On the public citation graph

Enhanced noradrenergic axon regeneration into schwann cell‐filled PVDF‐TrFE conduits after complete spinal cord transection

0 signed · 136 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/ana.410140302openalex-snapshot

Dopamine-containing neurons in the spinal cord: Anatomy and some functional aspects

inferredcites →https://doi.org/10.1002/anie.200604646openalex-snapshot

Electrospinning: A Fascinating Method for the Preparation of Ultrathin Fibers

inferredcites →https://doi.org/10.1002/bit.24788openalex-snapshot

Fiber alignment directs cell motility over chemotactic gradients

inferredcites →https://doi.org/10.1002/cne.903510113openalex-snapshot

Axonal regeneration into Schwann cell‐seeded guidance channels grafted into transected adult rat spinal cord

inferredcites →https://doi.org/10.1002/jbm.a.32675openalex-snapshot

Guidance of neurite outgrowth on aligned electrospun polypyrrole/poly(styrene‐β‐isobutylene‐β‐styrene) fiber platforms

inferredcites →https://doi.org/10.1002/jbm.a.34551openalex-snapshot

Electrospun silk fibroin nanofibers in different diameters support neurite outgrowth and promote astrocyte migration

inferredcites →https://doi.org/10.1002/jbm.b.32676openalex-snapshot

Electrospun bio‐composite P(LLA‐CL)/collagen I/collagen III scaffolds for nerve tissue engineering

inferredcites →https://doi.org/10.1002/jcp.21431openalex-snapshot

Small applied electric fields guide migration of hippocampal neurons

inferredcites →https://doi.org/10.1002/jgm.1628openalex-snapshot

The assessment of adeno‐associated vectors as potential intrinsic treatments for brainstem axon regeneration

inferredcites →https://doi.org/10.1006/exnr.1995.1056openalex-snapshot

A Combination of BDNF and NT-3 Promotes Supraspinal Axonal Regeneration into Schwann Cell Grafts in Adult Rat Thoracic Spinal Cord

inferredcites →https://doi.org/10.1007/978-1-61779-301-1_20openalex-snapshot

Preparation of Spinal Cord Injured Tissue for Light and Electron Microscopy Including Preparation for Immunostaining

inferredcites →https://doi.org/10.1007/bf02368241openalex-snapshot

Biased cell migration of fibroblasts exhibiting contact guidance in oriented collagen gels

inferredcites →https://doi.org/10.1007/s12015-014-9518-zopenalex-snapshot

Directed Migration of Embryonic Stem Cell-derived Neural Cells In An Applied Electric Field

inferredcites →https://doi.org/10.1016/0006-8993(87)91570-8openalex-snapshot

Piezoelectric guidance channels enhance regeneration in the mouse sciatic nerve after axotomy

inferredcites →https://doi.org/10.1016/0006-8993(92)90583-uopenalex-snapshot

GFAP expression of human Schwann cells in tissue culture

inferredcites →https://doi.org/10.1016/0142-9612(91)90029-aopenalex-snapshot

Improved nerve regeneration through piezoelectric vinylidenefluoride-trifluoroethylene copolymer guidance channels

inferredcites →https://doi.org/10.1016/0142-9612(92)90069-zopenalex-snapshot

Electrically charged polymeric substrates enhance nerve fibre outgrowth In vitro

inferredcites →https://doi.org/10.1016/j.actbio.2010.02.039openalex-snapshot

Synergistic effects of electrospun PLLA fiber dimension and pattern on neonatal mouse cerebellum C17.2 stem cells

inferredcites →https://doi.org/10.1016/j.actbio.2010.03.035openalex-snapshot

Characterization and in vitro cytocompatibility of piezoelectric electrospun scaffolds

inferredcites →https://doi.org/10.1016/j.actbio.2011.07.013openalex-snapshot

Neurite extension of primary neurons on electrospun piezoelectric scaffolds

inferredcites →https://doi.org/10.1016/j.actbio.2015.07.010openalex-snapshot

Piezoelectric materials for tissue regeneration: A review

inferredcites →https://doi.org/10.1016/j.biomaterials.2009.04.042openalex-snapshot

Polypyrrole-coated electrospun PLGA nanofibers for neural tissue applications

inferredcites →https://doi.org/10.1016/j.biomaterials.2011.05.006openalex-snapshot

