review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Ahna R Skop | |
Marisa S Otegui | |||
Koen J Verbrugghe | |||
P2860 | cites work | The APC-associated protein EB1 associates with components of the dynactin complex and cytoplasmic dynein intermediate chain | Q22009478 |
Central spindle assembly and cytokinesis require a kinesin-like protein/RhoGAP complex with microtubule bundling activity | Q24292120 | ||
Dissection of the mammalian midbody proteome reveals conserved cytokinesis mechanisms. | Q24294556 | ||
Phosphorylation by Aurora B Converts MgcRacGAP to a RhoGAP during Cytokinesis | Q24299695 | ||
Human mitotic spindle-associated protein PRC1 inhibits MgcRacGAP activity toward Cdc42 during the metaphase | Q24306385 | ||
Bni1p, a yeast formin linking cdc42p and the actin cytoskeleton during polarized morphogenesis | Q24310527 | ||
The mammalian passenger protein TD-60 is an RCC1 family member with an essential role in prometaphase to metaphase progression | Q24315803 | ||
Aurora B -TACC1 protein complex in cytokinesis | Q24324208 | ||
A minus-end-directed kinesin with plus-end tracking protein activity is involved in spindle morphogenesis | Q24521334 | ||
Ablation of PRC1 by small interfering RNA demonstrates that cytokinetic abscission requires a central spindle bundle in mammalian cells, whereas completion of furrowing does not | Q24556579 | ||
The Caenorhabditis elegans Aurora B kinase AIR-2 phosphorylates and is required for the localization of a BimC kinesin to meiotic and mitotic spindles | Q24557446 | ||
Cell cycle-dependent translocation of PRC1 on the spindle by Kif4 is essential for midzone formation and cytokinesis | Q24557528 | ||
Mutations in the kinesin-like protein Eg5 disrupting localization to the mitotic spindle | Q24562852 | ||
Essential roles of KIF4 and its binding partner PRC1 in organized central spindle midzone formation | Q24563319 | ||
Plant formin AtFH5 is an evolutionarily conserved actin nucleator involved in cytokinesis. | Q46375768 | ||
The vegetative vacuole proteome of Arabidopsis thaliana reveals predicted and unexpected proteins | Q46931449 | ||
Depletion of syntaxins in the early Caenorhabditis elegans embryo reveals a role for membrane fusion events in cytokinesis | Q47069088 | ||
SPD-1 is required for the formation of the spindle midzone but is not essential for the completion of cytokinesis in C. elegans embryos | Q47069180 | ||
Syntaxin 5 is required for cytokinesis and spermatid differentiation in Drosophila. | Q47070982 | ||
Assembly of ring canals in the male germ line from structural components of the contractile ring. | Q47071871 | ||
Interactions of tobacco microtubule-associated protein MAP65-1b with microtubules | Q47334290 | ||
A new class of microtubule-associated proteins in plants. | Q47823275 | ||
TKRP125, a kinesin-related protein involved in the centrosome-independent organization of the cytokinetic apparatus in tobacco BY-2 cells | Q48055976 | ||
Identification and dynamics of two classes of aurora-like kinases in Arabidopsis and other plants | Q48149761 | ||
Syntaxin specificity of cytokinesis in Arabidopsis | Q48247313 | ||
A kinesin-like protein is essential for oriented deposition of cellulose microfibrils and cell wall strength | Q48270378 | ||
NPSN11 is a cell plate-associated SNARE protein that interacts with the syntaxin KNOLLE. | Q48297919 | ||
Dynamics of the endoplasmic reticulum during early development of Drosophila melanogaster | Q48834402 | ||
Members of the Arabidopsis dynamin-like gene family, ADL1, are essential for plant cytokinesis and polarized cell growth. | Q52107211 | ||
Furrow-specific endocytosis during cytokinesis of zebrafish blastomeres. | Q52115211 | ||
Three-dimensional analysis of syncytial-type cell plates during endosperm cellularization visualized by high resolution electron tomography. | Q52129775 | ||
The kinesin-related protein Kip1p of Saccharomyces cerevisiae is bipolar. | Q52573199 | ||
Electron tomographic analysis of post-meiotic cytokinesis during pollen development in Arabidopsis thaliana | Q58478797 | ||
Kinesin-related cut7 protein associates with mitotic and meiotic spindles in fission yeast | Q59082519 | ||
Distinct nuclear and spindle pole body populations of cyclin–cdc2 in fission yeast | Q59096969 | ||
