Axon degeneration mechanisms: commonality amid diversity

Alzheimer's Disease Is a Synaptic Failure

Selkoe, D. J. (2002) · Science · doi:10.1126/science.1074069 · Cited by 4,420

Axonal transection in the lesions of multiple sclerosis

Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029

Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP

Feng, G., Mellor, R. H., Bernstein, M., Keller-Peck, C., Nguyen, Q. T., Wallace, M., Nerbonne, J. M., Lichtman, J. W., & Sanes, J. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00084-2 · Cited by 3,042

Axonal damage in acute multiple sclerosis lesions

Ferguson, B. (1997) · Brain · doi:10.1093/brain/120.3.393 · Cited by 1,532

Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man

Fischer, L. R., Culver, D. G., Tennant, P., Davis, A. A., Wang, M.-S., Castellano-Sanchez, A. A., Khan, J., Polak, M. A., & Glass, J. D. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2003.10.004 · Cited by 1,383

Death by design: apoptosis, necrosis and autophagy

Edinger, A. L., & Thompson, C. B. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.09.011 · Cited by 1,362

Axonopathy and Transport Deficits Early in the Pathogenesis of Alzheimer’s Disease

Stokin, G. B., Lillo, C., Falzone, T. L., Brusch, R. G., Rockenstein, E., Mount, S. L., Raman, R., Davies, P., Masliah, E., Williams, D. S., et al. (2005) · Science · doi:10.1126/science.1105681 · Cited by 1,214

Increased Nuclear NAD Biosynthesis and SIRT1 Activation Prevent Axonal Degeneration

Araki, T., Sasaki, Y., & Milbrandt, J. (2004) · Science · doi:10.1126/science.1098014 · Cited by 1,060

Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination

Lappe-Siefke, C., Goebbels, S., Gravel, M., Nicksch, E., Lee, J., Braun, P. E., Griffiths, I. R., & Nave, K.-A. (2003) · Nature Genetics · doi:10.1038/ng1095 · Cited by 1,036

Erythropoietin prevents neuronal apoptosis after cerebral ischemia and metabolic stress

Sirén, A., Fratelli, M., Brines, M. L., Goemans, C. G., Casagrande, S., Lewczuk, P., Keenan, S., Gleiter, C. H., Pasquali, C., Capobianco, A., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051606598 · Cited by 1,019

Oxidative signaling thresholds shape vulnerability in the central and peripheral nervous systems

Wakatsuki, S., & Araki, T. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3004032 · Cited by 1

A Neurite Quality Index and Machine Vision Software for Improved Quantification of Neurodegeneration

Romero, P. L., Miller, T., & Garakani, A. (2009) · BioTechniques · doi:10.2144/000113305 · Cited by 1

Autoimmunity

Kilpatrick, T. J., Ransohoff, R. M., & Wesselingh, S. L. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9781139195805.006 · Cited by 1

Identification of compounds that cause axonal dieback without cytotoxicity in dorsal root ganglia explants and intervertebral disc cells with potential to treat pain via denervation

Lee, F. S., Nguyen, U. N., Munns, E. J., & Wachs, R. A. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300254 · Cited by 1

High-Field 3 T Imaging of Alzheimer Disease

Luccichenti, G., Péran, P., Cherubini, A., Giugni, E., Scarabino, T., Hagberg, G. E., & Sabatini, U. (2006) · Springer eBooks · doi:10.1007/3-540-31776-7_17 · Cited by 1

Morphological Assessments Following Spinal Cord Injury

Walker, C. L., & Xu, X. (2012) · Springer protocols handbooks/Springer protocols · doi:10.1007/978-1-61779-782-8_36 · Cited by 1

Degenerative and Regenerative Events in the Central and Peripheral Nervous System

Dennis, K., & Valentine, W. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.02189-9 · Cited by 1

High-Field 3 T Imaging of Alzheimer’s Disease

Caligiuri, M. E., Cherubini, A., Scarabino, T., & Sabatini, U. (2017) · Springer eBooks · doi:10.1007/978-3-319-44174-0_18 · Cited by 1