Robust CNS regeneration after complete spinal cord transection using aligned poly-l-lactic acid microfibers

inferredcites →https://doi.org/10.1016/j.colsurfb.2012.03.014openalex-snapshot

Piezoelectric PU/PVDF electrospun scaffolds for wound healing applications

inferredcites →https://doi.org/10.1016/j.expneurol.2011.02.001openalex-snapshot

GDNF modifies reactive astrogliosis allowing robust axonal regeneration through Schwann cell-seeded guidance channels after spinal cord injury

inferredcites →https://doi.org/10.1016/j.jcyt.2013.03.012openalex-snapshot

Safety and possible outcome assessment of autologous Schwann cell and bone marrow mesenchymal stromal cell co-transplantation for treatment of patients with chronic spinal cord injury

inferredcites →https://doi.org/10.1016/j.nano.2013.09.001openalex-snapshot

Alignment of multiple glial cell populations in 3D nanofiber scaffolds: Toward the development of multicellular implantable scaffolds for repair of neural injury

inferredcites →https://doi.org/10.1016/j.neulet.2008.07.041openalex-snapshot

Treatment of chronic thoracic spinal cord injury patients with autologous Schwann cell transplantation: An interim report on safety considerations and possible outcomes

inferredcites →https://doi.org/10.1016/j.neulet.2008.08.092openalex-snapshot

Combinatorial strategies with Schwann cell transplantation to improve repair of the injured spinal cord

inferredcites →https://doi.org/10.1016/s0014-4886(03)00188-2openalex-snapshot

Glial cell line-derived neurotrophic factor-enriched bridging transplants promote propriospinal axonal regeneration and enhance myelination after spinal cord injury

inferredcites →https://doi.org/10.1016/s0161-4754(99)70049-7openalex-snapshot

A review of biomechanics of the central nervous system—Part I: Spinal canal deformations resulting from changes in posture

inferredcites →https://doi.org/10.1016/s0161-4754(99)70065-5openalex-snapshot

A review of biomechanics of the central nervous system—Part II: Spinal cord strains from postural loads

inferredcites →https://doi.org/10.1016/s0161-4754(99)70086-2openalex-snapshot

A review of biomechanics of the central nervous system—part III: Spinal cord stresses from postural loads and their neurologic effects

inferredcites →https://doi.org/10.1016/s0361-9230(99)00072-6openalex-snapshot

The glial scar and central nervous system repair

inferredcites →https://doi.org/10.1021/acsami.5b10073openalex-snapshot

Thermo-electromechanical Behavior of Piezoelectric Nanofibers

inferredcites →https://doi.org/10.1023/a:1018557923309openalex-snapshot

Bridging Schwann cell transplants promote axonal regeneration from both the rostral and caudal stumps of transected adult rat spinal cord

inferredcites →https://doi.org/10.1038/ncomms2639openalex-snapshot

High performance piezoelectric devices based on aligned arrays of nanofibers of poly(vinylidenefluoride-co-trifluoroethylene)

inferredcites →https://doi.org/10.1038/nrm2729openalex-snapshot

Random versus directionally persistent cell migration

inferredcites →https://doi.org/10.1038/nrn1326openalex-snapshot

Regeneration beyond the glial scar

inferredcites →https://doi.org/10.1038/sc.2015.142openalex-snapshot

Co-transplantation of autologous bone marrow mesenchymal stem cells and Schwann cells through cerebral spinal fluid for the treatment of patients with chronic spinal cord injury: safety and possible outcome

inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00591.xopenalex-snapshot

Regrowth of axons into the distal spinal cord through a Schwann‐cell‐seeded mini‐channel implanted into hemisected adult rat spinal cord

inferredcites →https://doi.org/10.1089/neu.2004.21.1415openalex-snapshot

Basic Fibroblast Growth Factor Promotes Neuronal Survival but Not Behavioral Recovery in the Transected and Schwann Cell Implanted Rat Thoracic Spinal Cord

inferredcites →https://doi.org/10.1089/neu.2006.23.496openalex-snapshot

Bioengineered Strategies for Spinal Cord Repair

inferredcites →https://doi.org/10.1089/neu.2009.0948openalex-snapshot

Biomaterial Design Strategies for the Treatment of Spinal Cord Injuries

inferredcites →https://doi.org/10.1089/neu.2009.1177openalex-snapshot

A Systematic Review of Cellular Transplantation Therapies for Spinal Cord Injury

inferredcites →https://doi.org/10.1089/ten.tea.2011.0540openalex-snapshot

The Influence of Piezoelectric Scaffolds on Neural Differentiation of Human Neural Stem/Progenitor Cells

