Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: LPIN1[original query] |
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Association of lipin 1 gene polymorphisms with measures of energy and glucose metabolism. Obesity (Silver Spring, Md.) 2007 Nov 15 (11): 2723-32. Loos Ruth J F, Rankinen Tuomo, Pérusse Louis, Tremblay Angelo, Després Jean-Pierre, Bouchard Clau |
Genetic variants within the LPIN1 gene, encoding lipin, are influencing phenotypes of the metabolic syndrome in humans. Diabetes 2008 Jan 57 (1): 209-17. Wiedmann Silke, Fischer Marcus, Koehler Martina, Neureuther Katharina, Riegger Guenter, Doering Angela, Schunkert Heribert, Hengstenberg Christian, Baessler Andr |
LPIN1 genetic variation is associated with rosiglitazone response in type 2 diabetic patients. Molecular genetics and metabolism 0 95 (1-2): 96-100. Kang Eun Seok, Park Se Eun, Han Seung Jin, Kim So Hun, Nam Chung Mo, Ahn Chul Woo, Cha Bong Soo, Kim Kyung Sub, Lee Hyun Ch |
Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations. Diabetes 2008 Sep 57 (9): 2527-33. Fawcett Katherine A, Grimsey Neil, Loos Ruth J F, Wheeler Eleanor, Daly Allan, Soos Maria, Semple Robert, Syddall Holly, Cooper Cyrus, Siniossoglou Symeon, O'Rahilly Stephen, Wareham Nicholas J, Barroso In |
Association of a polymorphism in the lipin 1 gene with systolic blood pressure in men. American journal of hypertension 2008 May 21 (5): 539-45. Ong K L, Leung Raymond Y H, Wong Louisa Y F, Cherny Stacey S, Sham P C, Lam T H, Lam Karen S L, Cheung Bernard M |
The associations of LPIN1 gene expression in adipose tissue with metabolic phenotypes in the Chinese population. Obesity (Silver Spring, Md.) 2009 Jun . Chang YC, Chang LY, Chang TJ, Jiang YD, Lee KC, Kuo SS, Lee WJ, Chuang LM |
Studies of association between LPIN1 variants and common metabolic phenotypes among 17,538 Danes. European journal of endocrinology / European Federation of Endocrine Societies 2010 Jul 163 (1): 81-7. Burgdorf Kristoffer Sølvsten, Sandholt Camilla Helene, Sparsø Thomas, Andersen Gitte, Witte Daniel R, Jørgensen Torben, Sandbaek Anelli, Lauritzen Torsten, Sørensen Thorkild I A, Madsbad Sten, Hansen Torben, Pedersen Ol |
Adipogenic gene variants in patients with HIV-associated lipodystrophy. Pharmacogenetics and genomics 2011 Feb 21 (2): 76-83. Pushpakom Sudeep P, Owen Andrew, Vilar F Javier, Castro Hannah, Dunn David T, Back David J, Pirmohamed Mun |
LPIN1 rs13412852 polymorphism in pediatric nonalcoholic fatty liver disease. Journal of pediatric gastroenterology and nutrition 2012 May 54 (5): 588-93. Valenti Luca, Motta Benedetta Maria, Alisi Anna, Sartorelli Rita, Buonaiuto Giulia, Dongiovanni Paola, Rametta Raffaela, Pelusi Serena, Fargion Silvia, Nobili Valer |
Association of PPARG and LPIN1 gene polymorphisms with metabolic syndrome and type 2 diabetes. Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina 2011 Feb 8 (1): 76-83. Bego Tamer, Dujic Tanja, Mlinar Barbara, Semiz Sabina, Malenica Maja, Prnjavorac Besim, Ostanek Barbara, Marc Janja, Causevi? Adli |
