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Comparative Proteomic Analysis of Differentially Expressed Proteins between Peripheral Sensory and Motor Nerves
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.1929.02710220063037openalex-snapshot
Degeneration and Regeneration of the Nervous System.
inferredcites →https://doi.org/10.1002/(sici)1096-9896(199909)189:1<4::aid-path332>3.0.co;2-popenalex-snapshot
The role of CD146 (Mel-CAM) in biology and pathology
inferredcites →https://doi.org/10.1002/glia.20340openalex-snapshot
Schwann cells genetically engineered to express PSA show enhanced migratory potential without impairment of their myelinating ability in vitro
inferredcites →https://doi.org/10.1002/jnr.20146openalex-snapshot
Reexpression of vimentin in differentiated neuroblastoma cells enhances elongation of axonal neurites
inferredcites →https://doi.org/10.1002/pmic.200600422openalex-snapshot
Protein labeling by iTRAQ: A new tool for quantitative mass spectrometry in proteome research
inferredcites →https://doi.org/10.1007/978-1-4419-1170-4_10openalex-snapshot
Signaling Pathways Involved in NCAM-Induced Neurite Outgrowth
inferredcites →https://doi.org/10.1007/978-1-4419-1170-4_16openalex-snapshot
Role of NCAM in Spine Dynamics and Synaptogenesis
inferredcites →https://doi.org/10.1007/978-1-4684-5754-4_32openalex-snapshot
Calretinin and Other CaBPs in the Nervous System
inferredcites →https://doi.org/10.1007/s00702-010-0403-xopenalex-snapshot
Proteome analysis of lumbar spinal cord from rats submitted to peripheral lesion during neonatal period
inferredcites →https://doi.org/10.1016/0014-5793(91)80915-popenalex-snapshot
Molecular cloning of cDNA encoding the rat neural cell adhesion molecule L1 Two L1 isoforms in the cytoplasmic region are produced by differential splicing
inferredcites →https://doi.org/10.1016/0092-8674(90)90662-xopenalex-snapshot
CNS stem cells express a new class of intermediate filament protein
inferredcites →https://doi.org/10.1016/0092-8674(92)90121-ropenalex-snapshot
F-spondin: A gene expressed at high levels in the floor plate encodes a secreted protein that promotes neural cell adhesion and neurite extension
inferredcites →https://doi.org/10.1016/0301-0082(89)90036-1openalex-snapshot
Nerve regeneration through artificial tubular implants
inferredcites →https://doi.org/10.1016/0306-4522(89)90434-xopenalex-snapshot
Two calcium-binding proteins mark many chick sensory neurons
inferredcites →https://doi.org/10.1016/0736-5748(93)90003-vopenalex-snapshot
Peripheral nerve regeneration: Role of growth factors and their receptors
inferredcites →https://doi.org/10.1016/0955-0674(94)90113-9openalex-snapshot
Neurofilament function and dysfunction: involvement in axonal growth and neuronal disease
inferredcites →https://doi.org/10.1016/j.brainres.2006.12.053openalex-snapshot
Differential RIP antigen (CNPase) expression in peripheral ensheathing glia
inferredcites →https://doi.org/10.1016/j.expneurol.2009.05.037openalex-snapshot
The nerve regenerative microenvironment: Early behavior and partnership of axons and Schwann cells
inferredcites →https://doi.org/10.1016/j.neuron.2005.01.023openalex-snapshot
Vimentin-Dependent Spatial Translocation of an Activated MAP Kinase in Injured Nerve
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.06.060openalex-snapshot
Differentially expressed genes in the rat cochlear nucleus
inferredcites →https://doi.org/10.1016/j.neuroscience.2008.02.017openalex-snapshot
Different protein profiles in inferior colliculus and cerebellum: A comparative proteomic study
inferredcites →https://doi.org/10.1016/s0025-6196(12)60711-3openalex-snapshot
Wound Healing: Biochemical and Clinical Aspects
inferredcites →https://doi.org/10.1016/s0301-0082(00)00045-9openalex-snapshot
Role of integrins in the peripheral nervous system
inferredcites →https://doi.org/10.1016/s0896-6273(00)00033-7openalex-snapshot
Analysis of the L1-Deficient Mouse Phenotype Reveals Cross-Talk between Sema3A and L1 Signaling Pathways in Axonal Guidance
inferredcites →https://doi.org/10.1016/s0896-6273(02)00617-7openalex-snapshot
