Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: CLC[original query] |
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Lack of association of variants of the renal salt reabsorption-related genes SLC12A3 and ClC-Kb and hypertension in Mongolian and Han populations in Inner Mongolia. Genetics and molecular research : GMR 2011 10 (2): 948-54. Chang P Y, Zhang X G, Su X |
Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. Proceedings of the National Academy of Sciences of the United States of America 2011 Feb 108 (6): 2456-61. Cappola Thomas P, Matkovich Scot J, Wang Wei, van Booven Derek, Li Mingyao, Wang Xuexia, Qu Liming, Sweitzer Nancy K, Fang James C, Reilly Muredach P, Hakonarson Hakon, Nerbonne Jeanne M, Dorn Gerald |
A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defect. Genetic testing and molecular biomarkers 2012 Aug 16 (8): 984-7. Xuan Chao, Wang Bin-Bin, Gao Ge, Bai Xiao-Yan, Yang Qin, Liu Xiao-Cheng, Jing Wen-Bin, Ma Xu, He Guo-W |
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencing. Journal of medical genetics 2012 Dec 49 (12): 756-67. Halbritter Jan, Diaz Katrina, Chaki Moumita, Porath Jonathan D, Tarrier Brendan, Fu Clementine, Innis Jamie L, Allen Susan J, Lyons Robert H, Stefanidis Constantinos J, Omran Heymut, Soliman Neveen A, Otto Edgar |
Identification of two novel mutations of the HOMEZ gene in Chinese patients with isolated ventricular septal defect. Genetic testing and molecular biomarkers 2013 May 17 (5): 390-4. Xuan Chao, Jia Ke-Gang, Wang Bin-Bin, Bai Xiao-Yan, Gao Ge, Yang Qin, Wang Xiu-Li, Liu Xiao-Cheng, Ma Xu, He Guo-W |
Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology 2013 Mar 80 (12): 1078-85. Chen Tim T, Klassen Tara L, Goldman Alica M, Marini Carla, Guerrini Renzo, Noebels Jeffrey |
Genetic variations in the osteopontin promoters T-443C and G-156GG increase carotid intima-media thickness. International journal of general medicine 2016 9 117-22. Yueniwati Yuyun, Yurina Valentina, Sobah Nurus, Rahayu Enda |
The rs3737964 single-nucleotide polymorphism of the chloride channel-6 gene as a risk factor for coronary heart disease. Molecular genetics & genomic medicine 2015 Nov 3 (6): 537-42. Zhang Li, Zhang Tao, Xiang Zhengkai, Lu Shengqia |
Genetic Variants of Cytochrome CYP2D6 in Two Mixed Chilean Populations. Human heredity 2017 Jul 82 (1-2): 16-20. Acuña Mónica, Pinto Eric, Olivares Paulina, Ríos Caroli |
Clinicopathological, radiologic, and molecular study of 23 combined hepatocellular-cholangiocarcinomas with stem cell features, cholangiolocellular type. Human pathology 2017 Apr . Chen Jun, He Jian, Deng Min, Wu Hong-Yan, Shi Jiong, Mao Liang, Sun Qi, Tang Min, Fan Xiang-Shan, Qiu Yu-Dong, Huang Q |
A silent mutation in human alpha-A crystallin gene in patients with age-related nuclear or cortical cataract. Bosnian journal of basic medical sciences 2017 Feb . Mynampati Bharani K, Muthukumarappa Thungapathra, Ghosh Sujata, Ram Jag |
Significance of 3'UTR and Pathogenic Haplotype in Glucose-6-Phosphate Deficiency. Laboratory medicine 2017 Feb 48 (1): 73-88. Chaowanathikhom Mallika, Nuchnoi Pornlada, Palasuwan Duangd |
