Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Michelle, Kuzma"'
Autor:
Vijaya L. Damaraju, Maral Aminpour, Michelle Kuzma, Philip Winter, Jordane Preto, Jack Tuszynski, Alexander B.J. McEwan, Michael B. Sawyer
Publikováno v:
Clinical and Translational Science, Vol 14, Iss 3, Pp 847-858 (2021)
Positron emission tomography (PET) using 2‐deoxy‐2‐[18F]fluoro‐d‐glucose ([18F]FDG), a marker of energy metabolism and cell proliferation, is routinely used in the clinic to assess patient response to chemotherapy and to monitor tumor growt
Externí odkaz:
https://doaj.org/article/0ee71f90bba14c2d88d2155aa4242963
Autor:
Jack A. Tuszynski, Michael B. Sawyer, Vijaya L. Damaraju, Philip Winter, Jordane Preto, Alexander B.J. McEwan, Maral Aminpour, Michelle Kuzma
Publikováno v:
Clinical and Translational Science, Vol 14, Iss 3, Pp 847-858 (2021)
Positron emission tomography (PET) using 2-deoxy-2-[18 F]fluoro-d-glucose ([18 F]FDG), a marker of energy metabolism and cell proliferation, is routinely used in the clinic to assess patient response to chemotherapy and to monitor tumor growth. Treat
Autor:
Vijaya L, Damaraju, Maral, Aminpour, Michelle, Kuzma, Philip, Winter, Jordane, Preto, Jack, Tuszynski, Alexander B J, McEwan, Michael B, Sawyer
Publikováno v:
Clinical and Translational Science
Positron emission tomography (PET) using 2‐deoxy‐2‐[18F]fluoro‐d‐glucose ([18F]FDG), a marker of energy metabolism and cell proliferation, is routinely used in the clinic to assess patient response to chemotherapy and to monitor tumor growt
Publikováno v:
Biochemical Pharmacology. 155:162-171
Tyrosine kinase inhibitors (TKIs) have advanced cancer treatment and prognosis but have also resulted in adverse effects such as fatigue, diarrhea, hypothyroidism, and other toxicities. We investigated TKI effects on skeletal muscle as a possible exp
Publikováno v:
Journal of Biological Chemistry. 291:18809-18817
Human nucleoside transporters (hNTs) mediate cellular influx of anticancer nucleoside drugs, including cytarabine, cladribine, and fludarabine. BCR-ABL tyrosine kinase inhibitors (TKIs) imatinib and dasatinib inhibit fludarabine and cytarabine uptake
Publikováno v:
Cancer Chemotherapy and Pharmacology. 76:1093-1098
Effects of tyrosine kinase inhibitors (TKIs) on equilibrative nucleobase transport (ENBT) and sodium-dependent nucleobase transport (SNBT) activities were investigated in normal human renal proximal tubule epithelial cells (hRPTECs) and in pig kidney
Autor:
Michelle Kuzma, Anderson J. Ryan, Carol E. Cass, Tara Scriver, Delores Mowles, Michael B. Sawyer, Vijaya L. Damaraju
Publikováno v:
Clinical Cancer Research. 20:176-186
Purpose: Combinations of tyrosine kinase inhibitors (TKI) with gemcitabine have been attempted with little added benefit to patients. We hypothesized that TKIs designed to bind to ATP-binding pockets of growth factor receptors also bind to transporte
Autor:
Michelle Kuzma, Carol E. Cass, Vijaya L. Damaraju, Marnie Wilson, Michael B. Sawyer, Delores Mowles
Publikováno v:
Biochemistry and Cell Biology. 91:419-427
The goal of this study was to understand roles of nucleoside and nucleobase transport processes in capecitabine pharmacology in cells derived from human renal proximal tubule cells (hRPTCs) and three human renal cell carcinoma (RCC) cell lines, A498,
Publikováno v:
The Journal of biological chemistry. 291(36)
Human nucleoside transporters (hNTs) mediate cellular influx of anticancer nucleoside drugs, including cytarabine, cladribine, and fludarabine. BCR-ABL tyrosine kinase inhibitors (TKIs) imatinib and dasatinib inhibit fludarabine and cytarabine uptake
Autor:
Vickie E. Baracos, Vijaya L. Damaraju, Linda J. McCargar, Tony Reiman, Michelle Kuzma, Carla M. Prado, Michael B. Sawyer, John R. Mackey, Isac S. F. Lima, Robert R. Bies
Publikováno v:
Cancer Chemotherapy and Pharmacology. 67:93-101
Although body composition has emerged as an important predictor of drug efficacy and toxicity, explanations for this association are unclear. Our goal was to investigate relationships between lean body mass (LBM), liver size/function and epirubicin p