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VP-16

Known as: VP16, drug vp 16, VP 16 
National Institutes of Health

Papers overview

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Highly Cited
2003
Highly Cited
2003
The herpes simplex virus 1 (HSV-1) replicative cycle begins by binding of the viral activator, VP16, to a set of sequences in the… 
Highly Cited
1998
Highly Cited
1998
The relationship between chemosensitivity and p53 is currently considered from two mutually exclusive points of view: (1) wt p53… 
Highly Cited
1998
Highly Cited
1998
Apoptosis is cellular suicide functionally opposite of mitosis. It plays an important role in tissue growth control and removal… 
Highly Cited
1992
Highly Cited
1992
We have recently demonstrated that bufalin is a new potent inducer of the differentiation of human myeloid leukemia cells. The… 
Highly Cited
1992
Highly Cited
1992
We have overproduced and purified the carboxy-terminal transactivation domain of Vmw65 (VP16) of herpes simplex virus, and… 
Highly Cited
1990
Highly Cited
1990
The clastogenic effect of etoposide, an anti‐cancer chemotherapeutic drug, was investigated in vitro on lymphocytes of 5 healthy… 
Highly Cited
1987
Highly Cited
1987
In a phase I/II study, 47 patients (median age, 24 years) with hematologic malignancies (33 patients with acute leukemia not in… 
Highly Cited
1986
Highly Cited
1986
Etoposide (VP16) pharmacokinetics was investigated in three groups of cancer patients: a control group of 18 patients with renal… 
Highly Cited
1984
Highly Cited
1984
The clinical pharmacokinetics of etoposide were studied in eight pediatric patients with refractory solid tumors. The alpha-phase… 
Highly Cited
1983
Highly Cited
1983
The effects of the anticancer drugs 4′-demethylepipodophyllotoxin thenylidene β-d-glucoside and 4′-demethylepipodophyllotoxin…