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Axon degeneration: context defines distinct pathways

https://doi.org/10.1016/j.conb.2016.05.002
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2 of the 62 references listed on this page are in the Retraction Watch database as retracted (export 2026-10-21): 10.1038/nature07767 (notice 2023-12-18), 10.1074/jbc.m114.611574 (notice 2016-10-28).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/dbio.1994.1234openalex-snapshot
Neurites Can Remain Viable after Destruction of the Neuronal Soma by Programmed Cell Death (Apoptosis)
inferredcites →https://doi.org/10.1007/bf01195555openalex-snapshot
Prolonged survival of transected nerve fibres in C57BL/Ola mice is an intrinsic characteristic of the axon
inferredcites →https://doi.org/10.1016/0006-8993(89)91197-9openalex-snapshot
Death of sensory ganglion neurons after acute withdrawal of nerve growth factor in dissociated cell cultures
inferredcites →https://doi.org/10.1016/j.cell.2014.11.053openalex-snapshot
Pathological Axonal Death through a MAPK Cascade that Triggers a Local Energy Deficit
inferredcites →https://doi.org/10.1016/j.cell.2016.01.032openalex-snapshot
Axon Degeneration Gated by Retrograde Activation of Somatic Pro-apoptotic Signaling
inferredcites →https://doi.org/10.1016/j.celrep.2013.04.013openalex-snapshot
The Phr1 Ubiquitin Ligase Promotes Injury-Induced Axon Self-Destruction
inferredcites →https://doi.org/10.1016/j.celrep.2013.07.015openalex-snapshot
XIAP Regulates Caspase Activity in Degenerating Axons
inferredcites →https://doi.org/10.1016/j.celrep.2015.02.060openalex-snapshot
Absence of SARM1 Rescues Development and Survival of NMNAT2-Deficient Axons
inferredcites →https://doi.org/10.1016/j.celrep.2015.11.032openalex-snapshot
Wallerian Degeneration Is Executed by an NMN-SARM1-Dependent Late Ca2+ Influx but Only Modestly Influenced by Mitochondria
inferredcites →https://doi.org/10.1016/j.conb.2013.06.007openalex-snapshot
Neurite pruning and neuronal cell death: spatial regulation of shared destruction programs
inferredcites →https://doi.org/10.1016/j.nbd.2013.03.009openalex-snapshot
Calpains mediate axonal cytoskeleton disintegration during Wallerian degeneration
inferredcites →https://doi.org/10.1016/j.neuron.2006.07.014openalex-snapshot
Identification of E2/E3 Ubiquitinating Enzymes and Caspase Activity Regulating Drosophila Sensory Neuron Dendrite Pruning
inferredcites →https://doi.org/10.1016/j.neuron.2013.08.034openalex-snapshot
Regulation of Axon Degeneration after Injury and in Development by the Endogenous Calpain Inhibitor Calpastatin
inferredcites →https://doi.org/10.1016/j.neuron.2015.08.029openalex-snapshot
New Views on the Misconstrued: Executioner Caspases and Their Diverse Non-apoptotic Roles
inferredcites →https://doi.org/10.1016/j.neuron.2015.12.023openalex-snapshot
Axon Self-Destruction: New Links among SARM1, MAPKs, and NAD+ Metabolism
inferredcites →https://doi.org/10.1016/j.tcb.2014.04.003openalex-snapshot
Diverse cellular and molecular modes of axon degeneration
inferredcites →https://doi.org/10.1016/j.tibs.2011.08.009openalex-snapshot
BAX unleashed: the biochemical transformation of an inactive cytosolic monomer into a toxic mitochondrial pore
inferredcites →https://doi.org/10.1016/j.tins.2014.07.007openalex-snapshot
Preserve and protect: maintaining axons within functional circuits
inferredcites →https://doi.org/10.1016/s0896-6273(00)80173-7openalex-snapshot
BAX Is Required for Neuronal Death after Trophic Factor Deprivation and during Development
inferredcites →https://doi.org/10.1016/s0896-6273(03)00429-xopenalex-snapshot
Involvement of the Ubiquitin-Proteasome System in the Early Stages of Wallerian Degeneration
inferredcites →https://doi.org/10.1038/35037739openalex-snapshot
Apoptosis in the nervous system
inferredcites →https://doi.org/10.1038/cdd.2014.164openalex-snapshot
