Neuronal Intrinsic Mechanisms of Axon Regeneration

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Promoting Axon Regeneration in the Adult CNS by Modulation of the PTEN/mTOR Pathway

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Growing roles for the mTOR pathway

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Glial inhibition of CNS axon regeneration

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SOCS3: A common target for neuronal protection and axon regeneration after spinal cord injury

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Regulation of Microtubule Dynamics in Axon Regeneration: Insights from C. elegans

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Enhanced proliferation and differentiation of neural stem cells by peptide-containing temperature-sensitive hydrogel scaffold

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Electrospun decellularized extracellular matrix scaffolds promote the regeneration of injured neurons

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Effects of intravitreal injection of a Rho-GTPase inhibitor (BA-210), or CNTF combined with an analogue of cAMP, on the dendritic morphology of regenerating retinal ganglion cells

Drummond, E., Rodger, J., Penrose, M. A., Robertson, D., Hu, Y. J., & Harvey, A. R. (2014) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-130360 · Cited by 26

Down-regulation of NTPDase2 and ADP-sensitive P2 Purinoceptors Correlate with Severity of Symptoms during Experimental Autoimmune Encephalomyelitis

Jakovljevic, M., Lavrnja, I. C., Bozic, I. D., Savić, D. Z., Bjelobaba, I. M., Peković, S., Sévigny, J., Nedeljković, N., & Laketa, D. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00333 · Cited by 26

ARF6 and Rab11 as intrinsic regulators of axon regeneration

Nieuwenhuis, B., & Eva, R. (2018) · Small GTPases · doi:10.1080/21541248.2018.1457914 · Cited by 25

Plexina2 and CRMP2 Signaling Complex Is Activated by Nogo-A-Liganded Ngr1 to Restrict Corticospinal Axon Sprouting after Trauma

Sekine, Y., Algarate, P. T., Cafferty, W. B. J., & Strittmatter, S. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2996-18.2019 · Cited by 25

Selective expression of CSPG receptors PTPσ and LAR in poorly regenerating reticulospinal neurons of lamprey

Zhang, G., Hu, J., Li, S., Huang, L. A., & Selzer, M. E. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23529 · Cited by 25

In vivo imaging in mouse spinal cord reveals that microglia prevent degeneration of injured axons

Wu, W., He, Y., Chen, Y., Fu, Y., He, S., Liu, K., & Qu, J. Y. (2024) · Nature Communications · doi:10.1038/s41467-024-53218-0 · Cited by 25

Cytoskeletal Dynamics in Caenorhabditis elegans Axon Regeneration

Chisholm, A. D. (2013) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101512-122311 · Cited by 23

Boosted Regeneration and Reduced Denervated Muscle Atrophy by NeuroHeal in a Pre-clinical Model of Lumbar Root Avulsion with Delayed Reimplantation

Romeo-Guitart, D., Forés, J., Navarro, X., & Casas, C. (2017) · Scientific Reports · doi:10.1038/s41598-017-11086-3 · Cited by 27

Promoting axonal regeneration through exosomes: An update of recent findings on exosomal PTEN and mTOR modifiers

Tang, B. L. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.10.008 · Cited by 26

Inactivating Celsr2 promotes motor axon fasciculation and regeneration in mouse and human

Wen, Q., Weng, H., Liu, T., Yu, L., Zhao, T., Qin, J., Li, S., Wu, Q., Tissir, F., Qu, Y., et al. (2021) · Brain · doi:10.1093/brain/awab317 · Cited by 24

Interleukin-6 contributes to initiation of neuronal regeneration program in the remote dorsal root ganglia neurons after sciatic nerve injury

Dubový, P., Hradilová‐Svíženská, I., Klusáková, I., Brázda, V., & Joukal, M. (2019) · Histochemistry and Cell Biology · doi:10.1007/s00418-019-01779-3 · Cited by 24

Directed Axonal Outgrowth Using a Propagating Gradient of IGF‐1

Lee, W., Frank, C. W., & Park, J. (2014) · Advanced Materials · doi:10.1002/adma.201305995 · Cited by 23

The Biology, Limits, and Promotion of Peripheral Nerve Regeneration in Rats and Humans

Gordon, T. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-802653-3.00110-x · Cited by 24

A Conditioning Sciatic Nerve Lesion Triggers a Pro-regenerative State in Primary Sensory Neurons Also of Dorsal Root Ganglia Non-associated With the Damaged Nerve

Dubový, P., Klusáková, I., Hradilová‐Svíženská, I., Brázda, V., Kohoutková, M. H., & Joukal, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00011 · Cited by 23

