Determinants of conduction velocity in myelinated nerve fibers

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(1976) · Medical Entomology and Zoology · Cited by 1,328

A theory of the effects of fibre size in medullated nerve

Rushton, W. A. H. (1951) · The Journal of Physiology · doi:10.1113/jphysiol.1951.sp004655 · Cited by 1,075

CONDUCTION VELOCITY AND DIAMETER OF NERVE FIBERS

Hursh, J. B. (1939) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1939.127.1.131 · Cited by 916

Evoked action potentials and conduction velocity in human sensory nerves

Buchthal, F., & Rosenfalck, A. (1966) · Brain Research · doi:10.1016/0006-8993(66)90056-4 · Cited by 748

Evidence for saltatory conduction in peripheral myelinated nerve fibres

Huxley, A. F., & Stämpeli, R. (1949) · The Journal of Physiology · doi:10.1113/jphysiol.1949.sp004335 · Cited by 665

Peripheral Neuropathy.

(1976) · Annals of Internal Medicine · doi:10.7326/0003-4819-85-1-141_2 · Cited by 636

AXON DIAMETERS IN RELATION TO THE SPIKE DIMENSIONS AND THE CONDUCTION VELOCITY IN MAMMALIAN A FIBERS

Gasser, H. S., & Grundfest, H. (1939) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1939.127.2.393 · Cited by 452

Relative conduction velocities of small myelinated and non-myelinated fibres in the central nervous system

WAXMAN, S. G., & BENNETT, M. V. L. (1972) · Nature New Biology · doi:10.1038/newbio238217a0 · Cited by 444

Density of sodium channels in mammalian myelinated nerve fibers and nature of the axonal membrane under the myelin sheath.

Ritchie, J. M., & Rogart, R. B. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.1.211 · Cited by 350

THE RÔLE PLAYED BY THE SIZES OF THE CONSTITUENT FIBERS OF A NERVE TRUNK IN DETERMINING THE FORM OF ITS ACTION POTENTIAL WAVE

Gasser, H. S., & Erlanger, J. (1927) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1927.80.3.522 · Cited by 328

Axonal Neuregulin-1 Regulates Myelin Sheath Thickness

Michailov, G. V., Sereda, M. W., Brinkmann, B. G., Fischer, T. M., Haug, B., Birchmeier, C., Role, L. W., Lai, C., Schwab, M. H., & Nave, K. (2004) · Science · doi:10.1126/science.1095862 · Cited by 940

Axcaliber: A method for measuring axon diameter distribution from diffusion MRI

Assaf, Y., Blumenfeld‐Katzir, T., Yovel, Y., & Basser, P. J. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21577 · Cited by 849

Modeling the Excitability of Mammalian Nerve Fibers: Influence of Afterpotentials on the Recovery Cycle

McIntyre, C. C., Richardson, A. G., & Grill, W. M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00353.2001 · Cited by 764

Biomechanics of Sprint Running

Mero, A. A., Komi, P. V., & Gregor, R. J. (1992) · Sports Medicine · doi:10.2165/00007256-199213060-00002 · Cited by 688

Hierarchy of transcriptomic specialization across human cortex captured by structural neuroimaging topography

Burt, J. B., Demirtaş, M., Eckner, W. J., Navejar, N. M., Ji, J. L., Martin, W. J., Bernacchia, A., Anticevic, A., & Murray, J. D. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0195-0 · Cited by 657

Investigating white matter fibre density and morphology using fixel-based analysis.

