| scholarly article | Q13442814 |
| P50 | author | Dorota Wloga | Q58067989 |
| Jessica M Bryant | Q60721023 | ||
| P2093 | author name string | Neeraj Sharma | |
| Richard C Davis | |||
| Jacek Gaertig | |||
| Maria Jerka-Dziadosz | |||
| Rachel Donaldson | |||
| P2860 | cites work | Macronuclear genome sequence of the ciliate Tetrahymena thermophila, a model eukaryote | Q21146044 |
| Posttranslational glutamylation of alpha-tubulin | Q21994411 | ||
| Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing | Q24300949 | ||
| Tubulin polyglutamylase enzymes are members of the TTL domain protein family | Q24301967 | ||
| Monoclonal antibody ID5: epitope characterization and minimal requirements for the recognition of polyglutamylated alpha- and beta-tubulin. | Q48260321 | ||
| A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. | Q48371686 | ||
| A katanin-like protein regulates normal cell wall biosynthesis and cell elongation | Q48372257 | ||
| Katanin disrupts the microtubule lattice and increases polymer number in C. elegans meiosis. | Q51781699 | ||
| An alternating least squares approach to inferring phylogenies from pairwise distances. | Q52271424 | ||
| Monoclonal and polyclonal antibodies detect a new type of post-translational modification of axonemal tubulin | Q56903660 | ||
| Development of the ciliature of Tetrahymena thermophila. II. Spatial subdivision prior to cytokinesis | Q70941991 | ||
| Comparative immunogold analysis of tubulin isoforms in the mouse sperm flagellum: unique distribution of glutamylated tubulin | Q71678841 | ||
| Identification of elongation factor-1alpha as a Ca2+/calmodulin-binding protein in Tetrahymena cilia | Q73210414 | ||
| Polyglycylation domain of beta-tubulin maintains axonemal architecture and affects cytokinesis in Tetrahymena | Q77680794 | ||
| Microtubules cut and run | Q81124830 | ||
| Katanin is responsible for the M-phase microtubule-severing activity in Xenopus eggs | Q24648291 | ||
| Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function | Q24798261 | ||
| Microtubule acetylation promotes kinesin-1 binding and transport. | Q27919704 | ||
| Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia | Q28141185 | ||
| Differential binding regulation of microtubule-associated proteins MAP1A, MAP1B, and MAP2 by tubulin polyglutamylation | Q28208458 | ||
| Polyglycylation of tubulin: a posttranslational modification in axonemal microtubules | Q28242746 | ||
| Identification of katanin, an ATPase that severs and disassembles stable microtubules | Q28255544 | ||
| Tubulin tyrosination is a major factor affecting the recruitment of CAP-Gly proteins at microtubule plus ends. | Q28585847 | ||
| SEAVIEW and PHYLO_WIN: two graphic tools for sequence alignment and molecular phylogeny | Q29547654 | ||
| Oligomeric tubulin in large transporting complex is transported via kinesin in squid giant axons | Q31817842 | ||
| BOTERO1 is required for normal orientation of cortical microtubules and anisotropic cell expansion in Arabidopsis. | Q33335335 | ||
| Germline and somatic transformation of mating Tetrahymena thermophila by particle bombardment | Q33969895 | ||
| A robust inducible-repressible promoter greatly facilitates gene knockouts, conditional expression, and overexpression of homologous and heterologous genes in Tetrahymena thermophila | Q34019993 | ||
| Polarities of the centriolar structure: morphogenetic consequences | Q34289554 | ||
| Cellular deflagellation | Q34307853 | ||
| Members of the NIMA-related kinase family promote disassembly of cilia by multiple mechanisms | Q34661650 | ||
| The Caenorhabditis elegans microtubule-severing complex MEI-1/MEI-2 katanin interacts differently with two superficially redundant beta-tubulin isotypes | Q34785872 | ||
| MEI-1/MEI-2 katanin-like microtubule severing activity is required for Caenorhabditis elegans meiosis | Q35192719 | ||
| Intraflagellar Transport | Q35564826 | ||
| Three microtubule severing enzymes contribute to the "Pacman-flux" machinery that moves chromosomes | Q36118138 | ||
| Katanin controls mitotic and meiotic spindle length | Q36119429 | ||
| The morphogenesis of basal bodies and accessory structures of the cortex of the ciliated protozoan Tetrahymena pyriformis | Q36190466 | ||
| Microtubules containing acetylated alpha-tubulin in mammalian cells in culture | Q36215921 | ||
| Polyglycylation of tubulin is essential and affects cell motility and division in Tetrahymena thermophila | Q36327545 | ||