Local Delivery of Taxol From FGL-Functionalized Self-Assembling Peptide Nanofiber Scaffold Promotes Recovery After Spinal Cord Injury

Xiao, Z., Yao, Y., Wang, Z., Tian, Q., Wang, J., Gu, L., Li, B., Zheng, Q., & Wu, Y. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00820 · Cited by 23

Lack of the transcription factor C/EBPδ impairs the intrinsic capacity of peripheral neurons for regeneration

Heredia, L., & Magoulas, C. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.10.012 · Cited by 22

How reggies regulate regeneration and axon growth

Stuermer, C. A. O. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1343-6 · Cited by 22

Restoration versus reconstruction: cellular mechanisms of skin, nerve and muscle regeneration compared

Coletti, D., Teodori, L., Lin, Z., Beranudin, J., & Adamo, S. (2013) · Regenerative Medicine Research · doi:10.1186/2050-490x-1-4 · Cited by 23

Intrinsic Mechanisms Regulating Axon Regeneration

Eva, R., Andrews, M. R., Franssen, E. H. P., & Fawcett, J. W. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-407178-0.00004-1 · Cited by 23

Extracellular matrix constitution and function for tissue regeneration and repair

Caldeira, J., Sousa, A., Sousa, D. M., & Barros, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-100803-4.00002-4 · Cited by 24

Polycomb protein family member CBX7 regulates intrinsic axon growth and regeneration

Duan, R.-S., Tang, G.-B., Du, H., Hu, Y., Liu, P., Xu, Y., Zeng, Y.-Q., Zhang, S.-F., Wang, R., Teng, Z., et al. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0064-0 · Cited by 20

The Mechanisms of Peripheral Nerve Preconditioning Injury on Promoting Axonal Regeneration

Yang, X.-Y., Liu, R., Xu, Y., Ma, X., & Zhou, B. (2021) · Neural Plasticity · doi:10.1155/2021/6648004 · Cited by 20

Regeneration-associated macrophages: a novel approach to boost intrinsic regenerative capacity for axon regeneration

Kim, B. G., Kwon, M., & Yoon, H.-J. (2016) · Neural Regeneration Research · doi:10.4103/1673-5374.191194 · Cited by 21

Molecular mechanisms in the initiation phase of Wallerian degeneration

Chang, B., Quan, Q., Lu, S., Wang, Y., & Peng, J. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13250 · Cited by 22

Lanthionine ketimine ester promotes locomotor recovery after spinal cord injury by reducing neuroinflammation and promoting axon growth

Kotaka, K., Nagai, J., Hensley, K., & Ohshima, T. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.12.069 · Cited by 21

Cell-seeded porous silk fibroin scaffolds promotes axonal regeneration and myelination in spinal cord injury rats

You, K., Chang, H., Zhang, F., Shen, Y., Zhang, Y., Cai, F., Liu, L., & Liu, X. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.04.137 · Cited by 21

PTEN Blocking Stimulates Corticospinal and Raphespinal Axonal Regeneration and Promotes Functional Recovery After Spinal Cord Injury

Bhowmick, S., & Muneer, P. M. A. (2020) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaa147 · Cited by 21

Proteostasis impairment and ALS

Lambert-Smith, I. A., Saunders, D. N., & Yerbury, J. J. (2022) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2022.06.001 · Cited by 19

Report on the National Eye Institute Audacious Goals Initiative: Regenerating the Optic Nerve

Goldberg, J. L., Guido, W., & Participants, F. T. A. W. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-18500 · Cited by 20

The effects of Chinese medicines on cAMP/PKA signaling in central nervous system dysfunction

Li, L., Fan, X., Zhang, X.-T., Yue, S., Sun, Z.-Y., Zhu, J., Zhang, J., Gao, X., & Zhang, H. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.04.006 · Cited by 20

Cerebral imaging of post-stroke plasticity and tissue repair

Loubinoux, I., Brihmat, N., Castel-Lacanal, E., & Marqué, P. (2017) · Revue Neurologique · doi:10.1016/j.neurol.2017.09.007 · Cited by 25

Klf2-Vav1-Rac1 axis promotes axon regeneration after peripheral nerve injury

Wang, Q., Gong, L., Mao, S., Yao, C., Liu, M., Wang, Y., Yang, J. M., Yu, B., Chen, G., & Gu, X. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113788 · Cited by 20

Expedited Access to Vinaxanthone and Chemically Edited Derivatives Possessing Neuronal Regenerative Effects through Ynone Coupling Reactions

Chin, M. R., Zlotkowski, K., Han, M. N., Patel, S. N., Eliasen, A. M., Axelrod, A. J., & Siegel, D. R. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500237z · Cited by 19

Two Drosophila model neurons can regenerate axons from the stump or from a converted dendrite, with feedback between the two sites

Rao, K. S., & Rolls, M. M. (2017) · Neural Development · doi:10.1186/s13064-017-0092-3 · Cited by 19

Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others?