Aging and Parkinson’s Disease: Pathological Insight on Model Mice

Sato, S., & Hattori, N. (2022) · Springer eBooks · doi:10.1007/978-981-16-7977-3_23 · Cited by 1

Increased concentration of tumour necrosis factor alpha in the plasma of glaucoma patients

Trenkić-Božinović, M., Jevtović−Stoimenov, T., Bašić, J., Vasilijević, J., Ristić, D., Trenkić, M. S., Veselinovic, A., & Cvetanović, M. (2023) · Vojnosanitetski pregled · doi:10.2298/vsp230725062t · Cited by 1

Kinetic and statistical mechanical modeling of DNA unzipping and kinesin mechanochemistry

Herskowitz, L. (2011) · UNM’s Digital Repository (University of New Mexico) · Cited by 1

Molecular and Cellular Mechanisms Behind Juvenile Neuronal Ceroid Lipofuscinosis (JNCL, Batten disease)

Luiro, K. (2006) · Työväentutkimus Vuosikirja · Cited by 1

How to repair an ischemic brain injury? Value of experimental models in search of answers

Prieto, R., Pascual, J. M., González-Llanos, F., & Roda, J. M. (2011) · Neurología (English Edition) · doi:10.1016/s2173-5808(11)70016-5 · Cited by 1

Rehabilitation of Executive Dysfunction in Multiple Sclerosis: Cognitive, Behavioural and Neurophysiological Effects of Goal Management Training

Richard, N. M. (2013) · TSpace (University of Toronto) · Cited by 1

Deep learning to decipher the progression and morphology of axonal degenerationPreprint

Palumbo, A., Grüning, P., Landt, S. K., Heckmann, L., Bartram, L., Pabst, A., Flory, C., Ikhsan, M., Pietsch, S., Schulz, R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.26.269092 · Cited by 1

Neurological mechanism of sensory deficits after developmental exposure to non-dioxin-like polychlorinated biphenyls (PCBs)Preprint

Brun, N. R., Panlilio, J. M., Zhang, K., Zhao, Y., Ivashkin, E. G., Stegeman, J. J., & Goldstone, J. V. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.14.430009 · Cited by 1

Absolute Temperature

Wiltschko, W., Kramer, B., Winklhofer, M., Lohmann, K. J., Lohmann, C. M. F., Fransson, P., Ioannides, A. A., Boeke, H., Salcedo, E., Restrepo, D., et al. (2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_13 · Cited by 1

Alzheimer’s disease through the MR-eye; novel diagnostic markers and the road to clinical implementation

Clerx, L. (2014) · Research Publications (Maastricht University) · doi:10.26481/dis.20140516lc · Cited by 1

Zebrafish as a Model for the Study of Parkinson’s Disease

Xi, Y. (2011) · uO Research (University of Ottawa) · doi:10.20381/ruor-4585

Schwann Cell–Axon Interactions: The Molecular and Metabolic Link Between Schwann Cells and Axons

Ohno, N., Sakoh, T., Saitoh, Y., Terada, N., & Ohno, S. (2014) · Springer eBooks · doi:10.1007/978-4-431-54764-8_4

The interplay of JNK and SCG10 during cortical development and in excitotoxic responses in brain

Zdrojewska, J. (2014) · Doria (University of Helsinki)

The Role of Schwann Cell Mitochondrial Metabolism in Schwann Cell Biology and Axonal Survival

Viader, A. (2011) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7319sxj

Pathological and cognitive alterations in mouse models of traumatic brain injury and hypoperfusion

Spain, A. (2011) · ERA

Traumatic brain injury with particular reference to diffuse traumatic axonal injury subpopulations

al-Hasani, O. H. (2011) · ERA

Proteomic Approaches to Axon Injury – Postgenomic Approaches to a Posttranscriptional Process

Michaelevski, I., & Fainzilber, M. (2008) · Wiley eBooks · doi:10.1002/9783527622467.ch7

Axonal Regression in Corticospinal Slice Coculture

Yoshioka, N., Murabe, N., & Sakurai, M. (2013) · The Brain & Neural Networks · doi:10.3902/jnns.20.19