Fibrin Inhibits Peripheral Nerve Remyelination by Regulating Schwann Cell Differentiation
inferredcites →https://doi.org/10.1021/pr0503681openalex-snapshot
Characterization of the Mouse Brain Proteome Using Global Proteomic Analysis Complemented with Cysteinyl-Peptide Enrichment
inferredcites →https://doi.org/10.1021/pr060237fopenalex-snapshot
Focused Proteomics in Post-Mortem Human Spinal Cord
inferredcites →https://doi.org/10.1021/pr8010364openalex-snapshot
Comparative Proteomic Profiling of Membrane Proteins in Rat Cerebellum, Spinal Cord, and Sciatic Nerve
inferredcites →https://doi.org/10.1038/347762a0openalex-snapshot
Proliferation and differentiation of neuronal stem cells regulated by nerve growth factor
inferredcites →https://doi.org/10.1038/379451a0openalex-snapshot
Calcium-dependent interaction of N-type calcium channels with the synaptic core complex
inferredcites →https://doi.org/10.1038/ng1197-346openalex-snapshot
Disruption of the mouse L1 gene leads to malformations of the nervous system
inferredcites →https://doi.org/10.1046/j.1471-4159.1996.66062338.xopenalex-snapshot
A Nonneuronal Isoform of Cell Adhesion Molecule L1: Tissue‐Specific Expression and Functional Analysis
inferredcites →https://doi.org/10.1046/j.1523-1747.2003.12534.xopenalex-snapshot
Splice Site and Deletion Mutations in Keratin (KRT1 and KRT10) Genes: Unusual Phenotypic Alterations in Scandinavian Patients with Epidermolytic Hyperkeratosis
inferredcites →https://doi.org/10.1073/pnas.0602332103openalex-snapshot
Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells
inferredcites →https://doi.org/10.1073/pnas.0706211105openalex-snapshot
Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels
inferredcites →https://doi.org/10.1073/pnas.0711978105openalex-snapshot
Deletion of the mouse RegIIIβ (Reg2) gene disrupts ciliary neurotrophic factor signaling and delays myelination of mouse cranial motor neurons
inferredcites →https://doi.org/10.1073/pnas.1533187100openalex-snapshot
Axonal plasticity and functional recovery after spinal cord injury in mice deficient in both glial fibrillary acidic protein and vimentin genes
inferredcites →https://doi.org/10.1073/pnas.90.18.8514openalex-snapshot
Genomic organization of the melanoma-associated glycoprotein MUC18: implications for the evolution of the immunoglobulin domains.
inferredcites →https://doi.org/10.1073/pnas.94.3.997openalex-snapshot
Binding of the synaptic vesicle v-SNARE, synaptotagmin, to the plasma membrane t-SNARE, SNAP-25, can explain docked vesicles at neurotoxin-treated synapses
inferredcites →https://doi.org/10.1073/pnas.96.1.248openalex-snapshot
The voltage sensitive Lc-type Ca 2+ channel is functionally coupled to the exocytotic machinery
inferredcites →https://doi.org/10.1074/jbc.271.12.6567openalex-snapshot
Interaction of SNARE Complexes with P/Q-type Calcium Channels in Rat Cerebellar Synaptosomes
inferredcites →https://doi.org/10.1074/jbc.m305387200openalex-snapshot
Implications of Nectin-like Molecule-2/IGSF4/RA175/SgIGSF/TSLC1/SynCAM1 in Cell-Cell Adhesion and Transmembrane Protein Localization in Epithelial Cells
inferredcites →https://doi.org/10.1074/jbc.m400560200openalex-snapshot
Ectodomain Shedding of the Neural Recognition Molecule CHL1 by the Metalloprotease-disintegrin ADAM8 Promotes Neurite Outgrowth and Suppresses Neuronal Cell Death
inferredcites →https://doi.org/10.1074/mcp.m900243-mcp200openalex-snapshot
Quantitative Proteomics Analysis of Chondrogenic Differentiation of C3H10T1/2 Mesenchymal Stem Cells by iTRAQ Labeling Coupled with On-line Two-dimensional LC/MS/MS
inferredcites →https://doi.org/10.1083/jcb.146.5.1173openalex-snapshot
Heterophilic Binding of L1 on Unmyelinated Sensory Axons Mediates Schwann Cell Adhesion and Is Required for Axonal Survival
inferredcites →https://doi.org/10.1083/jcb.200109021openalex-snapshot
Conditional disruption of β1 integrin in Schwann cells impedes interactions with axons
inferredcites →https://doi.org/10.1083/jcb.200603161openalex-snapshot
New consensus nomenclature for mammalian keratins
