review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Andrea Musacchio | Q17715087 |
Luigi Nezi | Q63385204 | ||
P2860 | cites work | Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections | Q29619579 |
Tension between two kinetochores suffices for their bi-orientation on the mitotic spindle | Q34298424 | ||
P433 | issue | 6 | |
P304 | page(s) | 785-795 | |
P577 | publication date | 2009-10-19 | |
P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
P1476 | title | Sister chromatid tension and the spindle assembly checkpoint | |
P478 | volume | 21 |
Q34536926 | A conserved motif at the C terminus of sororin is required for sister chromatid cohesion |
Q27939065 | A conserved role for COMA/CENP-H/I/N kinetochore proteins in the spindle checkpoint. |
Q24338143 | APC15 drives the turnover of MCC-CDC20 to make the spindle assembly checkpoint responsive to kinetochore attachment |
Q52716392 | ATP depletion during mitotic arrest induces mitotic slippage and APC/CCdh1-dependent cyclin B1 degradation. |
Q58752763 | Absence of the Spindle Assembly Checkpoint Restores Mitotic Fidelity upon Loss of Sister Chromatid Cohesion |
Q57272751 | Adaptive Evolution of Centromeric Proteins |
Q44664422 | Altered expression of Aurora kinases in Arabidopsis results in aneu- and polyploidization |
Q26770399 | An Overview of Alternating Electric Fields Therapy (NovoTTF Therapy) for the Treatment of Malignant Glioma |
Q37591019 | Analysis and Modeling of Chromosome Congression During Mitosis in the Chemotherapy Drug Cisplatin |
Q35839779 | Aurora B controls kinetochore-microtubule attachments by inhibiting Ska complex-KMN network interaction |
Q26995347 | Aurora B hyperactivation by Bub1 overexpression promotes chromosome missegregation |
Q36252350 | Aurora B is regulated by acetylation/deacetylation during mitosis in prostate cancer cells |
Q36823669 | Aurora B prevents delayed DNA replication and premature mitotic exit by repressing p21(Cip1). |
Q27021024 | Aurora at the pole and equator: overlapping functions of Aurora kinases in the mitotic spindle |
Q30495481 | Aurora-C kinase deficiency causes cytokinesis failure in meiosis I and production of large polyploid oocytes in mice |
Q24324197 | Beclin-1 is required for chromosome congression and proper outer kinetochore assembly. |
Q35610652 | Biophysics of mitosis |
Q37882877 | Bub1 and BubR1: at the interface between chromosome attachment and the spindle checkpoint |
Q27937206 | Bub1 kinase and Sgo1 modulate pericentric chromatin in response to altered microtubule dynamics |
Q35047487 | Bub1 overexpression induces aneuploidy and tumor formation through Aurora B kinase hyperactivation |
Q33603192 | Catch and release: how do kinetochores hook the right microtubules during mitosis? |
Q37671387 | Cdk1 inactivation terminates mitotic checkpoint surveillance and stabilizes kinetochore attachments in anaphase |
Q37999571 | Cell division control by the Chromosomal Passenger Complex |
Q34644085 | Centromere tension: a divisive issue |
Q30549643 | Characterization of novel MPS1 inhibitors with preclinical anticancer activity |
Q64062627 | Checkpoint Proteins Bub1 and Bub3 Delay Anaphase Onset in Response to Low Tension Independent of Microtubule-Kinetochore Detachment |
Q30577899 | Chk2 prevents mitotic exit when the majority of kinetochores are unattached |
Q44915590 | Clathrin heavy chain 1 is required for spindle assembly and chromosome congression in mouse oocytes |
Q38025305 | Connecting up and clearing out: how kinetochore attachment silences the spindle assembly checkpoint. |
Q35632434 | Correction of microtubule-kinetochore attachment errors: mechanisms and role in tumor suppression |
Q26991874 | DNA damage associated with mitosis and cytokinesis failure |
Q41608683 | DNA integrity, growth pattern, spindle formation, chromosomal constitution and imprinting patterns of mouse oocytes from vitrified pre-antral follicles |
Q35130588 | Defining genome maintenance pathways using functional genomic approaches |
Q35867731 | Dispensability of the SAC Depends on the Time Window Required by Aurora B to Ensure Chromosome Biorientation |
Q40459343 | Dissecting the first and the second meiotic divisions using a marker-less drug-hypersensitive fission yeast. |
Q39363632 | Dividing with Extra Centrosomes: A Double Edged Sword for Cancer Cells. |
Q33687283 | E-cadherin is required for centrosome and spindle orientation in Drosophila male germline stem cells |