Rodemer, W., Hu, J., Selzer, M. E., & Shifman, M. I. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.270298 · Cited by 19

Impairments of cortico-cortical connectivity in fine tactile sensation after stroke

Zhou, S., Huang, Y., Jiao, J., Hu, J., Hsing, C., Lai, Z., Yang, Y., & Hu, X. (2021) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-021-00821-7 · Cited by 19

CNS axon regeneration inhibitors stimulate an immediate early gene response via MAP kinase-SRF signaling

Stern, S., & Knöll, B. (2014) · Molecular Brain · doi:10.1186/s13041-014-0086-6 · Cited by 19

Maf1 regulates axonal regeneration of retinal ganglion cells after injury

Chen, D., Sun, Y., Zhou, L.-Y., Yang, S., Hong, F.-Y., Liu, X., Sun, Z.-L., Huang, J., & Feng, D. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113948 · Cited by 18

Functional Hydrogel Co‐Remolding Migration and Differentiation Microenvironment for Severe Spinal Cord Injury Repair

Liu, D., Shen, H., Zhang, K., Shen, Y., Wen, R., He, X., Long, G., & Li, X. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202301662 · Cited by 18

The small molecule mimetic agonist trimebutine of adhesion molecule L1 contributes to functional recovery after spinal cord injury in mice

Xu, J., Hu, C., Jiang, Q., Pan, H., Shen, H., & Schachner, M. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.029801 · Cited by 18

A Drosophila In Vivo Injury Model for Studying Neuroregeneration in the Peripheral and Central Nervous System

Li, D., Li, F., Guttipatti, P., & Song, Y. (2018) · Journal of Visualized Experiments · doi:10.3791/57557 · Cited by 18

The effects of electrical stimulation on neurite outgrowth of goldfish retinal explants

Ou, Y.-T., Lu, M. S.-C., & Chiao, C. (2012) · Brain Research · doi:10.1016/j.brainres.2012.08.041 · Cited by 18

Do growth-stimulated retinal ganglion cell axons find their central targets after optic nerve injury? New insights by three-dimensional imaging of the visual pathway

Diekmann, H., Leibinger, M., & Fischer, D. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.06.021 · Cited by 17

Lhx2 promotes axon regeneration of adult retinal ganglion cells and rescues neurodegeneration in mouse models of glaucoma

Li, C., Wu, S., Yong-quan, S., Peng, X.-Q., Gong, M., Du, H., Zhang, J., Teng, Z., Wang, N., & Liu, C. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101554 · Cited by 18

Clickable, Thermally Responsive Hydrogels Enabled by Recombinant Spider Silk Protein and Spy Chemistry for Sustained Neurotrophin Delivery

Li, Y., Yang, C., Fang, S., Zhou, Y., Li, M., Liu, Z., Zhang, X., Duan, L., Liu, K., & Sun, F. (2024) · Advanced Materials · doi:10.1002/adma.202413957 · Cited by 17

Comparative analysis of the transcriptome of injured nerve segments reveals spatiotemporal responses to neural damage in mice

Shin, J. E., Ha, H., Cho, E. H., Kim, Y. K., & Cho, Y. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24404 · Cited by 16

The diversity and plasticity of descending motor pathways rewired after stroke and trauma in rodents

Inoue, T., & Ueno, M. (2025) · Frontiers in Neural Circuits · doi:10.3389/fncir.2025.1566562 · Cited by 21

A glycolytic shunt via the pentose phosphate pathway is a metabolic checkpoint for nervous system sensory homeostasis and axonal regeneration

Song, Y., Luengo-Gutierrez, L., Sági‐Kiss, V., Kong, G., Huang, H., Steinruecke, M., Zhou, L., Yuan, Z., Virgiliis, F. D., Pap, I. S., et al. (2026) · Cell · doi:10.1016/j.cell.2025.12.003 · Cited by 18

Microtubule deacetylation sets the stage for successful axon regeneration

Chen, L., & Rolls, M. M. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.175 · Cited by 16

N6-methyladenosine modification: A potential regulatory mechanism in spinal cord injury

