Reduced seed region-based off-target activity with lentivirus-mediated RNAi

Por Klinghoffer, Richard A., Magnus, Jill, Schelter, Janell, Mehaffey, Michele, Coleman, Casey, Cleary, Michele A.
Publicado em 2010

Using mixtures of biological samples as process controls for RNA-sequencing experiments

Por Parsons, Jerod, Munro, Sarah, Pine, P. Scott, McDaniel, Jennifer, Mehaffey, Michele, Salit, Marc
Publicado no BMC Genomics (2015)

Regulation and Expression of the ATP-binding Cassette Transporter ABCG2 in Human Embryonic Stem Cells

Por Padmanabhan, Raji, Chen, Kevin G., Gillet, Jean-Pierre, Handley, Misty, Mallon, Barbara S., Hamilton, Rebecca S., Park, Kyeyoon, Varma, Sudhir, Mehaffey, Michele G., Robey, Pamela G., McKay, Ronald D.G., Gottesman, Michael M.
Publicado em 2012

Plasmid-Based Materials as Multiplex Quality Controls and Calibrators for Clinical Next-Generation Sequencing Assays

Por Sims, David J., Harrington, Robin D., Polley, Eric C., Forbes, Thomas D., Mehaffey, Michele G., McGregor, Paul M., Camalier, Corinne E., Harper, Kneshay N., Bouk, Courtney H., Das, Biswajit, Conley, Barbara A., Doroshow, James H., Williams, P. Mickey, Lih, Chih-Jian
Publicado no J Mol Diagn (2016)

Robustness of Next Generation Sequencing on Older Formalin-Fixed Paraffin-Embedded Tissue

Por Carrick, Danielle Mercatante, Mehaffey, Michele G., Sachs, Michael C., Altekruse, Sean, Camalier, Corinne, Chuaqui, Rodrigo, Cozen, Wendy, Das, Biswajit, Hernandez, Brenda Y., Lih, Chih-Jian, Lynch, Charles F., Makhlouf, Hala, McGregor, Paul, McShane, Lisa M., Phillips Rohan, JoyAnn, Walsh, William D., Williams, Paul M., Gillanders, Elizabeth M., Mechanic, Leah E., Schully, Sheri D.
Publicado no PLoS One (2015)

Randomized trial of oral cyclophosphamide and veliparib in high-grade serous ovarian, primary peritoneal, or fallopian tube cancers, or BRCA-mutant ovarian cancer

Por Kummar, Shivaani, Oza, Amit M., Fleming, Gini F., Sullivan, Daniel M., Gandara, David R., Naughton, Michael J., Villalona-Calero, Miguel A., Morgan, Robert J., Szabo, Peter M., Youn, Ahrim, Chen, Alice P., Ji, Jiuping, Allen, Deborah E., Lih, Chih-Jian, Mehaffey, Michele G., Walsh, William D., McGregor, Paul M., Steinberg, Seth M., Williams, Paul M., Kinders, Robert J., Conley, Barbara A., Simon, Richard M., Doroshow, James H.
Publicado no Clin Cancer Res (2015)

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

Por Petrovski, Slavé, Küry, Sébastien, Myers, Candace T., Anyane-Yeboa, Kwame, Cogné, Benjamin, Bialer, Martin, Xia, Fan, Hemati, Parisa, Riviello, James, Mehaffey, Michele, Besnard, Thomas, Becraft, Emily, Wadley, Alexandrea, Politi, Anya Revah, Colombo, Sophie, Zhu, Xiaolin, Ren, Zhong, Andrews, Ian, Dudding-Byth, Tracy, Schneider, Amy L., Wallace, Geoffrey, Rosen, Aaron B.I., Schelley, Susan, Enns, Gregory M., Corre, Pierre, Dalton, Joline, Mercier, Sandra, Latypova, Xénia, Schmitt, Sébastien, Guzman, Edwin, Moore, Christine, Bier, Louise, Heinzen, Erin L., Karachunski, Peter, Shur, Natasha, Grebe, Theresa, Basinger, Alice, Nguyen, Joanne M., Bézieau, Stéphane, Wierenga, Klaas, Bernstein, Jonathan A., Scheffer, Ingrid E., Rosenfeld, Jill A., Mefford, Heather C., Isidor, Bertrand, Goldstein, David B.
Publicado no Am J Hum Genet (2016)