Mechanisms of Axonopathy in Krabbe Disease

Cantuti‐Castelvetri, L. (2012) · Figshare

Mouse embryonic stem cells as a new discovery tool in neurobiology

Plachta, N. (2006) · edoc (University of Basel) · doi:10.5451/unibas-004130499

Microdevices for Isolating Single Axons for the Study of Axonal Transport in Dopaminergic Neurons

Lu, X. (2013) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7ft8j1n

AXONAL RESPONSES TO INJURY

Fainzilber, M. (2008) · Elsevier eBooks · doi:10.1016/b978-012373994-0.50004-x

Retrograde trans-synaptic retinal ganglion cell loss following retrogeniculate lesions of human visual pathway identified using optical coherence tomography

Jindahra, P. (2011) · UCL Discovery (University College London)

Untersuchungen zu synaptischen Proteinen in einem Tiermodell für die Alzheimer-Krankheit

Wente, S. (2011) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1037

Cellular Interactions During Motor Nerve Regeneration

Rosenberg, A. F. (2014) · Scholarly Commons (University of Pennsylvania)

Immunoelectron microscopy reveals the presence of neurofilament proteins in retinal terminals undergoing dark degeneration

Marques, S. A., Mostacada, K., & Martinez, A. M. B. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.045

Axon Death Prevented: Wlds and Other Neuroprotective Molecules: A Dissertation

Avery, M. A. (2010) · eScholarship@UMassChan · doi:10.13028/ejya-6w71

Complex Roles of Constitutive Autophagy in the Neuron and the Axon: Protein Quality Control and Maintenance of Membrane Homeostasis

Yue, Z., Wang, Q. J., & Komatsu, M. (2008)

Prenatal Infection

Knuesel, I. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800228-5.00004-2

Molecular mechanisms of acute axonal degeneration in the rat optic nerve

Zhang, J.-N. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5410

Significance of Mechanism-Oriented Research Toward Neuronal Protection Therapy Against Neurodegenerative Disorders ~ ZNRF1 E3 Ubiquitin Ligase as a Critical Mediator for Wallerian Degeneration and Neuronal Apoptosis

Wakatsuki, S., & Araki, T. (2015) · Springer eBooks · doi:10.1007/978-4-431-54541-5_8

TITULACIÓN: MÁSTER EN INVESTIGACIÓN EN CIENCIAS DE LA SALUD: FARMACOLOGÍA, NEUROBIOLOGÍA Y NUTRICIÓN MOLECULAR

Medicina, F. D. (2013)

Aerobic capacity exercise effect on axon density and g-ratio during nerve regeneration

Park, J., 김종식, & 김동현 (2013) · Exercise Science · doi:10.15857/ksep.2013.22.2.163

Development of magnetic resonance imaging techniques for mouse models of Alzheimer's Disease

O’Callaghan, J. M. (2015) · UCL Discovery (University College London)

A survey of axonal transport function and motor behaviour in Drosophila models of amyotrophic lateral sclerosis

Baldwin, K. R. (2015) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)

Amnesi og herpes simplex encefalitt : en studie med diffusion tensor imaging og hjernemorfometri

Grydeland, H. (2009) · NORA - Norwegian Open Research Archives

Effects of Brief Electrical Stimulation on Embryonic Neurons Transplanted into Peripheral Nerve

Liu, Y. (2013)

The molecular intersection between axon-specific pruning and neuronal apoptosis

Cusack, C. L. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/rrx2-2p18

Mechanisms of axonal pathology in the context of traumatic brain injury

Dastgheyb, R. M., & Barbee, K. A. (2014) · doi:10.17918/etd-6332

Estudo prospectivo dos aspectos neuropsicológicos e da qualidade de vida de doentes com lesão axonial difusa traumática

Zaninotto, A. L. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2016.tde-06102016-095056

Quantitative analysis of neuropathological alterations in two transgenic mouse models of Alzheimer's disease

Kurdakova, A. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5882

Antibodies to Heterogenous Nuclear Ribonucleoprotein A1 Penetrate Neurons Leading to Multiple Downstream Effects Resulting in Neurodegeneration