Genetic variants of LPIN1 indicate an association with Type 2 diabetes mellitus in a Chinese population. Diabetic medicine : a journal of the British Diabetic Association 2013 Jan 30 (1): 118-22. Zhang R, Jiang F, Hu C, Yu W, Wang J, Wang C, Ma X, Tang S, Bao Y, Xiang K, Jia |
Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia. Journal of inherited metabolic disease 2012 Nov 35 (6): 1119-28. Michot Caroline, Hubert Laurence, Romero Norma B, Gouda Amr, Mamoune Asmaa, Mathew Suja, Kirk Edwin, Viollet Louis, Rahman Shamima, Bekri Soumeya, Peters Heidi, McGill James, Glamuzina Emma, Farrar Michelle, von der Hagen Maya, Alexander Ian E, Kirmse Brian, Barth Magalie, Laforet Pascal, Benlian Pascale, Munnich Arnold, JeanPierre Marc, Elpeleg Orly, Pines Ophry, Delahodde Agnès, de Keyzer Yves, de Lonlay Pasca |
Analyses of single nucleotide polymorphisms in selected nutrient-sensitive genes in weight-regain prevention: the DIOGENES study. The American journal of clinical nutrition 2012 May 95 (5): 1254-60. Larsen Lesli H, Angquist Lars, Vimaleswaran Karani S, Hager Jörg, Viguerie Nathalie, Loos Ruth J F, Handjieva-Darlenska Teodora, Jebb Susan A, Kunesova Marie, Larsen Thomas M, Martinez J Alfredo, Papadaki Angeliki, Pfeiffer Andreas F H, van Baak Marleen A, Sørensen Thorkild Ia, Holst Claus, Langin Dominique, Astrup Arne, Saris Wim H |
The role of genetic variants in CYP2C8, LPIN1, PPARGC1A and PPAR? on the trough steady-state plasma concentrations of rosiglitazone and on glycosylated haemoglobin A1c in type 2 diabetes. Pharmacogenetics and genomics 2013 Apr 23 (4): 219-27. Stage Tore B, Christensen Mette M H, Feddersen Søren, Beck-Nielsen Henning, Brøsen K |
A 4-polymorphism risk score predicts steatohepatitis in children with nonalcoholic fatty liver disease. Journal of pediatric gastroenterology and nutrition 2014 May 58 (5): 632-6. Nobili Valerio, Donati Benedetta, Panera Nadia, Vongsakulyanon Apirom, Alisi Anna, Dallapiccola Bruno, Valenti Lu |
Influence of SNPs in nutrient-sensitive candidate genes and gene-diet interactions on blood lipids: the DiOGenes study. The British journal of nutrition 2013 Jan . Brahe LK, Angquist L, Larsen LH, Vimaleswaran KS, Hager J, Viguerie N, Loos RJ, Handjieva-Darlenska T, Jebb SA, Hlavaty P, Larsen TM, Martinez JA, Papadaki A, Pfeiffer AF, van Baak MA, Sørensen TI, Holst C, Langin D, Astrup A, Saris WH |
Association of LPIN1 gene variations with markers of metabolic syndrome in population from Bosnia and Herzegovina. Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina 2015 Aug 12 (2): 113-21. Bego Tamer, Duji? Tanja, Mlinar Barbara, Semiz Sabina, Malenica Maja, Prnjavorac Besim, Ostanek Barbara, Marc Janja, ?auševi?-Ramoševac Anida, ?auševi? Adli |
Dietary polyunsaturated fatty acids and the Pro12Ala polymorphisms of PPARG regulate serum lipids through divergent pathways: a randomized crossover clinical trial. Genes & nutrition 2015 Nov 10 (6): 43. Pihlajamäki Jussi, Schwab Ursula, Kaminska Dorota, Ågren Jyrki, Kuusisto Johanna, Kolehmainen Marjukka, Paananen Jussi, Laakso Markku, Uusitupa Mat |
