tea1 and the microtubular cytoskeleton are important for generating global spatial order within the fission yeast cell.
about
Hsp70-Hsp40 chaperone complex functions in controlling polarized growth by repressing Hsf1-driven heat stress-associated transcriptionMuskelin, a novel intracellular mediator of cell adhesive and cytoskeletal responses to thrombospondin-1Cytokinesis in prokaryotes and eukaryotes: common principles and different solutionsMolecular phylogeny of the kelch-repeat superfamily reveals an expansion of BTB/kelch proteins in animalsRga6 is a Fission Yeast Rho GAP Involved in Cdc42 Regulation of Polarized Growth.Regulation of fission yeast morphogenesis by PP2A activator pta2The Vip1 inositol polyphosphate kinase family regulates polarized growth and modulates the microtubule cytoskeleton in fungiA unique Kelch domain phosphatase in Plasmodium regulates ookinete morphology, motility and invasionPKA antagonizes CLASP-dependent microtubule stabilization to re-localize Pom1 and buffer cell size upon glucose limitationWall mechanics and exocytosis define the shape of growth domains in fission yeastA polarised population of dynamic microtubules mediates homeostatic length control in animal cellsCytokinesis-based constraints on polarized cell growth in fission yeastThe kinetochore protein Kis1/Eic1/Mis19 ensures the integrity of mitotic spindles through maintenance of kinetochore factors Mis6/CENP-I and CENP-ADynamics of cell shape inheritance in fission yeastYeast Cdk1 translocates to the plus end of cytoplasmic microtubules to regulate bud cortex interactions.Spatial segregation of polarity factors into distinct cortical clusters is required for cell polarity controlA protein interaction map for cell polarity development.Identification of Kel1p, a kelch domain-containing protein involved in cell fusion and morphology in Saccharomyces cerevisiaeSaccharomyces cerevisiae Kelch proteins and Bud14 protein form a stable 520-kDa formin regulatory complex that controls actin cable assembly and cell morphogenesisA role for cell polarity proteins in mitotic exit.Fusion of a fission yeastContribution of actin filaments and microtubules to cell elongation and alignment depends on the grating depth of microgratingsThe cell end marker Tea4 regulates morphogenesis and pathogenicity in the basidiomycete fungus Ustilago maydis.The cell end marker protein TeaC is involved in growth directionality and septation in Aspergillus nidulansFission yeast Pob1p, which is homologous to budding yeast Boi proteins and exhibits subcellular localization close to actin patches, is essential for cell elongation and separation.Multistep and multimode cortical anchoring of tea1p at cell tips in fission yeast.Noncore components of the fission yeast gamma-tubulin complex.Regulation of cell diameter, For3p localization, and cell symmetry by fission yeast Rho-GAP Rga4pApical sterol-rich membranes are essential for localizing cell end markers that determine growth directionality in the filamentous fungus Aspergillus nidulans.Force- and kinesin-8-dependent effects in the spatial regulation of fission yeast microtubule dynamicsReorganization of the growth pattern of Schizosaccharomyces pombe in invasive filament formation.Physical mechanisms redirecting cell polarity and cell shape in fission yeast.Characterization of Mug33 reveals complementary roles for actin cable-dependent transport and exocyst regulators in fission yeast exocytosisOscillatory dynamics of Cdc42 GTPase in the control of polarized growth.Casein kinase 1γ ensures monopolar growth polarity under incomplete DNA replication downstream of Cds1 and calcineurin in fission yeast.The roles of fission yeast ase1 in mitotic cell division, meiotic nuclear oscillation, and cytokinesis checkpoint signalingDynein supports motility of endoplasmic reticulum in the fungus Ustilago maydisIdentification of Nd1, a novel murine kelch family protein, involved in stabilization of actin filaments.Improved tools for efficient mapping of fission yeast genes: identification of microtubule nucleation modifier mod22-1 as an allele of chromatin- remodelling factor gene swr1A systematic screen for morphological abnormalities during fission yeast sexual reproduction identifies a mechanism of actin aster formation for cell fusion.