Douglas, J. N. (2016) · doi:10.21007/etd.cghs.2016.0402

Clinical Symptoms in Parkinson's and Huntington's Diseases Reflect Loss of Connectivity Rather than Loss of Neurons

Brady, S. T. (2012)

Estudo prospectivo dos aspectos neuropsicológicos e da qualidade de vida de doentes com lesão axonial difusa traumática

Paiva, W. S., & Paulo, S. (2016)

Tumour-Suppressor Knockdown as a Strategy for Peripheral Nerve Regeneration: The Effects of PTEN and Rb

Eaton, S. (2016) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28532

Einfluss der Rho-Kinase-Hemmung auf Mikrogliazellen im SOD1-G93A-Mausmodell der Amyotrophen Lateralsklerose

Jansen, J. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6353

Understanding Injury, Health, and Adaptations of the Musculoskeletal System

O'Donnell, M. (2012) · Orthopaedic Section, APTA, Inc. eBooks · doi:10.17832/isc.2012.22.1.1

Cellular pathology and apoptosis in experimental and human acute and chronic compressive myelopathy.

Newcombe, R. (2010) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

New Approaches in Glial Biology

Nikić, I., Misgeld, T., & Kerschensteiner, M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00093-9

Insight into the Cargo Recognition Mechanism of Kinesin Light Chain 1

Lee, H. Y. (2011) · TSpace (University of Toronto)

A DLK And JNK Dependent Axon Self-Destruction Program Promotes Wallerian Degeneration

Miller, B. R. (2011) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k79k4889

In-vivo-Untersuchungen der axonalen Degeneration im Tiermodell der Multiplen Sklerose

Ruhe, J. (2017) · doi:10.53846/goediss-6637

Perfil da expressão dos retrovírus endógenos humanos da família W em pacientes com esclerose múltipla

Nali, L. H. D. S. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.99.2018.tde-26042018-115451

Elucidating regulators and biomarkers of synaptic stability during neurodegeneration

Hurtado, M. L. (2018)

WHITE MATTER AT VARIOUS STAGES OF ALZHEIMER’S DISEASE

Karami, V., Nittari, G., & Amenta, F. (2019) · EPH - International Journal of Applied Science · doi:10.53555/eijas.v5i1.85

Primary Open-Angle Glaucoma, Trans-Lamina Cribrosa Pressure Difference, and Central Nerve System

Fan, N., Liu, G., Zhang, X., & Liu, X. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-2137-5_5

Facteurs cellulaires et moléculaires influençant la régénération axonale dans les systèmes nerveux central et périphérique

Barrette, B. (2008) · Corpus Université Laval (Université Laval)

Estudo sequencial da expressão de citocinas na plasticidade de nervo periférico de ratos utilizando a tubulização látero-terminal

Miguel, V. T. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2019.tde-08082019-100009

The diffusion-tensor MRI data analysis for cerebral microangiopathy influence detection on the integrity of the brain white matter in Alzheimer’s disease patients

Гридин, В. Н., Андреевич, П. В., Солодовников, В. И., & Yakhno, N. N. (2019) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1368/5/052042

Investigating cellular stress in industry and medicine

Hyland, R. A. (2012)

Optic atrophy

Tagg, N. T., & Kardon, R. H. (2010) · Elsevier eBooks · doi:10.1016/b978-0-7020-2983-7.00044-9

On the neurobiology of apathy and depression in cerebral small vessel disease

Tay, J. (2019) · Apollo (University of Cambridge) · doi:10.17863/cam.56769

Magnetic resonance tractography exhibiting retrograde degeneration of the corticospinal tract in a patient with a unilateral spinal cord tumor

Osaki, Y., Sako, W., Harada, M., & Izumi, Y. (2021) · Brain and Behavior · doi:10.1002/brb3.2020

Pathogenic impact of immune cells in mouse models of neuronal ceroid lipofuscinosis

Groh, J. (2013) · Online Publication Service of Würzburg University (Würzburg University)

