Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and SLC12A3[original query] |
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| Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms. Diabetes 2003 Nov 52 (11): 2848-53. Tanaka Nobue, Babazono Tetsuya, Saito Susumu, Sekine Akihiro, Tsunoda Tatsuhiko, Haneda Masakazu, Tanaka Yasushi, Fujioka Tomoaki, Kaku Kohei, Kawamori Ryuzou, Kikkawa Ryuichi, Iwamoto Yasuhiko, Nakamura Yusuke, Maeda Shi |
| SLC12A3 (solute carrier family 12 member [sodium/chloride] 3) polymorphisms are associated with end-stage renal disease in diabetic nephropathy. Diabetes 2006 Mar 55 (3): 843-8. Kim Jae Hyeon, Shin Hyoung Doo, Park Byung Lae, Moon Min Kyong, Cho Young Min, Hwang Young Hwan, Oh Kook Whan, Kim Seong Yeon, Lee Hong Kyu, Ahn Curie, Park Kyong S |
| Genetic variation at the SLC12A3 locus is unlikely to explain risk for advanced diabetic nephropathy in Caucasians with type 2 diabetes. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008 Jul 23 (7): 2260-4. Ng Daniel P K, Nurbaya Siti, Choo Serena, Koh David, Chia Kee-Seng, Krolewski Andrzej |
| Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2011 Oct 165 (4): 665-73. Balavoine A S, Bataille P, Vanhille P, Azar R, Noël C, Asseman P, Soudan B, Wémeau J L, Vantyghem M |
| Genetic and biological effects of sodium-chloride cotransporter (SLC12A3) in diabetic nephropathy. American journal of nephrology 2014 40 (5): 408-16. Abu Seman Norhashimah, He Bing, Ojala Juha R M, Wan Mohamud Wan Nazaimoon, Östenson Claes-Göran, Brismar Kerstin, Gu Harvest |
| Mutation profile and treatment of Gitelman syndrome in Chinese patients. Clinical and experimental nephrology 2016 May . Wang Fen, Shi Chuan, Cui Yunying, Li Chunyan, Tong An |
| Clinical and genetic analyses of Chinese patients with Gitelman syndrome. Genetics and molecular research : GMR 2016 15 (2): . Miao M, Zhao C Q, Wang X L, Shan Z |
| Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome. Journal of Korean medical science 2016 Jan 31 (1): 47-54. Lee Jae Wook, Lee Jeonghwan, Heo Nam Ju, Cheong Hae Il, Han Jin S |
| Arg913Gln of SLC12A3 gene promotes development and progression of end-stage renal disease in Chinese type 2 diabetes mellitus. Molecular and cellular biochemistry 2017 Jul . Zhang Rong, Zhuang Langen, Li Ming, Zhang Juan, Zhao Weijing, Ge Xiaoxu, Chen Yating, Wang Feng, Wang Niansong, Bao Yuqian, Liu Limei, Liu Yanjun, Jia Weipi |
| SLC12A3 variants modulate LDL cholesterol levels in the Mongolian population. Lipids in health and disease 2017 Feb 16 (1): 29. An Caiyan, Zhang Kejin, Su Xiul |
| Genetic variants of SLC12A3 modulate serum lipid profiles in a group of Mongolian pedigree population. Lipids in health and disease 2018 Apr 17 (1): 83. An Caiyan, Liang Junqing, Zhang Kejin, Su Xiul |
| [Association of sodium ion transporter gene polymorphisms with essential hypertension among ethnic Koreans from Mudanjiang]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 Feb 35 (1): 116-120. Shi Jiayi, Zhang Chunjun, Bu Xiaobo, Han Yanlong, Deng Daiqian, Song J |
| Polymorphisms in PCSK9, LDLR, BCMO1, SLC12A3, and KCNJ1 are Associated with Serum Lipid Profile in Chinese Han Population. International journal of environmental research and public health 2019 Sep 16 (17): . Li Zheng, Zhao Tianyu, Tan Xiaohua, Lei Song, Huang Liu, Yang L |
| The single nucleotide polymorphism rs11643718 in SLC12A3 is associated with the development of diabetic kidney disease in Chinese people with type 2 diabetes. Diabetic medicine : a journal of the British Diabetic Association 2020 Jul . Yang J-F, Xiong X-F, Xiao Y, Wei L, Li L, Yang M, Han Y-C, Zhao H, Li C-R, Jiang N, Xiong S, Zeng L-F, Zhou Z-G, Liu S-P, Wang N-S, Fan Y, Sun |
| Impact on Longevity of Genetic Cardiovascular Risk and Lifestyle including Red Meat Consumption. Oxidative medicine and cellular longevity 2020 7 2020 1305413. Pereira da Silva Alda, Costa Maria do Céu, Aguiar Laura, Matos Andreia, Gil Ângela, Gorjão-Clara J, Polónia Jorge, Bicho Manu |
| Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report. Medicine 2020 7 99 (29): e21123. He Guangyu, Gang Xiaokun, Sun Zhonghua, Wang Ping, Wang Guixia, Guo Weiyi |
| Model of genetic and environmental factors associated with type 2 diabetes mellitus in a Chinese Han population. BMC public health 2020 7 20 (1): 1024. Li Zheng, Ye Cheng-Yin, Zhao Tian-Yu, Yang L |
| Multi-centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children. Clinical genetics 2020 12 99 (4): 558-564. Shen Qian, Chen Jiemei, Yu Minghui, Lin Zhi, Nan Xiaojuan, Dong Beijun, Fang Xiaoyan, Chen Jing, Ding Guixia, Zhang Aihua, Gao Chunlin, Miao Li, Xu Yuanyuan, Jiang Xiaoyun, Bai Haitao, Zhuang Jieqiu, Gao Xiaojie, Xu Hong, |
| Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases. Scientific reports 2021 8 11 (1): 16099. Kondo Atsushi, Nagano China, Ishiko Shinya, Omori Takashi, Aoto Yuya, Rossanti Rini, Sakakibara Nana, Horinouchi Tomoko, Yamamura Tomohiko, Nagai Sadayuki, Okada Eri, Shima Yuko, Nakanishi Koichi, Ninchoji Takeshi, Kaito Hiroshi, Takeda Hiroki, Nagase Hiroaki, Morisada Naoya, Iijima Kazumoto, Nozu Kand |
| Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA. Journal of the American Society of Nephrology : JASN 2021 10 33 (2): 305-325. Viering Daan, Schlingmann Karl P, Hureaux Marguerite, Nijenhuis Tom, Mallett Andrew, Chan Melanie M Y, van Beek André, van Eerde Albertien M, Coulibaly Jean-Marie, Vallet Marion, Decramer Stéphane, Pelletier Solenne, Klaus Günter, Kömhoff Martin, Beetz Rolf, Patel Chirag, Shenoy Mohan, Steenbergen Eric J, Anderson Glenn, Bongers Ernie M H F, Bergmann Carsten, Panneman Daan, Rodenburg Richard J, Kleta Robert, Houillier Pascal, Konrad Martin, Vargas-Poussou Rosa, Knoers Nine V A M, Bockenhauer Detlef, de Baaij Jeroen H F, |
| Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. Frontiers in genetics 2022 8 13 886038. Alaamery Manal, Alghamdi Jahad, Massadeh Salam, Alsawaji Mona, Aljawini Nora, Albesher Nour, Alghamdi Bader, Almutairi Mansour, Hejaili Fayez, Alfadhel Majid, Baz Batoul, Almuzzaini Bader, Almutairi Adel F, Abdullah Mubarak, Quintana Francisco J, Sayyari Abdull |
| Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes. Genes 2022 3 13 (3): . Peces Ramón, Peces Carlos, Mena Rocío, Cuesta Emilio, García-Santiago Fe Amalia, Ossorio Marta, Afonso Sara, Lapunzina Pablo, Nevado Juli |
| Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis. PLoS medicine 2022 02 19 (2): e1003897. Yarmolinsky James, Díez-Obrero Virginia, Richardson Tom G, Pigeyre Marie, Sjaarda Jennifer, Paré Guillaume, Walker Venexia M, Vincent Emma E, Tan Vanessa Y, Obón-Santacana Mireia, Albanes Demetrius, Hampe Jochen, Gsur Andrea, Hampel Heather, Pai Rish K, Jenkins Mark, Gallinger Steven, Casey Graham, Zheng Wei, Amos Christopher I, , , , Smith George Davey, Martin Richard M, Moreno Vict |
| Recent Progress in Genetics and Epigenetics Research on Diabetic Nephropathy in Malaysia. Journal of diabetes research 2023 5 2023 9053580. Norhashimah Abu Seman, Siti Haslina Othm |
| Genetic Etiology Investigation in Treatment-Resistant Nocturnal Enuresis Children: A descriptive study. Urology journal 2024 12 . Sevim Yener, Metin Es |
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