Canlyniadau Chwilio - Scherer, Steven E

Growth Factor-Induced Transcription of GluR1 Increases Functional AMPA Receptor Density in Glial Progenitor Cells gan Chew, Li-Jin, Fleck, Mark W., Wright, Paul, Scherer, Steven E., Mayer, Mark L., Gallo, Vittorio

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Accuracy and applications of sequencing and genotyping approaches for CYP2A6 and homologous genes gan Langlois, Alec W.R., El-Boraie, Ahmed, Fukunaga, Koya, Mushiroda, Taisei, Kubo, Michiaki, Lerman, Caryn, Knight, Jo, Scherer, Steven E., Chenoweth, Meghan J., Tyndale, Rachel F.

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Differentially Expressed Gene Transcripts Using RNA Sequencing from the Blood of Immunosuppressed Kidney Allograft Recipients gan Dorr, Casey, Wu, Baolin, Guan, Weihua, Muthusamy, Amutha, Sanghavi, Kinjal, Schladt, David P., Maltzman, Jonathan S., Scherer, Steven E., Brott, Marcia J., Matas, Arthur J., Jacobson, Pamala A., Oetting, William S., Israni, Ajay K.

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Pharmacogenomic Next-Generation DNA Sequencing: Lessons from the Identification and Functional Characterization of Variants of Unknown Significance in CYP2C9 and CYP2C19 gan Devarajan, Sandhya, Moon, Irene, Ho, Ming-Fen, Larson, Nicholas B., Neavin, Drew R., Moyer, Ann M., Black, John L., Bielinski, Suzette J., Scherer, Steven E., Wang, Liewei, Weinshilboum, Richard M., Reid, Joel M.

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A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome gan Hampton, Oliver A., Den Hollander, Petra, Miller, Christopher A., Delgado, David A., Li, Jian, Coarfa, Cristian, Harris, Ronald A., Richards, Stephen, Scherer, Steven E., Muzny, Donna M., Gibbs, Richard A., Lee, Adrian V., Milosavljevic, Aleksandar

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Novel CYP2A6 diplotypes identified through next-generation sequencing are associated with in vitro and in vivo nicotine metabolism gan Tanner, Julie-Anne, Zhu, Andy Z., Claw, Katrina G., Prasad, Bhagwat, Korchina, Viktoriya, Hu, Jianhong, Doddapaneni, HarshaVardhan, Muzny, Donna M., Schuetz, Erin G., Lerman, Caryn, Thummel, Kenneth E., Scherer, Steven E., Tyndale, Rachel F.

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Pharmacogenomics of Nicotine Metabolism: Novel CYP2A6 and CYP2B6 Genetic Variation Patterns in Alaska Native and American Indian Populations gan Claw, Katrina G, Beans, Julie A, Lee, Seung-Been, Avey, Jaedon P, Stapleton, Patricia A, Scherer, Steven E, El-Boraie, Ahmed, Tyndale, Rachel F, Nickerson, Deborah A, Dillard, Denise A, Thummel, Kenneth E, Robinson, Renee F

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Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young gan Methner, D. Nicole R., Scherer, Steven E., Welch, Katherine, Walkiewicz, Magdalena, Eng, Christine M., Belmont, John W., Powell, Mark C., Korchina, Viktoriya, Doddapaneni, Harsha Vardhan, Muzny, Donna M., Gibbs, Richard A., Wolf, Dwayne A., Sanchez, Luis A., Kahn, Roger

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Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes gan Liu, Duan, Ho, Ming-Fen, Schaid, Daniel J., Scherer, Steven E., Kalari, Krishna, Liu, Mohan, Biernacka, Joanna, Yee, Vivien, Evans, Jared, Carlson, Erin, Goetz, Matthew P., Kubo, Michiaki, Wickerham, D. Lawrence, Wang, Liewei, Ingle, James N., Weinshilboum, Richard M.

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Targeted Genotyping in Clinical Pharmacogenomics: What Is Missing? gan Lopes, Jaime L., Harris, Kimberley, Karow, Mary Beth, Peterson, Sandra E., Kluge, Michelle L., Kotzer, Katrina E., Lopes, Guilherme S., Larson, Nicholas B., Bielinski, Suzette J., Scherer, Steven E., Wang, Liewei, Weinshilboum, Richard M., Black, John L., Moyer, Ann M.

