Works matching IS 00778923 AND DT 1999 AND VI 886 AND IP 1
Results: 48
Anti-HER2 Immunoliposomes for Targeted Drug Delivery.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 293, doi. 10.1111/j.1749-6632.1999.tb09440.x
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Telomerase: A Target for Anticancer Therapy.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 1, doi. 10.1111/j.1749-6632.1999.tb09395.x
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Activation of Apoptosis and Its Inhibition.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 132, doi. 10.1111/j.1749-6632.1999.tb09408.x
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Homeodomain-Derived Peptides: In and Out of the Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 172, doi. 10.1111/j.1749-6632.1999.tb09410.x
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Selective Inhibition of ras-Transformed Cell Growth by a Novel Fatty Acid-Based Chloromethyl Ketone Designed to Target Ras Endoprotease.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 103, doi. 10.1111/j.1749-6632.1999.tb09405.x
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Induction of Apoptosis by Gelsolin Truncates.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 217, doi. 10.1111/j.1749-6632.1999.tb09420.x
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The Farnesyltransferase Inhibitor L-744,832 Inhibits the Growth of Astrocytomas through a Combination of Antiproliferative, Antiangiogenic, and Proapoptotic Activities.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 257, doi. 10.1111/j.1749-6632.1999.tb09430.x
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Homologous Recombination between Heterologs during Repair of a Double-Strand Break: Suppression of Translocations in Normal Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 183, doi. 10.1111/j.1749-6632.1999.tb09412.x
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Recombinant Cytotoxins Specific for Cancer Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 297, doi. 10.1111/j.1749-6632.1999.tb09441.x
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Cellular Effects of a New Farnesyltransferase Inhibitor, RPR-115135, in a Human Isogenic Colon Cancer Cell Line Model System HCT-116.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 252, doi. 10.1111/j.1749-6632.1999.tb09429.x
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Selection of Genetic Suppressor Elements Conferring Resistance to DNA Topoisomerase II Inhibitors.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 187, doi. 10.1111/j.1749-6632.1999.tb09413.x
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A Paradigm for Cancer Treatment Using the Retinoblastoma Gene in a Mouse Model.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 12, doi. 10.1111/j.1749-6632.1999.tb09396.x
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Trichostatin and Leptomycin: Inhibition of Histone Deacetylation and Signal-Dependent Nuclear Export.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 23, doi. 10.1111/j.1749-6632.1999.tb09397.x
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Immunotherapy of Cancer.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 67, doi. 10.1111/j.1749-6632.1999.tb09401.x
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Farnesyltransferase Inhibitors: Preclinical Development.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 91, doi. 10.1111/j.1749-6632.1999.tb09404.x
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Strategies to Adapt Adenoviral Vectors for Targeted Delivery.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 158, doi. 10.1111/j.1749-6632.1999.tb09409.x
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Construction of a Cell-Permeable CDC42 Binding Fragment of ACK That Inhibits v-Ha-Ras Transformation.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 285, doi. 10.1111/j.1749-6632.1999.tb09438.x
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RPR 130401, a Nonpeptidomimetic Farnesyltransferase Inhibitor with in Vivo Activity.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 249, doi. 10.1111/j.1749-6632.1999.tb09428.x
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Rational Development of Cell-Penetrating High Affinity SH3 Domain Binding Peptides That Selectively Disrupt the Signal Transduction of Crk Family Adapters.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 289, doi. 10.1111/j.1749-6632.1999.tb09439.x
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Truncated Form of β-Catenin and Reduced Expression of Wild-Type Catenins Feature HepG2 Human Liver Cancer Cells.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 212, doi. 10.1111/j.1749-6632.1999.tb09419.x
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Intracellular Signaling of the TGF-β Superfamily by Smad Proteins.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 73, doi. 10.1111/j.1749-6632.1999.tb09402.x
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The Dual Role of Cytoskeletal Anchor Proteins in Cell Adhesion and Signal Transduction.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 37, doi. 10.1111/j.1749-6632.1999.tb09398.x
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Cytoskeletal Tumor Suppressors That Block Oncogenic RAS Signaling.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 48, doi. 10.1111/j.1749-6632.1999.tb09399.x
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Selective Induction of Cyclin-Dependent Kinase Inhibitors and Their Roles in Cell Cycle Arrest Caused by Trichostatin A, an Inhibitor of Histone Deacetylase.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 200, doi. 10.1111/j.1749-6632.1999.tb09416.x
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Plasmin-Depletion Therapy A New Approach to Overcoming Tumor Cell Drug Resistance.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 240, doi. 10.1111/j.1749-6632.1999.tb09426.x
