On the public citation graph
Microtubule Organization in Striated Muscle Cells
0 signed · 337 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbin.10016openalex-snapshot
Association of nucleus and centrosome: magnet or velcro?
inferredcites →https://doi.org/10.1002/cm.20042openalex-snapshot
Reorganization of microtubule nucleation during muscle differentiation
inferredcites →https://doi.org/10.1002/dneu.22751openalex-snapshot
Nucleating microtubules in neurons: Challenges and solutions
inferredcites →https://doi.org/10.1002/humu.21106openalex-snapshot
The genetic basis of long QT and short QT syndromes: A mutation update
inferredcites →https://doi.org/10.1002/jmor.1051790103openalex-snapshot
Perinuclear microtubules in postnatal rat heart
inferredcites →https://doi.org/10.1007/112_2013_12openalex-snapshot
The Cardiomyocyte Cell Cycle in Hypertrophy, Tissue Homeostasis, and Regeneration
inferredcites →https://doi.org/10.1007/978-3-030-23173-6_4openalex-snapshot
Role of Intracellular Transport in the Centriole-Dependent Formation of Golgi Ribbon
inferredcites →https://doi.org/10.1007/978-3-030-23173-6_5openalex-snapshot
RhoA Pathway and Actin Regulation of the Golgi/Centriole Complex
inferredcites →https://doi.org/10.1007/978-3-030-23173-6_7openalex-snapshot
Positioning of the Centrosome and Golgi Complex
inferredcites →https://doi.org/10.1007/bf02619489openalex-snapshot
Rat myocardial cells in vitro: Mitosis and differentiated properties
inferredcites →https://doi.org/10.1007/s00018-017-2570-5openalex-snapshot
Routes and machinery of primary cilium biogenesis
inferredcites →https://doi.org/10.1007/s00223-014-9915-yopenalex-snapshot
Skeletal Muscle: A Brief Review of Structure and Function
inferredcites →https://doi.org/10.1007/s00249-017-1244-4openalex-snapshot
Mitotic spindle: kinetochore fibers hold on tight to interpolar bundles
inferredcites →https://doi.org/10.1007/s00294-019-01033-2openalex-snapshot
Help or hindrance: how do microtubule-based forces contribute to genome damage and repair?
inferredcites →https://doi.org/10.1007/s10815-016-0652-1openalex-snapshot
The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertility
inferredcites →https://doi.org/10.1016/0092-8674(93)90721-2openalex-snapshot
Reversal of terminal differentiation and control of DNA replication: Cyclin A and cdk2 specifically localize at subnuclear sites of DNA replication
inferredcites →https://doi.org/10.1016/0378-1119(86)90333-1openalex-snapshot
Differential expression of several neurospecific β-tubulin mRNAs in the mouse brain during development
inferredcites →https://doi.org/10.1016/b978-0-12-405943-6.00001-4openalex-snapshot
Molecular and Cellular Regulation of Skeletal Myogenesis
inferredcites →https://doi.org/10.1016/bs.ircmb.2015.03.001openalex-snapshot
Nuclear Envelope and Chromatin, Lock and Key of Genome Integrity
inferredcites →https://doi.org/10.1016/j.ceb.2014.03.002openalex-snapshot
KASHing up with the nucleus: novel functional roles of KASH proteins at the cytoplasmic surface of the nucleus
inferredcites →https://doi.org/10.1016/j.ceb.2016.09.003openalex-snapshot
Microtubule-organizing centers: from the centrosome to non-centrosomal sites
inferredcites →https://doi.org/10.1016/j.ceb.2019.10.004openalex-snapshot
Generation and regulation of microtubule network asymmetry to drive cell polarity
inferredcites →https://doi.org/10.1016/j.cell.2007.06.025openalex-snapshot
Self-Organization of MTOCs Replaces Centrosome Function during Acentrosomal Spindle Assembly in Live Mouse Oocytes
inferredcites →https://doi.org/10.1016/j.cell.2012.01.007openalex-snapshot
Cortical Dynein Controls Microtubule Dynamics to Generate Pulling Forces that Position Microtubule Asters
inferredcites →https://doi.org/10.1016/j.cell.2012.12.044openalex-snapshot
Branching Microtubule Nucleation in Xenopus Egg Extracts Mediated by Augmin and TPX2
inferredcites →https://doi.org/10.1016/j.cell.2013.02.047openalex-snapshot
Phospholipase Cε Hydrolyzes Perinuclear Phosphatidylinositol 4-Phosphate to Regulate Cardiac Hypertrophy
inferredcites →https://doi.org/10.1016/j.cell.2014.03.032openalex-snapshot
The Oxygen-Rich Postnatal Environment Induces Cardiomyocyte Cell-Cycle Arrest through DNA Damage Response
inferredcites →https://doi.org/10.1016/j.cell.2014.03.053openalex-snapshot
High-Resolution Microtubule Structures Reveal the Structural Transitions in αβ-Tubulin upon GTP Hydrolysis
inferredcites →https://doi.org/10.1016/j.cell.2016.01.019openalex-snapshot
Graded Control of Microtubule Severing by Tubulin Glutamylation
inferredcites →https://doi.org/10.1016/j.cell.2016.07.025openalex-snapshot
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex
inferredcites →https://doi.org/10.1016/j.cell.2017.05.028openalex-snapshot
The Centrosome Is a Selective Condensate that Nucleates Microtubules by Concentrating Tubulin
inferredcites →https://doi.org/10.1016/j.celrep.2018.06.093openalex-snapshot
