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Proceedings of the National Academy of Sciences of the United States of America|August 29, 1995
Isolation and characterization of pokeweed antiviral protein mutations in Saccharomyces cerevisiae: identification of residues important for toxicityY Hur, D J Hwang, O Zoubenko, et al.Cancer Research|March 15, 1993
Radiation damage repair capacity of primary clonogenic blasts in acute lymphoblastic leukemiaF M Uckun, M Chandan-Langlie, W Jaszcz, et al.The Journal of Biological Chemistry|March 29, 1996
Signal transduction through the beta1 integrin family surface adhesion molecules VLA-4 and VLA-5 of human B-cell precursors activates CD19 receptor-associated protein-tyrosine kinasesJ Xiao, Y Messinger, J Jin, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 29, 1998
Calphostin C triggers calcium-dependent apoptosis in human acute lymphoblastic leukemia cellsD M Zhu, R K Narla, W H Fang, et al.Blood|August 1, 1989
Leukemic B-cell precursors constitutively express functional receptors for human interleukin-1F M Uckun, D E Myers, A S Fauci, et al.Leukemia & Lymphoma|August 28, 1998
Treatment of human B-cell precursor leukemia in SCID mice by using a combination of the anti-CD19 immunotoxin B43-PAP with the standard chemotherapeutic drugs vincristine, methylprednisolone, and L-asparaginaseO Ek, P Gaynon, T Zeren, et al.Blood|November 15, 1989
Cell-type-specific cytotoxicity of anti-CD4 and anti-CD8 ricin immunotoxins against human alloreactive T-cell clonesF M Uckun, D E Myers, J A Ledbetter, et al.Anti-Cancer Drugs|May 4, 2001
Vanadocenes as potent anti-proliferative agents disrupting mitotic spindle formation in cancer cellsC S Navara, A Benyumov, A Vassilev, et al.Blood|August 15, 1993
Reactive oxygen intermediates activate NF-kappa B in a tyrosine kinase-dependent mechanism and in combination with vanadate activate the p56lck and p59fyn tyrosine kinases in human lymphocytesG L Schieven, J M Kirihara, D E Myers, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO seriesR Vig, C Mao, T K Venkatachalam, et al.Pageof 233