Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Disease and POMC[original query] |
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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 |
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 |
Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology. Neuroscience letters 2006 Sep 405 (3): 212-6. Shadrina Maria, Nikopensius Tiit, Slominsky Petr, Illarioshkin Sergei, Bagyeva Gulbahar, Markova Elene, Ivanova-Smolenskaia Irina, Kurg Ants, Limborska Svetlana, Metspalu Andr |
Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways. Mutation research 2009 Jan 660 (1-2): 12-21. Slattery Martha L, Wolff Roger K, Curtin Karen, Fitzpatrick Frank, Herrick Jennifer, Potter John D, Caan Bette J, Samowitz Wade |
Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech population. Heart and vessels 2009 Mar 24 (2): 131-7. Bienertová-Vask? Julie Anna, Spinarová Lenka, Bienert Petr, Vask? An |
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.
PLoS genetics 2011 Sep 7 (9): e1002293. Bradfield Jonathan P, Qu Hui-Qi, Wang Kai, Zhang Haitao, Sleiman Patrick M, Kim Cecilia E, Mentch Frank D, Qiu Haijun, Glessner Joseph T, Thomas Kelly A, Frackelton Edward C, Chiavacci Rosetta M, Imielinski Marcin, Monos Dimitri S, Pandey Rahul, Bakay Marina, Grant Struan F A, Polychronakos Constantin, Hakonarson Hak |
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 |
The USP8 mutational status may predict drug susceptibility in corticotroph adenomas of Cushing's disease. European journal of endocrinology / European Federation of Endocrine Societies 2015 Nov . Hayashi Kyohei, Inoshita Naoko, Kawaguchi Kohei, Ardisasmita Arif Ibrahim, Suzuki Hisanori, Fukuhara Noriaki, Okada Mitsuo, Nishioka Hiroshi, Takeuchi Yasuhiro, Komada Masayuki, Takeshita Akira, Yamada Sho |
Whole-exome sequencing analysis in twin sibling males with an anterior cruciate ligament rupture. Injury 2016 Sep 47 Suppl 3 S41-S50. Caso Enrique, Maestro Antonio, Sabiers Cristina C, Godino Manuel, Caracuel Zaira, Pons Joana, Gonzalez F Jesus, Bautista Rocio, Claros M Gonzalo, Caso-Onzain Jaime, Viejo-Allende Elena, Giannoudis Peter V, Alvarez Sara, Maietta Paolo, Guerado Enriq |
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 |
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 |
Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity. Frontiers in endocrinology 2022 13 832911. Šket Robert, Kotnik Primož, Bizjan Barbara Jenko, Kocen Valentina, Mlinari? Matej, Tesovnik Tine, Debeljak Maruša, Battelino Tadej, Kova? Jern |
The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar. Obesity facts 2022 1 15 (3): 357-365. AbouHashem Nadien, Zaied Roan E, Al-Shafai Kholoud, Nofal Mariam, Syed Najeeb, Al-Shafai Masha |
Polymorphisms in Corticotrophin-releasing Hormone-Proopiomalanocortin (CRH-POMC) System Genes: Neuroimmune contributions to Psoriasis Disease. Journal of the European Academy of Dermatology and Venereology : JEADV 2023 6 . Elvira Galimova, Ranno Rätsep, Tanel Traks, Alexandr Chernov, Darya Gaysina, Külli Kingo, Sulev Kõ |
PAM variants in patients with thyrotrophinomas, cyclical Cushing's disease and prolactinomas. Frontiers in endocrinology 2023 12 14 1305606. Sunita M C De Sousa, Angeline Shen, Christopher J Yates, Roderick Clifton-Bligh, Stephen Santoreneos, James King, John Toubia, Giampaolo Trivellin, Andrea G Lania, Constantine A Stratakis, David J Torpy, Hamish S Sco |
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- Page last updated:Apr 16, 2024
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