Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 36 Records) |
| Query Trace: Disease and ENPP1[original query] |
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| PC-1 (ENPP1) K121Q polymorphism in overweight and obese type 2 diabetic coronary heart disease patients. Acta cardiologica 2008 Jun 63 (3): 323-30. Lazarevic Gordana, Milojkovic Maja, Tasic Ivan, Najman Stevo, Antic Slobodan, Stefanovic Vladis |
| Effect of ENPP1/PC-1-K121Q and PPARgamma-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population. Diabetes research and clinical practice 2008 Sep 81 (3): 278-83. Bouhaha R, Meyre D, Kamoun H Abid, Ennafaa H, Vaillant E, Sassi R, Baroudi T, Vatin V, Froguel P, Elgaaied A, Vaxillaire |
| The K121Q polymorphism of ENPP1 and peripheral arterial disease. Heart and vessels 2008 Mar 23 (2): 104-7. Eller Philipp, Schgoer Wilfried, Mueller Thomas, Tancevski Ivan, Demetz Egon, Duwensee Kristina, Ritsch Andreas, Haltmayer Meinhard, Patsch Josef |
| Candidate gene association study conditioning on individual ancestry in patients with type 2 diabetes and metabolic syndrome from Mexico City. Diabetes/metabolism research and reviews 2010 May 26 (4): 261-70. Cruz M, Valladares-Salgado A, Garcia-Mena J, Ross K, Edwards M, Angeles-Martinez J, Ortega-Camarillo C, de la Peña J Escobedo, Burguete-Garcia A I, Wacher-Rodarte N, Ambriz R, Rivera R, D'artote A L, Peralta J, Parra Esteban J, Kumate |
| [ENPP1 K121Q polymorphism and ischemic heart disease in diabetic patients]. Arquivos brasileiros de cardiologia 2010 Feb 94 (2): 157-61, 168-73, 159-63. Moehlecke Milene, Kramer Caroline K, Leitão Cristiane B, Krahe Ana Luiza, Balbosco Ivaldir, Azevedo Mirela Jobim de, Gross Jorge L, Canani Luis Henriq |
| Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease. Gut 2010 Feb 59 (2): 267-73. Dongiovanni P, Valenti L, Rametta R, Daly A K, Nobili V, Mozzi E, Leathart J B S, Pietrobattista A, Burt A D, Maggioni M, Fracanzani A L, Lattuada E, Zappa M A, Roviaro G, Marchesini G, Day C P, Fargion |
| ENPP1 K121Q Genotype Not Associated with Coronary Artery Calcification in Korean Patients with Type 2 Diabetes Mellitus. Korean diabetes journal 2010 Oct 34 (5): 320-6. Jeong Dae Joon, Lee Dong Gyu, Kim Hee-Jung, Cho Eun Hee, Kim Sang-Wo |
| a-Actinin-3 deficiency is associated with reduced bone mass in human and mouse. Bone 2011 Oct 49 (4): 790-8. Yang Nan, Schindeler Aaron, McDonald Michelle M, Seto Jane T, Houweling Peter J, Lek Monkol, Hogarth Marshall, Morse Alyson R, Raftery Joanna M, Balasuriya Dominic, MacArthur Daniel G, Berman Yemima, Quinlan Kate G R, Eisman John A, Nguyen Tuan V, Center Jacqueline R, Prince Richard L, Wilson Scott G, Zhu Kathy, Little David G, North Kathryn |
| Insulin resistance and left ventricular hypertrophy in end-stage renal disease: association between the ENPP1 gene and left ventricular concentric remodelling. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Feb 27 (2): 661-6. Spoto Belinda, Testa Alessandra, Parlongo Rosa M, Tripepi Giovanni, Trischitta Vincenzo, Mallamaci Francesca, Zoccali Carmi |