p34cdc2 kinase is localized to distinct domains within the mitotic apparatus | Q68645461 | ||
A kinesin-like protein, KatAp, in the cells of arabidopsis and other plants | Q70992273 | ||
Functions of the Golgi complex in cell division: formation of cell-matrix contacts and cell-cell communication channels in the terminal phase of cytokinesis | Q72343725 | ||
The exocyst complex in plants | Q73228153 | ||
Two kinesin-related proteins associated with the cold-stable cytoskeleton of carrot cells: characterization of a novel kinesin, DcKRP120-2 | Q73338631 | ||
Cytokinesis failure in clathrin-minus cells is caused by cleavage furrow instability | Q73552853 | ||
Role of microtubules in the organization of the Golgi complex | Q77928235 | ||
Aberrant cell plate formation in the Arabidopsis thaliana microtubule organization 1 mutant | Q81489012 | ||
D-TACC: a novel centrosomal protein required for normal spindle function in the early Drosophila embryo | Q24602580 | ||
The bipolar kinesin, KLP61F, cross-links microtubules within interpolar microtubule bundles of Drosophila embryonic mitotic spindles | Q24670581 | ||
PRC1 is a microtubule binding and bundling protein essential to maintain the mitotic spindle midzone | Q24672475 | ||
Relocation of Aurora B from centromeres to the central spindle at the metaphase to anaphase transition requires MKlp2 | Q24676654 | ||
Brefeldin A: deciphering an enigmatic inhibitor of secretion | Q24678924 | ||
Peripheral Golgi protein GRASP65 is a target of mitotic polo-like kinase (Plk) and Cdc2 | Q24680026 | ||
Isolation and initial characterization of the mammalian midbody | Q24681405 | ||
Parallel chemical genetic and genome-wide RNAi screens identify cytokinesis inhibitors and targets | Q24794040 | ||
Evidence for the involvement of KIF4 in the anterograde transport of L1-containing vesicles | Q27863665 | ||
Two microtubule-associated proteins required for anaphase spindle movement in Saccharomyces cerevisiae | Q27931082 | ||
The molecular function of Ase1p: evidence for a MAP-dependent midzone-specific spindle matrix. Microtubule-associated proteins | Q27932270 | ||
Cytokinesis in flowering plants: more than one way to divide a cell | Q28143674 | ||
Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor | Q28183531 | ||
Chromosomal passengers and the (aurora) ABCs of mitosis | Q28199592 | ||
Mitotic kinases as regulators of cell division and its checkpoints | Q28202545 | ||
Vesicle tethering complexes in membrane traffic | Q28206189 | ||
Kinesin superfamily protein member 4 (KIF4) is localized to midzone and midbody in dividing cells | Q28251408 | ||
Dynamic recruitment of Cdc2 to specific microtubule structures during mitosis | Q28345518 | ||
A novel plant kinesin-related protein specifically associates with the phragmoplast organelles | Q28363613 | ||
Syntaxin 2 and endobrevin are required for the terminal step of cytokinesis in mammalian cells | Q28571407 | ||
Cdc2 kinase directly phosphorylates the cis-Golgi matrix protein GM130 and is required for Golgi fragmentation in mitosis | Q28573476 | ||
TAC-1, a regulator of microtubule length in the C. elegans embryo | Q28611313 | ||
cyk-1: a C. elegans FH gene required for a late step in embryonic cytokinesis | Q28611334 | ||
Polo-like kinases and the orchestration of cell division | Q29616759 | ||
The cellular geography of aurora kinases | Q29617749 | ||
Ase1p organizes antiparallel microtubule arrays during interphase and mitosis in fission yeast | Q30475810 | ||
Regulated Expression of the Centrosomal Protein DdCP224 Affects Microtubule Dynamics and Reveals Mechanisms for the Control of Supernumerary Centrosome Number | Q30480604 | ||
Terminal cytokinesis events uncovered after an RNAi screen | Q30495347 | ||
The large GTPase dynamin associates with the spindle midzone and is required for cytokinesis | Q30540862 | ||
Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex | Q30542170 | ||
The 65-kDa carrot microtubule-associated protein forms regularly arranged filamentous cross-bridges between microtubules | Q30829099 | ||
The roles of fission yeast ase1 in mitotic cell division, meiotic nuclear oscillation, and cytokinesis checkpoint signaling | Q30856513 | ||
In vivo dynamics and differential microtubule-binding activities of MAP65 proteins | Q33209194 | ||