The HAUS Complex Is a Key Regulator of Non-centrosomal Microtubule Organization during Neuronal Development
inferredcites →https://doi.org/10.1016/j.celrep.2019.01.020openalex-snapshot
Structural and Molecular Basis for Katanin-Mediated Severing of Glutamylated Microtubules
inferredcites →https://doi.org/10.1016/j.cub.2007.12.055openalex-snapshot
The Mammalian SPD-2 Ortholog Cep192 Regulates Centrosome Biogenesis
inferredcites →https://doi.org/10.1016/j.cub.2012.02.044openalex-snapshot
A Role for the Centrosome and PAR-3 in the Hand-Off of MTOC Function during Epithelial Polarization
inferredcites →https://doi.org/10.1016/j.cub.2012.06.027openalex-snapshot
Nek9 Phosphorylation of NEDD1/GCP-WD Contributes to Plk1 Control of γ-Tubulin Recruitment to the Mitotic Centrosome
inferredcites →https://doi.org/10.1016/j.cub.2014.11.025openalex-snapshot
Microtubule Nucleation in Mitosis by a RanGTP-Dependent Protein Complex
inferredcites →https://doi.org/10.1016/j.cub.2015.06.001openalex-snapshot
SPD-2/CEP192 and CDK Are Limiting for Microtubule-Organizing Center Function at the Centrosome
inferredcites →https://doi.org/10.1016/j.cub.2017.05.090openalex-snapshot
A Splice Variant of Centrosomin Converts Mitochondria to Microtubule-Organizing Centers
inferredcites →https://doi.org/10.1016/j.cub.2017.08.031openalex-snapshot
Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells
inferredcites →https://doi.org/10.1016/j.devcel.2007.02.020openalex-snapshot
A Double-Assurance Mechanism Controls Cell Cycle Exit upon Terminal Differentiation in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2007.04.002openalex-snapshot
Asymmetric CLASP-Dependent Nucleation of Noncentrosomal Microtubules at the trans-Golgi Network
inferredcites →https://doi.org/10.1016/j.devcel.2010.03.015openalex-snapshot
A Developmentally Regulated Two-Step Process Generates a Noncentrosomal Microtubule Network in Drosophila Tracheal Cells
inferredcites →https://doi.org/10.1016/j.devcel.2014.02.013openalex-snapshot
The Centrosome-Specific Phosphorylation of Cnn by Polo/Plk1 Drives Cnn Scaffold Assembly and Centrosome Maturation
inferredcites →https://doi.org/10.1016/j.devcel.2016.08.009openalex-snapshot
Molecular Pathway of Microtubule Organization at the Golgi Apparatus
inferredcites →https://doi.org/10.1016/j.devcel.2018.08.014openalex-snapshot
Human β-Tubulin Isotypes Can Regulate Microtubule Protofilament Number and Stability
inferredcites →https://doi.org/10.1016/j.devcel.2018.10.026openalex-snapshot
Oxidative Stress in Cells with Extra Centrosomes Drives Non-Cell-Autonomous Invasion
inferredcites →https://doi.org/10.1016/j.devcel.2019.04.002openalex-snapshot
The Emerging Link between Centrosome Aberrations and Metastasis
inferredcites →https://doi.org/10.1016/j.gde.2020.01.003openalex-snapshot
Control of cell shape during epithelial morphogenesis: recent advances
inferredcites →https://doi.org/10.1016/j.jacbts.2016.02.002openalex-snapshot
Microtubule-Mediated Misregulation of Junctophilin-2 Underlies T-Tubule Disruptions and Calcium Mishandling in mdx Mice
inferredcites →https://doi.org/10.1016/j.molcel.2014.06.016openalex-snapshot
The Cep192-Organized Aurora A-Plk1 Cascade Is Essential for Centrosome Cycle and Bipolar Spindle Assembly
inferredcites →https://doi.org/10.1016/j.neuron.2012.10.008openalex-snapshot
Golgi Outposts Shape Dendrite Morphology by Functioning as Sites of Acentrosomal Microtubule Nucleation in Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2014.04.019openalex-snapshot
Microtubule Minus-End Binding Protein CAMSAP2 Controls Axon Specification and Dendrite Development
inferredcites →https://doi.org/10.1016/j.neuron.2015.05.046openalex-snapshot
Building the Neuronal Microtubule Cytoskeleton
inferredcites →https://doi.org/10.1016/j.semcdb.2017.11.005openalex-snapshot
Nuclear positioning in skeletal muscle
inferredcites →https://doi.org/10.1016/j.semcdb.2017.11.008openalex-snapshot
LINC complexes and nuclear positioning
inferredcites →https://doi.org/10.1016/j.tcb.2017.02.005openalex-snapshot
Moonlighting Motors: Kinesin, Dynein, and Cell Polarity
inferredcites →https://doi.org/10.1016/j.tcb.2018.08.004openalex-snapshot
Kinesin-5 Regulation and Function in Mitosis
inferredcites →https://doi.org/10.1016/j.tcb.2020.01.002openalex-snapshot
Getting into Position: Nuclear Movement in Muscle Cells
inferredcites →https://doi.org/10.1016/j.tibs.2020.02.002openalex-snapshot
Activation and Regulation of Cytoplasmic Dynein
inferredcites →https://doi.org/10.1016/j.tins.2018.07.006openalex-snapshot
Walking Forward with Kinesin
inferredcites →https://doi.org/10.1016/j.yjmcc.2019.07.005openalex-snapshot
Pseudo-bipolar spindle formation and cell division in postnatal binucleated cardiomyocytes
inferredcites →https://doi.org/10.1016/s0021-9258(18)90982-8openalex-snapshot
The kinetics of microtubule assembly. Evidence for a two-stage nucleation mechanism.
