Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: DHX58[original query] |
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Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes. Scientific reports 2019 Jun 9 (1): 9171. Vidmar Lovro, Maver Ales, Drulovi? Jelena, Sep?i? Juraj, Novakovi? Ivana, Risti? Smiljana, Šega Saša, Peterlin Bor |
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta neuropathologica 2019 Feb . Pottier Cyril, Ren Yingxue, Perkerson Ralph B, Baker Matt, Jenkins Gregory D, van Blitterswijk Marka, DeJesus-Hernandez Mariely, van Rooij Jeroen G J, Murray Melissa E, Christopher Elizabeth, McDonnell Shannon K, Fogarty Zachary, Batzler Anthony, Tian Shulan, Vicente Cristina T, Matchett Billie, Karydas Anna M, Hsiung Ging-Yuek Robin, Seelaar Harro, Mol Merel O, Finger Elizabeth C, Graff Caroline, Öijerstedt Linn, Neumann Manuela, Heutink Peter, Synofzik Matthis, Wilke Carlo, Prudlo Johannes, Rizzu Patrizia, Simon-Sanchez Javier, Edbauer Dieter, Roeber Sigrun, Diehl-Schmid Janine, Evers Bret M, King Andrew, Mesulam M Marsel, Weintraub Sandra, Geula Changiz, Bieniek Kevin F, Petrucelli Leonard, Ahern Geoffrey L, Reiman Eric M, Woodruff Bryan K, Caselli Richard J, Huey Edward D, Farlow Martin R, Grafman Jordan, Mead Simon, Grinberg Lea T, Spina Salvatore, Grossman Murray, Irwin David J, Lee Edward B, Suh EunRan, Snowden Julie, Mann David, Ertekin-Taner Nilufer, Uitti Ryan J, Wszolek Zbigniew K, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Hodges John R, Piguet Olivier, Geier Ethan G, Yokoyama Jennifer S, Rissman Robert A, Rogaeva Ekaterina, Keith Julia, Zinman Lorne, Tartaglia Maria Carmela, Cairns Nigel J, Cruchaga Carlos, Ghetti Bernardino, Kofler Julia, Lopez Oscar L, Beach Thomas G, Arzberger Thomas, Herms Jochen, Honig Lawrence S, Vonsattel Jean Paul, Halliday Glenda M, Kwok John B, White Charles L, Gearing Marla, Glass Jonathan, Rollinson Sara, Pickering-Brown Stuart, Rohrer Jonathan D, Trojanowski John Q, Van Deerlin Vivianna, Bigio Eileen H, Troakes Claire, Al-Sarraj Safa, Asmann Yan, Miller Bruce L, Graff-Radford Neill R, Boeve Bradley F, Seeley William W, Mackenzie Ian R A, van Swieten John C, Dickson Dennis W, Biernacka Joanna M, Rademakers Ro |
Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population.
Scientific reports 2020 Jan 10 (1): 152. Hebbar Prashantha, Abu-Farha Mohamed, Alkayal Fadi, Nizam Rasheeba, Elkum Naser, Melhem Motasem, John Sumi Elsa, Channanath Arshad, Abubaker Jehad, Bennakhi Abdullah, Al-Ozairi Ebaa, Tuomilehto Jaakko, Pitkaniemi Janne, Alsmadi Osama, Al-Mulla Fahd, Thanaraj Thangavel Alphon |
Polymorphisms of RIG-I-like receptor influence HBV clearance in Chinese Han population. Journal of medical virology 2021 Mar . Yao Yinan, Shen Yan, Shao Haifeng, Liu Yuchang, Ji Yan, Du Guoming, Ye Xiangyu, Huang Peng, Chen Haimi |
DNA methylation and single-nucleotide polymorphisms in DDX58 are associated with hand, foot and mouth disease caused by enterovirus 71. PLoS neglected tropical diseases 2022 1 16 (1): e0010090. Li Ya-Ping, Liu Chen-Rui, Deng Hui-Ling, Wang Mu-Qi, Tian Yan, Chen Yuan, Zhang Yu-Feng, Dang Shuang-Suo, Zhai So |
Genetic variants of IFIH1 and DHX58 affect the chronicity of hepatitis C in the Chinese Han population. PeerJ 2023 2 11 e14740. Huang Peng, Wu Jing-Jing, Zhang Jin-Wei, Hou Yu-Qing, Zhu Ping, Yin Rong, Yu Rong-Bin, Zhang Yun, Yue Ming, Hou W |
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- Page last updated:Apr 29, 2024
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