Cholangiolocellular Carcinoma With "Ductal Plate Malformation" Pattern May Be Characterized by ARID1A Genetic Alterations. The American journal of surgical pathology 2018 12 43 (3): 352-360. Sasaki Motoko, Sato Yasunori, Nakanuma Yasu |
A somatic mutation in CLCN2 identified in a sporadic aldosterone-producing adenoma. European journal of endocrinology 2019 9 181 (5): K37-K41. Dutta Ravi Kumar, Arnesen Thomas, Heie Anette, Walz Martin, Alesina Piero, Söderkvist Peter, Gimm Oliv |
Myotonia congenita: mutation spectrum of CLCN1 in Spanish patients. Journal of genetics 2019 9 98 . Milla Carmen Palma, De Castro Carmen Prior, Gómez-González Clara, Martínez-Montero Paloma, Pascual Pascual Samuel I, Molano Mateos Jes |
Comprehensive genetic analysis of cholangiolocellular carcinoma with a coexistent hepatocellular carcinoma-like area and metachronous hepatocellular carcinoma. Hepatology research : the official journal of the Japan Society of Hepatology 2019 7 49 (12): 1466-1474. Kawai-Kitahata Fukiko, Asahina Yasuhiro, Kaneko Shun, Tsuchiya Jun, Sato Ayako, Miyoshi Masato, Tsunoda Tomoyuki, Inoue-Shinomiya Emi, Murakawa Miyako, Nitta Sayuri, Itsui Yasuhiro, Nakagawa Mina, Azuma Seishin, Kakinuma Sei, Tanabe Minoru, Sugawara Emiko, Takemoto Akira, Ojima Hidenori, Sakamoto Michiie, Muraoka Masaru, Takano Shinichi, Maekawa Shinya, Enomoto Nobuyuki, Watanabe Mamo |
Distinctive clinicopathological features and KRAS and IDH1/2 mutation status of cholangiolocellular carcinoma. Hepatology research : the official journal of the Japan Society of Hepatology 2019 Nov . Kusano Hironori, Naito Yoshiki, Mihara Yutaro, Kondo Reiichiro, Ogasawara Sachiko, Akiba Jun, Nakashima Osamu, Yano Hirohi |
A sputum 6-gene signature predicts future exacerbations of poorly controlled asthma. The Journal of allergy and clinical immunology 2019 1 144 (1): 51-60.e11. Fricker Michael, Gibson Peter G, Powell Heather, Simpson Jodie L, Yang Ian A, Upham John W, Reynolds Paul N, Hodge Sandra, James Alan L, Jenkins Christine, Peters Matthew J, Marks Guy B, Baraket Melissa, Baines Katherine |
Lipoprotein(a) concentration, genetic variants, apo(a) isoform size, and cellular cholesterol efflux in patients with elevated Lp(a) and coronary heart disease submitted or not to lipoprotein apheresis: An Italian case-control multicenter study on Lp(a). Journal of clinical lipidology 2020 May . Stefanutti Claudia, Pisciotta Livia, Favari Elda, Di Giacomo Serafina, Vacondio Federica, Zenti Maria Grazia, Morozzi Claudia, Berretti Daniele, Mesce Dario, Vitale Marco, Pasta Andrea, Ronca Annalisa, Garuti Anna, Manfredini Matteo, Anglés-Cano Eduardo, Marcovina Santica Marija, Watts Gerald Francis, |
HDL-Mediated Cholesterol Efflux and Plasma Loading Capacities Are Altered in Subjects with Metabolically- but Not Genetically Driven Non-Alcoholic Fatty Liver Disease (NAFLD). Biomedicines 2020 12 8 (12): . Di Costanzo Alessia, Ronca Annalisa, D'Erasmo Laura, Manfredini Matteo, Baratta Francesco, Pastori Daniele, Di Martino Michele, Ceci Fabrizio, Angelico Francesco, Del Ben Maria, Pavanello Chiara, Turri Marta, Calabresi Laura, Favari Elda, Arca Marcel |