A rise in NAD precursor nicotinamide mononucleotide (NMN) after injury promotes axon degeneration
inferredcites →https://doi.org/10.1038/cdd.2014.47openalex-snapshot
Programmed cell death during neuronal development: the sympathetic neuron model
inferredcites →https://doi.org/10.1038/cr.2009.11openalex-snapshot
A retrograde apoptotic signal originating in NGF-deprived distal axons of rat sympathetic neurons in compartmented cultures
inferredcites →https://doi.org/10.1038/nature07767openalex-snapshot
RETRACTED ARTICLE: APP binds DR6 to trigger axon pruning and neuron death via distinct caspases
inferredcites →https://doi.org/10.1038/ncomms2910openalex-snapshot
Distinct pathways mediate axon degeneration during apoptosis and axon-specific pruning
inferredcites →https://doi.org/10.1038/nmeth777openalex-snapshot
A microfluidic culture platform for CNS axonal injury, regeneration and transport
inferredcites →https://doi.org/10.1038/nn.2290openalex-snapshot
A dual leucine kinase–dependent axon self-destruction program promotes Wallerian degeneration
inferredcites →https://doi.org/10.1038/nn770openalex-snapshot
Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene
inferredcites →https://doi.org/10.1038/nrn3680openalex-snapshot
Wallerian degeneration: an emerging axon death pathway linking injury and disease
inferredcites →https://doi.org/10.1038/sj.cdd.4401147openalex-snapshot
The proapoptotic proteins Bax and Bak are not involved in Wallerian degeneration
inferredcites →https://doi.org/10.1038/sj.cdd.4402024openalex-snapshot
Apoptosome dependent caspase-3 activation pathway is non-redundant and necessary for apoptosis in sympathetic neurons
inferredcites →https://doi.org/10.1073/pnas.1211074110openalex-snapshot
DLK initiates a transcriptional program that couples apoptotic and regenerative responses to axonal injury
inferredcites →https://doi.org/10.1073/pnas.1216204109openalex-snapshot
SCG10 is a JNK target in the axonal degeneration pathway
inferredcites →https://doi.org/10.1073/pnas.1508337112openalex-snapshot
Local axonal protection by WldS as revealed by conditional regulation of protein stability
inferredcites →https://doi.org/10.1073/pnas.74.10.4516openalex-snapshot
Local control of neurite development by nerve growth factor
inferredcites →https://doi.org/10.1074/jbc.m114.611574openalex-snapshot
Spy1 Protein Mediates Phosphorylation and Degradation of SCG10 Protein in Axonal Degeneration
inferredcites →https://doi.org/10.1083/jcb.200307130openalex-snapshot
Critical function of endogenous XIAP in regulating caspase activation during sympathetic neuronal apoptosis
inferredcites →https://doi.org/10.1083/jcb.200504028openalex-snapshot
A local mechanism mediates NAD-dependent protection of axon degeneration
inferredcites →https://doi.org/10.1083/jcb.200708086openalex-snapshot
Chromatin modification of Apaf-1 restricts the apoptotic pathway in mature neurons
inferredcites →https://doi.org/10.1083/jcb.201103153openalex-snapshot
DLK induces developmental neuronal degeneration via selective regulation of proapoptotic JNK activity
inferredcites →https://doi.org/10.1083/jcb.201108111openalex-snapshot
Axon degeneration: Molecular mechanisms of a self-destruction pathway
inferredcites →https://doi.org/10.1111/j.1471-4159.2005.03676.xopenalex-snapshot
The BH3‐only protein Puma is both necessary and sufficient for neuronal apoptosis induced by DNA damage in sympathetic neurons
inferredcites →https://doi.org/10.1126/science.1098014openalex-snapshot
Increased Nuclear NAD Biosynthesis and SIRT1 Activation Prevent Axonal Degeneration
inferredcites →https://doi.org/10.1126/science.1223899openalex-snapshot
dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway
inferredcites →https://doi.org/10.1126/science.1258366openalex-snapshot
SARM1 activation triggers axon degeneration locally via NAD + destruction
inferredcites →https://doi.org/10.1128/mcb.21.14.4713-4724.2001openalex-snapshot