P2860
Q21563355-EF9419AD-EF60-417F-936A-CD7465A80868Q24533305-DDA4E586-0D0F-4DFB-BFCD-3BFE3734CE53Q24548470-477DCF72-B29C-410D-89A9-9A2623C3E716Q24804994-85C195F9-9FAC-4743-90D7-A7316F290E0EQ27304852-D72765B2-AD86-442E-8F8B-984EE571757DQ27307800-E61E0F00-28E9-4FD6-8E99-16B8230D6BABQ27313776-3CE1BB5C-B1A8-470A-AE65-0E29AF6DD94CQ27319927-F44E5C63-E713-4F74-9CCA-A9DA5ED9F2E3Q27322471-4B722DE4-4F0D-44C8-B9CB-B63475ECCD04Q27322497-74D6EBF0-EF44-484D-BCDF-51187A29631BQ27322844-B8E307CA-66D9-4D17-906A-CCBF22D86B89Q27330538-04F1845A-A77B-411D-BF07-83ECEBB44F73Q27331943-A36B9221-54D0-4326-A111-57C9E252EF11Q27348941-FED28F51-FD2A-464F-B76E-337A4C4E5D7FQ27932858-05C76FBD-E154-4CA7-8709-2A405AA1D399Q27933969-51C895D2-86C6-4F92-85B3-EDFE06179C39Q27934870-FD81F833-A956-45F1-95DC-FE1172E3401EQ27935230-0FD69818-A7AE-439E-94E5-4D131E340731Q27935950-CE41976F-9F7F-4AD8-A13B-E5C0D72E42D7Q27936619-34A34199-D433-42E8-991E-3C21F999A410Q28293542-C2D483DC-FB72-4B62-983C-C1B2A6CCE2FFQ28833776-C8B0D312-DA90-4B83-9595-FC2F70795FD8Q30009450-C88B05B5-9CF3-4A7B-AA28-9B17D2320730Q30157259-A0FBA7F2-7C69-45B6-B989-C6BA53FDDD6AQ30175385-7279033A-5293-428B-8F48-EEFEB89CA872Q30476340-7CA0206A-8E52-4161-9019-6C4A13F3D1BCQ30478405-EEA20ED9-AB00-43B8-85E4-789BE80C3279Q30479491-47E133C4-E5A8-4608-83FA-8EE5C6042182Q30480990-74000E45-2D7F-4FE3-9BD8-9FB5F55D1840Q30487153-812EBA82-D3CB-433B-B30D-E90B1204C961Q30497316-B4DD32AD-4B72-40DB-B528-479C6D00353DQ30497591-8B9254EA-A477-4CE6-B352-812AC77F9FE8Q30501053-552B9FD4-CC70-4678-83E2-7B02CDBBE45BQ30540610-170DFEA5-2B6D-41C3-BE16-863CBCD7CA83Q30636315-C59D2043-EF57-4C7E-B2CA-0D0ABF66AFADQ30856513-4FD2DF64-8ACD-49CF-B45A-8457DCF11890Q30857136-7B7FEF32-DCCA-4631-92D2-EFD6E15077D4Q31108300-27700230-2C57-4679-9E95-EC29872AB468Q33401806-3BBE07BF-D31F-4F67-90EC-091FA42AFDE4Q33615825-F0C256D3-5D5A-4E09-80D0-6269B65D9247
P2860
tea1 and the microtubular cytoskeleton are important for generating global spatial order within the fission yeast cell.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
tea1 and the microtubular cyto ...... within the fission yeast cell.
@en
tea1 and the microtubular cyto ...... within the fission yeast cell.
@nl
type
label
tea1 and the microtubular cyto ...... within the fission yeast cell.
@en
tea1 and the microtubular cyto ...... within the fission yeast cell.
@nl
prefLabel
tea1 and the microtubular cyto ...... within the fission yeast cell.
@en
tea1 and the microtubular cyto ...... within the fission yeast cell.
@nl
P1433
P1476
tea1 and the microtubular cyto ...... within the fission yeast cell.
@en
P2093
P304
P356
10.1016/S0092-8674(00)80279-2
P407
P50
P577
1997-06-01T00:00:00Z