Electron tomographic analysis of somatic cell plate formation in meristematic cells of Arabidopsis preserved by high-pressure freezing. | Q33339822 | ||
EB1 reveals mobile microtubule nucleation sites in Arabidopsis | Q38349273 | ||
NQK1/NtMEK1 is a MAPKK that acts in the NPK1 MAPKKK-mediated MAPK cascade and is required for plant cytokinesis. | Q39895295 | ||
Characterization of a 200 kDa microtubule-associated protein of tobacco BY-2 cells, a member of the XMAP215/MOR1 family | Q40498993 | ||
Alteration of microtubule dynamic instability during preprophase band formation revealed by yellow fluorescent protein-CLIP170 microtubule plus-end labeling | Q40666784 | ||
Golgi membranes are absorbed into and reemerge from the ER during mitosis | Q40909932 | ||
Trafficking through Rab11 endosomes is required for cellularization during Drosophila embryogenesis | Q42452062 | ||
The growing cell plate of higher plants is a site of both actin assembly and vinculin-like antigen recruitment | Q42686051 | ||
Diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene. | Q42687958 | ||
MOR1/GEM1 has an essential role in the plant-specific cytokinetic phragmoplast. | Q42949963 | ||
Flp1, a fission yeast orthologue of the s. cerevisiae CDC14 gene, is not required for cyclin degradation or rum1p stabilisation at the end of mitosis | Q43781967 | ||
Actomyosin promotes cell plate alignment and late lateral expansion in Tradescantia stamen hair cells | Q43908514 | ||
Fragmentation and dispersal of the pericentriolar Golgi complex is required for entry into mitosis in mammalian cells | Q43997060 | ||
Characterization of AtCDC48. Evidence for multiple membrane fusion mechanisms at the plane of cell division in plants | Q44213642 | ||
The Arabidopsis microtubule-associated protein AtMAP65-1: molecular analysis of its microtubule bundling activity. | Q44992507 | ||
The S. pombe Cdc14-like phosphatase Clp1p regulates chromosome biorientation and interacts with Aurora kinase | Q45138476 | ||
Localization of two homologous Arabidopsis kinesin-related proteins in the phragmoplast | Q46137558 | ||
Involvement of the actin cytoskeleton and homotypic membrane fusion in ER dynamics in Caenorhabditis elegans | Q33768439 | ||
Profilin-mediated competition between capping protein and formin Cdc12p during cytokinesis in fission yeast | Q33768492 | ||
The plant microtubule-associated protein AtMAP65-3/PLE is essential for cytokinetic phragmoplast function | Q33842288 | ||
Antagonistic microtubule-sliding motors position mitotic centrosomes in Drosophila early embryos | Q33880076 | ||
Control of microtubule dynamics by the antagonistic activities of XMAP215 and XKCM1 in Xenopus egg extracts | Q33885622 | ||
MOR1 is essential for organizing cortical microtubules in plants. | Q33949237 | ||
The multiprotein exocyst complex is essential for cell separation in Schizosaccharomyces pombe. | Q33953693 | ||
Search, capture and signal: games microtubules and centrosomes play | Q34124566 | ||
Targeting of Nir2 to lipid droplets is regulated by a specific threonine residue within its PI-transfer domain | Q34149069 | ||
Mitotic phosphorylation of the peripheral Golgi protein Nir2 by Cdk1 provides a docking mechanism for Plk1 and affects cytokinesis completion. | Q34318559 | ||
Feo, the Drosophila homolog of PRC1, is required for central-spindle formation and cytokinesis | Q34345003 | ||
Deconstructing Golgi inheritance | Q34368497 | ||
Membrane traffic: a driving force in cytokinesis | Q34391536 | ||
The molecular requirements for cytokinesis | Q34404139 | ||
Animal cell cytokinesis | Q34425177 | ||
The Ran GTPase system in fission yeast affects microtubules and cytokinesis in cells that are competent for nucleocytoplasmic protein transport | Q34443582 | ||
Vesicle traffic in the endomembrane system: a tale of COPs, Rabs and SNAREs. | Q34977149 | ||
Telophase disc: a new mammalian mitotic organelle that bisects telophase cells with a possible function in cytokinesis | Q34977771 | ||
Surfing on microtubule ends | Q35125633 | ||
Cell-cycle-specific Golgi fragmentation: how and why? | Q35189422 | ||
Microtubule organization and function in epithelial cells | Q35607716 | ||
MAPping the eukaryotic tree of life: structure, function, and evolution of the MAP215/Dis1 family of microtubule-associated proteins | Q35909198 | ||