Raffelt, D. A., Tournier, J.-D., Smith, R. E., Vaughan, D. N., Jackson, G., Ridgway, G. R., & Connelly, A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.029 · Cited by 620

Accelerated microstructure imaging via Convex Optimization (AMICO) from diffusion MRI data

Daducci, A., Canales-Rodríguez, E. J., Zhang, H., Dyrby, T. B., Alexander, D. C., & Thiran, J.-P. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.026 · Cited by 593

Apparent Fibre Density: A novel measure for the analysis of diffusion-weighted magnetic resonance images

Raffelt, D., Tournier, J.-D., Rose, S., Ridgway, G., Henderson, R., Crozier, S., Salvado, O., & Connelly, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.045 · Cited by 616

Autism as a neural systems disorder: A theory of frontal-posterior underconnectivity

Just, M. A., Keller, T. A., Malave, V. L., Kana, R. K., & Varma, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.02.007 · Cited by 578

Training of Working Memory Impacts Structural Connectivity

Takeuchi, H., Sekiguchi, A., Taki, Y., Yokoyama, S., Yomogida, Y., Komuro, N., Yamanouchi, T., Suzuki, S., & Kawashima, R. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4611-09.2010 · Cited by 531

Mild respiratory COVID can cause multi-lineage neural cell and myelin dysregulation

Fernández-Castañeda, A., Lu, P., Geraghty, A. C., Song, E., Lee, M.-H., Wood, J., O’Dea, M. R., Dutton, S., Shamardani, K., Nwangwu, K., et al. (2022) · Cell · doi:10.1016/j.cell.2022.06.008 · Cited by 521

Cognitive processing speed and the structure of white matter pathways: Convergent evidence from normal variation and lesion studies

Turken, U., Whitfield-Gabrieli, S., Bammer, R., Baldo, J. V., Dronkers, N. F., & Gabrieli, J. D. E. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.057 · Cited by 500

Myelin-Associated Glycoprotein Is a Myelin Signal that Modulates the Caliber of Myelinated Axons

Yin, X., Crawford, T. O., Griffin, J. W., Tu, P., Lee, V. M. ‐., Li, C. C., Roder, J., & Trapp, B. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-06-01953.1998 · Cited by 491

Growth of white matter in the adolescent brain: Myelin or axon?

Paus, T. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2009.06.002 · Cited by 424

Polarized Domains of Myelinated Axons

Salzer, J. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00628-7 · Cited by 416

Aβ-fiber nociceptive primary afferent neurons: a review of incidence and properties in relation to other afferent A-fiber neurons in mammals

Djouhri, L., & Lawson, S. N. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.07.015 · Cited by 398

The social brain in adolescence: evidence from functional magnetic resonance imaging and behavioural studies

Burnett, S., Sebastian, C., Cohen Kadosh, K., & Blakemore, S.-J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.011 · Cited by 391

In vivo measurement of axon diameter distribution in the corpus callosum of rat brain

Barazany, D., Basser, P. J., & Assaf, Y. (2009) · Brain · doi:10.1093/brain/awp042 · Cited by 400

Schwann Cell MyelinationPreprint

Salzer, J. L. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020529 · Cited by 392

Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models

Chrast, R., Saher, G., Nave, K.-A., & Verheijen, M. H. G. (2011) · Journal of Lipid Research · doi:10.1194/jlr.r009761 · Cited by 314

Change of conduction velocity by regional myelination yields constant latency irrespective of distance between thalamus and cortex

Salami, M., Itami, C., Tsumoto, T., & Kimura, F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0937380100 · Cited by 314

αβγ-Synuclein triple knockout mice reveal age-dependent neuronal dysfunction

Greten-Harrison, B., Polydoro, M., Morimoto‐Tomita, M., Diao, L., Williams, A. M., Nie, E. H., Makani, S., Tian, N., Castillo, P. E., Buchman, V. L., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005005107 · Cited by 305

Altered white matter connectivity as a neural substrate for social impairment in Autism spectrum disorder

Ameis, S. H., & Catani, M. (2015) · Cortex · doi:10.1016/j.cortex.2014.10.014 · Cited by 301

Oligodendroglial myelination requires astrocyte-derived lipids

Camargo, N., Goudriaan, A., van Deijk, A.-L. F., Otte, W. M., Brouwers, J. F., Lodder, H., Gutmann, D. H., Nave, K.-A., Dijkhuizen, R. M., Mansvelder, H. D., et al. (2017) · PLOS Biology · doi:10.1371/journal.pbio.1002605 · Cited by 296

Tuning of Ranvier node and internode properties in myelinated axons to adjust action potential timing

