HuGE Literature Finder
Records 1-51
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Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity.
Obesity surgery 2019 Oct . Cooiman M I, Kleinendorst L, Aarts E O, Janssen I M C, van Amstel H K Ploos, Blakemore A I, Hazebroek E J, Meijers-Heijboer H J, van der Zwaag B, Berends F J, van Haelst M |
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Identification of genetic basis of obesity and mechanistic link of genes and lipids in Pakistani population.
Bioscience reports 2018 May . Shabana N M, Shahid Saleem Ullah, Hasnain Shahi |
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The Canine POMC Gene, Obesity in Labrador Retrievers and Susceptibility to Diabetes Mellitus.
Journal of veterinary internal medicine 2017 Feb . Davison L J, Holder A, Catchpole B, O'Callaghan C |
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The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.
Translational psychiatry 2017 Jan 7 (1): e1007. Amare A T, Schubert K O, Klingler-Hoffmann M, Cohen-Woods S, Baune B |
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Next-generation sequencing of the monogenic obesity genes LEP, LEPR, MC4R, PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls.
Molecular genetics and metabolism 2017 05 121 (1): 51-56. Nordang Gry B N, Busk Øyvind L, Tveten Kristian, Hanevik Hans Ivar, Fell Anne Kristin M, Hjelmesæth Jøran, Holla Øystein L, Hertel Jens |
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Polymorphisms of the GR and HSD11B1genes influence body mass index and weight gain during hormone replacement treatment in patients with Addison's disease.
Clinical endocrinology 2016 Jan . Molnár Ágnes, Kövesdi Annamária, Szücs Nikolette, Tóth Miklós, Igaz Péter, Rácz Károly, Patócs Atti |
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A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.
PloS one 2016 11 (6): e0157776. Volkov Petr, Olsson Anders H, Gillberg Linn, Jørgensen Sine W, Brøns Charlotte, Eriksson Karl-Fredrik, Groop Leif, Jansson Per-Anders, Nilsson Emma, Rönn Tina, Vaag Allan, Ling Charlot |
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Exome sequencing in Thai patients with familial obesity.
Genetics and molecular research : GMR 2016 15 (2): . Kaewsutthi S, Santiprabhob J, Phonrat B, Tungtrongchitr A, Lertrit P, Tungtrongchitr |
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Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity.
Human genetics 2016 08 135 (8): 869-80. Sajuthi Satria P, Sharma Neeraj K, Chou Jeff W, Palmer Nicholette D, McWilliams David R, Beal John, Comeau Mary E, Ma Lijun, Calles-Escandon Jorge, Demons Jamehl, Rogers Samantha, Cherry Kristina, Menon Lata, Kouba Ethel, Davis Donna, Burris Marcie, Byerly Sara J, Ng Maggie C Y, Maruthur Nisa M, Patel Sanjay R, Bielak Lawrence F, Lange Leslie A, Guo Xiuqing, Sale Michèle M, Chan Kei Hang K, Monda Keri L, Chen Gary K, Taylor Kira, Palmer Cameron, Edwards Todd L, North Kari E, Haiman Christopher A, Bowden Donald W, Freedman Barry I, Langefeld Carl D, Das Swapan |
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Prevalence of POMC R236G mutation in Pakistan.
Obesity research & clinical practice 2015 Oct . Shabana , Hasnain Shahi |
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Analysis of MC4R rs17782313, POMC rs1042571, APOE-Hha1 and AGRP rs3412352 genetic variants with susceptibility to obesity risk in North Indians.
Annals of human biology 2015 Jul 1-4. Srivastava Apurva, Mittal Balraj, Prakash Jai, Srivastava Pranjal, Srivastava Nee |
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IGF2, LEPR, POMC, PPARG, and PPARGC1 gene variants are associated with obesity-related risk phenotypes in Brazilian children and adolescents.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas me?dicas e biolo?gicas / Sociedade Brasileira de Biofi?sica ... [et al.] 2015 Jul 48 (7): 595-602. Queiroz E M, Cândido A P C, Castro I M, Bastos A Q A, Machado-Coelho G L L, Freitas R |
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A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.
