Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: SLC5A2[original query] |
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A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria. Scientific reports 0 6 33920. Zhao Xiangzhong, Cui Li, Lang Yanhua, Liu Ting, Lu Jingru, Wang Cui, Tuffery-Giraud Sylvie, Bottillo Irene, Wang Xinsheng, Shao Lepi |
Common variation in the sodium/glucose cotransporter 2 gene SLC5A2 does neither affect fasting nor glucose-suppressed plasma glucagon concentrations. PloS one 2017 12 (5): e0177148. Ordelheide Anna-Maria, Böhm Anja, Kempe-Teufel Daniela, Wagner Robert, Machicao Fausto, Heni Martin, Stefan Norbert, Fritsche Andreas, Häring Hans-Ulrich, Staiger Hara |
Influence of common polymorphisms in the SLC5A2 gene on metabolic traits in subjects at increased risk of diabetes and on response to empagliflozin treatment in patients with diabetes. Pharmacogenetics and genomics 2017 Jan . Zimdahl Heike, Haupt Axel, Brendel Michael, Bour Louis, Machicao Fausto, Salsali Afshin, Broedl Uli C, Woerle Hans-Juergen, Häring Hans-Ulrich, Staiger Hara |
Identification of ten novel SLC5A2 mutations and determination of the renal threshold for glucose excretion in Chinese patients with familial renal glucosuria. Clinica chimica acta; international journal of clinical chemistry 2018 12 490 102-106. Wang Sai, Zhao Xiangzhong, Zhang Ruixiao, Wang Cui, Han Yue, Shao Lepi |
Sequence variants associating with urinary biomarkers.
Human molecular genetics 2019 04 28 (7): 1199-1211. Benonisdottir Stefania, Kristjansson Ragnar P, Oddsson Asmundur, Steinthorsdottir Valgerdur, Mikaelsdottir Evgenia, Kehr Birte, Jensson Brynjar O, Arnadottir Gudny A, Sulem Gerald, Sveinbjornsson Gardar, Kristmundsdottir Snaedis, Ivarsdottir Erna V, Tragante Vinicius, Gunnarsson Bjarni, Runolfsdottir Hrafnhildur Linnet, Arthur Joseph G, Deaton Aimee M, Eyjolfsson Gudmundur I, Davidsson Olafur B, Asselbergs Folkert W, Hreidarsson Astradur B, Rafnar Thorunn, Thorleifsson Gudmar, Edvardsson Vidar, Sigurdsson Gunnar, Helgadottir Anna, Halldorsson Bjarni V, Masson Gisli, Holm Hilma, Onundarson Pall T, Indridason Olafur S, Benediktsson Rafn, Palsson Runolfur, Gudbjartsson Daniel F, Olafsson Isleifur, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
Are SGLT2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis. Bioscience reports 2019 Apr . Drexel Heinz, Leiherer Andreas, Saely Christoph H, Brandtner Eva Maria, Geiger Kathrin, Vonbank Alexander, Fraunberger Pater, Muendlein Ax |
Clinical and genetic determinants of urinary glucose excretion in patients with diabetes mellitus. Journal of diabetes investigation 2020 9 12 (5): 728-737. Monobe Keisuke, Noso Shinsuke, Babaya Naru, Hiromine Yoshihisa, Taketomo Yasunori, Niwano Fumimaru, Yoshida Sawa, Yasutake Sara, Minohara Tatsuro, Kawabata Yumiko, Ikegami Hiros |
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PloS one 2020 6 15 (6): e0234246. Zhang Rong, Gehlen Jan, Kawalia Amit, Melissari Maria-Theodora, Dakal Tikam Chand, Menon Athira M, Höfele Julia, Riedhammer Korbinian, Waffenschmidt Lea, Fabian Julia, Breuer Katinka, Kalanithy Jeshurun, Hilger Alina Christine, Sharma Amit, Hölscher Alice, Boemers Thomas M, Pauly Markus, Leutner Andreas, Fuchs Jörg, Seitz Guido, Ludwikowski Barbara M, Gomez Barbara, Hubertus Jochen, Heydweiller Andreas, Kurz Ralf, Leonhardt Johannes, Kosch Ferdinand, Holland-Cunz Stefan, Münsterer Oliver, Ure Beno, Schmiedeke Eberhard, Neser Jörg, Degenhardt Petra, Märzheuser Stefanie, Kleine Katharina, Schäfer Mattias, Spychalski Nicole, Deffaa Oliver J, Gosemann Jan-Hendrik, Lacher Martin, Heilmann-Heimbach Stefanie, Zwink Nadine, Jenetzky Ekkehart, Ludwig Michael, Grote Phillip, Schumacher Johannes, Thiele Holger, Reutter Hei |
Common variation at 16p11.2 is associated with glycosuria in pregnancy: findings from a genome-wide association study in European women.
