about
A conserved mechanism for Bni1- and mDia1-induced actin assembly and dual regulation of Bni1 by Bud6 and profilinGuanylic nucleotide starvation affects Saccharomyces cerevisiae mother-daughter separation and may be a signal for entry into quiescenceMutations in the yeast Myb-like protein Bas1p resulting in discrimination between promoters in vivo but notin vitro.Saccharomyces cerevisiae Kelch proteins and Bud14 protein form a stable 520-kDa formin regulatory complex that controls actin cable assembly and cell morphogenesisQuiescent Saccharomyces cerevisiae forms telomere hyperclusters at the nuclear membrane vicinity through a multifaceted mechanism involving Esc1, the Sir complex, and chromatin condensation.Yeast formins regulate cell polarity by controlling the assembly of actin cables.Reversible cytoplasmic localization of the proteasome in quiescent yeast cells.Crystal structures of a Formin Homology-2 domain reveal a tethered dimer architectureExperimental relocation of the mitochondrial ATP9 gene to the nucleus reveals forces underlying mitochondrial genome evolutionActin bodies in yeast quiescent cells: an immediately available actin reserve?Polarized growth in the absence of F-actin in Saccharomyces cerevisiae exiting quiescence.Metabolic status rather than cell cycle signals control quiescence entry and exitMechanism and cellular function of Bud6 as an actin nucleation-promoting factor.A stable microtubule array drives fission yeast polarity reestablishment upon quiescence exit.An array of nuclear microtubules reorganizes the budding yeast nucleus during quiescenceMitochondrial F1F0-ATP synthase and organellar internal architecture.Microtubules move the nucleus to quiescenceA pharmaco-epistasis strategy reveals a new cell size controlling pathway in yeast.Meeting report--Imaging the Cell.Mitochondrial ATP synthases cluster as discrete domains that reorganize with the cellular demand for oxidative phosphorylation.Identification of genes affecting selenite toxicity and resistance in Saccharomyces cerevisiae.Yeast Cells Lacking the Mitochondrial Gene Encoding the ATP Synthase Subunit 6 Exhibit a Selective Loss of Complex IV and Unusual Mitochondrial MorphologyMitochondria reorganization upon proliferation arrest predicts individual yeast cell fateDeterminants of S. cerevisiae dynein localization and activation: implications for the mechanism of spindle positioningImaging fluorescence resonance energy transfer between two green fluorescent proteins in living yeastThe cell biology of quiescent yeast - a diversity of individual scenariosQuiescence, an individual journey
P50
Q24624729-B77E9BB2-E179-4E22-90A9-211B373F5649Q24811368-BAD153E1-F9CC-4498-A1E0-955B8E013E6DQ27935587-41A6A3B9-3EFF-4F09-BD03-4731F40AC0F1Q27935950-311DEE1F-6A96-4404-A06D-E4232190E516Q27936606-E6FDFDFA-0F5C-48C1-93E6-EBF5E68881AAQ27937210-6A996FD7-64BE-40EA-9CAB-CC2BF7F79EC3Q27940379-B36D9D1A-4A3A-4E9A-9FCE-16713B78D32AQ28248937-D3E6974E-E5EC-4820-A744-934F9CD02B3CQ30420609-9528BB25-23A4-42FD-A1E7-64FCC6924A70Q30478254-6F8FBFBE-5EE9-439B-B32A-E2AD4D9DC618Q33348556-CD06A485-A97E-4433-BB69-67E5F5563A46Q34712474-45A16373-C381-4130-A7F8-CF2FC873492AQ35474950-B10FA110-AF00-49C7-A5A9-45EEDFA487F7Q35826040-06A24046-B0D1-4746-8881-FC8648D279B0Q37343895-4DDE506E-FA01-4813-B167-8260EF0D0E92Q37585727-2CF3526C-AF1F-4045-A595-A14BC3AAC16DQ38196677-ACB2D745-2A6D-4B23-8112-F4D2AD0208A0Q40092854-8EA113A9-3A44-4009-A18E-FDA54E769C9BQ47973465-7B524C11-C4C5-43AC-82E7-248FEBECAE4AQ50466536-0ADD9AD3-D36A-48E8-ADC7-A4045BA0DFC9Q54049032-8B6CB6C8-16E1-4484-850C-E614F81DBF61Q57246529-8EFCB982-9F11-40A8-BA97-77888EF04D15Q57288459-D0440EA9-4BB7-4FA8-AC5F-48E37F2BF8BAQ73086391-5EC6DD03-76CC-419C-9A4B-84D8BEA3408BQ77369949-6520E4C7-334F-4D09-B7C8-CF88D39A3EF4Q90853382-4C0E2F7C-3ACC-4B30-AD22-83EC7F24E039Q91072912-0EA1E59D-9814-4844-91F7-0D5CB102EFAD
P50
description
researcher
@en
wetenschapper
@nl
name
Isabelle Sagot
@en
Isabelle Sagot
@nl
type
label
Isabelle Sagot
@en
Isabelle Sagot
@nl
prefLabel
Isabelle Sagot
@en
Isabelle Sagot
@nl
P106
P31
P496
0000-0003-2158-1783