inferredcites →https://doi.org/10.1089/ten.teb.2010.0561openalex-snapshot

Electric Field-Guided Neuron Migration:A Novel Approach in Neurogenesis

inferredcites →https://doi.org/10.1097/mat.0b013e3182a79151openalex-snapshot

Chitosan–Cross-Linked Nanofibrous PHBV Nerve Guide for Rat Sciatic Nerve Regeneration Across a Defect Bridge

inferredcites →https://doi.org/10.1097/mot.0000000000000026openalex-snapshot

Clinical translation of autologous Schwann cell transplantation for the treatment of spinal cord injury

inferredcites →https://doi.org/10.1152/physrev.1996.76.2.319openalex-snapshot

Degeneration and regeneration of axons in the lesioned spinal cord

inferredcites →https://doi.org/10.1163/1568562042459733openalex-snapshot

Characterization of neural stem cells on electrospun poly(L-lactic acid) nanofibrous scaffold

inferredcites →https://doi.org/10.1186/jbiol35openalex-snapshot

Astrocytes derived from glial-restricted precursors promote spinal cord repair

inferredcites →https://doi.org/10.1385/1-59259-141-8:259openalex-snapshot

HIV-Based Vectors: Preparation and Use

inferredcites →https://doi.org/10.1515/revneuro-2014-0068openalex-snapshot

Schwann cell transplantation for spinal cord injury repair: its significant therapeutic potential and prospectus

inferredcites →https://doi.org/10.1523/jneurosci.22-15-06670.2002openalex-snapshot

Schwann Cell But Not Olfactory Ensheathing Glia Transplants Improve Hindlimb Locomotor Performance in the Moderately Contused Adult Rat Thoracic Spinal Cord

inferredcites →https://doi.org/10.1523/jneurosci.2973-12.2013openalex-snapshot

A Novel Growth-Promoting Pathway Formed by GDNF-Overexpressing Schwann Cells Promotes Propriospinal Axonal Regeneration, Synapse Formation, and Partial Recovery of Function after Spinal Cord Injury

inferredcites →https://doi.org/10.3171/2011.6.spine10917openalex-snapshot

Safety of intramedullary Schwann cell transplantation for postrehabilitation spinal cord injuries: 2-year follow-up of 33 cases

inferredcites →https://doi.org/10.3233/rnn-2005-00317openalex-snapshot

Lentiviral vector-mediated transduction of neural progenitor cells before implantation into injured spinal cord and brain to detect their migration, deliver neurotrophic factors and repair tissue

inferredcites →https://doi.org/10.3390/polym3041684openalex-snapshot

Biodegradable Cell-Seeded Nanofiber Scaffolds for Neural Repair

inferredcites →https://doi.org/10.3727/096368912x633752openalex-snapshot

Transplantation of Autologous Activated Schwann Cells in the Treatment of Spinal Cord Injury: Six Cases, more than Five Years of Follow-up

inferredcites →https://doi.org/10.3727/096368913x674657openalex-snapshot

Permissive Schwann Cell Graft/Spinal Cord Interfaces for Axon Regeneration

inferredcites →https://doi.org/10.3727/096368914x685014openalex-snapshot

A Prospective Randomized Double-Blind Clinical Trial Using a Combination of Olfactory Ensheathing Cells and Schwann Cells for the Treatment of Chronic Complete Spinal Cord Injuries

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.4707196openalex-extracted

Corona Poling P(Vdf-Trfe) Films Enhance the Proliferation and Neurotrophic Factor Secretion of Schwann Cells

inferred← citeshttps://doi.org/10.2139/ssrn.4812094openalex-extracted

Corona Poling P(Vdf-Trfe) Films Enhance the Proliferation of Schwann Cells and Secretion of Neurotrophic Factor

inferred← citeshttps://doi.org/10.1002/adfm.201707077openalex-snapshot

3D Manufacture of Gold Nanocomposite Channels Facilitates Neural Differentiation and Regeneration

inferred← citeshttps://doi.org/10.1002/adfm.202003542openalex-snapshot

Simultaneous Regeneration of Bone and Nerves Through Materials and Architectural Design: Are We There Yet?

