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H + - and Na + -elicited swift changes of the microtubule system in the biflagellated green alga Chlamydomonas

https://doi.org/10.1101/121137
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inferredcites →https://doi.org/10.1002/(sici)1097-0169(1997)36:2<125::aid-cm3>3.0.co;2-8openalex-snapshot
How calcium causes microtubule depolymerization
inferredcites →https://doi.org/10.1002/(sici)1097-0169(199910)44:2<143::aid-cm6>3.0.co;2-3openalex-snapshot
An insertional mutant ofChlamydomonas reinhardtii with defective microtubule positioning
inferredcites →https://doi.org/10.1002/cm.10071openalex-snapshot
Reactivation of Ca2+‐dependent cytoplasmic contraction in permeabilized cell models of the heliozoon Echinosphaerium akamae
inferredcites →https://doi.org/10.1002/pro.5560051008openalex-snapshot
Cation selective promotion of tubulin polymerization by alkali metal chlorides
inferredcites →https://doi.org/10.1007/978-94-007-7500-8_2openalex-snapshot
Sodium and Potassium in Health and Disease
inferredcites →https://doi.org/10.1007/bf01210517openalex-snapshot
Fluorescence emission spectra of plant leaves and plant constituents
inferredcites →https://doi.org/10.1016/c2009-0-02778-0openalex-snapshot
The Chlamydomonas Sourcebook
inferredcites →https://doi.org/10.1016/j.biortech.2014.10.120openalex-snapshot
The selective breeding of the freshwater microalga Chlamydomonas reinhardtii for growth in salinity
inferredcites →https://doi.org/10.1016/j.bpj.2014.10.052openalex-snapshot
The Microtubule-Based Cytoskeleton Is a Component of a Mechanical Signaling Pathway in Fly Campaniform Receptors
inferredcites →https://doi.org/10.1016/j.ceb.2012.09.006openalex-snapshot
Microtubule catastrophe and rescue
inferredcites →https://doi.org/10.1016/j.cell.2012.02.049openalex-snapshot
EBs Recognize a Nucleotide-Dependent Structural Cap at Growing Microtubule Ends
inferredcites →https://doi.org/10.1016/j.cub.2003.10.058openalex-snapshot
The Microtubule Plus End-Tracking Protein EB1 Is Localized to the Flagellar Tip and Basal Bodies in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1016/j.cub.2013.08.006openalex-snapshot
An Atypical Tubulin Kinase Mediates Stress-Induced Microtubule Depolymerization in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2013.12.042openalex-snapshot
EB1 Accelerates Two Conformational Transitions Important for Microtubule Maturation and Dynamics
inferredcites →https://doi.org/10.1016/j.jsb.2011.07.009openalex-snapshot
plusTipTracker: Quantitative image analysis software for the measurement of microtubule dynamics
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.023openalex-snapshot
Unique Interweaved Microtubule Scaffold Mediates Osmosensory Transduction via Physical Interaction with TRPV1
inferredcites →https://doi.org/10.1016/j.tcb.2012.05.005openalex-snapshot
+TIPs: SxIPping along microtubule ends
inferredcites →https://doi.org/10.1016/j.tcb.2014.10.004openalex-snapshot
Post-translational modifications of tubulin: pathways to functional diversity of microtubules
inferredcites →https://doi.org/10.1016/j.tplants.2012.06.009openalex-snapshot
Proton channels in algae: reasons to be excited
inferredcites →https://doi.org/10.1016/s0021-9258(19)62723-7openalex-snapshot
Localization of the high affinity calcium-binding site on tubulin molecule.
inferredcites →https://doi.org/10.1016/s0021-9258(19)70212-9openalex-snapshot
Calcium ion induces endwise depolymerization of bovine brain microtubules.
