36 results on '"Greenberger, Lee"'
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2. High burden of clonal hematopoiesis in first responders exposed to the World Trade Center disaster
3. The efficacy of tixagevimab–cilgavimab prophylaxis against Omicron BA.5 variants in patients with hematological malignancies: insights from the Leukemia and Lymphoma Society Registry.
4. Distinct P-glycoprotein Precursors are Overproduced in Independently Isolated Drug-Resistant Cell Lines
5. Potent and sustained inhibition of HIF-1α and downstream genes by a polyethyleneglycol-SN38 conjugate, EZN-2208, results in anti-angiogenic effects
6. A highly selective, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor has potent activity in vitro and in vivo
7. Experimentally induced changes in the endocytic traffic of P-glycoprotein alter drug resistance of cancer cells
8. Development and comparison of two nonradioactive kinase assays for I kappa B kinase
9. Anti-spike antibody response to SARS-CoV-2 booster vaccination in patients with B cell-derived hematologic malignancies.
10. Antibody response to SARS-CoV-2 vaccines in patients with hematologic malignancies.
11. Two photoaffinity analogues of the tripeptide, hemiasterlin, exclusively label alpha-tubulin
12. Tumor cells resistant to a microtubule-depolymerizing hemiasterlin analogue, HTI-286, have mutations in alpha- or beta-tubulin and increased microtubule stability
13. EZN-2208 (PEG-SN38) Overcomes ABCG2-Mediated Topotecan Resistance in BRCA1-Deficient Mouse Mammary Tumors.
14. Two Photoaffinity Analogues of the Tripeptide, Hemiasterlin, Exclusively Label α-Tubulin.
15. Tumor Cells Resistant to a Microtubule-Depolymerizing Hemiasterlin Analogue, HTI-286, Have Mutations in α- or β-Tubulin and Increased Microtubule Stability.
16. Anticancer Agents from Unique Natural Products Sources.
17. Amplification of 4q21-q22 and the MXR gene in independently derived mitoxantrone-resistant cell lines.
18. Atypical multidrug resistance: breast cancer resistance protein messenger RNA expression in mitoxantrone-selected cell lines.
19. Stimulation of photoreceptor disc shedding and pigment epithelial phagocytosis by glutamate, aspartate, and other amino acids.
20. Electrophoretic Analysis of P-glycoproteins Produced by Mouse J774.2 and Chinese Hamster Ovary Multidrug-Resistant Cells2.
21. Biosynthesis of Multidrug Resistance-Associated Glycoproteins in J774.2 Multidrug Resistant Cells.
22. Design, Synthesis, and Evaluation of 3,4-Disubstituted Pyrazole Analogues as Antitumor CDK Inhibitors.
23. Synthesis and Biological Study of 4-Aminopyrimidine-5-carboxaldehyde Oximes as Antiproliferative VEGFR-2 Inhibitors.
24. Syntheses and EGFR Kinase Inhibitory Activity of 6-Substituted-4-anilino [1,7] and [1,8] Naphthyridine-3-carbonitriles.
25. Syntheses and EGFR and HER-2 Kinase Inhibitory Activities of 4-Anilinoquinoline-3-carbonitriles: Analogues of Three Important 4-Anilinoquinazolines Currently Undergoing Clinical Evaluation as Therapeutic Antitumor Agents.
26. ATP-binding cassette proteins: Common denominators between ion channels, transporters, and enzymes
27. ErbB3 Ablation Impairs PI3K/Akt-Dependent Mammary Tumorigenesis.
28. 4-Aminopyrimidine-5-carbaldehyde oximes as potent VEGFR-2 inhibitors. Part II
29. A novel 5-[1,3,4-oxadiazol-2-yl]-N-aryl-4,6-pyrimidine diamine having dual EGFR/HER2 kinase activity: Design, synthesis, and biological activity
30. Discovery of novel 4-amino-6-arylaminopyrimidine-5-carbaldehyde oximes as dual inhibitors of EGFR and ErbB-2 protein tyrosine kinases
31. Design, synthesis, and evaluation of 3,4-disubstituted pyrazole analogues as anti-tumor CDK inhibitors
32. Synthesis and evaluation of pyrazolo[3,4-b]pyridine CDK1 inhibitors as anti-tumor agents
33. Synthesis and biological study of 4-aminopyrimidine-5-carboxaldehyde oximes as antiproliferative VEGFR-2 inhibitors
34. D-piece modifications of the hemiasterlin analog HTI-286 produce potent tubulin inhibitors
35. Tubulin inhibitors. Synthesis and biological activity of HTI-286 analogs with B-segment heterosubstituents
36. Syntheses and EGFR and HER-2 kinase inhibitory activities of 4-anilinoquinoline-3-carbonitriles: analogues of three important 4-anilinoquinazolines currently undergoing clinical evaluation as therapeutic antitumor agents
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