Bilaketaren emaitzak - Matthews, Allison

Improving COVID-19 vaccine acceptance: Including insights from human decision-making under conditions of uncertainty and human-centered design nork Poland, Caroline M., Matthews, Allison K.S., Poland, Gregory A.

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A Tn-seq Screen of Streptococcus pneumoniae Uncovers DNA Repair as the Major Pathway for Desiccation Tolerance and Transmission nork Matthews, Allison J., Rowe, Hannah M., Rosch, Jason W., Camilli, Andrew

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A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta nork Inkster, Amy M., Yuan, Victor, Konwar, Chaini, Matthews, Allison M., Brown, Carolyn J., Robinson, Wendy P.

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Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders nork Tarailo-Graovac, Maja, Zhu, Jing Yun Alice, Matthews, Allison, van Karnebeek, Clara D M, Wasserman, Wyeth W

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Transcription and translation of the sigG gene is tuned for proper execution of the switch from early to late gene expression in the developing Bacillus subtilis spore nork Mearls, Elizabeth B., Jackter, Jacquelin, Colquhoun, Jennifer M., Farmer, Veronica, Matthews, Allison J., Murphy, Laura S., Fenton, Colleen, Camp, Amy H.

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Verbal Learning and Memory in Cannabis and Alcohol Users: An Event-Related Potential Investigation nork Smith, Janette L., De Blasio, Frances M., Iredale, Jaimi M., Matthews, Allison J., Bruno, Raimondo, Dwyer, Michelle, Batt, Tessa, Fox, Allison M., Solowij, Nadia, Mattick, Richard P.

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Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutation nork Bourne, Stephanie C., Townsend, Katelin N., Shyr, Casper, Matthews, Allison, Lear, Scott A., Attariwala, Raj, Lehman, Anna, Wasserman, Wyeth W., van Karnebeek, Clara, Sinclair, Graham, Vallance, Hilary, Gibson, William T.

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Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review nork Graham, Emma, Lee, Jessica, Price, Magda, Tarailo-Graovac, Maja, Matthews, Allison, Engelke, Udo, Tang, Jeffrey, Kluijtmans, Leo A. J., Wevers, Ron A., Wasserman, Wyeth W., van Karnebeek, Clara D. M., Mostafavi, Sara

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STAT3 restrains RANK- and TLR4-mediated signaling by suppressing expression of the E2 ubiquitin ligase Ubc13 nork Zhang, Huiyuan, Hu, Hongbo, Greeley, Nathaniel, Jin, Jin, Matthews, Allison J., Ohashi, Erika, Caetano, Mauricio S., Li, Haiyan S., Wu, Xuefeng, Mandal, Pijus K., McMurray, John S., Moghaddam, Seyed Javad, Sun, Shao-Cong, Watowich, Stephanie S.

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YY1 binding association with sex-biased transcription revealed through X-linked transcript levels and allelic binding analyses nork Chen, Chih-yu, Shi, Wenqiang, Balaton, Bradley P., Matthews, Allison M., Li, Yifeng, Arenillas, David J., Mathelier, Anthony, Itoh, Masayoshi, Kawaji, Hideya, Lassmann, Timo, Hayashizaki, Yoshihide, Carninci, Piero, Forrest, Alistair R. R., Brown, Carolyn J., Wasserman, Wyeth W.

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Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study nork Elliott, Alison M., Adam, Shelin, du Souich, Christèle, Lehman, Anna, Nelson, Tanya N., van Karnebeek, Clara, Alderman, Emily, Armstrong, Linlea, Aubertin, Gudrun, Blood, Katherine, Boelman, Cyrus, Boerkoel, Cornelius, Bretherick, Karla, Brown, Lindsay, Chijiwa, Chieko, Clarke, Lorne, Couse, Madeline, Creighton, Susan, Watts-Dickens, Abby, Gibson, William T., Gill, Harinder, Tarailo-Graovac, Maja, Hamilton, Sara, Heran, Harindar, Horvath, Gabriella, Huang, Lijia, Hulait, Gurdip K., Koehn, David, Lee, Hyun Kyung, Lewis, Suzanne, Lopez, Elena, Louie, Kristal, Niederhoffer, Karen, Matthews, Allison, Meagher, Kirsten, Peng, Junran J., Patel, Millan S., Race, Simone, Richmond, Phillip, Rupps, Rosemarie, Salvarinova, Ramona, Seath, Kimberly, Selby, Kathryn, Steinraths, Michelle, Stockler, Sylvia, Tang, Kaoru, Tyson, Christine, van Allen, Margot, Wasserman, Wyeth, Mwenifumbo, Jill, Friedman, Jan M.

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