Liu, D., Fan, B., Li, J., Sun, T., Ma, J., Zhou, X., & Feng, S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.989637 · Cited by 16

Reshaping the chromatin landscape after spinal cord injury

Wong, J. K., & Zou, H. (2014) · Frontiers in Biology · doi:10.1007/s11515-014-1329-8 · Cited by 16

Cyclin-Dependent Kinase 5 in Axon Growth and Regeneration

Ye, T., Fu, A. K. Y., & Ip, N. Y. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-398309-1.00006-8 · Cited by 17

Paxillin phosphorylation counteracts proteoglycan-mediated inhibition of axon regeneration

Kuboyama, T., Luo, X., Park, K. K., Blackmore, M. G., Tojima, T., Tohda, C., Bixby, J. L., Lemmon, V., & Kamiguchi, H. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.06.011 · Cited by 17

A novel bioactive nerve conduit for the repair of peripheral nerve injury

Yin, Y., Li, B.-B., Yan, Q., Wang, X., & Li, S. (2016) · Neural Regeneration Research · doi:10.4103/1673-5374.175062 · Cited by 16

The Plasminogen Activation System Promotes Neurorepair in the Ischemic Brain

Yepes, M. (2018) · Current Drug Targets · doi:10.2174/1389450120666181211144550 · Cited by 16

Electrical Stimulation Therapy – Dedicated to the Perfect Plastic Repair

Deng, K., Luo, R., Chen, Y., Liu, X., Xi, Y., Usman, M., Jiang, X., Li, Z., & Zhang, J. (2024) · Advanced Science · doi:10.1002/advs.202409884 · Cited by 16

Regenerative Potential of Injured Spinal Cord in the Light of Epigenetic Regulation and Modulation

Gupta, S., Dutta, S., & Hui, S. P. (2023) · Cells · doi:10.3390/cells12131694 · Cited by 17

An effective pharmacological hydrogel induces optic nerve repair and improves visual function

Wang, L., Zhang, S., Han, Y., Tang, S., Li, J., Bu, L., Zhao, D., & Deng, H. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2394-3 · Cited by 15

Control of neurite growth and guidance by an inhibitory cell-body signal

Bicknell, B. A., Pujic, Z., Dayan, P., & Goodhill, G. J. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006218 · Cited by 15

Diversified Treatment Options of Adult Stem Cells for Optic Neuropathies

Tan, S., Yao, Y., Yang, Q., Yuan, X., Cen, L., & Ng, T. K. (2022) · Cell Transplantation · doi:10.1177/09636897221123512 · Cited by 15

Inhibition of kinesin-5 improves regeneration of injured axons by a novel microtubule-based mechanism

Baas, P., & Matamoros, A. J. (2015) · Neural Regeneration Research · doi:10.4103/1673-5374.158351 · Cited by 15

Deletion of Crmp4 attenuates CSPG-induced inhibition of axonal growth and induces nociceptive recovery after spinal cord injury

Nagai, J., Takaya, R., Piao, W., Goshima, Y., & Ohshima, T. (2016) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2016.03.006 · Cited by 16

Glycans in Regeneration

Babu, P. (2013) · ACS Chemical Biology · doi:10.1021/cb400784j · Cited by 15

The protocadherin alpha cluster is required for axon extension and myelination in the developing central nervous system

Wu, Q., Shen, Q., Lü, W.-C., Zhou, Y., Qiao, P., & Zheng, J. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.228724 · Cited by 14

CXCL1 and CXCL2 Inhibit the Axon Outgrowth in a Time- and Cell-Type-Dependent Manner in Adult Rat Dorsal Root Ganglia Neurons

Deftu, A. T., Ciorescu, R., Gheorghe, R., Mihailescu, D. F., & Ristoiu, V. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02861-x · Cited by 14

No simpler than mammals: axon and dendrite regeneration in Drosophila: Figure 1.Preprint

Nawabi, H., Zukor, K., & He, Z. (2012) · Genes & Development · doi:10.1101/gad.198150.112 · Cited by 14

Pharmacological intervention of early neuropathy in neurodegenerative diseases

Kwon, M. J., Kim, J., Kim, T. S., & Lee, S. B. (2017) · Pharmacological Research · doi:10.1016/j.phrs.2017.02.003 · Cited by 13

Retinoid X receptor α downregulation is required for tail and caudal spinal cord regeneration in the adult newt

Carlone, R. L., Walker, S. E., Nottrodt, R. E., Maddalena, L. G., Carter, C., & Spencer, G. E. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.233447 · Cited by 13

Degeneration of white matter and gray matter revealed by diffusion tensor imaging and pathological mechanism after spinal cord injury in canine