inferredcites →https://doi.org/10.1016/s0021-9258(19)40087-2openalex-snapshot
Increased microtubule assembly in bovine brain tubulin lacking the type III isotype of beta-tubulin.
inferredcites →https://doi.org/10.1016/s0021-9290(01)00201-9openalex-snapshot
Contribution of the nucleus to the mechanical properties of endothelial cells
inferredcites →https://doi.org/10.1016/s0022-2828(85)80087-0openalex-snapshot
Microtubules in the heart muscle of the postnatal and adult rat
inferredcites →https://doi.org/10.1016/s0022-2828(86)80981-6openalex-snapshot
Myocardial DNA content, ploidy level and cell number in geriatric hearts: Post-mortem examinations of human myocardium in old age
inferredcites →https://doi.org/10.1016/s0092-8674(01)00193-3openalex-snapshot
Ran Induces Spindle Assembly by Reversing the Inhibitory Effect of Importin α on TPX2 Activity
inferredcites →https://doi.org/10.1016/s0092-8674(01)00194-5openalex-snapshot
Importin β Is a Mitotic Target of the Small GTPase Ran in Spindle Assembly
inferredcites →https://doi.org/10.1016/s0304-3940(97)00412-6openalex-snapshot
Synaptically coupled central nervous system neurons lack centrosomal γ-tubulin
inferredcites →https://doi.org/10.1016/s0888-7543(03)00119-8openalex-snapshot
The centrosomal proteins pericentrin and kendrin are encoded by alternatively spliced products of one gene
inferredcites →https://doi.org/10.1016/s0960-9822(99)00276-6openalex-snapshot
Centrosome-independent mitotic spindle formation in vertebrates
inferredcites →https://doi.org/10.1016/s1534-5807(01)00110-1openalex-snapshot
Central Spindle Assembly and Cytokinesis Require a Kinesin-like Protein/RhoGAP Complex with Microtubule Bundling Activity
inferredcites →https://doi.org/10.1016/s1534-5807(02)00402-1openalex-snapshot
A RhoGEF and Rho Family GTPase-Activating Protein Complex Links the Contractile Ring to Cortical Microtubules at the Onset of Cytokinesis
inferredcites →https://doi.org/10.1016/s1534-5807(03)00193-xopenalex-snapshot
Polo-like Kinase 1 Regulates Nlp, a Centrosome Protein Involved in Microtubule Nucleation
inferredcites →https://doi.org/10.1021/bi00207a014openalex-snapshot
Polyglutamylation of Tubulin as a Progressive Regulator of in Vitro Interactions between the Microtubule-Associated Protein Tau and Tubulin
inferredcites →https://doi.org/10.1038/34465openalex-snapshot
Structure of the αβ tubulin dimer by electron crystallography
inferredcites →https://doi.org/10.1038/emboj.2009.47openalex-snapshot
Microtubule nucleation at the cis‐side of the Golgi apparatus requires AKAP450 and GM130
inferredcites →https://doi.org/10.1038/nature04589openalex-snapshot
Analysis of a RanGTP-regulated gradient in mitotic somatic cells
inferredcites →https://doi.org/10.1038/nature10914openalex-snapshot
MAP and kinesin-dependent nuclear positioning is required for skeletal muscle function
inferredcites →https://doi.org/10.1038/nature13277openalex-snapshot
Oncogene-like induction of cellular invasion from centrosome amplification
inferredcites →https://doi.org/10.1038/ncb1206openalex-snapshot
Coupling of ER exit to microtubules through direct interaction of COPII with dynactin
inferredcites →https://doi.org/10.1038/ncb1349openalex-snapshot
GCP-WD is a γ-tubulin targeting factor required for centrosomal and chromatin-mediated microtubule nucleation
inferredcites →https://doi.org/10.1038/ncb2591openalex-snapshot
Subdiffraction imaging of centrosomes reveals higher-order organizational features of pericentriolar material
inferredcites →https://doi.org/10.1038/ncb2597openalex-snapshot
Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization
inferredcites →https://doi.org/10.1038/ncb3241openalex-snapshot
Complementary activities of TPX2 and chTOG constitute an efficient importin-regulated microtubule nucleation module
inferredcites →https://doi.org/10.1038/ncb3481openalex-snapshot
Tubulin acetylation protects long-lived microtubules against mechanical ageing
inferredcites →https://doi.org/10.1038/ncomms12187openalex-snapshot
Non-centrosomal nucleation mediated by augmin organizes microtubules in post-mitotic neurons and controls axonal microtubule polarity
inferredcites →https://doi.org/10.1038/ncomms8929openalex-snapshot
Mto2 multisite phosphorylation inactivates non-spindle microtubule nucleation complexes during mitosis
inferredcites →https://doi.org/10.1038/ncomms9526openalex-snapshot
Detyrosinated microtubules modulate mechanotransduction in heart and skeletal muscle
inferredcites →https://doi.org/10.1038/ng1657openalex-snapshot
Mutations in dynamin 2 cause dominant centronuclear myopathy
inferredcites →https://doi.org/10.1038/nrm.2016.162openalex-snapshot
Mitotic spindle assembly in animal cells: a fine balancing act
inferredcites →https://doi.org/10.1038/nrm.2017.21openalex-snapshot
The development and functions of multiciliated epithelia
inferredcites →https://doi.org/10.1038/nrm2410openalex-snapshot
