Blanché H, James RW, Garin MC, Vaisse C, Charpentier G, Cohen N, Morabia A, Passa P, Froguel P. PMID: 7564671.
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PubMed Mentions:
54 Fields:
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Humans
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Genetic variation in the beta 3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesity. N Engl J Med. 1995 Aug 10; 333(6):352-4.
Clément K, Vaisse C, Manning BS, Basdevant A, Guy-Grand B, Ruiz J, Silver KD, Shuldiner AR, Froguel P, Strosberg AD. PMID: 7609752.
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97 Fields:
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HumansCells
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A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus. Nat Genet. 1995 Mar; 9(3):299-304.
Hager J, Hansen L, Vaisse C, Vionnet N, Philippi A, Poller W, Velho G, Carcassi C, Contu L, Julier C, et al. PMID: 7773293.
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PubMed Mentions:
36 Fields:
Translation:
Humans
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Expression and regulation of adrenodoxin and P450scc mRNA in rodent tissues. DNA Cell Biol. 1991 Jun; 10(5):339-47.
Mellon SH, Kushner JA, Vaisse C. PMID: 1863358.
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PubMed Mentions:
1 Fields:
Translation:
HumansAnimalsCells
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The human placental protein 14 (PP14) gene is localized on chromosome 9q34. Hum Genet. 1991 Mar; 86(5):515-8.
Van Cong N, Vaisse C, Gross MS, Slim R, Milgrom E, Bernheim A. PMID: 2016092.
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PubMed Mentions:
5 Fields:
Translation:
HumansAnimalsCells
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Human placental protein 14 gene: sequence and characterization of a short duplication. DNA Cell Biol. 1990 Jul-Aug; 9(6):401-13.
Vaisse C, Atger M, Potier B, Milgrom E. PMID: 2206398.
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PubMed Mentions:
13 Fields:
Translation:
HumansAnimalsCells
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cAMP regulates P450scc gene expression by a cycloheximide-insensitive mechanism in cultured mouse Leydig MA-10 cells. Proc Natl Acad Sci U S A. 1989 Oct; 86(20):7775-9.
Mellon SH, Vaisse C. PMID: 2554289; PMCID: PMC298153.
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PubMed Mentions:
15 Fields:
Translation:
AnimalsCells