inferred← citeshttps://doi.org/10.1002/adhm.201700002openalex-snapshot

Remote Control of Cellular Functions: The Role of Smart Nanomaterials in the Medicine of the Future

inferred← citeshttps://doi.org/10.1002/adhm.202100806openalex-snapshot

Formation of 3D Self‐Organized Neuron‐Glial Interface Derived from Neural Stem Cells via Mechano‐Electrical Stimulation

inferred← citeshttps://doi.org/10.1002/adhm.202301494openalex-snapshot

State of the Art and Current Challenges on Electroactive Biomaterials and Strategies for Neural Tissue Regeneration

inferred← citeshttps://doi.org/10.1002/adma.202008788openalex-snapshot

A Self‐Powered Piezo‐Bioelectric Device Regulates Tendon Repair‐Associated Signaling Pathways through Modulation of Mechanosensitive Ion Channels

inferred← citeshttps://doi.org/10.1002/adma.202209769openalex-snapshot

Manipulation of Heterogeneous Surface Electric Potential Promotes Osteogenesis by Strengthening RGD Peptide Binding and Cellular Mechanosensing

inferred← citeshttps://doi.org/10.1002/admi.202500552openalex-snapshot

Piezoelectric Stimulation of Neural Cells: Exploring the Synergistic Potential of Hybrid Scaffolds for Enhanced Regeneration

inferred← citeshttps://doi.org/10.1002/adtp.202400506openalex-snapshot

Insights on Advances in 3D Bioprinting for Peripheral Nerve Regeneration

inferred← citeshttps://doi.org/10.1002/advs.202510349openalex-snapshot

Open Challenges and Opportunities in Piezoelectricity for Tissue Regeneration

inferred← citeshttps://doi.org/10.1002/bit.27459openalex-snapshot

Fabrication of a biomimetic spinal cord tissue construct with heterogenous mechanical properties using intrascaffold cell assembly

inferred← citeshttps://doi.org/10.1002/glia.23769openalex-snapshot

Gpr126/Adgrg6 contributes to the terminal Schwann cell response at the neuromuscular junction following peripheral nerve injury

inferred← citeshttps://doi.org/10.1002/jbm.a.37595openalex-snapshot

Review on electrically conductive smart nerve guide conduit for peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1002/mabi.202000197openalex-snapshot

Development of a Piezoelectric PVDF‐TrFE Fibrous Scaffold to Guide Cell Adhesion, Proliferation, and Alignment

inferred← citeshttps://doi.org/10.1007/s12274-017-1549-8openalex-snapshot

Electrospun poly(vinylidene fluoride-trifluoroethylene)/zinc oxide nanocomposite tissue engineering scaffolds with enhanced cell adhesion and blood vessel formation

inferred← citeshttps://doi.org/10.1016/b978-0-12-813477-1.00006-2openalex-snapshot

Biomaterials and scaffolds for the treatment of spinal cord injury

inferred← citeshttps://doi.org/10.1016/b978-0-12-821551-7.00012-9openalex-snapshot

Biomimetic biocompatible ferroelectric polymer materials with an active response for implantology and regenerative medicine

inferred← citeshttps://doi.org/10.1016/b978-0-323-95486-0.00175-7openalex-snapshot

Functional Polymers for Tissue Engineering Applications

inferred← citeshttps://doi.org/10.1016/b978-0-323-99690-7.00004-2openalex-snapshot

Polymers and composites for peripheral nerve repair

inferred← citeshttps://doi.org/10.1016/bs.irn.2022.09.008openalex-snapshot

Cell transplantation to repair the injured spinal cord

inferred← citeshttps://doi.org/10.1016/j.addr.2017.12.012openalex-snapshot

Electroactive biomaterials: Vehicles for controlled delivery of therapeutic agents for drug delivery and tissue regeneration

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.06.022openalex-snapshot

Research trends of piezoelectric materials in neurodegenerative disease applications

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.01.012openalex-snapshot

Scaffold-facilitated locomotor improvement post complete spinal cord injury: Motor axon regeneration versus endogenous neuronal relay formation

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2023.122421openalex-snapshot

Biomaterials and bioelectronics for self-powered neurostimulation

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2024.122528openalex-snapshot