Spatial and temporal coordination of mitosis by Ran GTPase
inferredcites →https://doi.org/10.1038/nrm3118openalex-snapshot
Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis
inferredcites →https://doi.org/10.1038/nrm4062openalex-snapshot
Centrosome function and assembly in animal cells
inferredcites →https://doi.org/10.1038/s41556-018-0091-6openalex-snapshot
XMAP215 is a microtubule nucleation factor that functions synergistically with the γ-tubulin ring complex
inferredcites →https://doi.org/10.1038/s41556-018-0100-9openalex-snapshot
XMAP215 joins microtubule nucleation team
inferredcites →https://doi.org/10.1038/s41556-020-0470-7openalex-snapshot
A perinuclear microtubule-organizing centre controls nuclear positioning and basement membrane secretion
inferredcites →https://doi.org/10.1038/s41569-019-0331-xopenalex-snapshot
Cardiomyocyte maturation: advances in knowledge and implications for regenerative medicine
inferredcites →https://doi.org/10.1038/s41580-018-0004-3openalex-snapshot
The cytoplasmic dynein transport machinery and its many cargoes
inferredcites →https://doi.org/10.1038/s41580-018-0067-1openalex-snapshot
Actin–microtubule crosstalk in cell biology
inferredcites →https://doi.org/10.1038/s41580-020-0214-3openalex-snapshot
The tubulin code and its role in controlling microtubule properties and functions
inferredcites →https://doi.org/10.1038/s41591-018-0046-2openalex-snapshot
Suppression of detyrosinated microtubules improves cardiomyocyte function in human heart failure
inferredcites →https://doi.org/10.1038/s41598-019-50728-6openalex-snapshot
Nesprin-1-alpha2 associates with kinesin at myotube outer nuclear membranes, but is restricted to neuromuscular junction nuclei in adult muscle
inferredcites →https://doi.org/10.1042/bst20170149openalex-snapshot
Nesprin-1/2: roles in nuclear envelope organisation, myogenesis and muscle disease
inferredcites →https://doi.org/10.1042/bst20180350openalex-snapshot
Parts list for a microtubule depolymerising kinesin
inferredcites →https://doi.org/10.1042/cs20180560openalex-snapshot
Advances in heart regeneration based on cardiomyocyte proliferation and regenerative potential of binucleated cardiomyocytes and polyploidization
inferredcites →https://doi.org/10.1042/ebc20180028openalex-snapshot
Microtubule nucleation by γ-tubulin complexes and beyond
inferredcites →https://doi.org/10.1073/pnas.0500711102openalex-snapshot
Syne proteins anchor muscle nuclei at the neuromuscular junction
inferredcites →https://doi.org/10.1073/pnas.0500748102openalex-snapshot
Function and regulation of Tumbleweed (RacGAP50C) in neuroblast proliferation and neuronal morphogenesis
inferredcites →https://doi.org/10.1073/pnas.0901587106openalex-snapshot
The augmin complex plays a critical role in spindle microtubule generation for mitotic progression and cytokinesis in human cells
inferredcites →https://doi.org/10.1073/pnas.1004736107openalex-snapshot
Kinesin-1 heavy chain mediates microtubule sliding to drive changes in cell shape
inferredcites →https://doi.org/10.1073/pnas.1520638113openalex-snapshot
CAMSAP3 orients the apical-to-basal polarity of microtubule arrays in epithelial cells
inferredcites →https://doi.org/10.1074/jbc.m011380200openalex-snapshot
Differential Binding Regulation of Microtubule-associated Proteins MAP1A, MAP1B, and MAP2 by Tubulin Polyglutamylation
inferredcites →https://doi.org/10.1074/jbc.m110.105965openalex-snapshot
Conserved Motif of CDK5RAP2 Mediates Its Localization to Centrosomes and the Golgi Complex
inferredcites →https://doi.org/10.1074/jbc.r117.001324openalex-snapshot
Kinesin-2 motors: Kinetics and biophysics
inferredcites →https://doi.org/10.1080/15384101.2015.1004937openalex-snapshot
Neuronal cell cycle: the neuron itself and its circumstances
inferredcites →https://doi.org/10.1080/19490992.2015.1106061openalex-snapshot
Composite biopolymer scaffolds shape muscle nucleus: Insights and perspectives fromDrosophila
inferredcites →https://doi.org/10.1080/19491034.2018.1454168openalex-snapshot
Causes and consequences of genomic instability in laminopathies: Replication stress and interferon response
inferredcites →https://doi.org/10.1083/jcb.100.1.35openalex-snapshot
Fate of microtubule-organizing centers during myogenesis in vitro.
inferredcites →https://doi.org/10.1083/jcb.101.2.630openalex-snapshot
The Golgi apparatus remains associated with microtubule organizing centers during myogenesis.
inferredcites →https://doi.org/10.1083/jcb.120.2.399openalex-snapshot
Changes in architecture of the Golgi complex and other subcellular organelles during myogenesis.
inferredcites →https://doi.org/10.1083/jcb.124.5.783openalex-snapshot
PCM-1, A 228-kD centrosome autoantigen with a distinct cell cycle distribution
inferredcites →https://doi.org/10.1083/jcb.132.4.657openalex-snapshot
Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis.
