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Characterization of neuronal synaptopodin reveals a myosin V-dependent mechanism of synaptopodin clustering at the post-synaptic sites
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(20000306)418:2<164::aid-cne4>3.0.co;2-0openalex-snapshot
Actin-associated protein synaptopodin in the rat hippocampal formation: Localization in the spine neck and close association with the spine apparatus of principal neurons
inferredcites →https://doi.org/10.1002/cne.20651openalex-snapshot
Postnatal development of synaptopodin expression in the rodent hippocampus
inferredcites →https://doi.org/10.1002/cne.21445openalex-snapshot
Loss of the cisternal organelle in the axon initial segment of cortical neurons in synaptopodin‐deficient mice
inferredcites →https://doi.org/10.1007/s12551-010-0040-5openalex-snapshot
Synaptopodin family of natively unfolded, actin binding proteins: physical properties and potential biological functions
inferredcites →https://doi.org/10.1016/j.cell.2008.09.057openalex-snapshot
Myosin Vb Mobilizes Recycling Endosomes and AMPA Receptors for Postsynaptic Plasticity
inferredcites →https://doi.org/10.1016/j.celrep.2014.05.028openalex-snapshot
Synaptic Control of Secretory Trafficking in Dendrites
inferredcites →https://doi.org/10.1016/j.celrep.2015.09.062openalex-snapshot
Positioning of AMPA Receptor-Containing Endosomes Regulates Synapse Architecture
inferredcites →https://doi.org/10.1016/j.celrep.2015.12.024openalex-snapshot
A Dendritic Golgi Satellite between ERGIC and Retromer
inferredcites →https://doi.org/10.1016/j.conb.2016.03.004openalex-snapshot
Specialization of biosynthetic membrane trafficking for neuronal form and function
inferredcites →https://doi.org/10.1016/j.cub.2009.12.052openalex-snapshot
Mixed Microtubules Steer Dynein-Driven Cargo Transport into Dendrites
inferredcites →https://doi.org/10.1016/j.jneumeth.2011.06.006openalex-snapshot
An efficient method for the long-term and specific expression of exogenous cDNAs in cultured Purkinje neurons
inferredcites →https://doi.org/10.1016/j.mcn.2011.06.010openalex-snapshot
In vitro maturation of the cisternal organelle in the hippocampal neuron's axon initial segment
inferredcites →https://doi.org/10.1016/j.neuron.2008.11.013openalex-snapshot
Dynamic Microtubules Regulate Dendritic Spine Morphology and Synaptic Plasticity
inferredcites →https://doi.org/10.1016/j.neuron.2012.11.027openalex-snapshot
TRAK/Milton Motor-Adaptor Proteins Steer Mitochondrial Trafficking to Axons and Dendrites
inferredcites →https://doi.org/10.1016/j.neuron.2018.01.036openalex-snapshot
α-Actinin Anchors PSD-95 at Postsynaptic Sites
inferredcites →https://doi.org/10.1016/j.neuron.2018.01.046openalex-snapshot
Caldendrin Directly Couples Postsynaptic Calcium Signals to Actin Remodeling in Dendritic Spines
inferredcites →https://doi.org/10.1016/j.neuropharm.2004.07.022openalex-snapshot
The dynamic turnover and functional roles of α-actinin in dendritic spines
inferredcites →https://doi.org/10.1038/379466a0openalex-snapshot
Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry
inferredcites →https://doi.org/10.1038/ncb2132openalex-snapshot
Myosin-Va transports the endoplasmic reticulum into the dendritic spines of Purkinje neurons
inferredcites →https://doi.org/10.1038/ng1295-369openalex-snapshot
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
inferredcites →https://doi.org/10.1038/nm.1857openalex-snapshot
The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nn.4593openalex-snapshot
Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems
inferredcites →https://doi.org/10.1038/nn2063openalex-snapshot
Motor protein–dependent transport of AMPA receptors into spines during long-term potentiation
inferredcites →https://doi.org/10.1038/nprot.2006.357openalex-snapshot
Time-lapse imaging of dendritic spines in vitro
inferredcites →https://doi.org/10.1038/sj.gt.3301905openalex-snapshot
Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00552.xopenalex-snapshot
Regulated expression of an actin‐associated protein, synaptopodin, during long‐term potentiation
inferredcites →https://doi.org/10.1073/pnas.082243699openalex-snapshot
A monomeric red fluorescent protein
inferredcites →https://doi.org/10.1073/pnas.0905110106openalex-snapshot
