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VP-16
Known as:
VP16
, drug vp 16
, VP 16
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National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
Etoposide
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
Inhibition of herpes simplex virus 1 gene expression by designer zinc-finger transcription factors
M. Papworth
,
M. Moore
,
M. Isalan
,
M. Minczuk
,
Y. Choo
,
A. Klug
Proceedings of the National Academy of Sciences…
2003
Corpus ID: 29972915
The herpes simplex virus 1 (HSV-1) replicative cycle begins by binding of the viral activator, VP16, to a set of sequences in the…
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Highly Cited
1998
Highly Cited
1998
Acute overexpression of wt p53 facilitates anticancer drug‐induced death of cancer and normal cells
M. Blagosklonny
,
W. El-Deiry
International Journal of Cancer
1998
Corpus ID: 35768898
The relationship between chemosensitivity and p53 is currently considered from two mutually exclusive points of view: (1) wt p53…
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Highly Cited
1998
Highly Cited
1998
Involvement of Bcl-2 cleavage in the acceleration of VP-16-induced U937 cell apoptosis.
Naoya Fujita
,
Takashi Tsuruo
,
Takashi Tsuruo
Biochemical and Biophysical Research…
1998
Corpus ID: 38030037
Apoptosis is cellular suicide functionally opposite of mitosis. It plays an important role in tissue growth control and removal…
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Highly Cited
1992
Highly Cited
1992
Induction by bufalin of differentiation of human leukemia cells HL60, U937, and ML1 toward macrophage/monocyte-like cells and its potent synergistic effect on the differentiation of human leukemia…
Lisha Zhang
,
Kazuyasu Nakaya
,
Takemi Yoshida
,
Yukio Kuroiwa
Cancer Research
1992
Corpus ID: 8845789
We have recently demonstrated that bufalin is a new potent inducer of the differentiation of human myeloid leukemia cells. The…
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Highly Cited
1992
Highly Cited
1992
Structural studies of the acidic transactivation domain of the Vmw65 protein of herpes simplex virus using 1H NMR.
P. O’Hare
,
G. Williams
Biochemistry
1992
Corpus ID: 34924103
We have overproduced and purified the carboxy-terminal transactivation domain of Vmw65 (VP16) of herpes simplex virus, and…
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Highly Cited
1990
Highly Cited
1990
Chromosome aberrations induced by etoposide (VP‐16) are not random
Joëlle Maraschin
,
B. Dutrillaux
,
A. Aurias
International Journal of Cancer
1990
Corpus ID: 31218102
The clastogenic effect of etoposide, an anti‐cancer chemotherapeutic drug, was investigated in vitro on lymphocytes of 5 healthy…
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Highly Cited
1987
Highly Cited
1987
Total body irradiation and high-dose etoposide: a new preparatory regimen for bone marrow transplantation in patients with advanced hematologic malignancies [published erratum appears in Blood 1987…
KG Blume
,
SJ Forman
,
+7 authors
GE Metter
1987
Corpus ID: 208313764
In a phase I/II study, 47 patients (median age, 24 years) with hematologic malignancies (33 patients with acute leukemia not in…
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Highly Cited
1986
Highly Cited
1986
Pharmacokinetics of etoposide in patients with abnormal renal and hepatic function.
Maurizio D'Incaici
,
Cosmo Rossi
,
+5 authors
Cristiana Sessa
Cancer Research
1986
Corpus ID: 12220828
Etoposide (VP16) pharmacokinetics was investigated in three groups of cancer patients: a control group of 18 patients with renal…
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Highly Cited
1984
Highly Cited
1984
Pharmacokinetics of etoposide (VP16) in children and adolescents with refractory solid tumors.
J. Sinkule
,
P. Hutson
,
F. A. Hayes
,
E. Etcubanas
,
W. Evans
Cancer Research
1984
Corpus ID: 20928428
The clinical pharmacokinetics of etoposide were studied in eight pediatric patients with refractory solid tumors. The alpha-phase…
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Highly Cited
1983
Highly Cited
1983
Genetic, biochemical, and cross-resistance studies with mutants of Chinese hamster ovary cells resistant to the anticancer drugs, VM-26 and VP16-213.
R. Gupta
Cancer Research
1983
Corpus ID: 16683502
The effects of the anticancer drugs 4′-demethylepipodophyllotoxin thenylidene β-d-glucoside and 4′-demethylepipodophyllotoxin…
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