Search Results - "AVRAMIS, V. I"

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  1. 1

    Structure-function relationships and clinical applications of L-asparaginases by Labrou, N E, Papageorgiou, A C, Avramis, V I

    Published in Current medicinal chemistry (01-07-2010)
    “…L-asparaginase (L-ASNase, EC 3.5.1.1) catalyzes the hydrolysis of the non-essential amino acid L-Asn to LAsp and ammonia and is widely used for the treatment…”
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  2. 2

    Phase I trial of 13-cis-retinoic acid in children with neuroblastoma following bone marrow transplantation by Villablanca, J G, Khan, A A, Avramis, V I, Seeger, R C, Matthay, K K, Ramsay, N K, Reynolds, C P

    Published in Journal of clinical oncology (01-04-1995)
    “…Treatment of neuroblastoma cell lines with 13-cis-retinoic acid (cis-RA) can cause sustained inhibition of proliferation. Since cis-RA has demonstrated…”
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  3. 3

    Taxotere and vincristine inhibit the secretion of the angiogenesis inducing vascular endothelial growth factor (VEGF) by wild-type and drug-resistant human leukemia T-cell lines by Avramis, I A, Kwock, R, Avramis, V I

    Published in Anticancer research (01-07-2001)
    “…Recent studies have shown that angiogenesis, which is induced by VEGF, may be involved in the pathogenesis of hematopoietic malignancies. A human leukemia…”
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    NONMEM population pharmacokinetic studies of cytosine arabinoside after high-dose and after loading bolus followed by continuous infusion of the drug in pediatric patients with leukemias by PERICLOU, A. P, AVRAMIS, V. I

    “…We examined the population pharmacokinetics (PPK) of cytosine arabinoside (ara-C) after high-dose ara-C (HDara-C) (3 g/m2 every 12 h) and after a loading bolus…”
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  6. 6

    Increased p21/WAF-1 and p53 protein levels following sequential three drug combination regimen of fludarabine, cytarabine and docetaxel induces apoptosis in human leukemia cells by Avramis, V I, Nandy, P, Kwock, R, Solorzano, M M, Mukherjee, S K, Danenberg, P, Cohen, L J

    Published in Anticancer research (01-07-1998)
    “…Combinations of nucleoside analog drugs, such as F-araA and ara-C, combined with Topoisomerase II inhibitors, such as anthracyclines, are synergistic against…”
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  7. 7

    Treatment of human B-cell precursor leukemia in SCID mice using a combination of the investigational biotherapeutic agent B43-PAP with cytosine arabinoside by MESSINGER, Y, YANISHEVSKI, Y, AVRAMIS, V. I, EK, O, CHELSTROM, L. M, GUNTHER, R, MYERS, D. E, IRVIN, J. D, EVANS, W, UCKUN, F. M

    Published in Clinical cancer research (01-09-1996)
    “…Combined immunochemotherapy regimens using the investigational biotherapeutic agent B43(anti-CD19)-poke-weed antiviral protein (PAP) immunotoxin may offer an…”
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  8. 8

    Biochemical pharmacology and DNA methylation studies of arabinosyl 5-azacytidine and 5,6-dihydro-5-azacytidine in two human leukemia cell lines PER-145 and PER-163 by Kees, U R, Avramis, V I

    Published in Anti-cancer drugs (01-04-1995)
    “…1-beta-D-arabinofuranosyl-5-azacytosine (ara-AC) and 5,6-dihydro-5-azacytidine (DHAC) are two new antitumor agents under clinical investigations, which exhibit…”
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  9. 9

    Protein phosphatase 1α-mediated stimulation of apoptosis is associated with dephosphorylation of the retinoblastoma protein by WANG, Rui-Hong, LIU, Cathy W. Y, AVRAMIS, Vassilios I, BERNDT, Norbert

    Published in Oncogene (27-09-2001)
    “…Protein phosphatase 1 (PP1) plays important roles in many different aspects of cellular activities including cell cycle control. One important function of PP1…”
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  10. 10

    Biochemical pharmacology of zidovudine in human T-lymphoblastoid cells (CEM) by Avramis, V I, Markson, W, Jackson, R L, Gomperts, E

    Published in AIDS (London) (01-07-1989)
    “…HIV is the causative agent of AIDS. The purpose of this study was to examine the biochemical pharmacology of the anti-viral agent zidovudine (AZT) in the…”
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  11. 11