Progress in the development of piezoelectric biomaterials for tissue remodeling

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2025.123385openalex-snapshot

Bioelectric and physicochemical foundations of bioelectronics in tissue regeneration

inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112529openalex-snapshot

Advanced approaches to regenerate spinal cord injury: The development of cell and tissue engineering therapy and combinational treatments

inferred← citeshttps://doi.org/10.1016/j.ejpb.2022.02.016openalex-snapshot

Emerging approaches of neural regeneration using physical stimulations solely or coupled with smart piezoelectric nano-biomaterials

inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111663openalex-snapshot

Electrospun nanofiber nerve guidance conduits for peripheral nerve regeneration: A review

inferred← citeshttps://doi.org/10.1016/j.jmbbm.2021.104669openalex-snapshot

Recent advances of polymer-based piezoelectric composites for biomedical applications

inferred← citeshttps://doi.org/10.1016/j.mtbio.2023.100740openalex-snapshot

Physical stimuli-emitting scaffolds: The role of piezoelectricity in tissue regeneration

inferred← citeshttps://doi.org/10.1016/j.mtbio.2024.100950openalex-snapshot

Revealing an important role of piezoelectric polymers in nervous-tissue regeneration: A review

inferred← citeshttps://doi.org/10.1016/j.mtchem.2022.100944openalex-snapshot

Review of advances in electrospinning-based strategies for spinal cord regeneration

inferred← citeshttps://doi.org/10.1016/j.nanoen.2019.104411openalex-snapshot

3D structured self-powered PVDF/PCL scaffolds for peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.polymer.2026.130211openalex-snapshot

Engineering piezoelectric polymers and peptides for soft biomedical interfaces

inferred← citeshttps://doi.org/10.1016/j.tibtech.2019.07.002openalex-snapshot

Electric Phenomenon: A Disregarded Tool in Tissue Engineering and Regenerative Medicine

inferred← citeshttps://doi.org/10.1016/j.trsl.2026.07.009openalex-snapshot

Electroactive scaffolds for spinal cord injury repair: Modulating the electrophysiological homeostasis

inferred← citeshttps://doi.org/10.1021/acsabm.3c01032openalex-snapshot

Magnetoactive Composite Conduits Based on Poly(3-hydroxybutyrate) and Magnetite Nanoparticles for Repair of Peripheral Nerve Injury

inferred← citeshttps://doi.org/10.1021/acsami.7b04323openalex-snapshot

Piezoelectric Effects of Materials on Bio-Interfaces

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.3c01989openalex-snapshot

Scaffold-Based Poly(Vinylidene Fluoride) and Its Copolymers: Materials, Fabrication Methods, Applications, and Perspectives

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.5c00814openalex-snapshot

3D-Printed Stent-Like Polymeric Structures with Tunable Mechanical Properties and Ionic Conductivity for Reinforced Nerve Guidance Conduits

inferred← citeshttps://doi.org/10.1038/s41536-023-00334-yopenalex-snapshot

Enhanced peripheral nerve regeneration by mechano-electrical stimulation

inferred← citeshttps://doi.org/10.1038/s41598-017-09432-6openalex-snapshot

Combinatory repair strategy to promote axon regeneration and functional recovery after chronic spinal cord injury

inferred← citeshttps://doi.org/10.1039/d0tb01842bopenalex-snapshot

Design of hydrogel-based scaffolds for the treatment of spinal cord injuries

inferred← citeshttps://doi.org/10.1039/d1tb00686jopenalex-snapshot

Electroactive nanomaterials in the peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1039/d2tb01582jopenalex-snapshot

Advances in applications of piezoelectronic electrons in cell regulation and tissue regeneration

inferred← citeshttps://doi.org/10.1039/d4bm00904eopenalex-snapshot

Piezoelectric PVDF and its copolymers in biomedicine: innovations and applications

inferred← citeshttps://doi.org/10.1063/5.0245674openalex-snapshot

Organ synergy in poly(vinylidene fluoride)-based piezoelectrical materials for tissue engineering

inferred← citeshttps://doi.org/10.1088/1741-2552/aac77fopenalex-snapshot

Aligned fibrous PVDF-TrFE scaffolds with Schwann cells support neurite extension and myelination in vitro