inferredcites →https://doi.org/10.1083/jcb.143.6.1575openalex-snapshot
Centriole Disassembly In Vivo and Its Effect on Centrosome Structure and Function in Vertebrate Cells
inferredcites →https://doi.org/10.1083/jcb.153.1.237openalex-snapshot
Centrosomes Enhance the Fidelity of Cytokinesis in Vertebrates and Are Required for Cell Cycle Progression
inferredcites →https://doi.org/10.1083/jcb.200202047openalex-snapshot
The kinetically dominant assembly pathway for centrosomal asters in Caenorhabditis elegans is γ-tubulin dependent
inferredcites →https://doi.org/10.1083/jcb.200204023openalex-snapshot
Assembly of centrosomal proteins and microtubule organization depends on PCM-1
inferredcites →https://doi.org/10.1083/jcb.200408113openalex-snapshot
A standardized kinesin nomenclature
inferredcites →https://doi.org/10.1083/jcb.200509124openalex-snapshot
Coupling of the nucleus and cytoplasm: Role of the LINC complex
inferredcites →https://doi.org/10.1083/jcb.200512058openalex-snapshot
Tubulin tyrosination is a major factor affecting the recruitment of CAP-Gly proteins at microtubule plus ends
inferredcites →https://doi.org/10.1083/jcb.200609109openalex-snapshot
Desmoplakin: an unexpected regulator of microtubule organization in the epidermis
inferredcites →https://doi.org/10.1083/jcb.200902142openalex-snapshot
Motor-dependent microtubule disassembly driven by tubulin tyrosination
inferredcites →https://doi.org/10.1083/jcb.201001024openalex-snapshot
Tubulin polyglutamylation stimulates spastin-mediated microtubule severing
inferredcites →https://doi.org/10.1083/jcb.201012049openalex-snapshot
Rb and p130 control cell cycle gene silencing to maintain the postmitotic phenotype in cardiac myocytes
inferredcites →https://doi.org/10.1083/jcb.201106093openalex-snapshot
PLK1 phosphorylation of pericentrin initiates centrosome maturation at the onset of mitosis
inferredcites →https://doi.org/10.1083/jcb.201203166openalex-snapshot
Cortical dynein is critical for proper spindle positioning in human cells
inferredcites →https://doi.org/10.1083/jcb.201204102openalex-snapshot
Organelle positioning in muscles requires cooperation between two KASH proteins and microtubules
inferredcites →https://doi.org/10.1083/jcb.201210007openalex-snapshot
Mechanisms of spindle positioning
inferredcites →https://doi.org/10.1083/jcb.201304063openalex-snapshot
Microtubules that form the stationary lattice of muscle fibers are dynamic and nucleated at Golgi elements
inferredcites →https://doi.org/10.1083/jcb.201309038openalex-snapshot
Loss of centrioles causes chromosomal instability in vertebrate somatic cells
inferredcites →https://doi.org/10.1083/jcb.201408098openalex-snapshot
Nesprin provides elastic properties to muscle nuclei by cooperating with spectraplakin and EB1
inferredcites →https://doi.org/10.1083/jcb.201601099openalex-snapshot
Divergent regulation of functionally distinct γ-tubulin complexes during differentiation
inferredcites →https://doi.org/10.1083/jcb.201603050openalex-snapshot
The structured core of human β tubulin confers isotype-specific polymerization properties
inferredcites →https://doi.org/10.1083/jcb.201708137openalex-snapshot
Mechanotransduction via the LINC complex regulates DNA replication in myonuclei
inferredcites →https://doi.org/10.1083/jcb.201711090openalex-snapshot
Mechanism of how augmin directly targets the γ-tubulin ring complex to microtubules
inferredcites →https://doi.org/10.1083/jcb.201805044openalex-snapshot
Augmin accumulation on long-lived microtubules drives amplification and kinetochore-directed growth
inferredcites →https://doi.org/10.1083/jcb.201808176openalex-snapshot
The Drosophila Ninein homologue Bsg25D cooperates with Ensconsin in myonuclear positioning
inferredcites →https://doi.org/10.1083/jcb.201810155openalex-snapshot
Patronin-mediated minus end growth is required for dendritic microtubule polarity
inferredcites →https://doi.org/10.1083/jcb.201812170openalex-snapshot
Hook3 is a scaffold for the opposite-polarity microtubule-based motors cytoplasmic dynein-1 and KIF1C
inferredcites →https://doi.org/10.1083/jcb.39.3.544openalex-snapshot
THE EFFECT OF COLCHICINE ON MYOGENESIS IN VIVO IN RANA PIPIENS AND RHODNIUS PROLIXUS (HEMIPTERA)
inferredcites →https://doi.org/10.1091/mbc.12.4.795openalex-snapshot
Golgi Complex Reorganization during Muscle Differentiation: Visualization in Living Cells and Mechanism
inferredcites →https://doi.org/10.1091/mbc.12.7.2047openalex-snapshot
The Golgi Complex Is a Microtubule-organizing Organelle
inferredcites →https://doi.org/10.1091/mbc.7.4.631openalex-snapshot
Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites.