Ante Mortem Cerebrospinal Fluid Levels of Calsyntenin-1 and Neurexin-2a Reflect Post-Mortem TDP-43 Pathology in a Pathological Cohort of Frontotemporal Lobar DegenerationPreprint

González, A. C., Irwin, D. J., Alcolea, D. A., McMillan, C. T., Chen‐Plotkin, A. S., Wolk, D. A., Sirisi, S., Dols‐Icardo, O., Querol‐Vilaseca, M., Illán‐Gala, I., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-885718/v1

Regulation of Calcium Influx in Drosophila Motorneuron Axon Degeneration

Carson, R. (2014) · Deep Blue (University of Michigan)

Notes on Techniques

ten Donkelaar, H. J., Doorduin, J., Catani, M., & van den Heuvel, M. P. (2020) · Springer eBooks · doi:10.1007/978-3-030-41878-6_3

Role of autophagic protein ULK1 in axonal degeneration and regeneration in rat cortical neurons in vitro

Vahsen, B. F. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8894

Die Effekte des Wlds-Gens und der Gabe von Nikotinamid auf akute und chronisch-sekundäre Axon-Degeneration

Miesbach, T. A. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8730

Retrograde trans-synaptic axonal degeneration in post-geniculate lesions

Mohammed, R. V., Sujithra, H., Pillai, G. S., & Greeshma, C. R. (2022) · Indian Journal of Clinical and Experimental Ophthalmology · doi:10.18231/j.ijceo.2022.022

Multiple Sclerosis: Macrophages and Axonal Loss

Vereyken, E. J. F., Dijkstra, C. D., & Teunissen, C. E. (2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_3645

Spastic Paraplegia, Hereditary

Schüle, R., & Schöls, L. (2009) · Springer eBooks · doi:10.1007/978-3-540-29676-8_1645

Faculty Opinions recommendation of Mitofusin 2 regulates axonal transport of calpastatin to prevent neuromuscular synaptic elimination in skeletal muscles.

Morgan, B. P. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733645134.793552279

Effekte einer pharmakologischen Inhibition der ULK1-Kinase auf die akute axonalen Degeneration in vivo

Sundermeyer, J. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9423

New possibilities of cell and shock wave therapy in erectile function recovery in patients after radical prostatectomy: a review

Епифанова, М. В., Kostin, A. A., Gameeva, E. V., Грицкевич, А. А., Artemenko, S., & Epifanov, А. А. (2023) · Andrology and Genital Surgery · doi:10.17650/2070-9781-2023-24-2-41-48

Axonal transport of autophagosomes in models of neurodegeneration in vitro and in vivo

Luo, X. (2023) · doi:10.53846/goediss-10233

Additional file 1 of Neutral sphingomyelinase inhibition promotes local and network degeneration in vitro and in vivo

Risner, M. L., Ribeiro, M., McGrady, N. R., Kagitapalli, B. S., Chamling, X., Zack, D. J., & Calkins, D. J. (2023) · Figshare · doi:10.6084/m9.figshare.24465162

The regenerative role of mast cells and mesenchymal stem cells in histopathology of sciatic nerve and tibialis cranialis muscle, following denervation in ratsPreprint

Bakhtiary, Z., Shahrooz, R., Hobbenaghi, R., Azizi, S., Soltanalinejad, F., & Khoshfetrat, A. B. (2022) · Research Square · doi:10.21203/rs.3.rs-2312324/v1

Hemispheric Disconnection and Neurodegeneration: Cross-Disciplinary Approaches to Apraxias and Alzheimer’sPreprint

Sanna, M. (2025) · Preprints.org · doi:10.20944/preprints202501.1054.v1

Bridging the Gap: Contemporary Paradigms in Nerve Scaffolds and Regeneration

Hwang, C. D., Caragher, S. P., Bihun, R. J., & Eberlin, K. R. (2025) · Advances in Wound Care · doi:10.1089/wound.2024.0074

Degenerative and Regenerative Events in the Central and Peripheral Nervous System

Dennis, K., & Valentine, W. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.14003-3