| The ENPP1 Q121 variant predicts major cardiovascular events in high-risk individuals: evidence for interaction with obesity in diabetic patients. Diabetes 2011 Mar 60 (3): 1000-7. Bacci Simonetta, Rizza Stefano, Prudente Sabrina, Spoto Belinda, Powers Christine, Facciorusso Antonio, Pacilli Antonio, Lauro Davide, Testa Alessandra, Zhang Yuan-Yuan, Di Stolfo Giuseppe, Mallamaci Francesca, Tripepi Giovanni, Xu Rui, Mangiacotti Davide, Aucella Filippo, Lauro Renato, Gervino Ernest V, Hauser Thomas H, Copetti Massimiliano, De Cosmo Salvatore, Pellegrini Fabio, Zoccali Carmine, Federici Massimo, Doria Alessandro, Trischitta Vincen |
| Ectonucleotide pyrophosphatase/phosphodiesterase 1 K173Q polymorphism is associated with diabetic nephropathy in the Taiwanese population. Genetic testing and molecular biomarkers 2011 Apr 15 (4): 239-42. Lin Cheng-Chia, Wu Chun-Te, Wu Lawrence Shih-Hs |
| ATP acts as a survival signal and prevents the mineralization of aortic valve. Journal of molecular and cellular cardiology 2012 May 52 (5): 1191-202. Côté Nancy, El Husseini Diala, Pépin Andrée, Guauque-Olarte Sandra, Ducharme Valérie, Bouchard-Cannon Pascale, Audet Audrey, Fournier Dominique, Gaudreault Nathalie, Derbali Habib, McKee Marc D, Simard Chantale, Després Jean-Pierre, Pibarot Philippe, Bossé Yohan, Mathieu Patri |
| Evaluation of the ENPP1 and PLIN single nucleotide polymorphisms with type 2 diabetes in a Taiwanese population: evidence for replication and gene-gene interaction. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2012 Oct . Wang CH, Ke WS, Lin E |
| Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases. BMC medical genetics 2012 Oct 13 (1): 1. Huhn S, Bevier M, Rudolph A, Pardini B, Naccarati A, Hein R, Hoffmeister M, Vodickova L, Novotny J, Brenner H, Chang-Claude J, Vodicka P, Hemminki K, Försti A |
| Joint effect of insulin signaling genes on cardiovascular events and on whole body and endothelial insulin resistance. Atherosclerosis 2013 Jan 226 (1): 140-5. Bacci Simonetta, Prudente Sabrina, Copetti Massimiliano, Spoto Belinda, Rizza Stefano, Baratta Roberto, Di Pietro Natalia, Morini Eleonora, Di Paola Rosa, Testa Alessandra, Mallamaci Francesca, Tripepi Giovanni, Zhang Yuan-Yuan, Mercuri Luana, Di Silvestre Sara, Lauro Renato, Malatino Lorenzo, Consoli Agostino, Pellegrini Fabio, Pandolfi Assunta, Frittitta Lucia, Zoccali Carmine, Federici Massimo, Doria Alessandro, Trischitta Vincen |
| Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6. American journal of human genetics 2012 Jan 90 (1): 25-39. Nitschke Yvonne, Baujat Geneviève, Botschen Ulrike, Wittkampf Tanja, du Moulin Marcel, Stella Jacqueline, Le Merrer Martine, Guest Geneviève, Lambot Karen, Tazarourte-Pinturier Marie-Frederique, Chassaing Nicolas, Roche Olivier, Feenstra Ilse, Loechner Karen, Deshpande Charu, Garber Samuel J, Chikarmane Rashmi, Steinmann Beat, Shahinyan Tatevik, Martorell Loreto, Davies Justin, Smith Wendy E, Kahler Stephen G, McCulloch Mignon, Wraige Elizabeth, Loidi Lourdes, Höhne Wolfgang, Martin Ludovic, Hadj-Rabia Smaïl, Terkeltaub Robert, Rutsch Fra |
| Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia. Blood 2013 Apr 121 (16): 3237-45. Flanagan Jonathan M, Sheehan Vivien, Linder Heidi, Howard Thad A, Wang Yong-Dong, Hoppe Carolyn C, Aygun Banu, Adams Robert J, Neale Geoffrey A, Ware Russell |
| Genome-wide meta-analysis of genetic susceptible genes for Type 2 Diabetes. BMC systems biology 2012 6 Suppl 3 S16. Hale Paul J, López-Yunez Alfredo M, Chen Jake |