International journal of obesity (2005) 2015 Feb 39 (2): 295-302. Philippe J, Stijnen P, Meyre D, De Graeve F, Thuillier D, Delplanque J, Gyapay G, Sand O, Creemers J W, Froguel P, Bonnefond |
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Association between polymorphisms of the CRH and POMC genes with economic traits in Korean cattle (Hanwoo).
Genetics and molecular research : GMR 2015 14 (3): 10415-21. Seong J, Kong H |
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Association between rs155971 in the PCSK1 gene and the lipid profile of obese Thai children: a family-based study.
Genetics and molecular research : GMR 2015 14 (3): 9136-44. Kulanuwat S, Santiprabhob J, Phonrat B, Limwongse C, Tungtrongchitr A, Chongviriyaphan N, Tungtrongchitr |
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Many obesity-associated SNPs strongly associate with DNA methylation changes at proximal promoters and enhancers.
Genome medicine 2015 7 (1): 103. Voisin Sarah, Almén Markus Sällman, Zheleznyakova Galina Y, Lundberg Lina, Zarei Sanaz, Castillo Sandra, Eriksson Fia Ence, Nilsson Emil K, Blüher Matthias, Böttcher Yvonne, Kovacs Peter, Klovins Janis, Rask-Andersen Mathias, Schiöth Helgi |
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The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosa.
Journal of psychiatric research 2014 Aug 55 77-86. Yilmaz Zeynep, Kaplan Allan S, Tiwari Arun K, Levitan Robert D, Piran Sara, Bergen Andrew W, Kaye Walter H, Hakonarson Hakon, Wang Kai, Berrettini Wade H, Brandt Harry A, Bulik Cynthia M, Crawford Steven, Crow Scott, Fichter Manfred M, Halmi Katherine A, Johnson Craig L, Keel Pamela K, Klump Kelly L, Magistretti Pierre, Mitchell James E, Strober Michael, Thornton Laura M, Treasure Janet, Woodside D Blake, Knight Joanne, Kennedy James |
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Investigation of melanocortin system gene variants in antipsychotic-induced weight gain.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2014 Apr 15 (3): 251-8. Chowdhury Nabilah I, Souza Renan P, Tiwari Arun K, Brandl Eva J, Sicard Michelle, Meltzer Herbert Y, Lieberman Jeffrey A, Kennedy James L, Müller Daniel |
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.
Human molecular genetics 2013 Sep 22 (17): 3597-607. Graff Mariaelisa, Ngwa Julius S, Workalemahu Tsegaselassie, Homuth Georg, Schipf Sabine, Teumer Alexander, Völzke Henry, Wallaschofski Henri, Abecasis Goncalo R, Edward Lakatta, Francesco Cucca, Sanna Serena, Scheet Paul, Schlessinger David, Sidore Carlo, Xiao Xiangjun, Wang Zhaoming, Chanock Stephen J, Jacobs Kevin B, Hayes Richard B, Hu Frank, Van Dam Rob M, , Crout Richard J, Marazita Mary L, Shaffer John R, Atwood Larry D, Fox Caroline S, Heard-Costa Nancy L, White Charles, Choh Audrey C, Czerwinski Stefan A, Demerath Ellen W, Dyer Thomas D, Towne Bradford, Amin Najaf, Oostra Ben A, Van Duijn Cornelia M, Zillikens M Carola, Esko Tõnu, Nelis Mari, Nikopensius Tit, Metspalu Andres, Strachan David P, Monda Keri, Qi Lu, North Kari E, Cupples L Adrienne, Gordon-Larsen Penny, Berndt Sonja |
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Individual genetic variations related to satiety and appetite control increase risk of obesity in preschool-age children in the STRONG kids program.