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. International journal of molecular sciences 2020 1 21 (2): . Gianesello Lisa, Ceol Monica, Bertoldi Loris, Terrin Liliana, Priante Giovanna, Murer Luisa, Peruzzi Licia, Giordano Mario, Paglialonga Fabio, Cantaluppi Vincenzo, Musetti Claudio, Valle Giorgio, Del Prete Dorella, Anglani Franca, Network Dent Disease Itali |
Can Unlikely Neanderthal Chloride Channel CLC-2 Gene Variants Provide Insights in Modern Human Infertility? Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2021 6 55 (3): 301-310. Jeworutzki Elena, Tüttelmann Frank, Rothenberg Ina, Pusch Michael, Schreiber Julian A, Kliesch Sabine, Wünsch Bernhard, Strutz-Seebohm Nathalie, Seebohm Guisca |
The molecular and phenotypic spectrum of CLCN4-related epilepsy. Epilepsia 2021 5 62 (6): 1401-1415. He Hailan, Guzman Raul E, Cao Dezhi, Sierra-Marquez Juan, Yin Fei, Fahlke Christoph, Peng Jing, Stauber Tobi |
Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndrome. The Journal of allergy and clinical immunology 2021 3 148 (2): 585-598. Chen Yin-Huai, Zastrow Diane B, Metcalfe Riley D, Gartner Lisa, Krause Freia, Morton Craig J, Marwaha Shruti, Fresard Laure, Huang Yong, Zhao Chunli, McCormack Colleen, Bick David, Worthey Elizabeth A, Eng Christine M, Gold Jessica, Undiagnosed Diseases Network , Montgomery Stephen B, Fisher Paul G, Ashley Euan A, Wheeler Matthew T, Parker Michael W, Shanmugasundaram Veerabahu, Putoczki Tracy L, Schmidt-Arras Dirk, Laurence Arian, Bernstein Jonathan A, Griffin Michael D W, Uhlig Holm |
Kidney ion handling genes and their interaction in blood pressure control. Bioscience reports 2022 10 42 (11): . An Caiyan, Yang Liuyi, Han Tengfei, Song Huazhong, Li Zichao, Zhang Junjing, Zhang Kej |
Is nestin a diagnostic marker for combined hepatocellular-cholangiocarcinoma? Histopathology 2022 Jan . Sasaki M, Sato Y, Nakanuma |
Two Different Copy Number Variations of the CLCN2 Gene in Chinese Cattle and Their Association with Growth Traits. Animals : an open access journal from MDPI 2022 1 12 (1): . Tang Jia, Shen Xuemei, Yang Yu, Yang Haiyan, Qi Ao, Yang Shuling, Qu Kaixing, Lan Xianyong, Huang Bizhi, Chen Ho |
Novel genetic variants data for adaptation to hypoxia in native chickens. BMC research notes 2023 9 16 (1): 225. Atieh Moradi, Hamed Kharrati-Koopaee, Morteza Fardi, Mehdi Farahmandzadeh, Fatemeh Nowroo |
Genetic profile of thymic epithelial tumors in the Japanese population: an exploratory study examining potential therapeutic targets. Translational lung cancer research 2023 5 12 (4): 707-718. Midori Shimada, Hirokazu Taniguchi, Hiroyuki Yamaguchi, Hiroshi Gyotoku, Daisuke Sasaki, Norihito Kaku, Chikako Senju, Hiroaki Senju, Erika Imamura, Shinnosuke Takemoto, Kazuko Yamamoto, Noriho Sakamoto, Yasushi Obase, Tomoshi Tsuchiya, Minoru Fukuda, Hiroshi Soda, Kazuto Ashizawa, Junya Fukuoka, Takeshi Nagayasu, Katsunori Yanagihara, Hiroshi Muk |
Association of MGLL Intronic C>T Single Nucleotide Polymorphism (rs782440) with Borderline Personality Disorder: A Case-Control Study. Cell journal 2023 12 25 (11): 783-789. Nazanin Hatami Bavarsad, Leila Jahangard, Masood Saidijam, Seyed Asaad Karimi, Ali Reza Soltanian, Elahe Shahriari, Saeid Afshar, Abdolrahman Sari |
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- Page last updated:Apr 22, 2024
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