Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Robert Fram"'
Autor:
Justin Watts, Mikkael Sekeres, Atanas Radinoff, Montserrat Arnan, Marco Cerrano, Patricia Font Lopez, Joshua Zeidner, Maria Diez Campelo, Carlos Graux, Jane Liesveld, Dominik Selleslag, Nikolai Tzvetkov, Robert Fram, Dan Zhao, Sharon Friedlander, Kevin Galinsky, Douglas Faller, Lionel Adès
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 21:S227
Autor:
Timothy B. Lowinger, Jeremy M. Sen, William C. Zamboni, Robert Fram, Suzan K. Hanna, Aleksandr V. Yurkovetskiy, Carolina B. Cabral, S. Rawal, Mark D. Walsh
Publikováno v:
Clinical Cancer Research. 18:2591-2602
Purpose: To evaluate the pharmacokinetics and tissue disposition of macromolecular camptothecin (CPT) drug conjugate, XMT-1001, and irinotecan (CPT-11) in mice bearing HT-29 xenograft tumors. Experimental Design: The antitumor efficacy of XMT-1001 wa
Autor:
Robert Fram, Melissa A. Smrz, Cary T. Oien, Bruce Budowle, Robert B. Stacey, Danielle P. Seiger, Stephen Meagher, Stephen G. Bunch, Michael B. Smith, Greg L. Soltis, Maureen C. Bottrell, Peter E. Peterson, Diana Harrison
Publikováno v:
Journal of Forensic Sciences. 54:798-809
The forensic sciences are under review more so than ever before. Such review is necessary and healthy and should be a continuous process. It identifies areas for improvement in quality practices and services. The issues surrounding error, i.e., measu
Publikováno v:
Southern Medical Journal. 93:894-897
We describe the case of a patient with acquired immunodeficiency syndrome (AIDS) who had a CD4 cell count of 60/microL, bilateral hilar adenopathy, and hypercalcemia. Transbronchial biopsy showed T-cell anaplastic large cell lymphoma. Serology was ne
Autor:
Alexander V. Yurkovetskiy, Robert Fram
Publikováno v:
Advanced drug delivery reviews. 61(13)
An overview of XMT-1001 is provided in the context of other topoisomerase I inhibitors conjugated to polymers or encapsulated in liposomes. XMT-1001 is a novel polymeric pro-drug derivative of camptothecin (CPT) with a molecular weight of 70 kDa, in
Autor:
Corinne L, Reimer, Naoki, Agata, Jennifer G, Tammam, Michael, Bamberg, William M, Dickerson, George D, Kamphaus, Susan L, Rook, Michael, Milhollen, Robert, Fram, Raghu, Kalluri, Donald, Kufe, Surender, Kharbanda
Publikováno v:
Cancer research. 62(3)
Antiangiogenic therapy, although effective in shrinking tumors, has not yet been established as a standalone treatment for cancer. This therapeutic limitation can be overcome by combining angiogenesis inhibitors with chemotherapeutic agents. NM-3, a
Autor:
Donald Kufe, Lee F. Allen, Betty Razvillas, Robert Fram, Deborah Toppmeyer, Anthony A. Amato, Raja Velagapudi, Eric K. Rowinsky, Miguel A. Villalona-Calero, Daniel D. Von Hoff, Michael Myers, Kathleen Kagen-Hallet, Joseph Paul Eder
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 19(3)
PURPOSE: To determine the maximum-tolerated dose and characterize the pharmacokinetic behavior of LU79553, a novel bisnaphthalimide antineoplastic agent, when administered as a daily intravenous infusion for 5 days every 3 weeks. PATIENTS AND METHODS
Autor:
Jeffrey W. Clark, Jeffrey G. Supko, Donald Kufe, Lee F. Allen, Joseph Paul Eder, Thomas J. Lynch, Robert Fram, Raja Velagapudi
Publikováno v:
Cancer chemotherapy and pharmacology. 46(4)
Purpose: The dolastatins are a class of naturally occurring cytotoxic peptides which function by inhibiting microtubule assembly and tubulin polymerization. Cemadotin is a synthetic analogue of dolastatin 15 with potent antiproliferative and preclini
Autor:
C. Bethune, Lawrence E. Garbo, Edward A. Sausville, Glen J. Weiss, Dana Shkolny, Ramesh K. Ramanathan, Martin J. Edelman, Robert Fram, A. V. Yurkovetskiy
Publikováno v:
European Journal of Cancer Supplements. 8:180
Autor:
Robert Fram, Glen J. Weiss, C. Bethune, Ramesh K. Ramanathan, A. V. Yurkovetskiy, Edward A. Sausville, Dana Shkolny, Lawrence E. Garbo
Publikováno v:
Journal of Clinical Oncology. 28:e13121-e13121
e13121 Background: XMT-1001 is a water soluble macromolecular conjugate of camptothecin (CPT). In this novel CPT prodrug, CPT is conjugated with a 70 kDa biodegradable hydrophilic polyacetal, poly ...