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B4112, a Novel Tetramethylpiperidine-Substituted Phenazine That Inhibits the Proliferation of Multidrug-Resistant Cancer Cell Lines.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 280, doi. 10.1111/j.1749-6632.1999.tb09436.x
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Augmented Inhibition of Tumor Cell Proliferation in Combined Use of Electroporation with a Plant Toxin, Saporin.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 233, doi. 10.1111/j.1749-6632.1999.tb09424.x
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Activation of a 36-kD MBP Kinase, an Active Proteolytic Fragment of MST/Krs Proteins, during Anticancer Drug-Induced Apoptosis.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 273, doi. 10.1111/j.1749-6632.1999.tb09434.x
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Identification of a Novel Nuclear Export Signal Sensitive to Oxidative Stress in Yeast AP-1-Like Transcription Factor.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 204, doi. 10.1111/j.1749-6632.1999.tb09417.x
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Melanoma Cell Lines Contain a Proteasome-Sensitive, Nuclear Cytoskeleton-Associated Pool of β-Catenin.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 208, doi. 10.1111/j.1749-6632.1999.tb09418.x
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Azatyrosine: Mechanism of Action for Conversion of Transformed Phenotype to Normal.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 109, doi. 10.1111/j.1749-6632.1999.tb09406.x
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Introduction.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. xi, doi. 10.1111/j.1749-6632.1999.tb09394.x
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Bacterial Toxins Inhibiting or Activating Small GTP-Binding Proteins.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 83, doi. 10.1111/j.1749-6632.1999.tb09403.x
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Antiangiogenic Domains Shared by Thrombospondins and Metallospondins, a New Family of Angiogenic Inhibitors.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 58, doi. 10.1111/j.1749-6632.1999.tb09400.x
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Reexpression of the Major PKC Substrate, SSeCKS, Correlates with the Tumor-Suppressive Effects of SCH51344 on Rat-6/ src and Rat-6/ ras Fibroblasts but Not on Rat-6/ raf Fibroblasts.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 221, doi. 10.1111/j.1749-6632.1999.tb09421.x
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Isolation of Farnesyltransferase Inhibitors from Herbal Medicines.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 261, doi. 10.1111/j.1749-6632.1999.tb09431.x
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Polysulfated Heparinoids Selectively Inactivate Heparin-Binding Angiogenesis Factors.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 243, doi. 10.1111/j.1749-6632.1999.tb09427.x
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The Anti-RAS Cancer Drug MKT-077 Is an F-Actin Cross-Linker.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 283, doi. 10.1111/j.1749-6632.1999.tb09437.x
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In Vitro Evaluation of a Novel 2,6,9-Trisubstituted Purine Acting As a Cyclin-Dependent Kinase Inhibitor.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 180, doi. 10.1111/j.1749-6632.1999.tb09411.x
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Subtractive cDNA Cloning and Characterization of Genes Induced by All-Trans Retinoic Acid.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 225, doi. 10.1111/j.1749-6632.1999.tb09422.x
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Farnesyltransferase Inhibitor-Induced Regression of Mammary Tumors in TGFα and TGFα/ neu Transgenic Mice Correlates with Inhibition of Map Kinase and p70s6 Kinase Phosphorylation.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 265, doi. 10.1111/j.1749-6632.1999.tb09432.x
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BAP1, a Candidate Tumor Suppressor Protein That Interacts with BRCA1.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 191, doi. 10.1111/j.1749-6632.1999.tb09414.x
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SCH 51344, An Inhibitor of RAS/RAC-Mediated Cell Morphology Pathway.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 122, doi. 10.1111/j.1749-6632.1999.tb09407.x
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Expression of Matrix Metalloproteinases and Their Inhibitors in Human Brain Tumors.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 236, doi. 10.1111/j.1749-6632.1999.tb09425.x
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Peptides Mimicking Sialyl-Lewis A Isolated from a Random Peptide Library and Peptide Array.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 276, doi. 10.1111/j.1749-6632.1999.tb09435.x
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Purification and Functional Characterization of a Novel Protein Encoded by a Retinoic Acid-Induced Gene, RA28.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 229, doi. 10.1111/j.1749-6632.1999.tb09423.x
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Inhibition of Protein Tyrosine Kinase Activity by 1a-Docosahexaenoyl Mitomycin C.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 269, doi. 10.1111/j.1749-6632.1999.tb09433.x
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Histone Deacetylase Inhibitor Activates the p21/WAF1/Cip1 Gene Promoter through the Sp1 Sites.
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- Annals of the New York Academy of Sciences, 1999, v. 886, n. 1, p. 195, doi. 10.1111/j.1749-6632.1999.tb09415.x
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