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Calcium Plays an Essential Role in Early-Stage Dendrite Injury Detection
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-030-12457-1_22openalex-extracted
Calcium Signaling and Gene Expression
inferredcites →https://doi.org/10.1007/s13311-015-0415-1openalex-extracted
Electrical Stimulation to Enhance Axon Regeneration After Peripheral Nerve Injuries in Animal Models and Humans
inferredcites →https://doi.org/10.1016/j.ceca.2017.08.004openalex-extracted
Calcium signaling at the endoplasmic reticulum: fine-tuning stress responses
inferredcites →https://doi.org/10.1016/j.cell.2009.06.023openalex-extracted
The DLK-1 Kinase Promotes mRNA Stability and Local Translation in C. elegans Synapses and Axon Regeneration
inferredcites →https://doi.org/10.1016/j.cell.2013.10.004openalex-extracted
Injury-Induced HDAC5 Nuclear Export Is Essential for Axon Regeneration
inferredcites →https://doi.org/10.1016/j.celrep.2013.12.022openalex-extracted
Dendrite Injury Triggers DLK-Independent Regeneration
inferredcites →https://doi.org/10.1016/j.conb.2019.03.006openalex-extracted
Mechanisms of injury-induced axon degeneration
inferredcites →https://doi.org/10.1016/j.cub.2010.05.055openalex-extracted
Electrical Activity Suppresses Axon Growth through Cav1.2 Channels in Adult Primary Sensory Neurons
inferredcites →https://doi.org/10.1016/j.devcel.2023.03.007openalex-extracted
Gliotransmission and adenosine signaling promote axon regeneration
inferredcites →https://doi.org/10.1016/j.expneurol.2009.05.004openalex-extracted
Local calcium-dependent mechanisms determine whether a cut axonal end assembles a retarded endbulb or competent growth cone
inferredcites →https://doi.org/10.1016/j.gde.2017.01.009openalex-extracted
Intrinsic mechanisms for axon regeneration: insights from injured axons in Drosophila
inferredcites →https://doi.org/10.1016/j.inat.2021.101117openalex-extracted
Application of electrical stimulation for peripheral nerve regeneration: Stimulation parameters and future horizons
inferredcites →https://doi.org/10.1016/j.modgep.2006.03.007openalex-extracted
Drosophila protein kinase D is broadly expressed and a fraction localizes to the Golgi compartment
inferredcites →https://doi.org/10.1016/j.nbd.2015.02.014openalex-extracted
Cytoskeletal disruption activates the DLK/JNK pathway, which promotes axonal regeneration and mimics a preconditioning injury
inferredcites →https://doi.org/10.1016/j.neuron.2012.04.028openalex-extracted
Dual Leucine Zipper Kinase Is Required for Retrograde Injury Signaling and Axonal Regeneration
inferredcites →https://doi.org/10.1016/s0140-6736(10)61156-7openalex-extracted
Amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/nrn3609openalex-extracted
Axon–soma communication in neuronal injury
inferredcites →https://doi.org/10.1038/s41580-018-0052-8openalex-extracted
The machineries, regulation and cellular functions of mitochondrial calcium
inferredcites →https://doi.org/10.1038/s41583-018-0001-8openalex-extracted
Intrinsic mechanisms of neuronal axon regeneration
inferredcites →https://doi.org/10.1038/s41592-019-0435-6openalex-extracted
High-performance calcium sensors for imaging activity in neuronal populations and microcompartments
inferredcites →https://doi.org/10.1073/pnas.1523645113openalex-extracted
Promoting axon regeneration in the adult CNS by modulation of the melanopsin/GPCR signaling
inferredcites →https://doi.org/10.1073/pnas.2001563117openalex-extracted
Nasally delivered VEGFD mimetics mitigate stroke-induced dendrite loss and brain damage
inferredcites →https://doi.org/10.1074/jbc.273.42.27662openalex-extracted
Identification of in Vivo Phosphorylation Sites Required for Protein Kinase D Activation
inferredcites →https://doi.org/10.1080/01677060600569713openalex-extracted
TARGETED EXPRESSION OF IP3SPONGE AND IP3 DS RNA IMPAIRES SUGAR TASTE SENSATION INDROSOPHILA
inferredcites →https://doi.org/10.1083/jcb.201006039openalex-extracted
Protein turnover of the Wallenda/DLK kinase regulates a retrograde response to axonal injury
inferredcites →https://doi.org/10.1091/mbc.e08-09-0957openalex-extracted
Protein Kinase D Controls the Integrity of Golgi Apparatus and the Maintenance of Dendritic Arborization in Hippocampal Neurons
inferredcites →https://doi.org/10.1091/mbc.e09-11-0967openalex-extracted
Global Up-Regulation of Microtubule Dynamics and Polarity Reversal during Regeneration of an Axon from a Dendrite
inferredcites →https://doi.org/10.1091/mbc.e16-05-0287openalex-extracted
Spastin, atlastin, and ER relocalization are involved in axon but not dendrite regeneration
inferredcites →https://doi.org/10.1091/mbc.e20-04-0237-topenalex-extracted
Kinetochore proteins suppress neuronal microtubule dynamics and promote dendrite regeneration
inferredcites →https://doi.org/10.1093/bioinformatics/btr390openalex-extracted