inferred← citeshttps://doi.org/10.1088/1741-2552/ad0a00openalex-snapshot

A scaffold containing zinc oxide for Schwann cell-mediated axon growth

inferred← citeshttps://doi.org/10.1089/neu.2019.6939openalex-snapshot

Optimizing Olfactory Ensheathing Cell Transplantation for Spinal Cord Injury Repair

inferred← citeshttps://doi.org/10.1097/js9.0000000000002955openalex-snapshot

Application and challenge of Schwann cell transplantation in spinal cord injury and clinical trial

inferred← citeshttps://doi.org/10.1177/0391398818785049openalex-snapshot

Force induced piezoelectric effect of polyvinylidene fluoride and polyvinylidene fluoride-co-trifluoroethylene nanofibrous scaffolds

inferred← citeshttps://doi.org/10.1557/adv.2020.348openalex-snapshot

Wireless nanotechnologies light up the next frontier in cell Calcium signalling

inferred← citeshttps://doi.org/10.3171/2020.11.spine201433openalex-snapshot

Scalable culture techniques to generate large numbers of purified human Schwann cells for clinical trials in human spinal cord and peripheral nerve injuries

inferred← citeshttps://doi.org/10.3389/fbioe.2017.00080openalex-snapshot

Smart Materials Meet Multifunctional Biomedical Devices: Current and Prospective Implications for Nanomedicine

inferred← citeshttps://doi.org/10.3389/fbioe.2020.582646openalex-snapshot

Polymeric Guide Conduits for Peripheral Nerve Tissue Engineering

inferred← citeshttps://doi.org/10.3389/fncel.2022.926222openalex-snapshot

Biomaterial-Based Schwann Cell Transplantation and Schwann Cell-Derived Biomaterials for Nerve Regeneration

inferred← citeshttps://doi.org/10.3389/fphar.2025.1506552openalex-snapshot

Schwann cells in regeneration and cancer

inferred← citeshttps://doi.org/10.3390/biomimetics9010002openalex-snapshot

Innervation of an Ultrasound-Mediated PVDF-TrFE Scaffold for Skin-Tissue Engineering

inferred← citeshttps://doi.org/10.3390/cells14171336openalex-snapshot

Pathologic and Therapeutic Schwann Cells

inferred← citeshttps://doi.org/10.3390/ijms222111373openalex-snapshot

PVDF and P(VDF-TrFE) Electrospun Scaffolds for Nerve Graft Engineering: A Comparative Study on Piezoelectric and Structural Properties, and In Vitro Biocompatibility

inferred← citeshttps://doi.org/10.3390/jfb17040172openalex-snapshot

Electrical Microenvironment Reconstruction and the Application of Biomaterials in Spinal Cord Injury

inferred← citeshttps://doi.org/10.3390/nano9070952openalex-snapshot

Electrospun Polyvinylidene Fluoride-Based Fibrous Scaffolds with Piezoelectric Characteristics for Bone and Neural Tissue Engineering

inferred← citeshttps://doi.org/10.3390/polym14204376openalex-snapshot

A Biomimetic Nonwoven-Reinforced Hydrogel for Spinal Cord Injury Repair

inferred← citeshttps://doi.org/10.34133/2022/9896274openalex-snapshot

Electrical Stimulation Enabled via Electrospun Piezoelectric Polymeric Nanofibers for Tissue Regeneration

inferred← citeshttps://doi.org/10.34133/bmef.0007openalex-snapshot

Tissue Engineering in Neuroscience: Applications and Perspectives

inferred← citeshttps://doi.org/10.3791/56077openalex-snapshot

Transplantation of Schwann Cells Inside PVDF-TrFE Conduits to Bridge Transected Rat Spinal Cord Stumps to Promote Axon Regeneration Across the Gap

inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-24-00061openalex-snapshot

Combinatorial therapies for spinal cord injury repair

inferred← citeshttps://doi.org/10.57634/rcr5037openalex-snapshot

Fluorine-containing ferroelectric polymers: applications in engineering and biomedicine

inferred← citeshttps://doi.org/10.5772/intechopen.109389openalex-snapshot

Frontier Electrospun Fibers for Nanomedical Applications

inferred← citeshttps://doi.org/10.70322/ism.2026.10010openalex-snapshot

Electrospun Scaffolds for Spinal Cord Injury Repair: Mechanisms, Strategies, and Advances

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.