Oscillatory nuclear movement in fission yeast meiotic prophase is driven by astral microtubules, as revealed by continuous observation of chromosomes and microtubules in living cells.
about
A quality control mechanism linking meiotic success to release of ascosporesInvolvement of rhp23, a Schizosaccharomyces pombe homolog of the human HHR23A and Saccharomyces cerevisiae RAD23 nucleotide excision repair genes, in cell cycle control and protein ubiquitinationCytokinesis in prokaryotes and eukaryotes: common principles and different solutionsDancing genomes: fungal nuclear positioningRibonuclease activity of Dis3 is required for mitotic progression and provides a possible link between heterochromatin and kinetochore functionThe dissection of meiotic chromosome movement in mice using an in vivo electroporation techniqueNuclear motility in glioma cells reveals a cell-line dependent role of various cytoskeletal componentsMechanism and regulation of rapid telomere prophase movements in mouse meiotic chromosomesMeiotic chromosome mobility in fission yeast is resistant to environmental stress.Self-organization of dynein motors generates meiotic nuclear oscillationsBqt2p is essential for initiating telomere clustering upon pheromone sensing in fission yeastDynamic positioning of the fission yeast cell division plane.A mutation in gamma-tubulin alters microtubule dynamics and organization and is synthetically lethal with the kinesin-like protein pkl1p.Noncore components of the fission yeast gamma-tubulin complex.Meiotic cohesins modulate chromosome compaction during meiotic prophase in fission yeast.Live observation of forespore membrane formation in fission yeastDynamic chromosome movements during meiosis: a way to eliminate unwanted connections?Live imaging of rapid chromosome movements in meiotic prophase I in maize.Physical mechanisms redirecting cell polarity and cell shape in fission yeast.Dynamic instability-driven centering/segregating mechanism in bacteriaInterdependency of fission yeast Alp14/TOG and coiled coil protein Alp7 in microtubule localization and bipolar spindle formation.Telomeres and centromeres have interchangeable roles in promoting meiotic spindle formation.The roles of fission yeast ase1 in mitotic cell division, meiotic nuclear oscillation, and cytokinesis checkpoint signalingMeasuring tubulin content in Toxoplasma gondii: a comparison of laser-scanning confocal and wide-field fluorescence microscopy.Mechanistic study of the photodynamic inactivation of Candida albicans by a cationic porphyrin.The fission yeast DNA structure checkpoint protein Rad26ATRIP/LCD1/UVSD accumulates in the cytoplasm following microtubule destabilizationVesicle-like biomechanics governs important aspects of nuclear geometry in fission yeast.The A78V mutation in the Mad3-like domain of Schizosaccharomyces pombe Bub1p perturbs nuclear accumulation and kinetochore targeting of Bub1p, Bub3p, and Mad3p and spindle assembly checkpoint functionInterorganelle interactions and inheritance patterns of nuclei and vacuoles in budding yeast meiosis.Cytoskeletal forces span the nuclear envelope to coordinate meiotic chromosome pairing and synapsis.Dissociation of the Nuf2-Ndc80 complex releases centromeres from the spindle-pole body during meiotic prophase in fission yeastEffects of {gamma}-tubulin complex proteins on microtubule nucleation and catastrophe in fission yeast.pkl1(+)and klp2(+): Two kinesins of the Kar3 subfamily in fission