The MLK Family Mediates c-Jun N-Terminal Kinase Activation in Neuronal Apoptosis
inferredcites →https://doi.org/10.1146/annurev-cellbio-100913-013038openalex-snapshot
Sculpting Neural Circuits by Axon and Dendrite Pruning
inferredcites →https://doi.org/10.1146/annurev.neuro.28.061604.135632openalex-snapshot
AXON RETRACTION AND DEGENERATION IN DEVELOPMENT AND DISEASE
inferredcites →https://doi.org/10.1146/annurev.neuro.28.061604.135659openalex-snapshot
GROWTH AND SURVIVAL SIGNALS CONTROLLING SYMPATHETIC NERVOUS SYSTEM DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.neuro.29.051605.112800openalex-snapshot
ADAPTIVE ROLES OF PROGRAMMED CELL DEATH DURING NERVOUS SYSTEM DEVELOPMENT
inferredcites →https://doi.org/10.1371/journal.pbio.1000300openalex-snapshot
Endogenous Nmnat2 Is an Essential Survival Factor for Maintenance of Healthy Axons
inferredcites →https://doi.org/10.1371/journal.pbio.1001440openalex-snapshot
The Highwire Ubiquitin Ligase Promotes Axonal Degeneration by Tuning Levels of Nmnat Protein
inferredcites →https://doi.org/10.1523/jneurosci.0922-10.2010openalex-snapshot
Axonal Degeneration Is Regulated by the Apoptotic Machinery or a NAD + -Sensitive Pathway in Insects and Mammals
inferredcites →https://doi.org/10.1523/jneurosci.1197-13.2013openalex-snapshot
Sarm1-Mediated Axon Degeneration Requires Both SAM and TIR Interactions
inferredcites →https://doi.org/10.1523/jneurosci.2039-12.2012openalex-snapshot
Spatially Coordinated Kinase Signaling Regulates Local Axon Degeneration
inferredcites →https://doi.org/10.1523/jneurosci.2320-06.2006openalex-snapshot
Stimulation of Nicotinamide Adenine Dinucleotide Biosynthetic Pathways Delays Axonal Degeneration after Axotomy
inferredcites →https://doi.org/10.1523/jneurosci.2484-15.2015openalex-snapshot
Live Imaging of Calcium Dynamics during Axon Degeneration Reveals Two Functionally Distinct Phases of Calcium Influx
inferredcites →https://doi.org/10.1523/jneurosci.2939-10.2010openalex-snapshot
Amyloid Precursor Protein Cleavage-Dependent and -Independent Axonal Degeneration Programs Share a Common Nicotinamide Mononucleotide Adenylyltransferase 1-Sensitive Pathway
inferredcites →https://doi.org/10.1523/jneurosci.3012-12.2012openalex-snapshot
A Caspase Cascade Regulating Developmental Axon Degeneration
inferredcites →https://doi.org/10.1523/jneurosci.3347-10.2011openalex-snapshot
Sensory Neuropathy Attributable to Loss of Bcl-w
inferredcites →https://doi.org/10.1523/jneurosci.3522-13.2014openalex-snapshot
Genetic Analysis Reveals that Amyloid Precursor Protein and Death Receptor 6 Function in the Same Pathway to Control Axonal Pruning Independent of β-Secretase

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/9781119432463.ch11openalex-snapshot
Molecular Mechanisms Regulating Wallerian Degeneration
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A multi‐layered nerve guidance conduit design adapted to facilitate surgical implantation
inferred← citeshttps://doi.org/10.1007/978-1-0716-0585-1_6openalex-snapshot
Planning and Analysis of Axon Degeneration Screening Experiments
inferred← citeshttps://doi.org/10.1007/978-1-0716-0585-1_7openalex-snapshot
A Microfluidic Culture Platform to Assess Axon Degeneration
inferred← citeshttps://doi.org/10.1007/s00018-018-2812-1openalex-snapshot
Neuronal autophagy and axon degeneration
inferred← citeshttps://doi.org/10.1007/s10072-021-05448-zopenalex-snapshot
Progression of optic atrophy in traumatic optic neuropathy: retrograde neuronal degeneration in humans
inferred← citeshttps://doi.org/10.1007/s12035-023-03494-6openalex-snapshot
Syntaphilin Inactivation Can Enhance Axonal Mitochondrial Transport to Improve Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/s12035-025-04835-3openalex-snapshot
SARM1: The Checkpoint of Axonal Degeneration in the Nervous System Disorders