inferredcites →https://doi.org/10.1091/mbc.e12-06-0458openalex-snapshot
Evidence for dynein and astral microtubule–mediated cortical release and transport of Gαi/LGN/NuMA complex in mitotic cells
inferredcites →https://doi.org/10.1091/mbc.e13-09-0515openalex-snapshot
γ-Tubulin controls neuronal microtubule polarity independently of Golgi outposts
inferredcites →https://doi.org/10.1091/mbc.e16-05-0271openalex-snapshot
A microtubule bestiary: structural diversity in tubulin polymers
inferredcites →https://doi.org/10.1091/mbc.e16-06-0405openalex-snapshot
Microtubule motors involved in nuclear movement during skeletal muscle differentiation
inferredcites →https://doi.org/10.1091/mbc.e17-02-0124openalex-snapshot
Tubulin isoform composition tunes microtubule dynamics
inferredcites →https://doi.org/10.1091/mbc.e17-03-0171openalex-snapshot
Increased lateral microtubule contact at the cell cortex is sufficient to drive mammalian spindle elongation
inferredcites →https://doi.org/10.1093/biolre/iox145openalex-snapshot
Meiotic spindle formation in mammalian oocytes: implications for human infertility†
inferredcites →https://doi.org/10.1093/cvr/cvy056openalex-snapshot
Cardiomyocyte binucleation is associated with aberrant mitotic microtubule distribution, mislocalization of RhoA and IQGAP3, as well as defective actomyosin ring anchorage and cleavage furrow ingression
inferredcites →https://doi.org/10.1093/hmg/ddp499openalex-snapshot
Nesprin 1 is critical for nuclear positioning and anchorage
inferredcites →https://doi.org/10.1093/nar/gkw1033openalex-snapshot
Genenames.org: the HGNC and VGNC resources in 2017
inferredcites →https://doi.org/10.1095/biolreprod.104.031245openalex-snapshot
Centrosome Reduction During Gametogenesis and Its Significance1
inferredcites →https://doi.org/10.1098/rsob.120104openalex-snapshot
Structured illumination of the interface between centriole and peri-centriolar material
inferredcites →https://doi.org/10.1098/rsob.190314openalex-snapshot
The crosstalk between microtubules, actin and membranes shapes cell division
inferredcites →https://doi.org/10.1098/rstb.2013.0453openalex-snapshot
Exploring the evolutionary history of centrosomes
inferredcites →https://doi.org/10.1098/rstb.2013.0459openalex-snapshot
Pericentriolar material structure and dynamics
inferredcites →https://doi.org/10.1098/rstb.2013.0462openalex-snapshot
The centrosome–Golgi apparatus nexus
inferredcites →https://doi.org/10.1098/rstb.2013.0467openalex-snapshot
Causes and consequences of centrosome abnormalities in cancer
inferredcites →https://doi.org/10.1098/rstb.2013.0469openalex-snapshot
Historical roots of centrosome research: discovery of Boveri's microscope slides in Würzburg
inferredcites →https://doi.org/10.1101/cshperspect.a022608openalex-snapshot
Microtubules and Microtubule-Associated Proteins
inferredcites →https://doi.org/10.1101/gad.1306705openalex-snapshot
p38 MAP kinase inhibition enables proliferation of adult mammalian cardiomyocytes
inferredcites →https://doi.org/10.1101/gad.894001openalex-snapshot
“It Takes Two to Tango”: understanding how centrosome duplication is regulated throughout the cell cycle
inferredcites →https://doi.org/10.1103/physreve.51.5058openalex-snapshot
Spontaneous nucleation of microtubules
inferredcites →https://doi.org/10.1111/apha.12287openalex-snapshot
Modular organization of cardiac energy metabolism: energy conversion, transfer and feedback regulation
inferredcites →https://doi.org/10.1111/j.1582-4934.2008.00439.xopenalex-snapshot
Features of cardiomyocyte proliferation and its potential for cardiac regeneration
inferredcites →https://doi.org/10.1111/tpj.12145openalex-snapshot
Evolution of microtubule organizing centers across the tree of eukaryotes
inferredcites →https://doi.org/10.1126/science.1056866openalex-snapshot
Requirement of a Centrosomal Activity for Cell Cycle Progression Through G 1 into S Phase
inferredcites →https://doi.org/10.1126/science.1068798openalex-snapshot
Visualization of a Ran-GTP Gradient in Interphase and Mitotic Xenopus Egg Extracts
inferredcites →https://doi.org/10.1126/science.1115964openalex-snapshot
Spatial Coordination of Spindle Assembly by Chromosome-Mediated Signaling Gradients
inferredcites →https://doi.org/10.1126/science.1182179openalex-snapshot
Axon Extension Occurs Independently of Centrosomal Microtubule Nucleation
inferredcites →https://doi.org/10.1126/science.1204824openalex-snapshot
The Structure of the Kinesin-1 Motor-Tail Complex Reveals the Mechanism of Autoinhibition
inferredcites →https://doi.org/10.1126/science.1209037openalex-snapshot
The Centrosome in Cells and Organisms
inferredcites →https://doi.org/10.1126/science.1214457openalex-snapshot
Centrosome Loss in the Evolution of Planarians
inferredcites →https://doi.org/10.1126/science.284.5418.1356openalex-snapshot
Self-Organization of Microtubule Asters Induced in Xenopus Egg Extracts by GTP-Bound Ran
inferredcites →https://doi.org/10.1126/science.aaa5111openalex-snapshot
Reversible centriole depletion with an inhibitor of Polo-like kinase 4
inferredcites →https://doi.org/10.1126/science.aaa9529openalex-snapshot
Error-prone chromosome-mediated spindle assembly favors chromosome segregation defects in human oocytes
inferredcites →https://doi.org/10.1126/science.aaf0659openalex-snapshot
Detyrosinated microtubules buckle and bear load in contracting cardiomyocytes
inferredcites →https://doi.org/10.1134/s0006297917070057openalex-snapshot
Intracellular cargo transport by kinesin-3 motors
inferredcites →https://doi.org/10.1146/annurev-cellbio-100616-060553openalex-snapshot