yeast perform different functions in both mitosis and meiosis.Two related kinesins, klp5+ and klp6+, foster microtubule disassembly and are required for meiosis in fission yeastThe meiotic checkpoint network: step-by-step through meiotic prophaseNuclear envelope attachment is not necessary for telomere function in fission yeastA single internal telomere tract ensures meiotic spindle formation.Fission yeast mutants affecting telomere clustering and meiosis-specific spindle pole body integrity.The meiotic bouquet promotes homolog interactions and restricts ectopic recombination in Schizosaccharomyces pombeMeiotic nuclear movements in fission yeast are regulated by the transcription factor Mei4 downstream of a Cds1-dependent replication checkpoint pathway
P2860
Q21090670-05E6706C-22BB-43FA-B0E2-0FAED9D1B596Q24548330-C0C36DAD-6A64-4BCB-AF85-3301F64B2ADAQ24548470-8658B75C-15B8-4F57-896F-7965155ACD32Q24657360-DB202DC4-26AC-4EC4-9BDA-371526C75F0EQ27303046-EE06CAC9-9D85-4887-B5FD-799F972AB08BQ27311658-428B9ACC-8FD8-4F2F-A12A-BA20CF2ADBC6Q27312089-F18D48FF-D7FA-41C0-9073-4F1F70F8696EQ27320760-E3A4BDBB-FA8A-45BD-9E41-B133F78C94FBQ27322714-4DF3BB87-FFEB-4A05-BA19-A33024456EBAQ27330851-C26192CB-F75F-4BA9-9DF3-D373902DF31FQ28756760-9B573FD2-8156-44AF-99C4-FC9841A3C7CEQ30475922-2EFE6730-8168-473C-A9FC-7CCAA17D403DQ30477485-4465F87A-544B-4619-8840-203939E98607Q30478405-D1CD37B3-5220-41C3-AA59-DD32C0901A76Q30480457-D9460F59-036B-4B27-829A-5D1791B82033Q30482879-F66279F9-643E-4A8F-BDAF-91AB2075358CQ30492148-5D316C52-92B9-4764-A372-07F728981B86Q30492271-DD1EDF6F-3596-44E8-A4EE-07BBBE621C84Q30497591-FC079348-A5BC-4ED4-9AFF-712EAC56EE8FQ30502251-C31A54C5-5BFF-4EAD-AF76-216EFAAF13DEQ30549682-B8CF57C6-38DF-4F0F-9F9D-FF6EEFD9C409Q30620665-774A76D9-A699-4F07-AF95-207B0E1CDA55Q30856513-395B7E91-BA5F-47C6-896C-A9396F1A6D05Q31037649-469273D7-1272-43C3-824E-4EFC9772B7A1Q31163998-F7F8D166-D1FF-40CB-A6F1-03B384D98A63Q33255128-7C24F90A-35DC-41C1-B90E-4EEF4EA8AA66Q33300359-3B73D306-F8C1-4D37-81B7-711937D4677CQ33565078-44FA80F8-3F32-4117-A1DD-814F58196AF9Q33577545-A21584E7-F07E-49FD-8D7C-5830B502D1BDQ33674350-70160382-1FAB-44ED-A420-1BD26E51E401Q33768498-533DA067-05EF-432F-A146-5189E783AF77Q33841383-4DD27E0F-3409-4090-A723-87EDBD860016Q33948516-9248E5A5-4834-48F6-BFBF-45CF7A085662Q33948791-C5C37807-261D-434A-BFD1-891C20ECCCDAQ34248122-BAC78BB1-C2A8-4F2B-BB41-8D78C028ADCAQ34521568-F618FCF1-5DC1-47E5-8379-BC6FE74F9E31Q34538394-7D1F8980-2460-4CC8-B8E3-6E0699813964Q34614492-ECF1F610-9B03-4CFE-98A9-179A68E8B5DCQ35038773-6FFF842B-FFD0-4200-BB49-9054C6F38C54Q35177578-5F7EFC22-9E27-4249-A99D-A7D9097B1486
P2860
Oscillatory nuclear movement in fission yeast meiotic prophase is driven by astral microtubules, as revealed by continuous observation of chromosomes and microtubules in living cells.
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Oscillatory nuclear movement i ...... microtubules in living cells.
@ast
Oscillatory nuclear movement i ...... microtubules in living cells.
@en
type
label
Oscillatory nuclear movement i ...... microtubules in living cells.
@ast
Oscillatory nuclear movement i ...... microtubules in living cells.
@en
prefLabel
Oscillatory nuclear movement i ...... microtubules in living cells.
@ast
Oscillatory nuclear movement i ...... microtubules in living cells.
@en
P2093
P1476
Oscillatory nuclear movement i ...... microtubules in living cells.
@en
P2093
Chikashige Y
Haraguchi T
P304
P407
P478
111 ( Pt 6)
P577
1998-03-01T00:00:00Z