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Neuropathy target esterase (NTE/PNPLA6) and organophosphorus compound-induced delayed neurotoxicity (OPIDN)
inferred← citeshttps://doi.org/10.1016/j.bbadis.2021.166117openalex-snapshot
Mechanisms and repair strategies for white matter degeneration in CNS injury and diseases
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.05.060openalex-snapshot
Genetic inhibition of CRMP2 phosphorylation delays Wallerian degeneration after optic nerve injury
inferred← citeshttps://doi.org/10.1016/j.biocel.2022.106264openalex-snapshot
Pivotal roles for membrane phospholipids in axonal degeneration
inferred← citeshttps://doi.org/10.1016/j.cogsys.2024.101260openalex-snapshot
Exploring biological challenges in building a thinking machine
inferred← citeshttps://doi.org/10.1016/j.conb.2018.07.002openalex-snapshot
An axonal stress response pathway: degenerative and regenerative signaling by DLK
inferred← citeshttps://doi.org/10.1016/j.cub.2019.12.065openalex-snapshot
Bidirectional Regulation of Sleep and Synapse Pruning after Neural Injury
inferred← citeshttps://doi.org/10.1016/j.exer.2018.03.007openalex-snapshot
Role of SARM1 and DR6 in retinal ganglion cell axonal and somal degeneration following axonal injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.113167openalex-snapshot
Intravitreal application of AAV-BDNF or mutant AAV-CRMP2 protects retinal ganglion cells and stabilizes axons and myelin after partial optic nerve injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114195openalex-snapshot
Presymptomatic macrophage targeting has a long-lasting therapeutic effect on treatment termination in a mouse model of Charcot-Marie-Tooth 1
inferred← citeshttps://doi.org/10.1016/j.fct.2020.111772openalex-snapshot
Chronic methylmercury exposure causes spinal cord impairment: Proteomic modulation and oxidative stress
inferred← citeshttps://doi.org/10.1016/j.ghres.2025.100005openalex-snapshot
Axonal spheroids are regulated by Schwann cells after peripheral nerve injury
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101647openalex-snapshot
FK506-binding protein-like and FK506-binding protein 8 regulate dual leucine zipper kinase degradation and neuronal responses to axon injury
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.06.030openalex-snapshot
Structural Evidence for an Octameric Ring Arrangement of SARM1
inferred← citeshttps://doi.org/10.1016/j.nbd.2019.104672openalex-snapshot
Axonal degeneration in an in vitro model of ischemic white matter injury
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.135595openalex-snapshot
New evidence for secondary axonal degeneration in demyelinating neuropathies
inferred← citeshttps://doi.org/10.1016/j.neures.2018.07.001openalex-snapshot
Metabolic aspects of neuronal degeneration: From a NAD+ point of view
inferred← citeshttps://doi.org/10.1016/j.neures.2018.07.008openalex-snapshot
Regulation of neuronal/axonal degeneration by ZNRF1 ubiquitin ligase
inferred← citeshttps://doi.org/10.1016/j.neures.2018.11.007openalex-snapshot
Apoptosis versus axon pruning: Molecular intersection of two distinct pathways for axon degeneration
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2017.11.052openalex-snapshot
Caspase-6 is a Dispensable Enabler of Adult Mammalian Axonal Degeneration
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.09.007openalex-snapshot
Caspases orchestrate microglia instrumental functions
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2019.07.002openalex-snapshot
Axon injury signaling and compartmentalized injury response in glaucoma
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.11.037openalex-snapshot
Physiological functions of non-apoptotic caspase activity in the nervous system
inferred← citeshttps://doi.org/10.1016/j.virol.2018.07.011openalex-snapshot
Strength in diversity: Understanding the pathways to herpes simplex virus reactivation
