ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
about
Novel agents for chronic lymphocytic leukemiaProteasome inhibitors evoke latent tumor suppression programs in pro-B MLL leukemias through MLL-AF4Noxa/Bcl-2 protein interactions contribute to bortezomib resistance in human lymphoid cellsSynthetic lethal interaction of combined BCL-XL and MEK inhibition promotes tumor regressions in KRAS mutant cancer modelsMcl-1 is critical for survival in a subgroup of non-small-cell lung cancer cell linesChemical genomics identifies small-molecule MCL1 repressors and BCL-xL as a predictor of MCL1 dependencySmall-Molecule Bcl2 BH4 Antagonist for Lung Cancer TherapyBcl-2 inhibitors: targeting mitochondrial apoptotic pathways in cancer therapySmall-molecule Bcl-2 antagonists as targeted therapy in oncologyMitochondria, cholesterol and cancer cell metabolismApoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategiesUpdate on rational targeted therapy in AMLCurrent challenges and novel treatment strategies in double hit lymphomasModulation of Protein-Protein Interactions for the Development of Novel TherapeuticsRegulation of Bim in Health and DiseaseTreatment Strategies that Enhance the Efficacy and Selectivity of Mitochondria-Targeted Anticancer AgentsBcl-2 antagonists: a proof of concept for CLL therapyChloroquine and hydroxychloroquine for cancer therapyTargeting BCL2-Proteins for the Treatment of Solid TumoursBcl-2 expression predicts sensitivity to chemotherapy in breast cancer: a systematic review and meta-analysisThe BCL2 Family: Key Mediators of the Apoptotic Response to Targeted Anticancer TherapeuticsNovel agents in mantle cell lymphomaHow cell death shapes cancerTargeting the apoptosis pathway in hematologic malignanciesGetting TRAIL back on track for cancer therapyNovel drug targets for personalized precision medicine in relapsed/refractory diffuse large B-cell lymphoma: a comprehensive reviewDynamics of Bcl-xL in water and membrane: molecular simulationsAutophagy suppresses RIP kinase-dependent necrosis enabling survival to mTOR inhibitionMito-priming as a method to engineer Bcl-2 addiction.BAX activation is initiated at a novel interaction siteConformational Changes in Bcl-2 Pro-survival Proteins Determine Their Capacity to Bind LigandsMcl-1-Bim complexes accommodate surprising point mutations via minor structural changesDeterminants of BH3 Binding Specificity for Mcl-1 versus Bcl-xLThe MCL-1 BH3 helix is an exclusive MCL-1 inhibitor and apoptosis sensitizerDiscovery and molecular characterization of a Bcl-2-regulated cell death pathway in schistosomesDiscovery of Potent Myeloid Cell Leukemia 1 (Mcl-1) Inhibitors Using Fragment-Based Methods and Structure-Based DesignExperimental and computational active site mapping as a starting point to fragment-based lead discoveryStructure-function analyses of the human SIX1–EYA2 complex reveal insights into metastasis and BOR syndromeDesign of Bcl-2 and Bcl-xL Inhibitors with Subnanomolar Binding Affinities Based upon a New ScaffoldStructure-Guided Rational Design of α/β-Peptide Foldamers with High Affinity for BCL-2 Family Prosurvival Proteins
P2860
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P2860
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@ast
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@en
type
label
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@ast
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@en
prefLabel
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@ast
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@en
P2093
P3181
P1433
P1476
ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor
@en
P2093
Anderson MG
Johnson EF
P304
P3181
P356
10.1158/0008-5472.CAN-07-5836
P407
P577
2008-05-01T00:00:00Z