Ford, M. C., Alexandrova, O., Cossell, L., Stange-Marten, A., Sinclair, J., Kopp‐Scheinpflug, C., Pecka, M., Attwell, D., & Grothe, B. (2015) · Nature Communications · doi:10.1038/ncomms9073 · Cited by 295

Quantitative magnetic resonance imaging of brain anatomy and in vivo histology

Weiskopf, N., Edwards, L., Helms, G., Mohammadi, S., & Kirilina, E. P. (2021) · Nature Reviews Physics · doi:10.1038/s42254-021-00326-1 · Cited by 309

Biology and pathology of nonmyelinating Schwann cells

Griffin, J. W., & Thompson, W. J. (2008) · Glia · doi:10.1002/glia.20778 · Cited by 293

Axotomy-induced alterations in the electrophysiological characteristics of neurons

Titmus, M. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90039-j · Cited by 273

The effects of SIFT on the reproducibility and biological accuracy of the structural connectome

Smith, R. E., Tournier, J.-D., Calamante, F., & Connelly, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.004 · Cited by 266

TIMING OF SYNAPTIC TRANSMISSION

Sabatini, B. L., & Regehr, W. G. (1999) · Annual Review of Physiology · doi:10.1146/annurev.physiol.61.1.521 · Cited by 260

Schwann cell functions in peripheral nerve development and repair

Bosch-Queralt, M., Fledrich, R., & Stassart, R. M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105952 · Cited by 257

Uniform olivocerebellar conduction time underlies Purkinje cell complex spike synchronicity in the rat cerebellum.

Sugihara, I., Lang, E. J., & Llinas, R. H. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019857 · Cited by 248

Regional modulation of neurofilament organization by myelination in normal axons

Hsieh, S., Kidd, G. J., Crawford, T., Xu, Z., Lin, W., Trapp, B., Cleveland, D. W., & Griffin, J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06392.1994 · Cited by 238

Regulation of conduction time along axons

Seidl, A. H. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.06.047 · Cited by 243

On Myelinated Axon Plasticity and Neuronal Circuit Formation and Function

Almeida, R. G., & Lyons, D. A. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3185-16.2017 · Cited by 221

White matter structures associated with creativity: Evidence from diffusion tensor imaging

Takeuchi, H., Taki, Y., Sassa, Y., Hashizume, H., Sekiguchi, A., Fukushima, A., & Kawashima, R. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.035 · Cited by 223

Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy

Powers, J. M., DeCiero, D. P., Ito, M., Moser, A. B., & Moser, H. W. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.2.89 · Cited by 204

Regulation of myelin structure and conduction velocity by perinodal astrocytes

Dutta, D. J., Woo, D. H., Lee, P. R., Pajevic, S., Bukalo, O., Huffman, W. C., Wake, H., Basser, P. J., SheikhBahaei, S., Lazarevic, V., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1811013115 · Cited by 203

Neuregulin 1–erbB Signaling Is Necessary for Normal Myelination and Sensory Function

Chen, S., Velardez, M. O., Warot, X. M., Yu, Z.-X., Miller, S. J., Cros, D. P., & Corfas, G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3785-05.2006 · Cited by 192

Dlg1-PTEN Interaction Regulates Myelin Thickness to Prevent Damaging Peripheral Nerve Overmyelination

Cotter, L., Özçelik, M., Jacob, C., Pereira, J. A., Locher, V., Baumann, R., Relvas, J. B., Suter, U., & Tricaud, N. (2010) · Science · doi:10.1126/science.1187735 · Cited by 191

AAEM minimonograph #14: The influence of temperature in clinical neurophysiology

Denys, E. H. (1991) · Muscle & Nerve · doi:10.1002/mus.880140902 · Cited by 189

Beyond faithful conduction: Short-term dynamics, neuromodulation, and long-term regulation of spike propagation in the axon

Bucher, D. M., & Goaillard, J. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.06.001 · Cited by 189

Myelin Dynamics Throughout Life: An Ever-Changing Landscape?