Human heredity 2013 75 (2-4): 152-9. Wang Yingying, Wang Anthony, Donovan Sharon M, Teran-Garcia Margarita, |
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Prevalence of metabolic syndrome in obese Chilean children and association with gene variants of the leptin-melanocortin system.
Journal of pediatric endocrinology & metabolism : JPEM 2013 26 (11-12): 1131-9. Suazo José, Hodgson María Isabel, Obregón Ana María, Valladares Macarena, Weisstaub Gerardo, Amador Paola, Santos José Lu |
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Gene-PUFA interactions and obesity risk.
The British journal of nutrition 2011 Oct 106 (8): 1263-72. Jourdan C, Kloiber S, Nieters A, Seiler H, Himmerich H, Kohli M A, Lucae S, Wolfram G, Gieger C, Wichmann H-E, Linseisen |
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Association study of POMC variants with body composition measures and nutrient choice.
European journal of pharmacology 2011 Jun 660 (1): 220-5. Ternouth Andrew, Brandys Marek K, van der Schouw Yvonne T, Hendriks Judith, Jansson John-Olov, Collier David, Adan Roger |
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Associations between anthropometrical measurements, body composition, single-nucleotide polymorphisms of the hypothalamus/pituitary/adrenal (HPA) axis and HPA axis functioning.
Clinical endocrinology 2011 Jun 74 (6): 679-86. Rutters Femke, Nieuwenhuizen Arie G, Lemmens Sofie G T, Bouwman Freek, Mariman Edwin, Westerterp-Plantenga Margriet |
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A large-scale candidate gene association study of age at menarche and age at natural menopause.
Human genetics 2010 Nov 128 (5): 515-27. He Chunyan, Kraft Peter, Chasman Daniel I, Buring Julie E, Chen Constance, Hankinson Susan E, Paré Guillaume, Chanock Stephen, Ridker Paul M, Hunter David |
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
Nature genetics 2010 Oct . Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Allen HL, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segrè AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpeläinen TO, Yang J, Bouatia-Naji N, Esko T, Feitosa MF, Kutalik Z, Mangino M, Raychaudhuri S, Scherag A, Smith AV, Welch R, Zhao JH, Aben KK, Absher DM, Amin N, Dixon AL, Fisher E, Glazer NL, Goddard ME, Heard-Costa NL, Hoesel V, Hottenga JJ, Johansson A, Johnson T, Ketkar S, Lamina C, Li S, Moffatt MF, Myers RH, Narisu N, Perry JR, Peters MJ, Preuss M, Ripatti S, Rivadeneira F, Sandholt C, Scott LJ, Timpson NJ, Tyrer JP, van Wingerden S, Watanabe RM, White CC, Wiklund F, Barlassina C, Chasman DI, Cooper MN, Jansson JO, Lawrence RW, Pellikka N, Prokopenko I, Shi J, Thiering E, Alavere H, Alibrandi MT, Almgren P, Arnold AM, Aspelund T, Atwood LD, Balkau B, Balmforth AJ, Bennett AJ, Ben-Shlomo Y, Bergman RN, Bergmann S, Biebermann H, Blakemore AI, Boes T, Bonnycastle LL, Bornstein SR, Brown MJ, Buchanan TA, Busonero F, Campbell H, Cappuccio FP, Cavalcanti-Proença C, Chen YD, Chen CM, Chines PS, Clarke R, Coin L, Connell J, Day IN, Heijer MD, Duan J, Ebrahim S, Elliott P, Elosua R, Eiriksdottir G, Erdos MR, Eriksson JG, Facheris