inferredcites →https://doi.org/10.1016/s0074-7696(08)61724-6openalex-snapshot
Cell Motility and Ionic Relations in Characean Cells as Revealed by Internal Perfusion and Cell Models
inferredcites →https://doi.org/10.1016/s0171-9335(99)80099-5openalex-snapshot
Direct measurement of cytosolic calcium and pH in living Chlamydomonas reinhardtii cells
inferredcites →https://doi.org/10.1021/bi00622a003openalex-snapshot
Binding sites for calcium on tubulin
inferredcites →https://doi.org/10.1021/bi00684a032openalex-snapshot
Ionic and nucleotide requirements for microtubule polymerization in vitro
inferredcites →https://doi.org/10.1038/277142a0openalex-snapshot
Are cardiac muscle cells ‘skinned’ by EGTA or EDTA?
inferredcites →https://doi.org/10.1038/312237a0openalex-snapshot
Dynamic instability of microtubule growth
inferredcites →https://doi.org/10.1038/314443a0openalex-snapshot
Carbon-dioxide-induced exocytotic insertion of H+ pumps in turtle-bladder luminal membrane: role of cell pH and calcium
inferredcites →https://doi.org/10.1038/emboj.2013.76openalex-snapshot
MAP1B regulates microtubule dynamics by sequestering EB1/3 in the cytosol of developing neuronal cells
inferredcites →https://doi.org/10.1038/nature04736openalex-snapshot
The depolymerizing kinesin MCAK uses lattice diffusion to rapidly target microtubule ends
inferredcites →https://doi.org/10.1038/ncb1609openalex-snapshot
Tension applied through the Dam1 complex promotes microtubule elongation providing a direct mechanism for length control in mitosis
inferredcites →https://doi.org/10.1038/ncb1703openalex-snapshot
EB1 regulates microtubule dynamics and tubulin sheet closure in vitro
inferredcites →https://doi.org/10.1038/ncb2214openalex-snapshot
Mechanoreception in motile flagella of Chlamydomonas
inferredcites →https://doi.org/10.1038/nmeth.1493openalex-snapshot
Analysis of microtubule dynamic instability using a plus-end growth marker
inferredcites →https://doi.org/10.1038/nmeth.2413openalex-snapshot
A bright monomeric green fluorescent protein derived from Branchiostoma lanceolatum
inferredcites →https://doi.org/10.1038/srep21076openalex-snapshot
Biomineral shell formation under ocean acidification: a shift from order to chaos
inferredcites →https://doi.org/10.1038/srep38228openalex-snapshot
MicroRNAs modulate adaption to multiple abiotic stresses in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1073/pnas.0308205100openalex-snapshot
Centrosome maturation: Measurement of microtubule nucleation throughout the cell cycle by using GFP-tagged EB1
inferredcites →https://doi.org/10.1073/pnas.1936192100openalex-snapshot
Channelrhodopsin-2, a directly light-gated cation-selective membrane channel
inferredcites →https://doi.org/10.1073/pnas.95.7.3661openalex-snapshot
Structural changes at microtubule ends accompanying GTP hydrolysis: Information from a slowly hydrolyzable analogue of GTP, guanylyl (α,β)methylenediphosphonate
inferredcites →https://doi.org/10.1074/jbc.m807173200openalex-snapshot
A Cation-regulated and Proton Gradient-dependent Cation Transporter from Chlamydomonas reinhardtii Has a Role in Calcium and Sodium Homeostasis
inferredcites →https://doi.org/10.1083/jcb.113.3.605openalex-snapshot
The colR4 and colR15 beta-tubulin mutations in Chlamydomonas reinhardtii confer altered sensitivities to microtubule inhibitors and herbicides by enhancing microtubule stability.
inferredcites →https://doi.org/10.1083/jcb.118.3.561openalex-snapshot
Osmotic stress and the yeast cytoskeleton: phenotype-specific suppression of an actin mutation.
inferredcites →https://doi.org/10.1083/jcb.124.6.985openalex-snapshot
Intrinsic microtubule stability in interphase cells
inferredcites →https://doi.org/10.1083/jcb.200202032openalex-snapshot
Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle
inferredcites →https://doi.org/10.1083/jcb.201009131openalex-snapshot
Asymmetric properties of the Chlamydomonas reinhardtii cytoskeleton direct rhodopsin photoreceptor localization
inferredcites →https://doi.org/10.1083/jcb.78.1.8openalex-snapshot
Flagellar elongation and shortening in Chlamydomonas. IV. Effects of flagellar detachment, regeneration, and resorption on the induction of flagellar protein synthesis.