APLP1 Interacts with SARM1 and Regulates Axonal Maintenance and Post-Injury Degeneration

Kang, M., Kim, H., Jeon, Y., Shin, Y. K., Park, H. T., & Shin, J. E. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05408-0

Aspectes moleculars de dues malalties de transport lisosòmic: la cistinosi i la malaltia de Niemann-Pick tipus C

Vidal, J. M. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Additional file 2 of In vivo imaging of injured cortical axons reveals a rapid onset form of Wallerian degeneration

Canty, A. J., Jackson, J., Huang, L., Trabalza, A., Bass, C., Little, G. E., Tortora, M., Khan, S., & Paola, V. D. (2020) · Figshare · doi:10.6084/m9.figshare.13257797

Additional file 5 of In vivo imaging of injured cortical axons reveals a rapid onset form of Wallerian degeneration

Canty, A. J., Jackson, J., Huang, L., Trabalza, A., Bass, C., Little, G. E., Tortora, M., Khan, S., & Paola, V. D. (2020) · Figshare · doi:10.6084/m9.figshare.13257803

Additional file 4 of In vivo imaging of injured cortical axons reveals a rapid onset form of Wallerian degeneration

Canty, A. J., Jackson, J., Huang, L., Trabalza, A., Bass, C., Little, G. E., Tortora, M., Khan, S., & Paola, V. D. (2020) · Figshare · doi:10.6084/m9.figshare.13257800

Additional file 1 of In vivo imaging of injured cortical axons reveals a rapid onset form of Wallerian degeneration

Canty, A. J., Jackson, J. S., Huang, L., Trabalza, A., Bass, C., Little, G. E., Tortora, M., Khan, S., & Paola, V. D. (2020) · Figshare · doi:10.6084/m9.figshare.13257794

Additional file 1 of Photobiomodulation improves the synapses and cognitive function and ameliorates epileptic seizure by inhibiting downregulation of Nlgn3

Hong, N., Kim, H. J., Kang, K., Park, J. O., Mun, S., Kim, H.-G., Kang, B. H., Chung, P.-S., Lee, M. Y., & Ahn, J.-C. (2023) · Figshare · doi:10.6084/m9.figshare.22610494

Epothilone B stabilizes microtubules via Tau to protect retinal ganglion cells and promote axon regeneration

Liang, Y., Chi, J., Sun, Y.-J., Li, Y.-Z., Li, G.-Y., & Li, G.-Y. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02733-2

The Neuroameliorative Effects of Enzymatically Modified Isoquercitrin and Sodium R-lipoate on the Rotenone rat Model of Parkinson’s Disease

Hassouna, I. A., Hassanein, O., El-Elaimy, I. A., & Ibrahim, H. M. (2026) · Neurochemical Research · doi:10.1007/s11064-026-04715-9

Metabolomic changes associated with behavioral and molecular findings: Triclocarban toxicity in the zebrafish model

Sulukan, E. (2026) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2026.110523

Etude de limplication de CaMKIα dans la régénération post-lésionnelle des neurones des ganglions rachidiens dorsaux.

Elzière, L. (2010) · theses.fr (ABES) · doi:10.70675/33df2c2azf851z46fdza011z322a433e963c

Acquired axonal degeneration and regeneration

Benarroch, E. E. (2015) · Neurology · doi:10.1212/wnl.0000000000001601 · Cited by 24

Axon degeneration: Molecular mechanisms of a self-destruction pathway

Wang, J. T., Medress, Z. A., & Barres, B. A. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201108111 · Cited by 464

Axonal degeneration as a therapeutic target in the CNS

Lingor, P., Koch, J. C., Tönges, L., & Bähr, M. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1362-3 · Cited by 119

Wallerian Degeneration in Injury and Diseases: Concepts and Prevention

Mietto, B. S., Rodrigo, M., de Lima, S., Sergio, T., & Martinez, A. M. B. (2011) · InTech eBooks · doi:10.5772/31927 · Cited by 5

Axon degeneration and rescue

Griffin, J. W., Höke, A., & Nguyen, T. T. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511545061.020 · Cited by 3