Q24297396 | Evidence that Aurora B is implicated in spindle checkpoint signalling independently of error correction |
Q38010323 | Geometry and force behind kinetochore orientation: lessons from meiosis |
Q92795230 | Helical Twist and Rotational Forces in the Mitotic Spindle |
Q47921014 | How Kinetochore Architecture Shapes the Mechanisms of Its Function |
Q51761068 | Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation. |
Q33590962 | INCENP-aurora B interactions modulate kinase activity and chromosome passenger complex localization |
Q41893477 | Insights from an erroneous kinetochore-microtubule attachment state |
Q50500643 | Interpolar microtubules are dispensable in fission yeast meiosis II. |
Q35754713 | Killing cells by targeting mitosis |
Q34987501 | Kinetochore function and chromosome segregation rely on critical residues in histones H3 and H4 in budding yeast |
Q28603755 | Kinetochore-microtubule attachment is sufficient to satisfy the human spindle assembly checkpoint |
Q24602097 | Kinetochore-microtubule interactions: steps towards bi-orientation |
Q38015243 | Let's huddle to prevent a muddle: centrosome declustering as an attractive anticancer strategy |
Q37616620 | Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins |
Q38026773 | Maturation of the kinetochore-microtubule interface and the meaning of metaphase. |
Q37838569 | Merotelic kinetochore attachment: causes and effects. |
Q38152747 | Microtubules and actin crosstalk in cell migration and division |
Q27008913 | Mitotic exit and separation of mother and daughter cells |
Q37818590 | Monitoring spindle orientation: Spindle position checkpoint in charge. |
Q36706361 | Mps1 and Ipl1/Aurora B act sequentially to correctly orient chromosomes on the meiotic spindle of budding yeast. |
Q50876082 | NQO1 prevents radiation-induced aneuploidy by interacting with Aurora-A. |
Q35979185 | Novel functions of endocytic player clathrin in mitosis |
Q27335480 | Overlap microtubules link sister k-fibres and balance the forces on bi-oriented kinetochores. |
Q34338531 | PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains |
Q24294588 | Phosphorylation at serine 331 is required for Aurora B activation. |
Q26822420 | Physiology of the read-write genome |
Q37838177 | Prevention and correction mechanisms behind anaphase synchrony: implications for the genesis of aneuploidy |
Q27007105 | Reconstituting the kinetochore–microtubule interface: what, why, and how |
Q38288071 | Regulation of sororin by Cdk1-mediated phosphorylation |
Q35273343 | Sgo1 is a potential therapeutic target for hepatocellular carcinoma |
Q28507814 | Sirt2 functions in spindle organization and chromosome alignment in mouse oocyte meiosis |
Q35409081 | Small GTPase Rab5 participates in chromosome congression and regulates localization of the centromere-associated protein CENP-F to kinetochores |
Q39209262 | Specialize and Divide (Twice): Functions of Three Aurora Kinase Homologs in Mammalian Oocyte Meiotic Maturation |
Q39015708 | Spindle and kinetochore-associated protein 1 is overexpressed in gastric cancer and modulates cell growth |
Q44943672 | Spindle assembly checkpoint satisfaction occurs via end-on but not lateral attachments under tension. |
Q37956287 | Spindle assembly checkpoint: the third decade |
Q27342956 | Stable kinetochore-microtubule attachment is sufficient to silence the spindle assembly checkpoint in human cells |
Q35803198 | Structural organization of the kinetochore-microtubule interface |
Q35049184 | System-level feedbacks make the anaphase switch irreversible |
Q27309241 | TRIP13PCH-2 promotes Mad2 localization to unattached kinetochores in the spindle checkpoint response |
Q35795073 | Targeting the p53 signaling pathway in cancer therapy - the promises, challenges and perils |
Q26777130 | The Aurora B Kinase in Chromosome Bi-Orientation and Spindle Checkpoint Signaling |
Q38661406 | The Janus soul of centrosomes: a paradoxical role in disease? |
Q34583129 | The fate of metaphase kinetochores is weighed in the balance of SUMOylation during S phase |
Q35793140 | The spatial arrangement of chromosomes during prometaphase facilitates spindle assembly |
Q35712127 | Timing of centrosome separation is important for accurate chromosome segregation |
Q30846736 | Ubiquitin Receptor Protein UBASH3B Drives Aurora B Recruitment to Mitotic Microtubules |
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