| Association between the ENPP1 K121Q polymorphism and risk of diabetic kidney disease: a systematic review and meta-analysis. PloS one 2015 10 (3): e0118416. Sortica Denise Alves, Buffon Marjorie Piucco, Souza Bianca Marmontel, Nicoletto Bruna Bellicanta, Santer Andressa, Assmann Tais Silveira, Crispim Daisy, Canani Luis Henriq |
| Is common genetic variation at IRS1, ENPP1 and TRIB3 loci associated with cardiometabolic phenotypes in type 2 diabetes? An exploratory analysis of the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 5. Nutrition, metabolism, and cardiovascular diseases : NMCD 2016 Mar 26 (3): 232-8. Trombetta M, Dauriz M, Bonetti S, Travia D, Boselli L, Santi L, Bonora E, Bonadonna R |
| Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population. Molecular genetics & genomic medicine 2015 Nov 3 (6): 558-69. Edelman Deborah, Kalia Harmit, Delio Maria, Alani Mustafa, Krishnamurthy Karthik, Abd Mortadha, Auton Adam, Wang Tao, Wolkoff Allan W, Morrow Bernice |
| ENPP1 121Q functional variant enhances susceptibility to coronary artery disease in South Indian patients with type 2 diabetes mellitus. Molecular and cellular biochemistry 2017 May . Sumi S, Ramachandran Surya, RamanKutty V, Patel Maulin M, Anand T N, Mullasari Ajit S, Kartha C |
| ENPP1 K121Q (rs1044498?C?>?A) genetic polymorphism confers a high risk of susceptibility to coronary heart disease: A PRISMA-compliant article. Medicine 2018 Jul 97 (27): e11236. Di Jia-Yin, Dai Meng-Lu, Zhang Zong-X |
| Genetic determinants of steatosis and fibrosis progression in paediatric non-alcoholic fatty liver disease. Liver international : official journal of the International Association for the Study of the Liver 2019 Mar 39 (3): 540-556. Hudert Christian A, Selinski Silvia, Rudolph Birgit, Bläker Hendrik, Loddenkemper Christoph, Thielhorn Ria, Berndt Nikolaus, Golka Klaus, Cadenas Cristina, Reinders Jörg, Henning Stephan, Bufler Philip, Jansen Peter L M, Holzhütter Hermann-Georg, Meierhofer David, Hengstler Jan G, Wiegand Susan |
| [Mutation analysis of four pedigrees affected with hypophosphatemic rickets through targeted next-generation sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 10 35 (5): 638-643. Bai Ying, Liu Ning, Shao Mingwei, Qin Guijun, Gao Xu, Kong Xiangdo |
| Genetic variants in cardiac calcification in Northern Sweden. Medicine 2019 4 98 (15): e15065. Hellman Urban, Mörner Stellan, Henein Micha |
| Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
| Association of the ENPP1/ENTPD1 Polymorphisms in Hemodialysis Patients. International journal of general medicine 2021 14 6401-6408. Zhang Xi, Wan Ziming, Cheng Si, Gan H |
| Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
| Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6. Gene 2024 6 927 148731. Clara Schott, Allison A Dilliott, Jian Wang, Adam D McIntyre, Surim Son, Samantha Colaiacovo, Cadence Baker, Lakshman Gunaratnam, Andrew A House, Shih-Han Susan Huang, Hariharan Iyer, John Johnson, Khaled Lotfy, Mario Masellis, Douglas P Munoz, Faisal Rehman, Pavel S Roshanov, Richard H Swartz, Matthew A Weir, Robert A Hegele, Dervla M Connaught |
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