Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: MED13[original query] |
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HLA-DRB1 and disease outcome in multiple sclerosis. Journal of neurology 2001 Apr 248 (4): 304-10. Weatherby S J, Thomson W, Pepper L, Donn R, Worthington J, Mann C L, Davies M B, Fryer A A, Boggild M D, Young C A, Jones P W, Strange R C, Ollier W E, Hawkins C |
Mutation analysis of components of the Mediator kinase module in MED12 mutation-negative uterine leiomyomas. British journal of cancer 2014 Apr 110 (9): 2246-9. Mäkinen N, Heinonen H-R, Sjöberg J, Taipale J, Vahteristo P, Aaltonen L |
Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms. The Prostate 2015 Sep . Kämpjärvi Kati, Kim Nam Hee, Keskitalo Salla, Clark Alison D, von Nandelstadh Pernilla, Turunen Mikko, Heikkinen Tuomas, Park Min Ju, Mäkinen Netta, Kivinummi Kati, Lintula Susanna, Hotakainen Kristina, Nevanlinna Heli, Hokland Peter, Böhling Tom, Bützow Ralf, Böhm Jan, Mecklin Jukka-Pekka, Järvinen Heikki, Kontro Mika, Visakorpi Tapio, Taipale Jussi, Varjosalo Markku, Boyer Thomas G, Vahteristo P |
Frameshift Mutations of HSPA4 and MED13 in Gastric and Colorectal Cancers. Pathology oncology research : POR 2016 Apr . Jo Yun Sol, Choi Mi Ryoung, Song Sang Yong, Kim Min Sung, Yoo Nam Jin, Lee Sug Hyu |
MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations. BMC cardiovascular disorders 2022 6 22 (1): 278. Lin Li-Rong, Hu Xue-Qun, Lu Li-Hong, Dai Jia-Zhen, Lin Ning-Ning, Wang Re-Hua, Xie Zhang-Xin, Chen Xue-M |
Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Frontiers in cardiovascular medicine 2022 2 8 811156. Zhou Yue, Bai Kai, Wang Yu, Meng Zhuo, Zhou Shuang, Jiang Shiwei, Wang Hualin, Wang Jian, Yang Mei, Wang Qingjie, Sun Kun, Chen S |
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Human genetics 2024 2 . Ashraf Yahia, Danyang Li, Sanna Lejerkrans, Shyam Rajagopalan, Nelli Kalnak, Kristiina Tammimi |
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- Page last updated:Mar 25, 2024
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