Cytokinesis: the central spindle takes center stage | Q35959019 | ||
Cytoskeletal motors in Arabidopsis. Sixty-one kinesins and seventeen myosins | Q35980443 | ||
Cytokinesis in higher plants | Q36110972 | ||
The Drosophila kinesin-like protein KLP3A is a midbody component required for central spindle assembly and initiation of cytokinesis | Q36235490 | ||
Partitioning of the Golgi apparatus during mitosis in living HeLa cells | Q36254732 | ||
Lava lamp, a novel peripheral golgi protein, is required for Drosophila melanogaster cellularization | Q36316531 | ||
Differential contribution of Bud6p and Kar9p to microtubule capture and spindle orientation in S. cerevisiae | Q36322729 | ||
Both midzone and astral microtubules are involved in the delivery of cytokinesis signals: insights from the mobility of aurora B. | Q36324485 | ||
Functional characterization of the KNOLLE-interacting t-SNARE AtSNAP33 and its role in plant cytokinesis | Q36380018 | ||
A novel role for clathrin in cytokinesis | Q36548632 | ||
Requirements of fission yeast septins for complex formation, localization, and function | Q37657358 | ||
P433 | issue | 8 | |
P304 | page(s) | 404-413 | |
P577 | publication date | 2005-08-01 | |
P1433 | published in | Trends in Cell Biology | Q1573994 |
P1476 | title | Midbodies and phragmoplasts: analogous structures involved in cytokinesis | |
P478 | volume | 15 |
Q33427806 | A complex cell division machinery was present in the last common ancestor of eukaryotes |
Q47136531 | A novel mode of cytokinesis without cell-substratum adhesion |
Q24321392 | ARF6 GTPase protects the post-mitotic midbody from 14-3-3-mediated disintegration |
Q57730339 | An inducible RNA interference system in Physcomitrella patens reveals a dominant role of augmin in phragmoplast microtubule generation |
Q34419568 | An integrated overview of spatiotemporal organization and regulation in mitosis in terms of the proteins in the functional supercomplexes. |
Q30482545 | Both daughter cells traffic and exocytose membrane at the cleavage furrow during mammalian cytokinesis |
Q37158871 | Breaking up is hard to do - membrane traffic in cytokinesis. |
Q28741421 | Cell differentiation and morphogenesis in the colony-forming choanoflagellate Salpingoeca rosetta |
Q37164565 | Cell division screens and dynamin |
Q24670163 | Cep55, a microtubule-bundling protein, associates with centralspindlin to control the midbody integrity and cell abscission during cytokinesis |
Q36850326 | Cep57 protein is required for cytokinesis by facilitating central spindle microtubule organization |
Q40583708 | Class I Arfs (Arf1 and Arf3) and Arf6 are localized to the Flemming body and play important roles in cytokinesis. |
Q53047134 | Cleavage of cytoplasm within the oligonucleate zoosporangia of allomyces macrogynus. |
Q33708397 | Cryoelectron tomography of eukaryotic cells. |
Q53090357 | DNA-PKcs associates with PLK1 and is involved in proper chromosome segregation and cytokinesis. |
Q34605374 | Dividing the spoils of growth and the cell cycle: The fission yeast as a model for the study of cytokinesis. |
Q57163396 | Dual localized kinesin-12 POK2 plays multiple roles during cell division and interacts with MAP65-3 |
Q42182021 | Dynamic actin gene family evolution in primates. |
Q36404509 | Dynamin and cytokinesis |
Q94453488 | ESCRT Machinery Mediates Cytokinetic Abscission in the Unicellular Red Alga Cyanidioschyzon merolae |
Q42182945 | Exo- and endocytotic trafficking of SCAMP2 |
Q35119229 | Germ cell intercellular bridges |
Q47424908 | Girdin locates in centrosome and midbody and plays an important role in cell division |
Q27321556 | Identification of Phosphoinositide-Binding Protein PATELLIN2 as a Substrate of Arabidopsis MPK4 MAP Kinase during Septum Formation in Cytokinesis |
Q24635641 | Interaction of antiparallel microtubules in the phragmoplast is mediated by the microtubule-associated protein MAP65-3 in Arabidopsis |
Q28271618 | Kinesins to the core: The role of microtubule-based motor proteins in building the mitotic spindle midzone |
Q45036715 | MICROTUBULE-ASSOCIATED PROTEIN65 is essential for maintenance of phragmoplast bipolarity and formation of the cell plate in Physcomitrella patens |
Q35253788 | MiCroKiTS 4.0: a database of midbody, centrosome, kinetochore, telomere and spindle |