inferredcites →https://doi.org/10.1093/brain/awl284openalex-snapshot
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton
inferredcites →https://doi.org/10.1093/brain/awm049openalex-snapshot
Adeno-associated virus-mediated L1 expression promotes functional recovery after spinal cord injury
inferredcites →https://doi.org/10.1093/brain/awn039openalex-snapshot
Intrinsic neuronal properties control selective targeting of regenerating motoneurons
inferredcites →https://doi.org/10.1093/hmg/3.10.1757openalex-snapshot
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1093/hmg/ddp562openalex-snapshot
Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy
inferredcites →https://doi.org/10.1097/00001756-199709290-00030openalex-snapshot
Enhancement of neurite outgrowth by the soluble form of human L1 (neural cell adhesion molecule)
inferredcites →https://doi.org/10.1097/00019052-199410000-00009openalex-snapshot
Peripheral nerve injury
inferredcites →https://doi.org/10.1111/j.1460-9568.1992.tb00171.xopenalex-snapshot
The L2/HNK‐1 Carbohydrate Epitope is Involved in the Preferential Outgrowth of Motor Neurons on Ventral Roots and Motor Nerves
inferredcites →https://doi.org/10.1113/jphysiol.1904.sp001042openalex-snapshot
The union of different kinds of nerve fibres
inferredcites →https://doi.org/10.1126/science.1072356openalex-snapshot
SynCAM, a Synaptic Adhesion Molecule That Drives Synapse Assembly
inferredcites →https://doi.org/10.1126/science.2830669openalex-snapshot
A Spatial-Temporal Model of Cell Activation
inferredcites →https://doi.org/10.1146/annurev.ne.13.030190.000355openalex-snapshot
Peripheral Nerve Regeneration
inferredcites →https://doi.org/10.1146/annurev.ne.14.030191.002531openalex-snapshot
Extracellular Matrix Molecules And Their Receptors: Functions In Neural Development
inferredcites →https://doi.org/10.1152/jn.00226.2007openalex-snapshot
Differential Effects of SNAP-25 Deletion on Ca2+-Dependent and Ca2+-Independent Neurotransmission
inferredcites →https://doi.org/10.1242/dev.112.1.69openalex-snapshot
Analysis of high PSA N-CAM expression during mammalian spinal cord and peripheral nervous system development
inferredcites →https://doi.org/10.1371/journal.pone.0012311openalex-snapshot
The Pancreatic and Duodenal Homeobox Protein PDX-1 Regulates the Ductal Specific Keratin 19 through the Degradation of MEIS1 and DNA Binding
inferredcites →https://doi.org/10.1523/jneurosci.08-03-01026.1988openalex-snapshot
Preferential reinnervation of motor nerves by regenerating motor axons
inferredcites →https://doi.org/10.1523/jneurosci.13-06-02730.1993openalex-snapshot
Motor axons preferentially reinnervate motor pathways
inferredcites →https://doi.org/10.1523/jneurosci.14-11-07180.1994openalex-snapshot
The L2/HNK-1 carbohydrate is preferentially expressed by previously motor axon-associated Schwann cells in reinnervated peripheral nerves
inferredcites →https://doi.org/10.1523/jneurosci.16-18-05698.1996openalex-snapshot
Reinnervation Accuracy of the Rat Femoral Nerve by Motor and Sensory Neurons
inferredcites →https://doi.org/10.1523/jneurosci.1620-06.2006openalex-snapshot
Schwann Cells Express Motor and Sensory Phenotypes That Regulate Axon Regeneration
inferredcites →https://doi.org/10.1523/jneurosci.18-21-08674.1998openalex-snapshot
Contributions of Pathway and Neuron to Preferential Motor Reinnervation
inferredcites →https://doi.org/10.1523/jneurosci.20-11-04177.2000openalex-snapshot
A MAP Kinase-Signaling Pathway Mediates Neurite Outgrowth on L1 and Requires Src-Dependent Endocytosis
inferredcites →https://doi.org/10.1523/jneurosci.22-12-04918.2002openalex-snapshot
The Neural Cell Adhesion Molecule L1 Potentiates Integrin-Dependent Cell Migration to Extracellular Matrix Proteins
inferredcites →https://doi.org/10.1523/jneurosci.22-15-06631.2002openalex-snapshot
Electrical Stimulation Promotes Motoneuron Regeneration without Increasing Its Speed or Conditioning the Neuron
inferredcites →https://doi.org/10.1523/jneurosci.3105-05.2005openalex-snapshot
Peripheral Pathways Regulate Motoneuron Collateral Dynamics
