Zobrazeno 1 - 10
of 49
pro vyhledávání: '"R L, Schilsky"'
Autor:
Paul Roepman, W. W. J. de Leng, Egbert F. Smit, L.R. Hoes, D.L. van der Velden, Derk Jan A. de Groot, H. van der Wijngaart, Niven Mehra, Alwin D. R. Huitema, C.M.L. van Herpen, Ann Hoeben, A.J. de Langen, J.M. van Berge Henegouwen, Ellen Kapiteijn, Mariette Labots, R. L. Schilsky, Stefan Sleijfer, Lot A. Devriese, Bastiaan Nuijen, Hans Gelderblom, Henk M.W. Verheul, Myriam Chalabi, Emile E. Voest, M.J.A. de Jonge, Edwin Cuppen, Petra M. Nederlof, E. van Werkhoven
Publikováno v:
Nature, 574(7776), 127-131. Nature Publishing Group
van der Velden, D L, Hoes, L R, van der Wijngaart, H, van Berge Henegouwen, J M, van Werkhoven, E, Roepman, P, Schilsky, R L, de Leng, W W J, Huitema, A D R, Nuijen, B, Nederlof, P M, van Herpen, C M L, de Groot, D J A, Devriese, L A, Hoeben, A, de Jonge, M J A, Chalabi, M, Smit, E F, de Langen, A J, Mehra, N, Labots, M, Kapiteijn, E, Sleijfer, S, Cuppen, E, Verheul, H M W, Gelderblom, H & Voest, E E 2019, ' The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs ', Nature, vol. 574, no. 7776, pp. 127-131 . https://doi.org/10.1038/s41586-019-1600-x
Nature, 574(7776), 127. Nature Publishing Group
Nature, 574, 7776, pp. 127
Nature, 574(7776), 127-+. Nature Publishing Group
Nature, 574, 127-131. Nature Publishing Group
Nature, 574(7776), 127
Nature, 574, 127
van der Velden, D L, Hoes, L R, van der Wijngaart, H, van Berge Henegouwen, J M, van Werkhoven, E, Roepman, P, Schilsky, R L, de Leng, W W J, Huitema, A D R, Nuijen, B, Nederlof, P M, van Herpen, C M L, de Groot, D J A, Devriese, L A, Hoeben, A, de Jonge, M J A, Chalabi, M, Smit, E F, de Langen, A J, Mehra, N, Labots, M, Kapiteijn, E, Sleijfer, S, Cuppen, E, Verheul, H M W, Gelderblom, H & Voest, E E 2019, ' The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs ', Nature, vol. 574, no. 7776, pp. 127-131 . https://doi.org/10.1038/s41586-019-1600-x
Nature, 574(7776), 127. Nature Publishing Group
Nature, 574, 7776, pp. 127
Nature, 574(7776), 127-+. Nature Publishing Group
Nature, 574, 127-131. Nature Publishing Group
Nature, 574(7776), 127
Nature, 574, 127
The large-scale genetic profiling of tumours can identify potentially actionable molecular variants for which approved anticancer drugs are available1–3. However, when patients with such variants are treated with drugs outside of their approved lab
Autor:
H. L. Kindler, R. L. Schilsky
Publikováno v:
Oncologic Therapies ISBN: 9783642628184
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3d7e04dcb33f14b9c0692da5729622f
https://doi.org/10.1007/978-3-642-55780-4_31
https://doi.org/10.1007/978-3-642-55780-4_31
Publikováno v:
Cancer. 92(6)
The purpose of this study was to determine the maximum tolerated dose and toxicity profile of gemcitabine given on a weekly schedule with continuous infusion 5-fluorouracil.Eligible patients with advanced solid tumors received escalating doses of gem
Publikováno v:
Cancer. 91(7)
The oral administration of 5-fluorouracil (5-FU) is hindered by erratic bioavailability due to catabolism of 5-FU by the enzyme dihydropyrimidine dehydrogenase (DPD) in the gastrointestinal tract. Eniluracil is a potent inactivator of DPD which resul
Autor:
S F, Williams, R L, Schilsky
Publikováno v:
Seminars in oncology. 27(6)
Cancer is the second leading cause of death in women during their reproductive years. Thus, antineoplastic drugs may be administered to pregnant women. The effects these agents have on the developing fetus depend on the type of agent and the timing o
Autor:
R L, Schilsky
Publikováno v:
Oncology (Williston Park, N.Y.). 14(9)
Capecitabine (Xeloda) is a new, orally administered, enzyme-activated fluoropyrimidine carbamate designed to generate high levels of fluorouracil (5-FU) in tumor cells. Selective tumor activation of 5'-deoxy-5-fluorouridine, the last enzymatic step o
Autor:
R L, Schilsky, M E, Dolan, D, Bertucci, R B, Ewesuedo, N J, Vogelzang, S, Mani, L R, Wilson, M J, Ratain
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(8)
O6-benzylguanine (BG) is a potent inactivator of the DNA repair protein O6-alkylguanine-DNA alkyltransferase (AGT) that enhances sensitivity to nitrosoureas in tumor cell lines and tumor-bearing animals. The major objectives of this study were to def
Autor:
E B, Lamont, R L, Schilsky
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 5(9)
A classic example of a rationally developed class of anticancer drugs, the fluoropyrimidines are now the focus of further rational approaches to cancer chemotherapy as they are transformed into oral formulations. Given alone, oral 5-fluorouracil (5-F
Autor:
R. L. Schilsky
Publikováno v:
Oncologic Therapies ISBN: 9783540781080
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d740c51b5e36f3987f2498c8015f2f6
https://doi.org/10.1007/978-3-642-97988-0_28
https://doi.org/10.1007/978-3-642-97988-0_28
Autor:
R L, Schilsky
Publikováno v:
Oncology (Williston Park, N.Y.). 12(10 Suppl 7)
The cellular and clinical pharmacology of fluoropyrimidines is characterized by marked interpatient variability in tumor response and patient tolerance. Understanding the metabolic pathways followed by 5-fluorouracil (5-FU) has led to new strategies