Search Results - "Stevens, Y W"

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    Structure, dissociation, and proteolysis of mammalian steroid receptors. Multiplicity of glucocorticoid receptor forms and proteolytic enzymes in rat liver and kidney cytosols by Sherman, M R, Moran, M C, Tuazon, F B, Stevens, Y W

    Published in The Journal of biological chemistry (10-09-1983)
    “…The forms of steroid receptors detected in mammalian tissue cytosols vary from a globular fragment, the mero-receptor, with a molecular weight (Mr) of…”
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    Phase I clinical and pharmacological study of merbarone by DIMAGGIO, J. J, WARRELL, R. P. JR, YOUNG, C. W, MUINDI, J, STEVENS, Y.-W, LEE, S. J, LOWENTHAL, D. A, HAINES, I, WALSH, T. D, BALTZER, L, YALDAEI, S

    Published in Cancer research (Chicago, Ill.) (15-02-1990)
    “…Merbarone, a nonsedating derivative of thiobarbituric acid, has demonstrated excellent activity against certain murine tumors, including L1210 and P388…”
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    In vitro differential metabolism of merbarone by xanthine oxidase and microsomal flavoenzymes. The role of reactive oxygen species by Muindi, J F, Stevens, Y W, Warrell, Jr, R P, Young, C W

    Published in Drug metabolism and disposition (01-05-1993)
    “…Merbarone (MB), a nonsedating derivative of thiobarbituric acid, was recently found to induce profound hypouricemia. When incubated with xanthine oxidase (XO)…”
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    Cancer policy framework for: public health assessment of carcinogens in the environment by DeRosa, C T, Stevens, Y W, Johnson, B L

    Published in Toxicology and industrial health (01-07-1993)
    “…Cancer remains at the forefront of public health concerns in the United States and throughout the world. Over the past 20 years a wide range of federal…”
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    Induction of profound hypouricemia by a non-sedating thiobarbiturate by Warrell, Jr, R P, Muindi, J, Stevens, Y W, Isaacs, M, Young, C W

    Published in Metabolism, clinical and experimental (01-06-1989)
    “…5-[N-phenylcarboxamido]-2-thiobarbituric acid (merbarone) is a non-sedating derivative of thiobarbituric acid originally developed for anticancer use. In the…”
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    The Agency for Toxic Substances and Disease Registry's role in development and application of biomarkers in public health practice by Derosa, C T, Stevens, Y W, Wilson, J D, Ademoyero, A A, Buchanan, S D, Cibulas, Jr, W, Duerksen-Hughes, P J, Mumtaz, M M, Neft, R E, Pohl, H R

    Published in Toxicology and industrial health (01-11-1993)
    “…An overview of the Agency for Toxic Substances and Disease Registry's (ATSDR) biomarker program is presented in the context of the paradigm for biomarkers…”
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    Multiple forms and fragments of cytosolic glucocorticoid receptors from human leukemic cells and normal lymphocytes by SHERMAN, M. R, YEE-WAN STEVENS, TUAZON, F. B

    Published in Cancer research (Chicago, Ill.) (01-09-1984)
    “…Therapy with glucocorticoids is generally more effective in acute lymphoblastic leukemia than in other types of human leukemia. Previous studies, however, have…”
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    Nuclear glucocorticoid binding in chronic lymphatic leukemia lymphocytes by Stevens, J, Stevens, Y W, Sloan, E, Rosenthal, R, Rhodes, J

    Published in Endocrine research communications (1978)
    “…A reliable procedure is described for isolating 3H-triamcinolone acetonide (3H-TA) receptor complexes from purified chronic lymphatic leukemia (CLL) lymphocyte…”
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    Cortisol-induced lymphocytolysis of P1798 tumor cells in glucose-free, pyruvate-free medium by Stevens, J, Stevens, Y W

    “…Exposure of corticoid-sensitive P1798 tumor lymphocytes to cortisol resulted in progressive cell dissolution either with or without exogenous glucose and…”
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    Agency for Toxic Substances and Disease Registry's 1997 priority list of hazardous substances. Latent effects—carcinogenesis, neurotoxicology, and developmental deficits in humans and animals by Ostrowski, S.R., Wilbur, S., Chou, C-H.S.J., Pohl, H.R., Stevens, Y-W., Allred, P.M., Roney, N., Fay, M., Tylenda, C.A.

    Published in Toxicology and industrial health (01-07-1999)
    “…In support of Superfund re-authorization legislation, the Division of Toxicology of the Agency for Toxic Substances and Disease Registry (ATSDR) prepared a…”
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    4-Demethoxydaunorubicin (idarubicin) in combination with 1-β-D-arabinofuranosylcytosine in the treatment of relapsed or refractory acute leukemia by BERMAN, E, RAYMOND, V, YOUNG, C, AIMAN DAGHESTANI, ARLIN, Z. A, GEE, T. S, KEMPIN, S, HANCOCK, C, WILLIAMS, L, YEE-WAN STEVENS, CLARKSON, B. D

    Published in Cancer research (Chicago, Ill.) (15-01-1989)
    “…We conducted a Phase I-II trial of 4-demethoxydaunorubicin (idarubicin, IDR) in combination with 1-beta-D-arabinofuranosylcytosine (ara-C) in 51 patients with…”
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    Phase I and clinical pharmacological study of 4-demethoxydaunorubicin (Idarubicin) in children with advanced cancer by TAN, C. T. C, HANCOCK, C, NIEDZWIECKI, D, STEVENS, Y.-W, STEINHERZ, P, BACHA, D. M, STEINHERZ, L, LUKS, E, WINICK, N, MEYERS, P, MONDORA, A, DANTIS, E

    Published in Cancer research (Chicago, Ill.) (01-06-1987)
    “…We conducted a phase I and pharmacokinetic study of i.v. idarubicin, a new anthracycline analogue, in 42 evaluable children 1-19 years old. Twenty-seven had…”
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