Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Stephanie G. Willis"'
Autor:
Oliver Hantschel, Richard D. Press, Michael W. Deininger, Ines Kaupe, Kim Hien T. Dao, Thoralf Lange, Lalita Prabha Turaga, Brian J. Druker, Stephanie G. Willis, Thomas Bumm, Daniel W. Sherbenou, Giulio Superti-Furga
Publikováno v:
Blood. 116:3278-3285
Point mutations in the kinase domain of BCR-ABL are the most common mechanism of drug resistance in chronic myeloid leukemia (CML) patients treated with ABL kinase inhibitors, including imatinib. It has also been shown in vitro that mutations outside
Autor:
Lucy C. Pemberton, Junia V. Melo, Thoralf Lange, Beth Wilmot, Michael W. Deininger, Mary MacPartlin, Christina A. Harrington, Gregory S. Yochum, Shannon K. McWeeney, Kristina Vartanian, Marc M. Loriaux, Stephanie G. Willis, Brian J. Druker, Yaron Turpaz, Stephen G. O'Brien, Raji Pillai, Jennifer Snead
Publikováno v:
Blood. 115:315-325
In chronic-phase chronic myeloid leukemia (CML) patients, the lack of a major cytogenetic response (< 36% Ph+ metaphases) to imatinib within 12 months indicates failure and mandates a change of therapy. To identify biomarkers predictive of imatinib f
Autor:
Richard D. Press, Stephanie G. Willis, Michael W. Deininger, Michael J. Mauro, Jennifer Laudadio
Publikováno v:
Blood. 114:2598-2605
In imatinib-treated chronic myeloid leukemia (CML), secondary drug resistance is often caused by mutations in the BCR-ABL kinase domain (KD). As alternative therapies are available for imatinib resistance, early identification of mutations may preven
Autor:
Marc M. Loriaux, Michael W. Deininger, Stephanie G. Willis, Michael Rutenberg-Schoenberg, Thomas O'Hare, Heidi Erickson, B. J. Druker, Jeffrey W. Tyner
Publikováno v:
Leukemia. 23:1345-1348
Therapies that are targeted to the molecular genetic defect of malignancies have proven more successful than conventional chemotherapeutic approaches.1, 2, 3, 4 A broad application of this strategy will require a detailed understanding of the genetic
Autor:
Michael W. Deininger, Amie S. Corbin, Jutta Deininger, Stephanie G. Willis, Marc M. Loriaux, Thomas O'Hare, Keiichi I. Nakayama, Brian J. Druker, Jonathan VanDyke, Anupriya Agarwal, Thomas Bumm
Publikováno v:
Blood. 112:1960-1970
BCR-ABL is proposed to impair cell-cycle control by disabling p27, a tumor suppressor that inhibits cyclin-dependent kinases. We show that in cell lines p27 expression is inversely correlated with expression of SKP2, the F-box protein of SCFSKP2 (SKP
Autor:
Jerald P. Radich, Marc A. Unger, Neil P. Shah, Ramesh Ramakrishnan, Stephanie G. Willis, Geoff Facer, Michael W. Deininger, Frank McCormick, Vivian G. Oehler, Carrie Cummings, Jian Qin, Antoine Daridon, Suchitra Ananthnarayan
Publikováno v:
Leukemia. 23:396-399
Absolute quantitative detection of ABL tyrosine kinase domain point mutations in chronic myeloid leukemia using a novel nanofluidic platform and mutation-specific PCR
Autor:
Tibor Kovacsovics, Stephanie G. Willis, Thoralf Lange, Jutta Deininger, Michael W. Deininger, Christopher A. Eide, Jeffrey W. Tyner, Heidi Erickson, Brian J. Druker, Norbert Gattermann, Marc M. Loriaux, Mary MacPartlin, Richard T. Maziarz
Publikováno v:
Leukemia. 23:406-409
High-throughput mutational screen of the tyrosine kinome in chronic myelomonocytic leukemia
Autor:
Stephanie G. Willis, Chad D. Galderisi, Carole Rempfer, Brian J. Druker, Rui Yang, Richard D. Press, Michael W. Deininger, Michael J. Mauro
Publikováno v:
Clinical Cancer Research. 13:6136-6143
Purpose: Imatinib induces a complete cytogenetic response (CCR) in most chronic myeloid leukemia patients in chronic phase. Although CCR is usually durable, a minority of patients relapse. Biomarkers capable of predicting those CCR patients with a hi
Autor:
Brian J. Druker, Lucy C. Crossman, Eric P. Stoffregen, Sandra Otto, Michael W. Deininger, Shannon K. McWeeney, Stephanie G. Willis, Byung Park, Dietger Niederwieser, Shadmehr Demehri, Thoralf Lange, Ines Kovacs
Publikováno v:
Blood. 106:2128-2137
Mutations in the kinase domain (KD) of BCR-ABL are the leading cause of acquired imatinib resistance. In some cases, identical mutations were detected at relapse and in pretherapeutic specimens, consistent with selection of resistant clones in the pr
Autor:
Juliette N. Rooney-Varga, Stephanie G. Willis, Richard Devereux, Mark E. Hines, Robert S. Evans, Stephanie D. Friedman, Barbara R. Sharak Genthner
Publikováno v:
Applied and Environmental Microbiology. 65:2209-2216
The population composition and biogeochemistry of sulfate-reducing bacteria (SRB) in the rhizosphere of the marsh grass Spartina alterniflora was investigated over two growing seasons by molecular probing, enumerations of culturable SRB, and measurem