Combining Genetic Variants to Improve Risk Prediction for NAFLD and Its Progression to Cirrhosis: A Proof of Concept Study. Canadian journal of gastroenterology & hepatology 2018 2018 7564835. Vespasiani-Gentilucci Umberto, Dell'Unto Chiara, De Vincentis Antonio, Baiocchini Andrea, Delle Monache Marco, Cecere Roberto, Pellicelli Adriano Maria, Giannelli Valerio, Carotti Simone, Galati Giovanni, Gallo Paolo, Valentini Francesco, Del Nonno Franca, Rosati Davide, Morini Sergio, Antonelli-Incalzi Raffaele, Picardi Anton |
Micro-ribonucleic acid-binding site variants of type 2 diabetes candidate loci predispose to gestational diabetes mellitus in Chinese Han women. Journal of diabetes investigation 2018 Jan . Wang Xiaojing, Li Wei, Ma Liangkun, Ping Fan, Liu Juntao, Wu Xueyan, Mao Jiangfeng, Wang Xi, Nie M |
Contribution of a genetic risk score to clinical prediction of hepatic steatosis in obese children and adolescents. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2019 Jun . Zusi Chiara, Mantovani Alessandro, Olivieri Francesca, Morandi Anita, Corradi Massimiliano, Miraglia Del Giudice Emanuele, Dauriz Marco, Valenti Luca, Byrne Christopher D, Targher Giovanni, Maffeis Claud |
The PNPLA3 rs738409 variant can increase the risk of liver toxicity in multiple sclerosis patients treated with beta-interferon. Clinical neurology and neurosurgery 2020 Aug 197 106166. Capone Fioravante, De Vincentis Antonio, Ferraro Elisabetta, Rossi Mariagrazia, Motolese Francesco, Picardi Antonio, Giannetti Barbara, Di Battista Giancarlo, Vespasiani-Gentilucci Umberto, Di Lazzaro Vincen |
Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia.
American journal of human genetics 2021 7 108 (8): 1478-1487. Li Quanlin, Chen Weifeng, Wang Cheng, Liu Zuqiang, Gu Yayun, Xu Xiaoyue, Xu Jiaxing, Jiang Tao, Xu Meidong, Wang Yifeng, Chen Congcong, Zhong Yunshi, Zhang Yiqun, Yao Liqing, Jin Guangfu, Hu Zhibin, Zhou Pingho |
Genetic Polymorphisms and Clinical Features in Diabetic Patients With Fatty Liver: Results From a Single-Center Experience in Southern Italy. Frontiers in medicine 2021 8 737759. Villani Rosanna, Magnati Grazia Pia, De Girolamo Giuseppe, Sangineto Moris, Romano Antonino Davide, Cassano Tommaso, Serviddio Gaeta |
Interaction between OCT1 and LPIN1 polymorphisms and response to pioglitazone-metformin tablets in patients with polycystic ovary syndrome. Chinese medical journal 2023 5 . Haixia Zeng, Yanting Huang, Dengke Liu, Tianqin Xie, Zheng Chen, Qiulan Huang, Xiaojun Zhou, Xiaoyang Lai, Jianping L |
Systemic corticosteroids for the treatment of acute episodes of rhabdomyolysis in lipin-1-deficient patients. Journal of inherited metabolic disease 2023 1 . Tuchmann-Durand Caroline, Roda Célina, Renard Perrine, Mortamet Guillaume, Bérat Claire-Marine, Altenburger Lucile, de Larauz Marie Hug, Thevenet Eloise, Cottart Charles-Henry, Moulin Florence, Bouchereau Juliette, Brassier Anais, Arnoux Jean-Baptiste, Schiff Manuel, Bednarek Nathalie, Lamireau Delphine, Garros Alexa, Mention Karine, Cano Aline, Finger Lionel, Pelosi Michele, Brochet Cécile Sergent, Caccavelli Laure, Raphalen Jean-Herlé, Renolleau Sylvain, Oualha Mehdi, de Lonlay Pasca |
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