inferredcites →https://doi.org/10.1085/jgp.108.4.351openalex-snapshot
Ca2+ influx activated by low pH in Chlamydomonas.
inferredcites →https://doi.org/10.1085/jgp.201411295openalex-snapshot
The ongoing search for the molecular basis of plant osmosensing
inferredcites →https://doi.org/10.1091/mbc.02-04-0210openalex-snapshot
EB1-Microtubule Interactions in Xenopus Egg Extracts: Role of EB1 in Microtubule Stabilization and Mechanisms of Targeting to Microtubules
inferredcites →https://doi.org/10.1091/mbc.e05-08-0810openalex-snapshot
A Complex of Two Centrosomal Proteins, CAP350 and FOP, Cooperates with EB1 in Microtubule Anchoring
inferredcites →https://doi.org/10.1091/mbc.e11-01-0017openalex-snapshot
Insights into EB1 structure and the role of its C-terminal domain for discriminating microtubule tips from the lattice
inferredcites →https://doi.org/10.1091/mbc.e14-04-0916openalex-snapshot
How Taxol/paclitaxel kills cancer cells
inferredcites →https://doi.org/10.1091/mbc.e15-08-0608openalex-snapshot
Single-particle imaging reveals intraflagellar transport–independent transport and accumulation of EB1 inChlamydomonasflagella
inferredcites →https://doi.org/10.1093/pcp/pcj090openalex-snapshot
Salt Stress Affects Cortical Microtubule Organization and Helical Growth in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcm123openalex-snapshot
Salt Tolerance Requires Cortical Microtubule Reorganization in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcp016openalex-snapshot
The Chlamydomonas Hatching Enzyme, Sporangin, is Expressed in Specific Phases of the Cell Cycle and is Localized to the Flagella of Daughter Cells Within the Sporangial Cell Wall
inferredcites →https://doi.org/10.1104/pp.108.4.1537openalex-snapshot
Potassium Fluxes in Chlamydomonas reinhardtii (II. Compartmental Analysis)
inferredcites →https://doi.org/10.1104/pp.15.01506openalex-snapshot
The Cytoskeleton and Its Regulation by Calcium and Protons
inferredcites →https://doi.org/10.1104/pp.82.2.594openalex-snapshot
Effect of Osmotic Stress on Carbon Metabolism in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1105/tpc.014977openalex-snapshot
Phospholipase D Activation Correlates with Microtubule Reorganization in Living Plant Cells[W]
inferredcites →https://doi.org/10.1105/tpc.104.026930openalex-snapshot
Encounters between Dynamic Cortical Microtubules Promote Ordering of the Cortical Array through Angle-Dependent Modifications of Microtubule Behavior[W]
inferredcites →https://doi.org/10.1105/tpc.111.089920openalex-snapshot
Salt Stress–Induced Disassembly of Arabidopsis Cortical Microtubule Arrays Involves 26S Proteasome–Dependent Degradation of SPIRAL1
inferredcites →https://doi.org/10.1105/tpc.112.104182openalex-snapshot
Phosphatidic Acid Regulates Microtubule Organization by Interacting with MAP65-1 in Response to Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1111/1462-2920.12372openalex-snapshot
Evolution of salt tolerance in a laboratory reared population of C hlamydomonas reinhardtii
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02222.xopenalex-snapshot
Molecular dissection of plant cytokinesis and phragmoplast structure: a survey of GFP‐tagged proteins
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03349.xopenalex-snapshot
Rapid spatiotemporal patterning of cytosolic Ca2+ underlies flagellar excision in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1111/j.1550-7408.1960.tb00715.xopenalex-snapshot
Sodium and Potassium in Normal and Paralyzed Chlamydomonas
inferredcites →https://doi.org/10.1111/j.1745-7270.2007.00350.xopenalex-snapshot
EDTA-induced Membrane Fluidization and Destabilization: Biophysical Studies on Artificial Lipid Membranes
inferredcites →https://doi.org/10.1111/tpj.12165openalex-snapshot