MF, Felix SB, Fischer-Posovszky P, Folsom AR, Friedrich N, Freimer NB, Fu M, Gaget S, Gejman PV, Geus EJ, Gieger C, Gjesing AP, Goel A, Goyette P, Grallert H, Gräßler J, Greenawalt DM, Groves CJ, Gudnason V, Guiducci C, Hartikainen AL, Hassanali N, Hall AS, Havulinna AS, Hayward C, Heath AC, Hengstenberg C, Hicks AA, Hinney A, Hofman A, Homuth G, Hui J, Igl W, Iribarren C, Isomaa B, Jacobs KB, Jarick I, Jewell E, John U, Jørgensen T, Jousilahti P, Jula A, Kaakinen M, Kajantie E, Kaplan LM, Kathiresan S, Kettunen J, Kinnunen L, Knowles JW, Kolcic I, König IR, Koskinen S, Kovacs P, Kuusisto J, Kraft P, Kvaløy K, Laitinen J, Lantieri O, Lanzani C, Launer LJ, Lecoeur C, Lehtimäki T, Lettre G, Liu J, Lokki ML, Lorentzon M, Luben RN, Ludwig B, Manunta P, Marek D, Marre M, Martin NG, McArdle WL, McCarthy A, McKnight B, Meitinger T, Melander O, Meyre D, Midthjell K, Montgomery GW, Morken MA, Morris AP, Mulic R, Ngwa JS, Nelis M, Neville MJ, Nyholt DR, O'Donnell CJ, O'Rahilly S, Ong KK, Oostra B, Paré G, Parker AN, Perola M, Pichler I, Pietiläinen KH, Platou CG, Polasek O, Pouta A, Rafelt S, Raitakari O, Rayner NW, Ridderstråle M, Rief W, Ruokonen A, Robertson NR, Rzehak P, Salomaa V, Sanders AR, Sandhu MS, Sanna S, Saramies J, Savolainen MJ, Scherag S, Schipf S, Schreiber S, Schunkert H, Silander K, Sinisalo J, Siscovick DS, Smit JH, Soranzo N, Sovio U, Stephens J, Surakka I, Swift AJ, Tammesoo ML, Tardif JC, Teder-Laving M, Teslovich TM, Thompson JR, Thomson B, Tönjes A, Tuomi T, van Meurs JB, van Ommen GJ, Vatin V, Viikari J, Visvikis-Siest S, Vitart V, Vogel CI, Voight BF, Waite LL, Wallaschofski H, Walters GB, Widen E, Wiegand S, Wild SH, Willemsen G, Witte DR, Witteman JC, Xu J, Zhang Q, Zgaga L, Ziegler A, Zitting P, Beilby JP, Farooqi IS, Hebebrand J, Huikuri HV, James AL, Kähönen M, Levinson DF, Macciardi F, Nieminen MS, Ohlsson C, Palmer LJ, Ridker PM, Stumvoll M, Beckmann JS, Boeing H, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Collins FS, Cupples LA, Smith GD, Erdmann J, Froguel P, Grönberg H, Gyllensten U, Hall P, Hansen T, Harris TB, Hattersley AT, Hayes RB, Heinrich J, Hu FB, Hveem K, Illig T, Jarvelin MR, Kaprio J, Karpe F, Khaw KT, Kiemeney LA, Krude H, Laakso M, Lawlor DA, Metspalu A, Munroe PB, Ouwehand WH, Pedersen O, Penninx BW, Peters A, Pramstaller PP, Quertermous T, Reinehr T, Rissanen A, Rudan I, Samani NJ, Schwarz PE, Shuldiner AR, Spector TD, Tuomilehto J, Uda M, Uitterlinden A, Valle TT, Wabitsch M, Waeber G, Wareham NJ, Watkins H, Wilson JF, Wright AF, Zillikens MC, Chatterjee N, McCarroll SA, Purcell S, Schadt EE, Visscher PM, Assimes TL, Borecki IB, Deloukas P, Fox CS, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, Mohlke KL, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, van Duijn CM, Wichmann HE, Frayling TM, Thorsteinsdottir U, Abecasis GR, Barroso I, Boehnke M, Stefansson K, North KE, I McCarthy M, Hirschhorn JN, Ingelsson E, Loos RJ |
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Genotype x nutrient association of common polymorphisms in obesity-related genes with food preferences and time structure of energy intake.