inferred← citeshttps://doi.org/10.1038/cddis.2017.338openalex-snapshot
JUN is important for ocular hypertension-induced retinal ganglion cell degeneration
inferred← citeshttps://doi.org/10.1038/s41380-020-0698-4openalex-snapshot
Hippocampal TNF-death receptors, caspase cell death cascades, and IL-8 in alcohol use disorder
inferred← citeshttps://doi.org/10.1038/s41419-019-1727-6openalex-snapshot
Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy
inferred← citeshttps://doi.org/10.1038/s41419-020-03373-1openalex-snapshot
p53 is required for nuclear but not mitochondrial DNA damage-induced degeneration
inferred← citeshttps://doi.org/10.1038/s41573-023-00823-1openalex-snapshot
Targeting synapse function and loss for treatment of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1042/ns20160007openalex-snapshot
Retrograde apoptotic signaling by the p75 neurotrophin receptor
inferred← citeshttps://doi.org/10.1073/pnas.2203824119openalex-snapshot
Autophagy protein ULK1 interacts with and regulates SARM1 during axonal injury
inferred← citeshttps://doi.org/10.1080/01913123.2020.1853865openalex-snapshot
The osmotic demyelination syndrome: the resilience of thalamic neurons is verified with transmission electron microscopy
inferred← citeshttps://doi.org/10.1089/ars.2018.7522openalex-snapshot
Nitrite Protects Neurons Against Hypoxic Damage Through S -nitrosylation of Caspase-6
inferred← citeshttps://doi.org/10.1093/brain/awac079openalex-snapshot
A new form of axonal pathology in a spinal model of neuromyelitis optica
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000001528openalex-snapshot
Axon degeneration: mechanistic insights lead to therapeutic opportunities for the prevention and treatment of peripheral neuropathy
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000001705openalex-snapshot
Neuromas and postamputation pain
inferred← citeshttps://doi.org/10.1101/2020.04.16.044875openalex-snapshot
Neuronal hyperexcitability is a DLK-dependent trigger of HSV-1 reactivation that can be induced by IL-1
inferred← citeshttps://doi.org/10.1101/2020.04.30.066209openalex-snapshot
Connectomes across development reveal principles of brain maturation
inferred← citeshttps://doi.org/10.1101/2021.08.20.457064openalex-snapshot
FKBPL and FKBP8 regulate DLK degradation and neuronal responses to axon injury
inferred← citeshttps://doi.org/10.1101/2022.02.17.479688openalex-snapshot
Specific attenuation of purinergic signaling during bortezomib-induced peripheral neuropathy
inferred← citeshttps://doi.org/10.1101/2022.11.09.515778openalex-snapshot
An in vitro microfluidic culture device for peripheral neurotoxicity prediction at low concentration based on deep learning
inferred← citeshttps://doi.org/10.1111/acel.70301openalex-snapshot
APP Induces AICD ‐Mediated Autophagy‐Dependent Axon Degeneration
inferred← citeshttps://doi.org/10.1136/practneurol-2020-002911openalex-snapshot
Wallerian degeneration as a mimic of recurrence of myelitis
inferred← citeshttps://doi.org/10.1139/bcb-2023-0224openalex-snapshot
Identification of critical mitochondrial hub gene for facial nerve regeneration
inferred← citeshttps://doi.org/10.1172/jci.insight.129920openalex-snapshot
Vincristine and bortezomib use distinct upstream mechanisms to activate a common SARM1-dependent axon degeneration program
inferred← citeshttps://doi.org/10.1242/dev.163592openalex-snapshot
JNK signaling coordinates with ecdysone signaling to promote dendrite pruning ofDrosophilasensory neurons
inferred← citeshttps://doi.org/10.14245/ns.2244976.488openalex-snapshot
Different Ways to Die: Cell Death Pathways and Their Association With Spinal Cord Injury
inferred← citeshttps://doi.org/10.1523/eneuro.0277-18.2018openalex-snapshot
NMNAT Proteins that Limit Wallerian Degeneration Also Regulate Critical Period Plasticity in the Visual Cortex
inferred← citeshttps://doi.org/10.1523/eneuro.0479-19.2020openalex-snapshot