Williamson, J., & Lyons, D. A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00424 · Cited by 194

Glial Regulation of the Neuronal Connectome through Local and Long-Distant Communication

Fields, R. D., Woo, D. H., & Basser, P. J. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.014 · Cited by 184

Can MRI measure myelin? Systematic review, qualitative assessment, and meta-analysis of studies validating microstructural imaging with myelin histology

Lazari, A., & Lipp, I. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117744 · Cited by 176

Noninvasive quantification of axon radii using diffusion MRI

Veraart, J., Nunes, D., Rudrapatna, U. S., Fieremans, E., Jones, D. K., Novikov, D. S., & Shemesh, N. (2020) · eLife · doi:10.7554/elife.49855 · Cited by 185

Methylcobalamin increases Erk1/2 and Akt activities through the methylation cycle and promotes nerve regeneration in a rat sciatic nerve injury model

Okada, K., Tanaka, H., Temporin, K., OKAMOTO, M. T., Kuroda, Y., Moritomo, H., Murase, T., & Yoshikawa, H. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2009.12.017 · Cited by 172

Remodeling myelination: implications for mechanisms of neural plasticity

Chang, K.-J., Redmond, S., & Chan, J. R. (2016) · Nature Neuroscience · doi:10.1038/nn.4200 · Cited by 171

The role of diffusion MRI in neuroscience

Assaf, Y., Johansen‐Berg, H., & Thiebaut de Schotten, M. (2019) · NMR in Biomedicine · doi:10.1002/nbm.3762 · Cited by 158

Compound action potentials recorded in the human spinal cord during neurostimulation for pain relief

Parker, J. L., Karantonis, D. M., Single, P. S., Obradovic, M., & Cousins, M. J. (2011) · Pain · doi:10.1016/j.pain.2011.11.023 · Cited by 158

Reliability of measuring isometric and isokinetic peak torque, rate of torque development, integrated electromyography, and tibial nerve conduction velocity

Sleivert, G. G., & Wenger, H. A. (1994) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/0003-9993(94)90279-8 · Cited by 155

White matter architecture rather than cortical surface area correlates with the EEG alpha rhythm

Valdes-Hernandez, P. A., Ojeda, A., Martínez‐Montes, E., Lage‐Castellanos, A., Virues-Alba, T. A., Valdés-Urrutia, L., & Valdes-Sosa, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.030 · Cited by 153

Cerebral White Matter Myelination and Relations to Age, Gender, and Cognition: A Selective Review

Buianova, I., & Arsalidou, M. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.662031 · Cited by 158

The relationship between axon diameter, myelin thickness and conduction velocity during atrophy of mammalian peripheral nerves

Gillespie, M. J., & Stein, R. B. (1983) · Brain Research · doi:10.1016/0006-8993(83)91065-x · Cited by 143

No evidence for chronic demyelination in spared axons after spinal cord injury in a mouse

Lasiene, J., Shupe, L., Perlmutter, S., & Horner, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4756-07.2008 · Cited by 133

The relationship between nerve conduction velocity and fiber morphology during peripheral nerve regeneration

Ikeda, M., & Oka, Y. (2012) · Brain and Behavior · doi:10.1002/brb3.61 · Cited by 131

Maladaptive myelination promotes generalized epilepsy progression

Knowles, J. K., Xu, H., Soane, C., Batra, A., Saucedo, T., Frost, E., Tam, L. T., Fraga, D. A., Ni, L., Villar, K., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01052-2 · Cited by 130

Potential use of glutathione for the prevention and treatment of diabetic neuropathy in the streptozotocin-induced diabetic rat

Bravenboer, B., Kappelle, A. C., Hamers, F. P. T., van Buren, T., Erkelens, D. W., & Gispen, W. H. (1992) · Diabetologia · doi:10.1007/bf00399926 · Cited by 129

Gene replacement in mice reveals that the heavily phosphorylated tail of neurofilament heavy subunit does not affect axonal caliber or the transit of cargoes in slow axonal transport

