Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Mary M Chen"'
Autor:
Tiffany F. Lin, Gary J. Schiller, Johnnie J. Orozco, Gail J. Roboz, Mohamed M. Hegazi, Laura Finn, Mary M Chen
Publikováno v:
Blood. 140:3336-3337
Background: Resistance to venetoclax, a BCL2 inhibitor, has been shown to be mediated by co-expression of other BCL2 proteins including BCLXL and MCL1 in relapsed/refractory AML (R/R AML). Therapeutic agents reducing resistance to BCL2 inhibitors and
Autor:
Sameem Abedin, Guru Subramanian Guru Murthy, Aniko Szabo, Mehdi Hamadani, Laura C. Michaelis, Karen-Sue Carlson, Lyndsey Runaas, Katelyn Gauger, Avinash G Desai, Mary M Chen, Alexandra M. Harrington, Ehab L. Atallah
Publikováno v:
Blood. 140:157-158
Autor:
Steve Lacroix, Paul A. Monach, Jerry Ware, Pierre Cunin, Yoichiro Iwakura, Tatiana G. Jones, Peter A. Nigrovic, Joseph E. Italiano, Mary M. Chen, Loka R. Penke, Eric Boilard, Jonathan N. Thon, Michael F. Gurish, Imene Melki, Margaret H. Chang
Publikováno v:
Journal of Clinical Investigation. 127:1714-1724
The growth factor receptor Kit is involved in hematopoietic and nonhematopoietic development. Mice bearing Kit defects lack mast cells; however, strains bearing different Kit alleles exhibit diverse phenotypes. Herein, we investigated factors underly
Publikováno v:
Teaching and Learning in Medicine. 28:320-328
The departure of physician-scientists from education and research into clinical practice is a growing challenge for the future of academic medicine. Junior faculty face competing demands for clinical productivity, teaching, research, and work-life in
Autor:
Paula Marlton, Helen M. Thackray, Daniel J. DeAngelo, Gavin Cull, Brian A. Jonas, Geoffrey L. Uy, Jane L. Liesveld, Harry P. Erba, Anjali S. Advani, Bhavana Bhatnagar, Mary M Chen, Eric J. Feldman, Brenda W. Cooper, William E. Fogler, John L. Magnani, Michael O'Dwyer, Pamela S. Becker, Michael B. Armstrong, Gerwin Huls
Publikováno v:
Blood. 134:2650-2650
Background Binding of E-selectin (E-sel) to sialyl Lex, the E-sel ligand, on the leukemic cell surface activates cell survival pathways and promotes chemotherapy resistance in AML. Higher expression of E-sel ligand is associated with relapse and poor
Autor:
Jane L. Liesveld, William E. Fogler, John L. Magnani, Daniel J. DeAngelo, Pamela S. Becker, Michael O'Dwyer, Helen M. Thackray, Eric J. Feldman, Mary M Chen, Brian A. Jonas, Anjali S. Advani, Dale L. Bixby, Paula Marlton
Publikováno v:
Blood. 134:2690-2690
Leukemic myeloblasts expressing E-selectin ligand (E-sel ligand) adhere to E-selectin on bone marrow endothelium resulting in environment-mediated drug resistance (EMDR). Uproleselan, a potent E-selectin inhibitor, disrupts the adhesion of AML cells
Autor:
Thomas Quertermous, Thomas Finsterbach, Michael Y Ho, David Charo, Mary M. Chen, Kavita V Ernst, Ramendra K. Kundu, Euan A. Ashley, Yen-Dong Ho, Masataka Kawana, Ahmad Y. Sheikh, Daniel Bernstein, Giovanni Fajardo, Hyung J. Chun, Nicholas J. Leeper
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 297:H1904-H1913
Studies have shown significant cardiovascular effects of exogenous apelin administration, including the potent activation of cardiac contraction. However, the role of the endogenous apelin-APJ pathway is less clear. To study the loss of endogenous ap
Autor:
Ingo Kutschka, Ziad A. Ali, Philip S. Tsao, Stephen L. Hendry, Mary M. Chen, Patrick Yue, Diego Ardigò, Ramendera K. Kundu, Marc P. Pelletier, Hyung J. Chun, Robert C. Robbins, Andrew J. Connolly, Ahmad Y. Sheikh, Alexander J. Glassford, Thomas Quertermous, Roger A. Wagner, Diem T. Huynh
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 294:H88-H98
Signaling by the peptide ligand apelin and its cognate G protein-coupled receptor APJ has a potent inotropic effect on cardiac contractility and modulates systemic vascular resistance through nitric oxide-dependent signaling. In addition, there is ev
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 15:424-428
Metabolic markers of bone metabolism may be useful for the diagnosis and monitoring of bone metastasis in breast cancer patients. Serum tartrate-resistant acid phosphatase 5b (TRACP5b) activity is a novel bone resorption marker. The treatment respons
Autor:
Tsu-Yi Chao, Jyh-Cherng Yu, Chih-Hung Ku, Mary M. Chen, Su-Huei Lee, Anthony J. Janckila, Lung T. Yam
Publikováno v:
Clinical Cancer Research. 11:544-550
Purpose: Previous studies showed that serum tartrate-resistant acid phosphatase 5b (TRACP5b) activity was increased in 70% to 94% of breast cancer (BC) patients with bone metastasis (BM). This study aims to determine whether serum TRACP5b is useful f