Assembly and Positioning of the Oocyte Meiotic Spindle
showing the first 200 of 271 · page through all 271
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4781335openalex-extracted
The Abl1 Tyrosine Kinase and p53 are Key Players in Doxorubicin-Induced Cardiomyopathy and Their Cell Death Signaling Differs in Atrial and Ventricular Cardiomyocytes
inferred← citeshttps://doi.org/10.1002/cm.21710openalex-snapshot
Reconstitution of muscle cell microtubule organization in vitro
inferred← citeshttps://doi.org/10.1002/jev2.12403openalex-snapshot
Dysregulation of extracellular vesicle protein cargo in female myalgic encephalomyelitis/chronic fatigue syndrome cases and sedentary controls in response to maximal exercise
inferred← citeshttps://doi.org/10.1007/978-3-032-16833-7_12openalex-snapshot
Insights into Microtubule Nucleation at the Golgi Apparatus
inferred← citeshttps://doi.org/10.1007/978-3-032-23779-8_6openalex-snapshot
Prokaryotic Cells and Endosymbiotic Origin of Eukaryotic Cells
inferred← citeshttps://doi.org/10.1007/s00418-021-01999-6openalex-snapshot
The Golgi apparatus is the main microtubule-organizing center in differentiating skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00240-6openalex-snapshot
Microtubules in Differentiated Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00274-1openalex-snapshot
Cytoskeleton and Motors: The Overview
inferred← citeshttps://doi.org/10.1016/j.biosystems.2021.104375openalex-snapshot
Archaeal Origins of Eukaryotic Cell and Nucleus
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.06.029openalex-snapshot
Sarcomere, troponin, and myosin X-ray diffraction signals can be resolved in single cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.ceb.2025.102517openalex-snapshot
Dysfunctional cardiomyocyte signalling and heart disease
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148945openalex-snapshot
PPP2R5E: New gene potentially involved in specific learning disorders and myopathy
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110630openalex-snapshot
Dynamic remodeling of septin structures fine-tunes myogenic differentiation
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111104openalex-snapshot
Alternatively spliced MAP4 isoforms have key roles in maintaining microtubule organization and skeletal muscle function
inferred← citeshttps://doi.org/10.1016/j.meatsci.2022.108804openalex-snapshot
Horse meat tenderization in relation to post-mortem evolution of the myofibrillar sub-proteome
inferred← citeshttps://doi.org/10.1016/j.tcb.2022.03.004openalex-snapshot
Centrosome heterogeneity in stem cells regulates cell diversity
inferred← citeshttps://doi.org/10.1021/acs.jproteome.2c00505openalex-snapshot
Phosphoproteomics Profiling Defines a Target Landscape of the Basophilic Protein Kinases AKT, S6K, and RSK in Skeletal Myotubes
inferred← citeshttps://doi.org/10.1038/s41419-026-08819-6openalex-snapshot
Emerin is necessary for microtubule-organizing center translocation to the nuclear envelope of muscle cells
inferred← citeshttps://doi.org/10.1038/s41536-026-00509-3openalex-snapshot
Skeletal muscle dedifferentiation requires centrosomes
inferred← citeshttps://doi.org/10.1038/s41569-022-00692-yopenalex-snapshot
The microtubule cytoskeleton in cardiac mechanics and heart failure
inferred← citeshttps://doi.org/10.1038/s41598-023-28896-3openalex-snapshot
Maternal diet induces persistent DNA methylation changes in the muscle of beef calves
inferred← citeshttps://doi.org/10.1038/s41598-024-64608-1openalex-snapshot
Loss of connectin novex-3 leads to heart dysfunction associated with impaired cardiomyocyte proliferation and abnormal nuclear mechanics
inferred← citeshttps://doi.org/10.1038/s42003-026-09537-7openalex-snapshot
WDR62 is required for proper proliferation and early differentiation of skeletal myoblasts
inferred← citeshttps://doi.org/10.1042/bst20221541openalex-snapshot
Nesprin-1: novel regulator of striated muscle nuclear positioning and mechanotransduction
inferred← citeshttps://doi.org/10.1063/5.0172423openalex-snapshot
Self-organizing behaviors of cardiovascular cells on synthetic nanofiber scaffolds
inferred← citeshttps://doi.org/10.1093/cvr/cvad052openalex-snapshot
Microtubule plus-end tracking proteins: novel modulators of cardiac sodium channels and arrhythmogenesis
inferred← citeshttps://doi.org/10.1098/rsob.240094openalex-snapshot
Tail-anchored membrane protein SLMAP3 is essential for targeting centrosomal proteins to the nuclear envelope in skeletal myogenesis
inferred← citeshttps://doi.org/10.1101/2021.04.19.440474openalex-snapshot
Alternative splicing of pericentrin contributes to cell cycle control in cardiomyocytes
inferred← citeshttps://doi.org/10.1101/2022.08.05.502981openalex-snapshot
Drosophila Tropomodulin is required for multiple actin-dependent processes in myofiber assembly and maintenance
inferred← citeshttps://doi.org/10.1101/2023.07.20.23292938openalex-snapshot
Deciphering the genetic architecture of atrial fibrillation offers insights into disease prediction, pathophysiology and downstream sequelae
inferred← citeshttps://doi.org/10.1101/2023.08.24.554594openalex-snapshot
Reorganization of Septin structures regulates early myogenesis
inferred← citeshttps://doi.org/10.1101/2024.06.17.599282openalex-snapshot
Myogenic dedifferentiation involves a p53-dependent reorganization of PLK4 localization during centrosome regeneration
inferred← citeshttps://doi.org/10.1101/2024.09.16.613201openalex-snapshot