Expanding the spectral palette of fluorescent proteins for the green microalga C hlamydomonas reinhardtii
inferredcites →https://doi.org/10.1111/tpj.12171openalex-snapshot
Microtubules and biotic interactions
inferredcites →https://doi.org/10.1111/tpj.12189openalex-snapshot
The evolution and diversification of plant microtubule‐associated proteins
inferredcites →https://doi.org/10.1126/science.1072068openalex-snapshot
Channelrhodopsin-1: A Light-Gated Proton Channel in Green Algae
inferredcites →https://doi.org/10.1126/science.1126551openalex-snapshot
Visualization of Cellulose Synthase Demonstrates Functional Association with Microtubules
inferredcites →https://doi.org/10.1126/science.1143609openalex-snapshot
The Chlamydomonas Genome Reveals the Evolution of Key Animal and Plant Functions
inferredcites →https://doi.org/10.1126/science.1152509openalex-snapshot
Coral Reefs Under Rapid Climate Change and Ocean Acidification
inferredcites →https://doi.org/10.1126/science.177.4054.1104openalex-snapshot
Microtubule Formation in vitro in Solutions Containing Low Calcium Concentrations
inferredcites →https://doi.org/10.1126/science.263.5152.1419openalex-snapshot
Cytosolic pH Gradients Associated with Tip Growth
inferredcites →https://doi.org/10.1134/s0006297911030047openalex-snapshot
Plant cortical microtubules are putative sensors under abiotic stresses
inferredcites →https://doi.org/10.1186/1742-4682-10-8openalex-snapshot
Is intracellular pH a clock for mitosis?
inferredcites →https://doi.org/10.1186/2046-2530-3-2openalex-snapshot
Reduction of meckelin leads to general loss of cilia, ciliary microtubule misalignment and distorted cell surface organization
inferredcites →https://doi.org/10.1199/tab.0179openalex-snapshot
Microtubules in Plants
inferredcites →https://doi.org/10.1242/jcs.03028openalex-snapshot
A kinesin-like calmodulin-binding protein inChlamydomonas: evidence for a role in cell division and flagellar functions
inferredcites →https://doi.org/10.1242/jcs.034488openalex-snapshot
Stress-regulated kinase pathways in the recovery of tip growth and microtubule dynamics following osmotic stress inS. pombe
inferredcites →https://doi.org/10.1242/jcs.062414openalex-snapshot
Microtubule +TIPs at a glance
inferredcites →https://doi.org/10.1242/jcs.124255openalex-snapshot
Flagellar regeneration requires cytoplasmic microtubule depolymerization and kinesin-13
inferredcites →https://doi.org/10.1242/jcs.129759openalex-snapshot
The microtubule end-binding protein EB2 is a central regulator of microtubule reorganisation in apico-basal epithelial differentiation
inferredcites →https://doi.org/10.1371/journal.pone.0007585openalex-snapshot
EB1 Recognizes the Nucleotide State of Tubulin in the Microtubule Lattice
inferredcites →https://doi.org/10.1371/journal.pone.0065694openalex-snapshot
Anti-Migratory Effect of Vinflunine in Endothelial and Glioblastoma Cells Is Associated with Changes in EB1 C-Terminal Detyrosinated/Tyrosinated Status
inferredcites →https://doi.org/10.1534/g3.116.034264openalex-snapshot
A Forward Genetic Screen and Whole Genome Sequencing Identify Deflagellation Defective Mutants inChlamydomonas, Including Assignment of ADF1 as a TRP Channel
inferredcites →https://doi.org/10.3233/jad-132315openalex-snapshot
Crosstalk between Axonal Classical Microtubule-Associated Proteins and End Binding Proteins during Axon Extension: Possible Implications in Neurodegeneration
inferredcites →https://doi.org/10.3389/fphys.2014.00043openalex-snapshot
Intracellular pH regulation by acid-base transporters in mammalian neurons
inferredcites →https://doi.org/10.3389/fpls.2015.00236openalex-snapshot
Cortical microtubule rearrangements and cell wall patterning
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