Human molecular genetics 2020 Jul 29 (12): 2098-2106. Lee Matthew A, McMahon George, Karhunen Ville, Wade Kaitlin H, Corbin Laura J, Hughes David A, Smith George Davey, Lawlor Debbie A, Jarvelin Marjo-Riitta, Timpson Nicholas |
Genetic variability in sodium-glucose cotransporter 2 influences glycemic control and risk for diabetic retinopathy in type 2 diabetes patients. Journal of medical biochemistry 2020 Sep 39 (3): 276-282. Klen Jasna, Goricar Katja, Dolžan Vi |
Pilot study in pharmacogenomic management of empagliflozin in type 2 diabetes mellitus patients. Journal of diabetes and metabolic disorders 2021 12 20 (2): 1407-1413. Jamalizadeh Mahdieh, Hasanzad Mandana, Sarhangi Negar, Sharifi Farshad, Nasli-Esfahani Ensieh, Larijani Bagh |
Genetic Variation in Sodium-glucose Cotransporter 2 and Heart Failure. Clinical pharmacology and therapeutics 2021 Jan . Katzmann Julius L, Mason Amy M, März Winfried, Kleber Marcus E, Niessner Alexander, Blüher Matthias, Speer Thimoteus, Laufs Ulri |
SGLT2 Inhibition, Choline Metabolites, and Cardiometabolic Diseases: A Mediation Mendelian Randomization Study. Diabetes care 2022 9 45 (11): 2718-2728. Xu Min, Zheng Jie, Hou Tianzhichao, Lin Hong, Wang Tiange, Wang Shuangyuan, Lu Jieli, Zhao Zhiyun, Li Mian, Xu Yu, Ning Guang, Bi Yufang, Wang Weiqi |
Hereditary renal glycosuria, diabetes and responses to SGLT2 inhibitor. Journal of diabetes 2022 3 14 (3): 216-220. Ren Qian, Gong Siqian, Han Xuyao, Ji Lino |
Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Annals of medicine 2022 10 54 (1): 3039-3051. Mota-Zamorano Sonia, González Luz M, Robles Nicolás R, Valdivielso José M, Arévalo-Lorido José C, López-Gómez Juan, Gervasini Guiller |
Genetic variation in SLC5A2 mimicking SGLT2-inhibition and risk of cardiovascular disease and all-cause mortality: reduced risk not explained by lower plasma glucose. Cardiovascular research 2023 7 . Louise E Bechmann, Frida Emanuelsson, Børge G Nordestgaard, Marianne Be |
Evaluation of the effect of sodium-glucose cotransporter 2 inhibition on fracture risk: evidence from Mendelian randomization and genetic association study. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 . Huajie Dai, Longyi Zheng, Zheng Zhu, Xin Geng, Tianzhichao Hou, Qi Wang, Yijie Zhu, Hong Lin, Shuangyuan Wang, Ruizhi Zheng, Zhiyun Zhao, Mian Li, Jieli Lu, Yu Xu, Tiange Wang, Jianmin Liu, Guang Ning, Weiqing Wang, Yufang Bi, Jie Zheng, Min |
Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome. medRxiv : the preprint server for health sciences 2023 10 . Hyejeong Hong, Katharina V Schulze, Ian E Copeland, Manasa Atyam, Kendra Kamp, Neil A Hanchard, John Belmont, Tamar Ringel-Kulka, Margaret Heitkemper, Robert J Shulm |
SGLT2 inhibition, circulating metabolites, and atrial fibrillation: a Mendelian randomization study. Cardiovascular diabetology 2023 10 22 (1): 278. Jiang Li, Yuefeng Yu, Ying Sun, Bowei Yu, Xiao Tan, Bin Wang, Yingli Lu, Ningjian Wa |
Role of SLC5A2 polymorphisms and effects of genetic polymorphism on sodium glucose cotransporter 2 inhibitorsinhibitor response. Molecular biology reports 2023 10 . Bo Xu, Shaoqian Li, Bo Kang, Shangzhi Fan, Canyu Chen, Weiyi Li, Jixiang Chen, Zunbo He, Fan Tang, Jiecan Zh |
Sodium-glucose cotransporter 2 inhibitors, inflammation, and heart failure: a two-sample Mendelian randomization study. Cardiovascular diabetology 2024 4 23 (1): 118. Wenqin Guo, Lingyue Zhao, Weichao Huang, Jing Chen, Tingting Zhong, Shaodi Yan, Wei Hu, Fanfang Zeng, Changnong Peng, Hongbing Y |
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- Page last updated:Apr 16, 2024
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