Zika virus NS3 drives the assembly of a viroplasm-like structure
inferred← citeshttps://doi.org/10.1111/febs.17212openalex-snapshot
Developmental and tissue‐specific roles of mammalian centrosomes
inferred← citeshttps://doi.org/10.1126/sciadv.abm2411openalex-snapshot
Spatiotemporal gating of Stat nuclear influx by Drosophila Npas4 in collective cell migration
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-120319-025356openalex-snapshot
Self-Organization of Cellular Units
inferred← citeshttps://doi.org/10.1152/ajpheart.00619.2023openalex-snapshot
Considering impact of age and sex on cardiac cytoskeletal components
inferred← citeshttps://doi.org/10.1161/circresaha.122.319808openalex-snapshot
Targeting Microtubules for the Treatment of Heart Disease
inferred← citeshttps://doi.org/10.1161/circulationaha.122.060985openalex-snapshot
Impaired Reorganization of Centrosome Structure Underlies Human Infantile Dilated Cardiomyopathy
inferred← citeshttps://doi.org/10.1186/s12964-024-01593-yopenalex-snapshot
Nesprin proteins: bridging nuclear envelope dynamics to muscular dysfunction
inferred← citeshttps://doi.org/10.1186/s12967-024-05623-8openalex-snapshot
The Abl1 tyrosine kinase is a key player in doxorubicin-induced cardiomyopathy and its p53/p73 cell death mediated signaling differs in atrial and ventricular cardiomyocytes
inferred← citeshttps://doi.org/10.1242/dev.199909openalex-snapshot
Microtubule-dependent subcellular organisation of pluripotent cells
inferred← citeshttps://doi.org/10.1242/dev.201194openalex-snapshot
Drosophila Tropomodulin is required for multiple actin-dependent processes within developing myofibers
inferred← citeshttps://doi.org/10.1242/jcs.258397openalex-snapshot
From tip to toe – dressing centrioles in γTuRC
inferred← citeshttps://doi.org/10.1242/jcs.263476openalex-snapshot
Diversity of microtubule arrays in animal cells at a glance
inferred← citeshttps://doi.org/10.1242/jcs.264166openalex-snapshot
Selective disruption of microtubule formation at the nuclear envelope impairs the bone resorption capacity of osteoclasts
inferred← citeshttps://doi.org/10.1247/csf.24067openalex-snapshot
The role of primary cilia in myoblast proliferation and cell cycle regulation during myogenesis
inferred← citeshttps://doi.org/10.1371/journal.pone.0283490openalex-snapshot
Histone methyltransferase SUV39H1 regulates the Golgi complex via the nuclear envelope-spanning LINC complex
inferred← citeshttps://doi.org/10.14814/phy2.15171openalex-snapshot
Switching in the expression pattern of actin isoforms marks the onset of contractility and distinct mechanodynamic behavior during cardiomyocyte differentiation
inferred← citeshttps://doi.org/10.3389/fcell.2021.690577openalex-snapshot
LINCing Nuclear Mechanobiology With Skeletal Muscle Mass and Function
inferred← citeshttps://doi.org/10.3389/fcell.2022.934586openalex-snapshot
Effects of mutant lamins on nucleo-cytoskeletal coupling in Drosophila models of LMNA muscular dystrophy
inferred← citeshttps://doi.org/10.3389/fendo.2023.1143067openalex-snapshot
Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses
inferred← citeshttps://doi.org/10.3389/fphys.2022.845504openalex-snapshot
Positional Context of Myonuclear Transcription During Injury-Induced Muscle Regeneration
inferred← citeshttps://doi.org/10.3390/cells10020318openalex-snapshot
Nuclear Mechanotransduction in Skeletal Muscle
inferred← citeshttps://doi.org/10.3390/cells11030354openalex-snapshot
Functional Coordination among the Golgi Complex, the Centrosome and the Microtubule Cytoskeleton during the Cell Cycle
inferred← citeshttps://doi.org/10.3390/cells14040237openalex-snapshot
NE-MTOC Formation in Skeletal Muscle Is Mbnl2-Dependent and Occurs in a Sequential and Gradual Manner
inferred← citeshttps://doi.org/10.3390/ijms222011226openalex-snapshot
In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies
inferred← citeshttps://doi.org/10.3390/ijms24032903openalex-snapshot
Insights into Cell-Specific Functions of Microtubules in Skeletal Muscle Development and Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms25052888openalex-snapshot
Deletion of Sarcolemmal Membrane-Associated Protein Isoform 3 (SLMAP3) in Cardiac Progenitors Delays Embryonic Growth of Myocardium without Affecting Hippo Pathway
inferred← citeshttps://doi.org/10.3390/jcdd8080087openalex-snapshot
Alternative Splicing of Pericentrin Contributes to Cell Cycle Control in Cardiomyocytes
inferred← citeshttps://doi.org/10.34117/bjdv7n6-438openalex-snapshot
Patogenia das doenças relacionadas ao citoesqueleto: uma revisão da literatura/ Pathogenics of cytoskeleton-related diseases: a review
inferred← citeshttps://doi.org/10.64898/2026.07.20.739552openalex-snapshot
Microtubule architecture and detyrosination bidirectionally modulate sarcomere shortening in skeletal muscle fibers
inferred← citeshttps://doi.org/10.70675/45004e64z3cdbz4307z818bz78f3b59c136eopenalex-snapshot
How cellulose and microtubules contribute to plant cell and organ growth : a temporal and spatial multi-scale analysis
inferred← citeshttps://doi.org/10.71548/13241openalex-snapshot
Defining the role of Xin and associated proteins in skeletal muscle health
inferred← citeshttps://doi.org/10.7554/elife.61669openalex-snapshot
AKAP6 orchestrates the nuclear envelope microtubule-organizing center by linking golgi and nucleus via AKAP9
inferred← citeshttps://doi.org/10.7554/elife.65672openalex-snapshot
Myogenin controls via AKAP6 non-centrosomal microtubule-organizing center formation at the nuclear envelope
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.