Rao, M. V., Garcia, M. L., Miyazaki, Y., Gotow, T., Yuan, A., Mattina, S., Ward, C. M., Calcutt, N. A., Uchiyama, Y., Nixon, R. A., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202037 · Cited by 128

Intrauterine growth restriction affects the maturation of myelin

Tolcos, M., Bateman, E., O'Dowd, R., Markwick, R., Vrijsen, K., Rehn, A., & Rees, S. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.08.002 · Cited by 125

Structural biology and molecular pharmacology of voltage-gated ion channels

Huang, J., Pan, X., & Yan, N. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00763-7 · Cited by 131

Org.2766 improves functional and electrophysiological aspects of regenerating sciatic nerve in the rat

Koning, P. D., & Gispen, W. H. (1987) · Peptides · doi:10.1016/0196-9781(87)90003-9 · Cited by 124

Mapping an index of the myelin g-ratio in infants using magnetic resonance imaging

Dean, D. C., O'Muircheartaigh, J., Dirks, H., Travers, B. G., Adluru, N., Alexander, A. L., & Deoni, S. C. L. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.040 · Cited by 121

Electrophysiological properties of axons in mice lacking neurofilament subunit genes: disparity between conduction velocity and axon diameter in absence of NF-H

Križ, J., Zhu, Q., Julien, J., & Padjen, A. L. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02899-7 · Cited by 121

The neurofilament middle molecular mass subunit carboxyl-terminal tail domains is essential for the radial growth and cytoskeletal architecture of axons but not for regulating neurofilament transport rate

Rao, M. V., Campbell, J., Yuan, A., Kumar, A. R., Gotow, T., Uchiyama, Y., & Nixon, R. A. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200308076 · Cited by 120

ERK1/2 Activation in Preexisting Oligodendrocytes of Adult Mice Drives New Myelin Synthesis and Enhanced CNS Function

Jeffries, M. A., Urbanek, K., Torres, L., Wendell, S. G., Rubio, M. E., & Fyffe-Maricich, S. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1444-16.2016 · Cited by 126

Nerve conduction velocity varies inversely with height

Campbell, W. W., Ward, L. C., & Swift, T. R. (1981) · Muscle & Nerve · doi:10.1002/mus.880040609 · Cited by 119

Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system

Figlia, G., Norrmén, C., Pereira, J. A., Gerber, D., & Suter, U. (2017) · eLife · doi:10.7554/elife.29241 · Cited by 116

Evidence for Myelin Sheath Remodeling in the CNS Revealed by In Vivo Imaging

Auer, F., Vagionitis, S., & Czopka, T. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.017 · Cited by 123

Age-related myelin dynamics revealed by increased oligodendrogenesis and short internodes

Lasiene, J., Matsui, A., Sawa, Y., Wong, F., & Horner, P. J. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00462.x · Cited by 111

Overexpression of Nerve Growth Factor in Skin Selectively Affects the Survival and Functional Properties of Nociceptors

Stucky, C. L., Koltzenburg, M., Schneider, M., Engle, M. G., Albers, K. M., & Davis, B. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08509.1999 · Cited by 111

Krüppel-like transcription factors in the nervous system: Novel players in neurite outgrowth and axon regeneration

Moore, D. L., Apara, A., & Goldberg, J. L. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.05.005 · Cited by 113

Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders

Blijham, P. J., Laak, H. J. T., Schelhaas, H. J., van Engelen, B. G. M., Stegeman, D. F., & Zwarts, M. J. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01009.2005 · Cited by 110

The membrane periodic skeleton is an actomyosin network that regulates axonal diameter and conduction

Costa, A. R., Sousa, S., Pinto‐Costa, R., Mateus, J. C., Lopes, C. D. F., Costa, A. C., Rosa, D., Machado, D., Pajuelo, L. S. M., Wang, X., et al. (2020) · eLife · doi:10.7554/elife.55471 · Cited by 109

Multimodal neuroimaging dissociates hemodynamic and electrophysiological correlates of error processing

Agam, Y., Hämäläinen, M., Lee, A. K. C., Dyckman, K. A., Friedman, J. S., Isom, M., Makris, N., & Manoach, D. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103475108 · Cited by 114