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Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma gan Cotton, Ronald T, Li, Donghui, Scherer, Steven E, Muzny, Donna M, Hodges, Sally E, Catania, Robbi L, Witkiewicz, Agnieszka K, Brody, Jonathan R, Kennedy, Eugene P, Yeo, Charles J, Brunicardi, F Charles, Gibbs, Richard A, Gingras, Marie-Claude, Fisher, William E

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High Frequency of PIK3R1 and PIK3R2 Mutations in Endometrial Cancer Elucidates a Novel Mechanism for Regulation of PTEN Protein Stability gan Cheung, Lydia W.T., Hennessy, Bryan T., Li, Jie, Yu, Shuangxing, Myers, Andrea P., Djordjevic, Bojana, Lu, Yiling, Stemke-Hale, Katherine, Zhang, Fan, Ju, Zhenlin, Cantley, Lewis C., Scherer, Steven E., Liang, Han, Lu, Karen H., Broaddus, Russell R., Mills, Gordon B.

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The ethics of conducting molecular autopsies in cases of sudden death in the young gan McGuire, Amy L., Moore, Quianta, Majumder, Mary, Walkiewicz, Magdalena, Eng, Christine M., Belmont, John W., Nassef, Salma, Darilek, Sandra, Rutherford, Katie, Pereira, Stacey, Scherer, Steven E., Sutton, V. Reid, Wolf, Dwayne, Gibbs, Richard A., Kahn, Roger, Sanchez, Luis A.

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Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy gan Xu, Tianhong, Yang, Zhao, Vatta, Matteo, Rampazzo, Alessandra, Beffagna, Giorgia, Pillichou, Kalliopi, Scherer, Steven E., Saffitz, Jeffrey, Kravitz, Joshua, Zareba, Wojciech, Danieli, Gian Antonio, Lorenzon, Alessandra, Nava, Andrea, Bauce, Barbara, Thiene, Gaetano, Basso, Cristina, Calkins, Hugh, Gear, Kathy, Marcus, Frank, Towbin, Jeffrey A.

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Prediction of Cochlear Implant Performance by Genetic Mutation: The Spiral Ganglion Hypothesis gan Eppsteiner, Robert W., Shearer, A. Eliot, Hildebrand, Michael S., DeLuca, Adam P., Ji, Haihong, Dunn, Camille C., Black-Ziegelbein, Elizabeth A., Casavant, Thomas L., Braun, Terry A., Scheetz, Todd E., Scherer, Steven E., Hansen, Marlan R., Gantz, Bruce J., Smith, Richard J.H.

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Genetic Alterations Associated With Progression From Pancreatic Intraepithelial Neoplasia to Invasive Pancreatic Tumor gan Murphy, Stephen J., Hart, Steven N., Lima, Joema Felipe, Kipp, Benjamin R., Klebig, Mitchell, Winters, Jennifer L, Szabo, Csilla, Zhang, Lizhi, Eckloff, Bruce W., Petersen, Gloria M., Scherer, Steven E., Gibbs, Richard A., McWilliams, Robert R., Vasmatzis, George, Couch, Fergus J.

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Whole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics gan Sá, Ana Caroline C., Webb, Amy, Gong, Yan, McDonough, Caitrin W., Datta, Somnath, Langaee, Taimour Y., Turner, Stephen T., Beitelshees, Amber L., Chapman, Arlene B., Boerwinkle, Eric, Gums, John G., Scherer, Steven E., Cooper-DeHoff, Rhonda M., Sadee, Wolfgang, Johnson, Julie A.

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Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes gan Lotta, Luca A, Wang, Mark, Yu, Jin, Martinelli, Ida, Yu, Fuli, Passamonti, Serena M, Consonni, Dario, Pappalardo, Emanuela, Menegatti, Marzia, Scherer, Steven E, Lewis, Lora L, Akbar, Humeira, Wu, Yuanqing, Bainbridge, Matthew N, Muzny, Donna M, Mannucci, Pier M, Gibbs, Richard A, Peyvandi, Flora

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Genome-Wide Prioritization and Transcriptomics Reveal Novel Signatures Associated with Thiazide Diuretics Blood Pressure Response gan Shahin, Mohamed H., Sá, Ana C., Webb, Amy, Gong, Yan, Langaee, Taimour, McDonough, Caitrin W., Riva, Alberto, Beitleshees, Amber L, Chapman, Arlene B., Gums, John G., Turner, Stephen T., Boerwinkle, Eric, Scherer, Steven E., Sadee, Wolfgang, Cooper-DeHoff, Rhonda M., Johnson, Julie A.

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Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies gan Sá, Ana Caroline C., Webb, Amy, Gong, Yan, McDonough, Caitrin W., Shahin, Mohamed H., Datta, Somnath, Langaee, Taimour Y., Turner, Stephen T., Beitelshees, Amber L., Chapman, Arlene B., Boerwinkle, Eric, Gums, John G., Scherer, Steven E., Cooper-DeHoff, Rhonda M., Sadee, Wolfgang, Johnson, Julie A.

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