The British journal of nutrition 2010 Feb 103 (3): 352-9. Bienertová-Vask? Julie, Bienert Petr, Forejt Martin, Tomandl Josef, Brázdová Zuzana, Vask? An |
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Severe obesity is associated with novel single nucleotide polymorphisms of the ESR1 and PPARgamma locus in Han Chinese.
The American journal of clinical nutrition 2009 Aug 90 (2): 255-62. Chen Hsin-Hung, Lee Wei-Jei, Fann Cathy S J, Bouchard Claude, Pan Wen-Ha |
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[Possible pathogenetic role of 11 beta-hydroxysteroid dehydrogenase type 1 (11betaHSD1) gene polymorphisms in arterial hypertension].
Revista médica de Chile 2008 Jun 136 (6): 701-10. Morales Mauricio A, Carvajal Cristián A, Ortiz Eugenia, Mosso Lorena M, Artigas Rocío A, Owen Gareth I, Fardella Carlos |
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Further Evidence For the Role of ENPP1 in Obesity: Association With Morbid Obesity in Finns.
Obesity (Silver Spring, Md.) 2008 Jun . Valli-Jaakola K, Suviolahti E, Schalin-Jäntti C, Ripatti S, Silander K, Oksanen L, Salomaa V, Peltonen L, Kontula K |
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Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Apr 17 (4): 1007-12. Doecke James D, Zhao Zhen Zhen, Stark Mitchell S, Green Adèle C, Hayward Nicholas K, Montgomery Grant W, Webb Penelope M, Whiteman David C, |
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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.
Pediatric research 2008 Feb 63 (2): 211-6. Dubern Beatrice, Lubrano-Berthelier Cecile, Mencarelli Monica, Ersoy Baran, Frelut Marie-Laure, Bouglé Dominique, Costes Bruno, Simon Chantal, Tounian Patrick, Vaisse Christian, Clement Kari |
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No association of defined variability in leptin, leptin receptor, adiponectin, proopiomelanocortin and ghrelin gene with food preferences in the Czech population.
Nutritional neuroscience 2008 Feb 11 (1): 2-8. Bienertova-Vasku Julie, Bienert Petr, Tomandl Josef, Forejt Martin, Vavrina Martin, Kudelkova Jana, Vasku An |
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A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2007 Jan 115 (1): 7-12. Rettenbacher E, Tarnow P, Brumm H, Prayer D, Wermter A-K, Hebebrand J, Biebermann H, Hinney A, Widhalm |
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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.
The Journal of clinical endocrinology and metabolism 2006 May 91 (5): 1811-8. Lubrano-Berthelier Cecile, Dubern Beatrice, Lacorte Jean-Marc, Picard Franck, Shapiro Astrid, Zhang Sumei, Bertrais Sandrine, Hercberg Serge, Basdevant Arnaud, Clement Karine, Vaisse Christi |
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Weight loss in obese children carrying the proopiomelanocortin R236G variant.
Journal of endocrinological investigation 2006 Mar 29 (3): 226-30. Santoro N, Perrone L, Cirillo G, Raimondo P, Amato A, Coppola F, Santarpia M, D'Aniello A, Miraglia Del Giudice |
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A POMC variant implicates beta-melanocyte-stimulating hormone in the control of human energy balance.
Cell metabolism 2006 Feb 3 (2): 135-40. Lee Yung Seng, Challis Ben G, Thompson Darren A, Yeo Giles S H, Keogh Julia M, Madonna Michael E, Wraight Vicki, Sims Matthew, Vatin Vincent, Meyre David, Shield Julian, Burren Christine, Ibrahim Zala, Cheetham Tim, Swift Peter, Blackwood Anthea, Hung Chiao-Chien Connie, Wareham Nicholas J, Froguel Philippe, Millhauser Glenn L, O'Rahilly Stephen, Farooqi I Sad |
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Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study.
Obesity research 2005 Sep 13 (9): 1491-8. Sutton Beth S, Langefeld Carl D, Williams Adrienne H, Norris Jill M, Saad Mohammed F, Haffner Steven M, Bowden Donald |
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Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
Diabetes 2005 Aug 54 (8): 2492-6. Baker M, Gaukrodger N, Mayosi BM, Imrie H, Farrall M, Watkins H, Connell JM, Avery PJ, Keavney B |
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Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy.