Somatodendritic Expression of JAM2 Inhibits Oligodendrocyte Myelination

Redmond, S., Mei, F., Eshed‐Eisenbach, Y., Osso, L. A., Leshkowitz, D., Shen, Y. A., Kay, J. N., Aurrand‐Lions, M., Lyons, D. A., Peles, E., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.021 · Cited by 115

Effects of Supramaximal Velocity on Biomechanical Variables in Sprinting

Mero, A. A., & Komi, P. V. (1985) · International Journal of Sport Biomechanics · doi:10.1123/ijsb.1.3.240 · Cited by 106

Remyelination reporter reveals prolonged refinement of spontaneously regenerated myelin

Powers, B. E., Sellers, D. L., Lovelett, E. A., Cheung, W., Aalami, S., Zapertov, N., Maris, D. O., & Horner, P. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210293110 · Cited by 112

A biomimetic 2D transistor for audiomorphic computing

Das, S., Dodda, A., & Das, S. (2019) · Nature Communications · doi:10.1038/s41467-019-11381-9 · Cited by 103

Mild respiratory SARS-CoV-2 infection can cause multi-lineage cellular dysregulation and myelin loss in the brainPreprint

Fernández-Castañeda, A., Lu, P., Geraghty, A. C., Song, E., Lee, M.-H., Wood, J., Yalçın, B., Taylor, K. R., Dutton, S., Acosta-Alvarez, L., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.07.475453 · Cited by 103

The distribution of conduction velocities (DCV) in peripheral nerves: A review

Dorfman, L. J. (1984) · Muscle & Nerve · doi:10.1002/mus.880070103 · Cited by 99

Electrospun nanofiber sheets incorporating methylcobalamin promote nerve regeneration and functional recovery in a rat sciatic nerve crush injury model

Suzuki, K., Tanaka, H., Ebara, M., Uto, K., Matsuoka, H., Nishimoto, S., Okada, K., Murase, T., & Yoshikawa, H. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.02.004 · Cited by 97

Activation of MAPK overrides the termination of myelin growth and replaces Nrg1/ErbB3 signals during Schwann cell development and myelinationPreprint

Sheean, M. E., McShane, E., Chéret, C., Walcher, J., Müller, T. H., Wulf-Goldenberg, A., Hoelper, S., Garratt, A. N., Krüger, M., Rajewsky, K., et al. (2014) · Genes & Development · doi:10.1101/gad.230045.113 · Cited by 103

Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review

Berciano, J., Garcı́a, A., Gallardo, E. C., Peeters, K., Pelayo‐Negro, A. L., Álvarez‐Paradelo, S., Gazulla, J., Martínez-Tames, M., Infante, J., & Jordanova, A. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8474-3 · Cited by 96

Neurofilament light chain polypeptide gene mutations in Charcot–Marie–Tooth disease: nonsense mutation probably causes a recessive phenotype

Abe, A., Numakura, C., Saito, K., Koide, H., Oka, N., Honma, A., Kishikawa, Y., & Hayasaka, K. (2009) · Journal of Human Genetics · doi:10.1038/jhg.2008.13 · Cited by 96

Individual prediction of white matter injury following traumatic brain injury

Hellyer, P. J., Leech, R., Ham, T. E., Bonnelle, V., & Sharp, D. J. (2012) · Annals of Neurology · doi:10.1002/ana.23824 · Cited by 95

Adaptive and maladaptive myelination in health and disease

Knowles, J. K., Batra, A., Xu, H., & Monje, M. (2022) · Nature Reviews Neurology · doi:10.1038/s41582-022-00737-3 · Cited by 97

The neurotrophin receptor p75NTR in Schwann cells is implicated in remyelination and motor recovery after peripheral nerve injury

Tomita, K., Kubo, T., Matsuda, K., 藤原敏宏, Yano, K., Winograd, J. M., Tohyama, M., & Hosokawa, K. (2007) · Glia · doi:10.1002/glia.20533 · Cited by 93