| A role for katanin-mediated axonemal severing during Chlamydomonas deflagellation | Q36872065 | ||
| Drugs affecting microtubule dynamics increase alpha-tubulin mRNA accumulation via transcription in Tetrahymena thermophila | Q36964541 | ||
| PF15p is the chlamydomonas homologue of the Katanin p80 subunit and is required for assembly of flagellar central microtubules | Q37226726 | ||
| Cell context-specific effects of the beta-tubulin glycylation domain on assembly and size of microtubular organelles | Q37497003 | ||
| Tau protects microtubules in the axon from severing by katanin. | Q40300939 | ||
| The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules | Q40436650 | ||
| Microtubule disassembly by ATP-dependent oligomerization of the AAA enzyme katanin | Q41697683 | ||
| Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastine | Q42068538 | ||
| Glutamylated tubulin: diversity of expression and distribution of isoforms. | Q42439193 | ||
| Structural inheritance in Paramecium: ultrastructural evidence for basal body and associated rootlets polarity transmission through binary fission⋆ | Q42441450 | ||
| Distribution of polyglutamylated tubulin in the flagellar apparatus of green flagellates | Q42495308 | ||
| Acetylation of lysine 40 in alpha-tubulin is not essential in Tetrahymena thermophila | Q42771369 | ||
| The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function. | Q47071071 | ||
| The A and B tubules of the outer doublets of sea urchin sperm axonemes are composed of different tubulin variants | Q48061028 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1065-1079 | |
| P577 | publication date | 2007-09-01 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Katanin regulates dynamics of microtubules and biogenesis of motile cilia | |
| P478 | volume | 178 |
| Q42479443 | A novel family of katanin-like 2 protein isoforms (KATNAL2), interacting with nucleotide-binding proteins Nubp1 and Nubp2, are key regulators of different MT-based processes in mammalian cells. |
| Q38151297 | Accumulation and post-translational modifications of plant tubulins |
| Q41377311 | Acetylation of microtubules influences their sensitivity to severing by katanin in neurons and fibroblasts |
| Q27334017 | An essential role for katanin p80 and microtubule severing in male gamete production |
| Q37429836 | Asymmetrically localized proteins stabilize basal bodies against ciliary beating forces |
| Q64094557 | Basalin is an evolutionarily unconstrained protein revealed via a conserved role in flagellum basal plate function |
| Q37999809 | Cellulose factories: advancing bioenergy production from forest trees. |
| Q91993978 | Ciliary Proteins: Filling the Gaps. Recent Advances in Deciphering the Protein Composition of Motile Ciliary Complexes |
| Q37369325 | Ciliary tubulin and its post-translational modifications |
| Q59620272 | Cilium structure, assembly, and disassembly regulated by the cytoskeleton |
| Q34141803 | Cytokinesis in bloodstream stage Trypanosoma brucei requires a family of katanins and spastin |
| Q30490376 | DYF-1 Is required for assembly of the axoneme in Tetrahymena thermophila |
| Q30273865 | Doublecortin associates with microtubules preferentially in regions of the axon displaying actin-rich protrusive structures |
| Q37142126 | Drosophila IKK-related kinase Ik2 and Katanin p60-like 1 regulate dendrite pruning of sensory neuron during metamorphosis. |
| Q30502887 | Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migration |
| Q33703159 | Electron Tomography and Immuno-labeling of Tetrahymena thermophila Basal Bodies |
| Q35795603 | Emergent Properties of the Metaphase Spindle |
| Q37216969 | Fidgetin-like 1 is a ciliogenesis-inhibitory centrosome protein |
| Q41879201 | Flagellar central pair assembly in Chlamydomonas reinhardtii. |
| Q28116771 | Graded Control of Microtubule Severing by Tubulin Glutamylation |
| Q27331566 | High-throughput generation of tagged stable cell lines for proteomic analysis |
| Q33585924 | Hyperglutamylation of tubulin can either stabilize or destabilize microtubules in the same cell |
| Q50630885 | KATNB1 in the human testis and its genetic variants in fertile and oligoasthenoteratozoospermic infertile men. |
| Q27336381 | KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome |
| Q47600921 | KTN80 confers precision to microtubule severing by specific targeting of katanin complexes in plant cells |
| Q36426507 | Katanin Severing and Binding Microtubules Are Inhibited by Tubulin Carboxy Tails |
| Q93892953 | Katanin cuts some, spares others |
