Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: XIRP2[original query] |
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Distinct Subtypes of Gastric Cancer Defined by Molecular Characterization Include Novel Mutational Signatures with Prognostic Capability. Cancer research 2016 04 76 (7): 1724-32. Li Xiangchun, Wu William K K, Xing Rui, Wong Sunny H, Liu Yuexin, Fang Xiaodong, Zhang Yanlin, Wang Mengyao, Wang Jiaqian, Li Lin, Zhou Yong, Tang Senwei, Peng Shaoliang, Qiu Kunlong, Chen Longyun, Chen Kexin, Yang Huanming, Zhang Wei, Chan Matthew T V, Lu Youyong, Sung Joseph J Y, Yu J |
Parkinson's disease: SNCA-, PARK2-, and LRRK2- targeting microRNAs elevated in cingulate gyrus. Parkinsonism & related disorders 2016 Sep . Tatura Roman, Kraus Theo, Giese Armin, Arzberger Thomas, Buchholz Malte, Höglinger Günter, Müller Ulri |
Polymorphisms in selected genes and analysis of their relationship with osteochondrosis in Polish sport horse breeds. Animal genetics 2018 8 49 (6): 623-627. Wypch?o M, Korwin-Kossakowska A, Bereznowski A, Hecold M, Lewczuk |
Genetic Variants Influencing Plasma Renin Activity in Hypertensive Patients From the PEAR Study (Pharmacogenomic Evaluation of Antihypertensive Responses).
Circulation. Genomic and precision medicine 2018 Apr 11 (4): e001854. McDonough Caitrin W, Magvanjav Oyunbileg, Sá Ana C C, El Rouby Nihal M, Dave Chintan, Deitchman Amelia N, Kawaguchi-Suzuki Marina, Mei Wenbin, Shen Yong, Singh Ravi Shankar Prasad, Solayman Mohamed, Bailey Kent R, Boerwinkle Eric, Chapman Arlene B, Gums John G, Webb Amy, Scherer Steven E, Sadee Wolfgang, Turner Stephen T, Cooper-DeHoff Rhonda M, Gong Yan, Johnson Julie |
Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. Birth defects research 2018 3 110 (7): 610-617. Matsunami Nori, Shanmugam Hari, Baird Lisa, Stevens Jeff, Byrne Janice L, Barnhart Douglas C, Rau Carrie, Feldkamp Marcia L, Yoder Bradley A, Leppert Mark F, Yost H Joseph, Brunelli Lu |
Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population. Journal of the American Heart Association 2018 01 7 (1): . Huang Lei, Wu Kuo-Ho, Zhang Liyong, Wang Qinchuan, Tang Shuangbo, Wu Qiuping, Jiang Pei-Hsiu, Lin Jim Jung-Ching, Guo Jian, Wang Lin, Loh Shih-Hurng, Cheng Jiandi |
Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients. Pediatric cardiology 2019 4 40 (5): 950-957. Dai Genyin, Pu Zhening, Cheng Xueying, Yin Jie, Chen Jun, Xu Ting, Zhang Han, Li Zewei, Chen Xuan, Chen Jinlong, Qin Yuming, Yang Shiw |
EP300 mutation is associated with tumor mutation burden and promotes antitumor immunity in bladder cancer patients. Aging 2020 Feb 12 . Zhu Gongmin, Pei Lijiao, Li Yuan, Gou X |
Whole exome sequencing of high-risk neuroblastoma identifies novel non-synonymous variants. PloS one 2022 17 (8): e0273280. Przyby?a Weronika, Gjersvoll Paulsen Kirsti Marie, Mishra Charitra Kumar, Nygård Ståle, Engebretsen Solveig, Ruud Ellen, Trøen Gunhild, Beiske Klaus, Baumbusch Lars Oliv |
Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells. Neurobiology of aging 2022 5 116 16-24. Ruf Wolfgang P, Hannon Eilis, Freischmidt Axel, Grozdanov Veselin, Brenner David, Müller Kathrin, Knehr Antje, Günther Kornelia, Dorst Johannes, Ammerpohl Ole, Danzer Karin M, Mill Jonathan, Ludolph Albert C, Weishaupt Jochen |
A genomic mutation spectrum of collecting duct carcinoma in the Chinese population. BMC medical genomics 2022 1 15 (1): 1. Zhang Huaru, Lu Xiaojun, Huang Gang, Hua Meimian, Zhang Wenhui, Wang Tao, Huang Liqun, Wang Ziwei, Chen Qing, Li Jing, Yang Qing, Yang Guoshe |
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- Page last updated:Apr 22, 2024
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