Collapsin Response Mediator Protein 4 (CRMP4) Facilitates Wallerian Degeneration and Axon Regeneration following Sciatic Nerve Injury
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Degeneration of Injured Axons and Dendrites Requires Restraint of a Protective JNK Signaling Pathway by the Transmembrane Protein Raw
inferred← citeshttps://doi.org/10.1523/jneurosci.0881-18.2019openalex-snapshot
Axonal Degeneration Is Mediated by Necroptosis Activation
inferred← citeshttps://doi.org/10.1523/jneurosci.2251-20.2021openalex-snapshot
The Ubiquitinated Axon: Local Control of Axon Development and Function by Ubiquitin
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An in vitro microfluidic culture device for peripheral neurotoxicity prediction at low concentrations based on deep learning
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Glia maturation factor-β: a potential therapeutic target in neurodegeneration and neuroinflammation
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Proposed Mechanisms of Photobiomodulation (PBM) Mediated via the Stimulation of Mitochondrial Activity in Peripheral Nerve Injuries
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Electrical welding technology in restoring the integrity of the injured peripheral nerve: review of literature and own experimental research
inferred← citeshttps://doi.org/10.3389/fmolb.2021.703532openalex-snapshot
A Novel NAD Signaling Mechanism in Axon Degeneration and its Relationship to Innate Immunity
inferred← citeshttps://doi.org/10.3389/fnagi.2021.650038openalex-snapshot
Mitochondrial Behavior in Axon Degeneration and Regeneration
inferred← citeshttps://doi.org/10.3389/fncel.2019.00419openalex-snapshot
Going Too Far Is the Same as Falling Short†: Kinesin-3 Family Members in Hereditary Spastic Paraplegia
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JNK Signaling Pathway Involvement in Spinal Cord Neuron Development and Death
inferred← citeshttps://doi.org/10.3390/ijms19071970openalex-snapshot
Schisandra chinensis Fructus and Its Active Ingredients as Promising Resources for the Treatment of Neurological Diseases
inferred← citeshttps://doi.org/10.3390/ijms22063202openalex-snapshot
Involvement of Bcl-xL in Neuronal Function and Development
inferred← citeshttps://doi.org/10.3390/ijms23073734openalex-snapshot
Specific Attenuation of Purinergic Signaling during Bortezomib-Induced Peripheral Neuropathy In Vitro
inferred← citeshttps://doi.org/10.3390/ijms27167301openalex-snapshot
Peripheral Neuropathy in Metabolic Stress
inferred← citeshttps://doi.org/10.3390/jdb6040024openalex-snapshot
The Role of Apoptotic Signaling in Axon Guidance
inferred← citeshttps://doi.org/10.4103/1673-5374.253520openalex-snapshot
Compartmentalized necroptosis activation in excitotoxicity-induced axonal degeneration: a novel mechanism implicated in neurodegenerative disease pathology
inferred← citeshttps://doi.org/10.4103/1673-5374.264463openalex-snapshot
Claudin-15 overexpression inhibits proliferation and promotes apoptosis of Schwann cells in vitro
inferred← citeshttps://doi.org/10.4103/1673-5374.286946openalex-snapshot
Oxidative stress battles neuronal Bcl-xL in a fight to the death
inferred← citeshttps://doi.org/10.60533/boss-2020-fqi7openalex-snapshot
Connectomes across development reveal principles of brain maturation
inferred← citeshttps://doi.org/10.70675/8c95aa8czda0ez4266z9deez38f393515833openalex-snapshot
A functionalizable nerve graft design based on an organized electrospun silk fibroin nanofiber biomaterial for peripheral nerve regeneration
inferred← citeshttps://doi.org/10.7554/elife.101093openalex-snapshot
Addressing burning questions on axon regeneration
inferred← citeshttps://doi.org/10.7554/elife.58037openalex-snapshot
Neuronal hyperexcitability is a DLK-dependent trigger of herpes simplex virus reactivation that can be induced by IL-1
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