Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cindy McCully"'
Autor:
Jette Tjørnelund, Cindy McCully, Frank M. Balis, Katherine E. Warren, Henrik Dvinge, Henri S. Lichenstein, Maxwell Sehested
Publikováno v:
Cancer Chemotherapy and Pharmacology. 62:433-437
Histone deacetylases (HDAC) are involved in the regulation of gene transcription. Aberrant HDAC activity has been associated with tumorigenesis, and, therefore, HDACs are potential targets for the treatment of cancers, including tumors of the central
Autor:
Karen Godwin, Barry D. Anderson, Philip A. Pizzo, Brigitta U. Mueller, Cindy McCully, Hiroaki Mitsuya, Judy Zuckerman, Frank M. Balis, Paul Jarosinski, Maureen Farley, Robert L. Murphy
Publikováno v:
Antimicrobial Agents and Chemotherapy. 42:1815-1818
KNI-272 is a human immunodeficiency virus (HIV) protease inhibitor with potent activity in vitro. We studied the pharmacokinetics of KNI-272 in the plasma and cerebrospinal fluid (CSF) of a nonhuman primate model and after intravenous and oral admini
Autor:
Cindy McCully, Katherine E. Warren, Nalini Jayaprakash, Anandani Nellan, Daniel W. Lee, Brigitte C. Widemann
Publikováno v:
Cancer Research. 76:1411-1411
Background: Cytokine release syndrome (CRS) is a life-threatening complication of effective immunotherapies, particularly chimeric antigen receptor (CAR) T-cells. CRS is characterized by fever, hypotension, cardiac dysfunction, and at times end organ
Autor:
Diane E. Cole, AeRang Kim, Elizabeth Fox, Raphael Cruz, Frank M. Balis, Cindy McCully, Brigitte C. Widemann
Publikováno v:
Investigational new drugs. 30(2)
Purpose Sorafenib is a small molecule inhibitor of multiple signaling kinases thought to contribute to the pathogenesis of many tumors including brain tumors. Clinical trials with sorafenib in primary and metastatic brain tumors are ongoing. We evalu
Publikováno v:
Cancer chemotherapy and pharmacology. 44(6)
Purpose: Raltitrexed (Tomudex™), ZD1694) is a novel quinazoline folate analog that selectively inhibits thymidylate synthase. Intracellularly, raltitrexed is polyglutamated to its active form which can be retained in cells for prolonged periods. Th
Autor:
AeRang Kim, Cindy McCully, Rafael Cruz, Diane E. Cole, Elizabeth Fox, Frank M. Balis, Brigitte C. Widemann
Publikováno v:
Cancer Research. 70:1672-1672
Background: Sorafenib is an oral multikinase inhibitor that targets intracellular and receptor protein kinases thought to be crucial in the pathogenesis and growth of many tumors including brain tumors. Sorafenib is FDA approved for advanced renal ce