Simple Neurite Tracer: open source software for reconstruction, visualization and analysis of neuronal processes
inferredcites →https://doi.org/10.1096/fj.04-1805fjeopenalex-extracted
Acute physiological response of mammalian central neurons to axotomy: ionic regulation and electrical activity
inferredcites →https://doi.org/10.1097/gox.0000000000004115openalex-extracted
Role of Electrical Stimulation in Peripheral Nerve Regeneration: A Systematic Review
inferredcites →https://doi.org/10.1101/gad.193243.112openalex-extracted
Regeneration of Drosophila sensory neuron axons and dendrites is regulated by the Akt pathway involving Pten and microRNA bantam
inferredcites →https://doi.org/10.1101/gad.282848.116openalex-extracted
In vivo dendrite regeneration after injury is different from dendrite development
inferredcites →https://doi.org/10.1101/gad.308270.117openalex-extracted
Dendrite regeneration of adult Drosophila sensory neurons diminishes with aging and is inhibited by epidermal-derived matrix metalloproteinase 2
inferredcites →https://doi.org/10.1111/j.1460-9568.1993.tb00531.xopenalex-extracted
Spatiotemporal Distribution of Ca2+ Following Axotomy and Throughout the Recovery Process of Cultured Aplysia Neurons
inferredcites →https://doi.org/10.1113/jphysiol.2009.168930openalex-extracted
Inositol‐1,4,5‐trisphosphate receptor‐mediated Ca2+ waves in pyramidal neuron dendrites propagate through hot spots and cold spots
inferredcites →https://doi.org/10.1126/science.1161566openalex-extracted
Promoting Axon Regeneration in the Adult CNS by Modulation of the PTEN/mTOR Pathway
inferredcites →https://doi.org/10.1126/science.1165527openalex-extracted
Axon Regeneration Requires a Conserved MAP Kinase Pathway
inferredcites →https://doi.org/10.1126/science.3715470openalex-extracted
Suppression of Neurite Elongation and Growth Cone Motility by Electrical Activity
inferredcites →https://doi.org/10.1152/jn.1993.69.1.151openalex-extracted
Alterations in membrane potential after axotomy at different distances from the soma of an identified neuron and the effect of depolarization on neurite outgrowth and calcium channel expression
inferredcites →https://doi.org/10.1152/jn.1995.74.6.2625openalex-extracted
Axotomy induces a transient and localized elevation of the free intracellular calcium concentration to the millimolar range
inferredcites →https://doi.org/10.1186/1471-213x-7-74openalex-extracted
Protein Kinase D regulates several aspects of development in Drosophila melanogaster
inferredcites →https://doi.org/10.1186/s13064-017-0092-3openalex-extracted
Two Drosophila model neurons can regenerate axons from the stump or from a converted dendrite, with feedback between the two sites
inferredcites →https://doi.org/10.1242/dev.129.12.2867openalex-extracted
Tiling of theDrosophilaepidermis by multidendritic sensory neurons
inferredcites →https://doi.org/10.1523/jneurosci.10-11-03564.1990openalex-extracted
The distribution of free calcium in transected spinal axons and its modulation by applied electrical fields
inferredcites →https://doi.org/10.1523/jneurosci.1291-08.2008openalex-extracted
Both the Establishment and Maintenance of Neuronal Polarity Require the Activity of Protein Kinase D in the Golgi Apparatus
inferredcites →https://doi.org/10.1523/jneurosci.1879-08.2008openalex-extracted
Protein Kinase D Regulates Trafficking of Dendritic Membrane Proteins in Developing Neurons
inferredcites →https://doi.org/10.1523/jneurosci.21-05-01523.2001openalex-extracted
Altered Electrical Properties inDrosophilaNeurons Developing without Synaptic Transmission
inferredcites →https://doi.org/10.1523/jneurosci.21-06-01923.2001openalex-extracted
Traumatic Axonal Injury Induces Calcium Influx Modulated by Tetrodotoxin-Sensitive Sodium Channels
inferredcites →https://doi.org/10.1523/jneurosci.4238-13.2014openalex-extracted
Neuronal Regeneration inC. elegansRequires Subcellular Calcium Release by Ryanodine Receptor Channels and Can Be Enhanced by Optogenetic Stimulation
inferredcites →https://doi.org/10.1523/jneurosci.4295-06.2007openalex-extracted
Extensive Turnover of Dendritic Spines and Vascular Remodeling in Cortical Tissues Recovering from Stroke
inferredcites →https://doi.org/10.1523/jneurosci.5464-09.2010openalex-extracted
Calcium and Cyclic AMP Promote Axonal Regeneration in Caenorhabditis elegans and Require DLK-1 Kinase
inferredcites →https://doi.org/10.3389/fcell.2020.00736openalex-extracted
Functional Electrical Stimulation and the Modulation of the Axon Regeneration Program
inferredcites →https://doi.org/10.3389/fncel.2020.613320openalex-extracted
Scrap and Build for Functional Neural Circuits: Spatiotemporal Regulation of Dendrite Degeneration and Regeneration in Neural Development and Disease
inferredcites →https://doi.org/10.4103/1673-5374.255957openalex-extracted
Remodeling dendritic spines for treatment of traumatic brain injury
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