inferredcites →https://doi.org/10.1523/jneurosci.4880-04.2005openalex-snapshot
Polysialylated Neural Cell Adhesion Molecule Is Necessary for Selective Targeting of Regenerating Motor Neurons
inferredcites →https://doi.org/10.2353/ajpath.2009.080743openalex-snapshot
Expression of a Soluble Isoform of Cell Adhesion Molecule 1 in the Brain and Its Involvement in Directional Neurite Outgrowth
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.4595470openalex-extracted
WGCNA Analysis of Gene Expression Difference between Afferent and Efferent Nerves in Mice During Development
inferred← citeshttps://doi.org/10.1002/cne.25018openalex-snapshot
A proteomic view on the differential phenotype of Schwann cells derived from mouse sensory and motor nerves
inferred← citeshttps://doi.org/10.1002/pmic.201200397openalex-snapshot
Understanding regeneration through proteomics
inferred← citeshttps://doi.org/10.1007/s10571-019-00650-2openalex-snapshot
Repair of Peripheral Nerve Sensory Impairments via the Transplantation of Bone Marrow Neural Tissue-Committed Stem Cell-Derived Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.11.078openalex-snapshot
Proteomic analysis of opossum Monodelphis domestica spinal cord reveals the changes of proteins related to neurodegenerative diseases during developmental period when neuroregeneration stops being possible
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2012.10.002openalex-snapshot
The proteomics of formalin-fixed wax-embedded tissue
inferred← citeshttps://doi.org/10.1016/j.expneurol.2023.114322openalex-snapshot
3D culture of the spinal cord with roots as an ex vivo model for comparative studies of motor and sensory nerve regeneration
inferred← citeshttps://doi.org/10.1016/j.neulet.2015.06.019openalex-snapshot
Expression and identification of olfactory receptors in sciatic nerve and dorsal root ganglia of rats
inferred← citeshttps://doi.org/10.1016/j.ymeth.2013.04.008openalex-snapshot
Recent advances in quantitative neuroproteomics
inferred← citeshttps://doi.org/10.1021/acs.jproteome.0c00639openalex-snapshot
Comparative Proteomic Analysis of Differentially Expressed Proteins between Injured Sensory and Motor Nerves after Peripheral Nerve Transection
inferred← citeshttps://doi.org/10.1021/pr4001064openalex-snapshot
Dimethyl-Labeling-Based Protein Quantification and Pathway Search: A Novel Method of Spinal Cord Analysis Applicable for Neurological Studies
inferred← citeshttps://doi.org/10.1038/s41598-018-30463-0openalex-snapshot
Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
inferred← citeshttps://doi.org/10.1159/000499126openalex-snapshot
Perinatal Ischemia Alters Global Expression of Synaptosomal Proteins Critical for Neural Plasticity in the Developing Mouse Brain
inferred← citeshttps://doi.org/10.1523/jneurosci.0585-18.2018openalex-snapshot
A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute to Schwann Cell Remyelination in the Central Nervous System
inferred← citeshttps://doi.org/10.3389/fmicb.2016.01754openalex-snapshot
Over-Expression of the Mycobacterial Trehalose-Phosphate Phosphatase OtsB2 Results in a Defect in Macrophage Phagocytosis Associated with Increased Mycobacterial-Macrophage Adhesion
inferred← citeshttps://doi.org/10.3389/fncel.2019.00182openalex-snapshot
Spatiotemporal Differences in Gene Expression Between Motor and Sensory Autografts and Their Effect on Femoral Nerve Regeneration in the Rat
inferred← citeshttps://doi.org/10.3389/fnins.2018.01016openalex-snapshot
Differential Gene Expression in Primary Cultured Sensory and Motor Nerve Fibroblasts
inferred← citeshttps://doi.org/10.4103/1673-5374.197148openalex-snapshot
Expression changes of nerve cell adhesion molecules L1 and semaphorin 3A after peripheral nerve injury
inferred← citeshttps://doi.org/10.4103/1673-5374.265556openalex-snapshot
Different protein expression patterns in rat spinal nerves during Wallerian degeneration assessed using isobaric tags for relative and absolute quantitation proteomics profiling
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