Changes in motor and sensory nerve conduction parameters with temperature in normal and diseased nerve

Diószeghy, P., & Stålberg, E. (1992) · Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section · doi:10.1016/0168-5597(92)90110-w · Cited by 91

Toward more rational nerve conduction interpreations: The effect of height

Rivener, M. H., Swift, T. R., Crout, B. O., & Rhodes, K. P. (1990) · Muscle & Nerve · doi:10.1002/mus.880130310 · Cited by 93

Anti‐myelin‐associated glycoprotein antibodies alter neurofilament spacing

Lunn, M. P., Crawford, T. O., Hughes, R. A., Griffin, J. W., & Sheikh, K. A. (2002) · Brain · doi:10.1093/brain/awf072 · Cited by 90

The effects of intrauterine growth retardation on the development of neuroglia in fetal guinea pigs. An immunohistochemical and an ultrastructural study

Nitsos, I., & Rees, S. M. (1990) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(90)90029-2 · Cited by 88

Comparative electrophysiological, functional, and histological studies of nerve lesions in rats

Wolthers, M., Moldovan, M., Binderup, T., Schmalbruch, H., & Krarup, C. (2005) · Microsurgery · doi:10.1002/micr.20156 · Cited by 87

Alterations in the oligodendrocyte lineage, myelin, and white matter in adult mice lacking the chemokine receptor CXCR2

Padovani-Claudio, D. A., Liu, L., Ransohoff, R. M., & Miller, R. H. (2006) · Glia · doi:10.1002/glia.20383 · Cited by 90

White matter maturation supports the development of reasoning ability through its influence on processing speed

Ferrer, E. E., Whitaker, K. J., Steele, J. S., Green, C. T., Wendelken, C., & Bunge, S. A. (2013) · Developmental Science · doi:10.1111/desc.12088 · Cited by 96

Increasing Internodal Distance in Myelinated Nerves Accelerates Nerve Conduction to a Flat Maximum

Wu, L. M. N., Williams, A., Delaney, A., Sherman, D. L., & Brophy, P. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.025 · Cited by 90

Axonal Thinning and Extensive Remyelination without Chronic Demyelination in Spinal Injured Rats

Powers, B. E., Lasiene, J., Plemel, J. R., Shupe, L., Perlmutter, S. I., Tetzlaff, W., & Horner, P. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0002-12.2012 · Cited by 88

Collagen VI regulates peripheral nerve myelination and function

Chen, P., Cescon, M., Megighian, A., & Ronaldo, P. (2013) · The FASEB Journal · doi:10.1096/fj.13-239533 · Cited by 84

Estimating axon conduction velocity in vivo from microstructural MRI

Drakesmith, M., Harms, R., Rudrapatna, S. U., Parker, G. D., Evans, C. J., & Jones, D. K. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116186 · Cited by 83

Phase-lags in large scale brain synchronization: Methodological considerations and in-silico analysis

Petkoski, S., Palva, J. M., & Jirsa, V. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006160 · Cited by 88

Study of conduction in a new model of the myelinated nerve fiber

Halter, J. A., & Clark, J. W. (2003) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.1989.96183 · Cited by 4

Conduction velocity and spike configuration in myelinated fibres: computed dependence on internode distance.

Brill, M. H., Waxman, S. G., Moore, J. W., & Joyner, R. W. (1977) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.40.8.769 · Cited by 213

[Neural conduction velocity, fiber size and internodal length of myelinated nerve fibers in animals of different sizes].

Spaan, G., Schnepp, G., Schnepp, P., Oksche, A., & Klussmann, F. W. (1969) · PubMed · Cited by 1

Simulation of the conduction velocity properties of nerve fibres by an electrical model

POLLAK, V., Ferbert, A., & Schulze-Clewing, J. (1993) · Medical & Biological Engineering & Computing · doi:10.1007/bf02446693 · Cited by 3

Myelinated nerve fibers: computed effect of myelin thickness on conduction velocity

Rs, S., & Koles, Z. J. (1970) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1970.219.5.1256 · Cited by 215