Myo10 is a key regulator of TNT formation in neuronal cells.
about
The Exocyst Complex in Health and DiseaseExploring the role of lipids in intercellular conduits: breakthroughs in the pipelineMechanisms of mesenchymal stem/stromal cell functionNovel microscopy-based screening method reveals regulators of contact-dependent intercellular transfer.Porcine Reproductive and Respiratory Syndrome Virus Utilizes Nanotubes for Intercellular SpreadTunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assembliesCell Connections by Tunneling Nanotubes: Effects of Mitochondrial Trafficking on Target Cell Metabolism, Homeostasis, and Response to Therapy.Linked in: immunologic membrane nanotube networksDifferential identity of Filopodia and Tunneling Nanotubes revealed by the opposite functions of actin regulatory complexes.RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns.Tunneling nanotubes: Diversity in morphology and structureInformation handling by the brain: proposal of a new "paradigm" involving the roamer type of volume transmission and the tunneling nanotube type of wiring transmission.Artificial Mitochondria Transfer: Current Challenges, Advances, and Future Applications.Potential Role of the Formation of Tunneling Nanotubes in HIV-1 Spread in Macrophages.Identification and Characterization of Tunneling Nanotubes for Intercellular Trafficking.Prion aggregates transfer through tunneling nanotubes in endocytic vesiclesTransfer of disrupted-in-schizophrenia 1 aggregates between neuronal-like cells occurs in tunnelling nanotubes and is promoted by dopamine.The spread of prion-like proteins by lysosomes and tunneling nanotubes: Implications for neurodegenerative diseases.Extracellular Vesicles, Tunneling Nanotubes, and Cellular Interplay: Synergies and Missing Links.Identification, modeling, and characterization studies of Tetrahymena thermophila myosin FERM domains suggests a conserved core fold but functional differences.Regulation of Osteoclast Differentiation by Myosin X.Dopamine transporter is enriched in filopodia and induces filopodia formation.The Role of Rho-GTPases and actin polymerization during Macrophage Tunneling Nanotube Biogenesis.Tunneling nanotubes spread fibrillar α-synuclein by intercellular trafficking of lysosomes.Tunneling Nanotubes are Novel Cellular Structures That Communicate Signals Between Trabecular Meshwork Cells.Tunneling Nanotubes and Gap Junctions-Their Role in Long-Range Intercellular Communication during Development, Health, and Disease Conditions.The Evidence for the Spread and Seeding Capacities of the Mutant Huntingtin Protein in in Vitro Systems and Their Therapeutic Implications.A Salutary Role of Reactive Oxygen Species in Intercellular Tunnel-Mediated Communication.Contact-dependent transfer of TiO₂ nanoparticles between mammalian cells.Emerging role of contact-mediated cell communication in tissue development and diseasesCellular and Molecular Networking Within the Ecosystem of Cancer Cell Communication via Tunneling Nanotubes
P2860
Q26752334-6E133977-9F9D-4968-8C7D-D3D92E56FD4AQ26823124-8D9D7639-B45F-4BE4-ABCA-1874597182CDQ28079649-4B88F075-8811-4772-819D-E5DA2939581FQ30661199-1F23B587-B654-45B9-ACF1-817AEBBDA4A5Q30754418-0286C7D0-03A9-47BE-AC17-BA3B0E41C243Q30827588-36274876-7C11-4B72-B1DC-0C62060502ACQ33808890-509EB593-4F32-404C-ACBC-CC28B235BE54Q37098075-DF0AA760-4AFC-423F-81E1-097818D68BB7Q37529495-1D89A7F5-BE05-444C-99A0-2F2DC68A4B5AQ37577398-FB421426-8AE2-4053-95EB-4A09CB65A21BQ38207996-D87D9B5B-D1EA-495F-9D7D-47ECBA675EFFQ38215360-2DD9A741-2E88-475B-93B6-50C616745D20Q38650633-5CA56F78-36FF-403F-AF20-B871CD5BC918Q38803122-2B675345-BB44-49AB-9CA8-3F08303EE826Q38865440-6B099A90-3E3F-4742-9D0D-9375C16720E5Q38872647-92F94A9C-27FD-4473-A482-56CB6F07CE7FQ38919714-CA1425C2-6936-479E-A141-81393B5A1CD5Q39445835-D30324A2-BDD5-45AD-90D0-F38D31E61BA8Q40097136-448F993A-FE5C-48BB-A48B-A9B9B55FC60BQ40402355-8AB6D495-2C0C-45F7-9AD1-0182B175E277Q41312017-7D4CFBF7-B153-4002-8F77-F1BD62C65F1DQ41337842-F69C9836-E2EB-4624-83CE-43C137853D4EQ41448310-D96A05B9-F80D-4088-A1FB-23B0BB236579Q42388077-F38CB75B-26E7-4EAD-8BD4-838708A8CBE1Q42631366-76DB89C6-A911-47BC-90BA-093F61115517Q45723587-0D4017E1-B564-4915-8F84-C08681A807BAQ47102449-682CF02B-91FC-4B3E-9FD5-E91FC10197B6Q50352962-0FEF2831-A8D6-4C8D-9079-4FA079CE24A7Q51742717-E6465D5B-38AC-4BD7-AC26-2EB03FC7B2D2Q57921405-ED6DA7C6-D34F-4714-92DE-78D56C1D66EFQ58586127-3BA1CE30-6E81-4163-9527-1765EA06F1CE
P2860
Myo10 is a key regulator of TNT formation in neuronal cells.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Myo10 is a key regulator of TNT formation in neuronal cells.
@en
Myo10 is a key regulator of TNT formation in neuronal cells.
@nl
type
label
Myo10 is a key regulator of TNT formation in neuronal cells.
@en
Myo10 is a key regulator of TNT formation in neuronal cells.
@nl
prefLabel
Myo10 is a key regulator of TNT formation in neuronal cells.
@en
Myo10 is a key regulator of TNT formation in neuronal cells.
@nl
P356
P1476
Myo10 is a key regulator of TNT formation in neuronal cells
@en
P2093
Ludovica Marzo
Pierre-Henri Commere
P304
P356
10.1242/JCS.129239
P407
P577
2013-07-25T00:00:00Z