Differential distribution of endoplasmic reticulum controls metabotropic signaling and plasticity at hippocampal synapses
inferredcites →https://doi.org/10.1073/pnas.1213677110openalex-snapshot
Synaptopodin regulates denervation-induced homeostatic synaptic plasticity
inferredcites →https://doi.org/10.1073/pnas.1832384100openalex-snapshot
Synaptopodin-deficient mice lack a spine apparatus and show deficits in synaptic plasticity
inferredcites →https://doi.org/10.1083/jcb.139.1.193openalex-snapshot
Synaptopodin: An Actin-associated Protein in Telencephalic Dendrites and Renal Podocytes
inferredcites →https://doi.org/10.1083/jcb.200410091openalex-snapshot
A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis
inferredcites →https://doi.org/10.1091/mbc.e02-11-0767openalex-snapshot
Myo6 Facilitates the Translocation of Endocytic Vesicles from Cell Peripheries
inferredcites →https://doi.org/10.1091/mbc.e17-01-0068openalex-snapshot
Dynein efficiently navigates the dendritic cytoskeleton to drive the retrograde trafficking of BDNF/TrkB signaling endosomes
inferredcites →https://doi.org/10.1093/nar/gku1003openalex-snapshot
STRING v10: protein–protein interaction networks, integrated over the tree of life
inferredcites →https://doi.org/10.1101/pdb.prot094888openalex-snapshot
Preparation of Slice Cultures from Rodent Hippocampus
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04342.xopenalex-snapshot
Dynamic distribution of endoplasmic reticulum in hippocampal neuron dendritic spines
inferredcites →https://doi.org/10.1111/j.1471-4159.2004.02888.xopenalex-snapshot
Synaptopodin, a molecule involved in the formation of the dendritic spine apparatus, is a dual actin/α‐actinin binding protein
inferredcites →https://doi.org/10.1172/jci200523371openalex-snapshot
Synaptopodin regulates the actin-bundling activity of α-actinin in an isoform-specific manner
inferredcites →https://doi.org/10.1172/jci23371openalex-snapshot
Synaptopodin regulates the actin-bundling activity of α-actinin in an isoform-specific manner
inferredcites →https://doi.org/10.1186/1475-925x-2-13openalex-snapshot
ScanImage: Flexible software for operating laser scanning microscopes
inferredcites →https://doi.org/10.1186/s40478-016-0311-xopenalex-snapshot
Rewiring neuronal microcircuits of the brain via spine head protrusions-a role for synaptopodin and intracellular calcium stores
inferredcites →https://doi.org/10.1371/journal.pgen.1005907openalex-snapshot
A Jacob/Nsmf Gene Knockout Results in Hippocampal Dysplasia and Impaired BDNF Signaling in Dendritogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0092349openalex-snapshot
Actin and Myosin-Dependent Localization of mRNA to Dendrites
inferredcites →https://doi.org/10.1371/journal.pone.0101770openalex-snapshot
α-Actinin-2 Mediates Spine Morphology and Assembly of the Post-Synaptic Density in Hippocampal Neurons
inferredcites →https://doi.org/10.1371/journal.pone.0119221openalex-snapshot
Optimal Cloning of PCR Fragments by Homologous Recombination in Escherichia coli
inferredcites →https://doi.org/10.1371/journal.pone.0148310openalex-snapshot
The Role of Synaptopodin in Membrane Protein Diffusion in the Dendritic Spine Neck
inferredcites →https://doi.org/10.1523/jneurosci.0381-14.2014openalex-snapshot
Synaptopodin Regulates Spine Plasticity: Mediation by Calcium Stores
inferredcites →https://doi.org/10.1523/jneurosci.2983-12.2013openalex-snapshot
Essential Role for Synaptopodin in Dendritic Spine Plasticity of the Developing Hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.5528-08.2009openalex-snapshot
Synaptopodin Regulates Plasticity of Dendritic Spines in Hippocampal Neurons
inferredcites →https://doi.org/10.3389/fnins.2015.00358openalex-snapshot
Diversifying the secretory routes in neurons
inferredcites →https://doi.org/10.7554/elife.39151openalex-snapshot
The fate of hippocampal synapses depends on the sequence of plasticity-inducing events
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41467-020-18889-5openalex-snapshot
Endoplasmic reticulum visits highly active spines and prevents runaway potentiation of synapses
inferred← citeshttps://doi.org/10.15252/embj.2018101183openalex-snapshot
F‐actin patches associated with glutamatergic synapses control positioning of dendritic lysosomes
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