Clinical chemistry 2005 Aug 51 (8): 1358-64. Buono Pasqualina, Pasanisi Fabrizio, Nardelli Carmela, Ieno Luigi, Capone Silvana, Liguori Rosario, Finelli Carmine, Oriani Giovannangelo, Contaldo Franco, Sacchetti Luc |
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Proopiomelanocortin gene variants are associated with serum leptin and body fat in a normal female population.
European journal of human genetics : EJHG 2005 Jun 13 (6): 772-80. Chen Yuanneng, Snieder Harold, Wang Xiaoling, Kaviya Bhavini, McCaffrey Clare, Spector Tim D, Carter Nicholas D, O'Dell Sandra |
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Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women.
Journal of human genetics 2005 50 (5): 235-40. Sudo Yoshihiro, Ezura Yoichi, Kajita Mitsuko, Yoshida Hideyo, Suzuki Takao, Hosoi Takayuki, Inoue Satoshi, Shiraki Masataka, Ito Hiromoto, Emi Mitsu |
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Gene variants and binge eating as predictors of comorbidity and outcome of treatment in severe obesity.
Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract 2004 Dec 8 (8): 971-81; discussion 981-2. Potoczna Natascha, Branson Ruth, Kral John G, Piec Grazyna, Steffen Rudolf, Ricklin Thomas, Hoehe Margret R, Lentes Klaus-Ulrich, Horber Fritz |
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An insertional polymorphism of the proopiomelanocortin gene is associated with fasting insulin levels in childhood obesity.
The Journal of clinical endocrinology and metabolism 2004 Oct 89 (10): 4846-9. Santoro Nicola, del Giudice Emanuele Miraglia, Cirillo Grazia, Raimondo Paolo, Corsi Ivana, Amato Alessandra, Grandone Anna, Perrone Lau |
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Binge eating as a major phenotype of melanocortin 4 receptor gene mutations.
The New England journal of medicine 2003 Mar 348 (12): 1096-103. Branson Ruth, Potoczna Natascha, Kral John G, Lentes Klaus-Ulrich, Hoehe Margret R, Horber Fritz |
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Polymorphisms in exon 3 of the proopiomelanocortin gene in relation to serum leptin, salivary cortisol, and obesity in Swedish men.
Metabolism: clinical and experimental 2002 May 51 (5): 642-4. Rosmond Roland, Ukkola Olavi, Bouchard Claude, Björntorp P |
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Sequence analysis of the pro-opiomelanocortin (POMC) gene in obese/diabetic Japanese.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2002 May 26 (5): 730-1. Ohshiro Y, Ueda K, Wakasaki H, Kosaka M, Nishi M, Sasaki H, Takasu N, Nanjo |
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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and alpha-melanocyte-stimulating hormone genes in severely obese children.
The Journal of pediatrics 2001 Aug 139 (2): 204-9. Dubern B, Clément K, Pelloux V, Froguel P, Girardet JP, Guy-Grand B, Tounian P |
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Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations.
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2001 Jan 25 (1): 61-7. Miraglia del Giudice E, Cirillo G, Santoro N, D'Urso L, Carbone M T, Di Toro R, Perrone |
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Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in caucasian families.
Diabetologia 2000 Dec 43 (12): 1554-7. Delplanque J, Barat-Houari M, Dina C, Gallina P, Clément K, Guy-Grand B, Vasseur F, Boutin P, Froguel |
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[Screening of mutations in genes of pro-opiomelanocortin in patients with constitutional exogenous obesity].
Voprosy medit?sinsko? khimii 0 48 (1): 121-30. Pankov Iu A, Iatsyshina S B, Karpova S K, Chekhranova M K, Popova Iu P, Grigorian O N, Rogaev E |
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- Page last updated:Feb 27, 2020
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