| Q37035129 | Katanin knockdown supports a role for microtubule severing in release of basal bodies before mitosis in Chlamydomonas. |
| Q27320598 | Katanin localization requires triplet microtubules in Chlamydomonas reinhardtii |
| Q37669220 | Katanin maintains meiotic metaphase chromosome alignment and spindle structure in vivo and has multiple effects on microtubules in vitro |
| Q47983792 | Katanin spiral and ring structures shed light on power stroke for microtubule severing |
| Q57462392 | Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos |
| Q30619248 | Kinesin-13 regulates the quantity and quality of tubulin inside cilia. |
| Q52599946 | Manipulating ciliary protein-encoding genes in Tetrahymena thermophila. |
| Q36554502 | Microtubule modifications and stability are altered by cilia perturbation and in cystic kidney disease |
| Q40166605 | Microtubule severing by katanin p60 AAA+ ATPase requires the C-terminal acidic tails of both α- and β-tubulins and basic amino acid residues in the AAA+ ring pore |
| Q33653810 | Microtubule-severing enzymes |
| Q26991651 | Microtubule-severing enzymes at the cutting edge |
| Q58104016 | Microtubule-severing enzymes: From cellular functions to molecular mechanism |
| Q36962006 | Models, Regulations, and Functions of Microtubule Severing by Katanin |
| Q24337446 | Multivalent Microtubule Recognition by Tubulin Tyrosine Ligase-like Family Glutamylases |
| Q37257945 | Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors |
| Q41993395 | N-terminal phosphorylation of p60 katanin directly regulates microtubule severing |
| Q46943230 | Overexpression of OsKTN80a, a katanin P80 ortholog, caused the repressed cell elongation and stalled cell division mediated by microtubule apparatus defects in primary root in Oryza sativa |
| Q36450993 | PF19 encodes the p60 catalytic subunit of katanin and is required for assembly of the flagellar central apparatus in Chlamydomonas |
| Q34182922 | Post-translational modifications of microtubules |
| Q34232911 | Post-translational regulation of the microtubule cytoskeleton: mechanisms and functions |
| Q39047528 | Posttranslational Modifications of Tubulin and Cilia |
| Q47228439 | Primary cilia proteins: ciliary and extraciliary sites and functions. |
| Q91957956 | Primary cilium loss in mammalian cells occurs predominantly by whole-cilium shedding |
| Q30397832 | Proteolysis-Dependent Remodeling of the Tubulin Homolog FtsZ at the Division Septum in Escherichia coli |
| Q34504269 | Quantitative analysis and modeling of katanin function in flagellar length control. |
| Q39303596 | Regulation of katanin activity in the ciliate Tetrahymena thermophila. |
| Q41408903 | Regulation of tubulin glutamylation plays cell-specific roles in the function and stability of sensory cilia |
| Q36846180 | Septins stabilize mitochondria in Tetrahymena thermophila. |
| Q60116381 | Severing enzymes amplify microtubule arrays through lattice GTP-tubulin incorporation. |
| Q34675241 | Soluble levels of cytosolic tubulin regulate ciliary length control |
| Q54920032 | Spatiotemporal manipulation of ciliary glutamylation reveals its roles in intraciliary trafficking and Hedgehog signaling. |
| Q88645890 | Structural basis for disassembly of katanin heterododecamers |
| Q46019045 | TTLL10 can perform tubulin glycylation when co-expressed with TTLL8. |
| Q93006545 | The LisH Domain-Containing N-Terminal Fragment is Important for the Localization, Dimerization, and Stability of Katnal2 in Tetrahymena |
| Q24633494 | The chemical complexity of cellular microtubules: tubulin post-translational modification enzymes and their roles in tuning microtubule functions |
| Q38111287 | The ciliary cytoskeleton |
| Q34679993 | The nphp-2 and arl-13 genetic modules interact to regulate ciliogenesis and ciliary microtubule patterning in C. elegans |
| Q37117060 | The role of protein phosphatase 4 in regulating microtubule severing in the Caenorhabditis elegans embryo |
| Q34888218 | The spindle assembly function of Caenorhabditis elegans katanin does not require microtubule-severing activity |
| Q36508546 | Tubulin modifications and their cellular functions. |
| Q28504801 | Tubulin polyglutamylation stimulates spastin-mediated microtubule severing |
| Q104482079 | Tubulin post-translational modifications control neuronal development and functions |
| Q91871690 | Who Needs a Contractile Actomyosin Ring? The Plethora of Alternative Ways to Divide a Protozoan Parasite |
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