Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: ME3[original query] |
---|
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. PloS one 2014 9 (7): e100776. Tang Wenbo, Kowgier Matthew, Loth Daan W, Soler Artigas María, Joubert Bonnie R, Hodge Emily, Gharib Sina A, Smith Albert V, Ruczinski Ingo, Gudnason Vilmundur, Mathias Rasika A, Harris Tamara B, Hansel Nadia N, Launer Lenore J, Barnes Kathleen C, Hansen Joyanna G, Albrecht Eva, Aldrich Melinda C, Allerhand Michael, Barr R Graham, Brusselle Guy G, Couper David J, Curjuric Ivan, Davies Gail, Deary Ian J, Dupuis Josée, Fall Tove, Foy Millennia, Franceschini Nora, Gao Wei, Gläser Sven, Gu Xiangjun, Hancock Dana B, Heinrich Joachim, Hofman Albert, Imboden Medea, Ingelsson Erik, James Alan, Karrasch Stefan, Koch Beate, Kritchevsky Stephen B, Kumar Ashish, Lahousse Lies, Li Guo, Lind Lars, Lindgren Cecilia, Liu Yongmei, Lohman Kurt, Lumley Thomas, McArdle Wendy L, Meibohm Bernd, Morris Andrew P, Morrison Alanna C, Musk Bill, North Kari E, Palmer Lyle J, Probst-Hensch Nicole M, Psaty Bruce M, Rivadeneira Fernando, Rotter Jerome I, Schulz Holger, Smith Lewis J, Sood Akshay, Starr John M, Strachan David P, Teumer Alexander, Uitterlinden André G, Völzke Henry, Voorman Arend, Wain Louise V, Wells Martin T, Wilk Jemma B, Williams O Dale, Heckbert Susan R, Stricker Bruno H, London Stephanie J, Fornage Myriam, Tobin Martin D, O'Connor George T, Hall Ian P, Cassano Patricia |
EZH2 inhibitory protein (EZHIP/Cxorf67) expression correlates strongly with H3K27me3 loss in posterior fossa ependymomas and is mutually exclusive with H3K27M mutations. Brain tumor pathology 2020 11 38 (1): 30-40. Nambirajan Aruna, Sharma Agrima, Rajeshwari Madhu, Boorgula Meher Tej, Doddamani Ramesh, Garg Ajay, Suri Vaishali, Sarkar Chitra, Sharma Mehar Cha |
Genetic Polymorphisms in Activating Transcription Factor 3 Binding Site and the Prognosis of Early-Stage Non-Small Cell Lung Cancer. Oncology 2021 2 99 (5): 336-344. Kang Hyo-Gyoung, Park Ji Eun, Lee Shin Yup, Choi Jin Eun, Do Sook Kyung, Hong Mi Jeong, Lee Jang Hyuck, Jeong Ji Yun, Do Young Woo, Lee Eung Bae, Shin Kyung Min, Lee Won Ki, Choi Sun Ha, Lee Yong Hoon, Seo Hye Won, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Cho Sukki, Jheon Sanghoon, Park Jae Yo |
Candidate Modifier Genes for the Penetrance of Leber's Hereditary Optic Neuropathy. International journal of molecular sciences 2022 10 23 (19): . Cheng Hui-Chen, Chi Sheng-Chu, Liang Chiao-Ying, Yu Jenn-Yah, Wang An-Gu |
Mitochondrial TXNRD2 and ME3 genetic risk scores are associated with specific primary open-angle glaucoma phenotypes. Ophthalmology 2023 2 . Aboobakar Inas F, Kinzy Tyler G, Zhao Yan, Fan Baojian, Pasquale Louis R, Qassim Ayub, Kolovos Antonia, Schmidt Joshua M, Craig Jamie E, Bailey Jessica N Cooke, Wiggs Janey L, |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: