MLN8054, a small-molecule inhibitor of Aurora A, causes spindle pole and chromosome congression defects leading to aneuploidy.
about
Novel E3 ligase component FBXL7 ubiquitinates and degrades Aurora A, causing mitotic arrestRecent advances in the development of Aurora kinases inhibitors in hematological malignanciesAurora Kinases and Potential Medical Applications of Aurora Kinase Inhibitors: A ReviewAurora at the pole and equator: overlapping functions of Aurora kinases in the mitotic spindleTACC3 Is Important for Correct Progression of Meiosis in Bovine OocytesA Cell Biologist's Field Guide to Aurora Kinase InhibitorsNEDD9 depletion destabilizes Aurora A kinase and heightens the efficacy of Aurora A inhibitors: implications for treatment of metastatic solid tumorsBPR1K653, a novel Aurora kinase inhibitor, exhibits potent anti-proliferative activity in MDR1 (P-gp170)-mediated multidrug-resistant cancer cellsAurora-A kinase is essential for bipolar spindle formation and early developmentRole of Filia, a maternal effect gene, in maintaining euploidy during cleavage-stage mouse embryogenesisInhibition of Aurora kinase B is important for biologic activity of the dual inhibitors of BCR-ABL and Aurora kinases R763/AS703569 and PHA-739358 in BCR-ABL transformed cellsAllosteric modulation of AURKA kinase activity by a small-molecule inhibitor of its protein-protein interaction with TPX2The UBXN-2/p37/p47 adaptors of CDC-48/p97 regulate mitosis by limiting the centrosomal recruitment of Aurora A.Benzo[e]pyridoindoles, novel inhibitors of the aurora kinases.Phase I study of the aurora A kinase inhibitor alisertib with induction chemotherapy in patients with acute myeloid leukemia.Aurora kinase inhibitors--rising stars in cancer therapeutics?Finding the middle ground: how kinetochores power chromosome congression.Clathrin heavy chain mediates TACC3 targeting to mitotic spindles to ensure spindle stability.SERS and MD simulation studies of a kinase inhibitor demonstrate the emergence of a potential drug discovery toolAurora kinases and protein phosphatase 1 mediate chromosome congression through regulation of CENP-E.Prophase I arrest and progression to metaphase I in mouse oocytes: comparison of resumption of meiosis and recovery from G2-arrest in somatic cellsThe aurora kinases in cell cycle and leukemiaGolgi partitioning controls mitotic entry through Aurora-A kinase.Phase 1 study of MLN8054, a selective inhibitor of Aurora A kinase in patients with advanced solid tumors.Update on aurora kinase inhibitors in gynecologic malignancies.Tripolin A, a novel small-molecule inhibitor of aurora A kinase, reveals new regulation of HURP's distribution on microtubules.Update on Aurora Kinase Targeted Therapeutics in Oncology.Generation and characterization of novel monoclonal antibodies against human aurora-A.The novel Aurora A kinase inhibitor MLN8237 is active in resistant chronic myeloid leukaemia and significantly increases the efficacy of nilotinibAurora-A inactivation causes mitotic spindle pole fragmentation by unbalancing microtubule-generated forcesAurora A and Aurora B jointly coordinate chromosome segregation and anaphase microtubule dynamics.Mitotic centromere-associated kinesin (MCAK): a potential cancer drug target.Mitotic entry: Non-genetic heterogeneity exposes the requirement for Plk1.Aurora kinase inhibitors as anticancer molecules.Aurora A is differentially expressed in gliomas, is associated with patient survival in glioblastoma and is a potential chemotherapeutic target in gliomas.Aurora-A inhibition offers a novel therapy effective against intracranial glioblastoma.Cell death signaling and anticancer therapyTargeting Aurora A kinase activity with the investigational agent alisertib increases the efficacy of cytarabine through a FOXO-dependent mechanism.Cucurbitacin-I inhibits Aurora kinase A, Aurora kinase B and survivin, induces defects in cell cycle progression and promotes ABT-737-induced cell death in a caspase-independent manner in malignant human glioma cellsAurora kinase A drives MTOC biogenesis but does not trigger resumption of meiosis in mouse oocytes matured in vivo.
P2860
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P2860
MLN8054, a small-molecule inhibitor of Aurora A, causes spindle pole and chromosome congression defects leading to aneuploidy.
description
2007 nî lūn-bûn
@nan
2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@ast
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@en
type
label
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@ast
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@en
prefLabel
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@ast
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@en
P2093
P2860
P356
P1476
MLN8054, a small-molecule inhi ...... defects leading to aneuploidy.
@en
P2093
Arijit Chakravarty
Claudia Rabino
Deborah Wysong
Douglas Bowman
Jeffrey A Ecsedy
Natalie Roy
P2860
P304
P356
10.1128/MCB.02364-06
P407
P577
2007-04-16T00:00:00Z