Q33506945 | MiCroKit 3.0: an integrated database of midbody, centrosome and kinetochore |
Q26830559 | Microtubule networks for plant cell division |
Q28589546 | Midbody and primary cilium of neural progenitors release extracellular membrane particles enriched in the stem cell marker prominin-1 |
Q33350278 | Mitogen-activated protein kinase 4 is involved in the regulation of mitotic and cytokinetic microtubule transitions in Arabidopsis thaliana |
Q37728172 | Mitotic Spindle Assembly in Land Plants: Molecules and Mechanisms |
Q34272397 | Molecular control of animal cell cytokinesis |
Q41988815 | Mutations in a gene encoding a midbody protein in binucleated Reed-Sternberg cells of Hodgkin lymphoma |
Q39870122 | NAT10, a nucleolar protein, localizes to the midbody and regulates cytokinesis and acetylation of microtubules |
Q34439714 | Nessun Dorma, a novel centralspindlin partner, is required for cytokinesis in Drosophila spermatocytes |
Q38177408 | New insights into the molecular mechanisms of mitosis and cytokinesis in trypanosomes |
Q34496748 | Not so divided: the common basis of plant and animal cell division |
Q37728644 | Optimized methods for imaging membrane nanotubes between T cells and trafficking of HIV-1. |
Q42083866 | Phosphorylation of NtMAP65-1 by a MAP kinase down-regulates its activity of microtubule bundling and stimulates progression of cytokinesis of tobacco cells |
Q35471362 | Phosphorylation of a mitotic kinesin-like protein and a MAPKKK by cyclin-dependent kinases (CDKs) is involved in the transition to cytokinesis in plants |
Q38504965 | Prediction of midbody, centrosome and kinetochore proteins based on gene ontology information |
Q38924455 | Proliferating versus differentiating stem and cancer cells exhibit distinct midbody-release behaviour. |
Q33363049 | ROS homeostasis as a prerequisite for the accomplishment of plant cytokinesis. |
Q46779754 | Rab-A2 and Rab-A3 GTPases define a trans-golgi endosomal membrane domain in Arabidopsis that contributes substantially to the cell plate |
Q30484752 | RanGAP1 is a continuous marker of the Arabidopsis cell division plane |
Q38067908 | Resurrecting remnants: the lives of post-mitotic midbodies |
Q27933531 | Role of Inn1 and its interactions with Hof1 and Cyk3 in promoting cleavage furrow and septum formation in S. cerevisiae. |
Q52720544 | Slow calcium waves mediate furrow microtubule reorganization and germ plasm compaction in the early zebrafish embryo. |
Q58430694 | Src Signaling Regulates Completion of Abscission in Cytokinesis through ERK/MAPK Activation at the Midbody |
Q39625937 | Strasburger's legacy to mitosis and cytokinesis and its relevance for the Cell Theory |
Q30481922 | Tektin 2 is required for central spindle microtubule organization and the completion of cytokinesis |
Q47830439 | TfVPS32 Regulates Cell Division in the Parasite Tritrichomonas foetus. |
Q50540459 | The Arabidopsis Exocyst Complex Is Involved in Cytokinesis and Cell Plate Maturation |
Q35537234 | The Chlamydomonas cell cycle. |
Q33280297 | The actin multigene family of Paramecium tetraurelia |
Q42366464 | The carboxyl-terminal tail of the stalk of Arabidopsis NACK1/HINKEL kinesin is required for its localization to the cell plate formation site |
Q30479948 | The concentration of Nuf, a Rab11 effector, at the microtubule-organizing center is cell cycle regulated, dynein-dependent, and coincides with furrow formation |
Q53164432 | The distribution of TPX2 in dividing leaf cells of the fern Asplenium nidus. |
Q38095625 | The evolution and diversification of plant microtubule-associated proteins |
Q27312259 | The maternal-effect gene cellular island encodes aurora B kinase and is essential for furrow formation in the early zebrafish embryo |
Q33641901 | Understanding cytokinesis: lessons from fission yeast |
Q37879607 | Universal rules for division plane selection in plants |
Q34772681 | Vertebrate maternal-effect genes: Insights into fertilization, early cleavage divisions, and germ cell determinant localization from studies in the zebrafish |
Q30482088 | Vesicles and actin are targeted to the cleavage furrow via furrow microtubules and the central spindle |
Q53568657 | Visualization of membrane-cytoskeletal interactions during plant cytokinesis. |
Q30416709 | What can plants do for cell biology? |