    Inhibition of ribonucleotide reductase by a new class of isoindole derivatives: drug synergism with cytarabine (Ara-C) and induction of cellular apoptosis by Nandy, P, Lien, E J, Avramis, V I

    Published in Anticancer research (01-05-1999)
    “…The hydroxyisoindole dione derivatives ISID and MISID are new compounds with structures resembling purines and possessing a hydroxamic acid moiety which is the…”
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  12. 12

    Phase I Study of Gemcitabine (Difluorodeoxycytidine) in Children with Relapsed or Refractory Leukemia (CCG-0955): A Report from the Children's Cancer Group by Steinherz, P.G., Seibel, N.L., Ames, M.M., Avramis, V.I., Krailo, M.D., Liu-Mares, W., Reid, J.M., Safgren, S.L., Reaman, G.H.

    Published in Leukemia & lymphoma (01-10-2002)
    “…To determine the maximum tolerated dose (MTD) and assess the toxicity profile and pharmacokinetics of weekly gemcitabine infusions in pediatric patients with…”
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  13. 13

    The combination regimen of idarubicin and taxotere is effective against human drug-resistant leukemic cell lines by Majlessipour, F, Avramis, I A, Kwock, R, Weinberg, K I, Avrami, V I

    Published in Anticancer research (01-05-2002)
    “…Up-regulation of Bcl-2 protein may contribute to drug resistance, by decreasing apoptosis after treatment, in pre-B and B-cell leukemias in pediatric patients…”
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  14. 14

    Pharmacokinetic studies of 13-cis-retinoic acid in pediatric patients with neuroblastoma following bone marrow transplantation by KHAN, A. A, VILLABLANCA, J. G, REYNOLDS, C. P, AVRAMIS, V. I

    “…A phase I clinical trial of 13-cis-retinoic acid (cis-RA) was undertaken to determine the maximally tolerated dose (MTD) and pharmacokinetics (PK) of cis-RA…”
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  15. 15

    Cytosine arabinoside (ara-C) resistance confers cross-resistance or collateral sensitivity to other classes of anti-leukemic drugs by Martin-Aragon, S, Mukherjee, S K, Taylor, B J, Ivy, S P, Fu, C H, Ardi, V C, Avramis, V I

    Published in Anticancer research (01-01-2000)
    “…The major limitation of treatment with antimetabolite drugs is that they produce resistant clones both in vitro and in patients who either do not respond to…”
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  16. 16

    Development of a double-drug-resistant human leukemia model to cytosine arabinoside and L-asparaginase: evaluation of cross-resistance to other treatment modalities by Majlessipour, F, Kwock, R, Martin-Aragon, S, Weinberg, K I, Avramis, V I

    Published in Anticancer research (01-01-2001)
    “…We have developed an in vitro model of 38 T-lymphoblastic leukemia lines resistant to cytosine arabinoside (ara-C) and L-asparaginase (ASNase). Of these, 26…”
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    Evidence of in vitro development of drug resistance to azidothymidine in T-lymphocytic leukemia cell lines (Jurkat E6-1/AZT-100) and in pediatric patients with HIV-1 infection by Avramis, V I, Kwock, R, Solorzano, M M, Gomperts, E

    “…Clinical reports indicate that the development of drug resistance to AZT after chronic administration is common. In order to study this phenomenon, the T-cell…”
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  19. 19

    Synergistic antiviral effect of PEG-asparaginase (ONCASPAR), with protease inhibitor alone and in combination with RT inhibitors against HIV-1 infected T-cells: a model of HIV-1-induced T-cell lymphoma by Avramis, V I, Kwock, R, Avramis, I A, Cohen, L J, Inderlied, C

    Published in In vivo (Athens) (01-01-2001)
    “…We evaluated the anti-HIV-1 activity of the T-cell-specific protein inhibitor PEG-asparaginase (PEG-ASNase) in human HIV-1-infected T-cells. We further…”
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  20. 20

    Synthesis and testing of new antileukemic schiff bases of N-hydroxy-N'-aminoguanidine against CCRF-CEM/0 human leukemia cells in vitro and synergism studies with cytarabine (Ara-C) by KONERU, P. B, LIEN, E. J, AVRAMIS, V. I

    Published in Pharmaceutical research (01-04-1993)
    “…A series of eight new N-hydroxy-N'-aminoguanidine (HAG) Schiff bases [ArCH = NNHC(= NH)NHOH.tosylate] was synthesized as potential antitumor agents through the…”
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