Liu, C., Yang, D., Zhang, X., Zhang, W., Li, D., Zhang, C., Qin, C., Du, L., Li, J., Gao, F., et al. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13044 · Cited by 13

Rodent Models of Spinal Cord Injury: From Pathology to Application

Liu, F., Huang, Y. M., & Wang, H. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03794-8 · Cited by 12

Microfluidic Manipulation for Biomedical Applications in the Central and Peripheral Nervous Systems

Li, Z., Jiang, Z., Lu, L., & Liu, Y. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15010210 · Cited by 12

Contrasting developmental axon regrowth and neurite sprouting of Drosophila mushroom body neurons reveals shared and unique molecular mechanisms

Marmor‐Kollet, N., & Schuldiner, O. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22312 · Cited by 12

Targeting Central Nervous System Regeneration with Cell Type Specificity

Anderson, M. A. (2021) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2021.03.011 · Cited by 12

Microtubule organization of vertebrate sensory neurons in vivo

Shorey, M., Rao, K. S., Stone, M. C., Mattie, F. J., Sagasti, A., & Rolls, M. M. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.06.007 · Cited by 12

Class II HDACs and Neuronal Regeneration

Tang, B. L. (2014) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24802 · Cited by 13

Cranial Pair II: The Optic Nerves

Herrera, E., Agudo‐Barriuso, M., & Murcia‐Belmonte, V. (2018) · The Anatomical Record · doi:10.1002/ar.23922 · Cited by 12

TC10, a Rho family GTPase, is required for efficient axon regeneration in a neuron‐autonomous manner

Koinuma, S., Negishi, R., Nomura, R., Sato, K., Kojima, T., Segi‐Nishida, E., Goitsuka, R., Iwakura, Y., Wada, N., Koriyama, Y., et al. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15235 · Cited by 13

Damage-induced basal epithelial cell migration modulates the spatial organization of redox signaling and sensory neuron regeneration

Fister, A. M., Horn, A. J., Lasarev, M. R., & Anna Huttenlocher, A. (2024) · eLife · doi:10.7554/elife.94995 · Cited by 11

Comparative gene expression profiling reveals the mechanisms of axon regeneration

Lee, J., & Cho, Y. (2020) · FEBS Journal · doi:10.1111/febs.15646 · Cited by 11

Unfolded protein response-induced expression of long noncoding RNA Ngrl1 supports peripheral axon regeneration by activating the PI3K-Akt pathway

Wang, D., Zheng, T., Ge, X., Xu, J., Feng, L., Jiang, C., Tao, J., Chen, Y., Liu, X., Yu, B., et al. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114025 · Cited by 11

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

Williams, R. R., Pearse, D. D., Tresco, P. A., & Bunge, M. B. (2011) · The Journal of Gene Medicine · doi:10.1002/jgm.1628 · Cited by 11

Regulation of axonal remodeling following spinal cord injury

Bareyre, F., & Jacobi, A. (2015) · Neural Regeneration Research · doi:10.4103/1673-5374.167748 · Cited by 11

Induction of axon growth in the adult brain: A new approach to restoration in Parkinson's disease

Padmanabhan, S., & Burke, R. E. (2017) · Movement Disorders · doi:10.1002/mds.27209 · Cited by 11

IPP5 inhibits neurite growth in primary sensory neurons by maintaining TGF- /Smad signaling

Han, Q., Gao, N.-N., Guo-QiangMa, Zhang, Z., Yu, W.-H., Pan, J., Wang, Q., Zhang, X., & Bao, L. (2012) · Journal of Cell Science · doi:10.1242/jcs.114280 · Cited by 11

The role of the immune system during regeneration of the central nervous system

Sabin, K. Z., & Echeverri, K. (2019) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2019.100023 · Cited by 10

Unlocking the potential for optic nerve regeneration over long distances: a multi-therapeutic intervention

Liu, Z.-G., Zhou, L.-Y., Yong-quan, S., Ma, Y., Liu, C.-M., & Zhang, B.-Y. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2024.1526973 · Cited by 12

Advances in electroactive bioscaffolds for repairing spinal cord injury

Liu, Z., Lai, J., Kong, D., Zhao, Y., Zhao, J., Dai, J., & Zhang, M. (2024) · Biomedical Materials · doi:10.1088/1748-605x/ad4079 · Cited by 13

DLK: The “Preconditioning” Signal for Axon Regeneration?

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Lentiviral mediated expression of a NGF-soluble Nogo receptor 1 fusion protein promotes axonal regeneration

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