Remodeling of the corticospinal innervation and spontaneous behavioral recovery after ischemic stroke in adult mice
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Background and Purpose— To elucidate how the motor pathways rewire the denervated tissue after stroke, we investigated remodeling of the corticospinal tract (CST) in transgenic mice with yellow fluorescent protein CST labeling in conjunction with transsynaptic pseudorabies virus retrograde tracing. Methods— Adult male CST-yellow fluorescent protein mice were subjected to permanent right middle cerebral artery occlusion (n=8/group). Foot-fault test was performed to monitor functional deficit and recovery. Pseudorabies virus tracer was injected into the left forelimb muscles at 1 or 4 weeks after middle cerebral artery occlusion (4 days before euthanasia), respectively. A third group of CST-yellow fluorescent protein mice without middle cerebral artery occlusion was used for normal control (n=6). The yellow fluorescent protein labeling of CST in the cervical cord and pseudorabies virus labeling of pyramidal neurons in the bilateral cortices were measured on vibratome sections using a confocal imaging system. Results— Compared with normal animals, axonal density in the stroke-affected side of the cervical cord was significantly decreased at 11 days ( P <0.001) and significantly increased at 32 days after stroke compared with the Day 11 values ( P <0.05). Pseudorabies virus labeling was significantly decreased in the ischemic hemisphere 11 days after middle cerebral artery occlusion ( P <0.001). In contrast, a significant increase was observed in pseudorabies virus labeling of bilateral cortices 32 days after stroke compared with 11 days ( P <0.05). The CST axonal density in the denervated spinal cord and pyramidal neuron labeling in the bilateral cortices were significantly correlated with behavioral recovery ( P <0.05). Conclusions— Spontaneous functional recovery after stroke may, at least in part, be attributed to neuronal remodeling in the corticospinal system.
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Stroke induces anterograde Wallerian degeneration of pyramidal tract axons, with degree depending on severity of ischaemic insult.
“Stroke induces anterograde Wallerian degeneration of pyramidal tract axons, the degree of which depends on the severity of the ischaemic insult (figure 1).19,21,22”
From Promoting brain remodelling and plasticity for stroke recovery: therapeutic promise and potential pitfalls of clinical translation (2012) · cites this paper as [22]
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Cites
A Semiautomated Method for Measuring Brain Infarct Volume
Swanson, R., Morton, M. T., Tsao-Wu, G., Savalos, R. A., Davidson, C., & Sharp, F. (1990) · Journal of Cerebral Blood Flow and Metabolism · doi:10.1038/jcbfm.1990.47 · Cited by 1,727 · see citing works
Glial inhibition of CNS axon regeneration
Yiu, G. C., & He, Z. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1956 · Cited by 1,500 · see citing works
The role of ipsilateral premotor cortex in hand movement after stroke
Johansen‐Berg, H., Rushworth, M. F. S., Bogdanovic, M. D., Kischka, U., Wimalaratna, S., & Matthews, P. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.222536799 · Cited by 785 · see citing works
Evolution of Cortical Activation During Recovery From Corticospinal Tract Infarction
Marshall, R. S., Perera, G. M., Lazar, R. M., Krakauer, J. W., Constantine, R. C., & DeLaPaz, R. L. (2000) · Stroke · doi:10.1161/01.str.31.3.656 · Cited by 617 · see citing works
Cellular and molecular mechanisms of neural repair after stroke: making waves
Carmichael, S. T. (2006) · Annals of Neurology · doi:10.1002/ana.20845 · Cited by 595 · see citing works
Atorvastatin Induction of VEGF and BDNF Promotes Brain Plasticity after Stroke in Mice
Chen, J., Zhang, C., Jiang, H., Li, Y., Zhang, L., Robin, A. M., Katakowski, M., Lü, M., & Chopp, M. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600034 · Cited by 451 · see citing works
Self-citationReorganization of the human ipsilesional premotor cortex after stroke
Fridman, E. A. (2004) · Brain · doi:10.1093/brain/awh082 · Cited by 435 · see citing works
Role of the Premotor Cortex in Recovery From Middle Cerebral Artery Infarction
Seitz, R. J., Höflich, P., Binkofski, F., Tellmann, L., Herzog, H. R., & Freund, H. (1998) · Archives of Neurology · doi:10.1001/archneur.55.8.1081 · Cited by 375 · see citing works
Nogo Receptor Antagonism Promotes Stroke Recovery by Enhancing Axonal Plasticity
Lee, J.-K., Kim, J., Sivula, M., & Strittmatter, S. M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1643-04.2004 · Cited by 338 · see citing works
Mechanisms for recovery of motor function following cortical damage
Nudo, R. J. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.004 · Cited by 332 · see citing works
Recovery recapitulates ontogeny
Cramer, S. C., & Chopp, M. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01562-9 · Cited by 326 · see citing works
Self-citationInfection and Spread of Alphaherpesviruses in the Nervous System
Enquist, L. W., Husak, P. J., Banfield, B. W., & Smith, G. A. (1998) · Advances in virus research · doi:10.1016/s0065-3527(08)60787-3 · Cited by 318 · see citing works
Contribution of the ipsilateral motor cortex to recovery after chronic stroke
Werhahn, K. J., Conforto, A. B., Kadom, N., Hallett, M., & Cohen, L. G. (2003) · Annals of Neurology · doi:10.1002/ana.10686 · Cited by 266 · see citing works
Inosine induces axonal rewiring and improves behavioral outcome after stroke
Chen, P., Goldberg, D. E., Kolb, B. E., Lanser, M. E., & Benowitz, L. I. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.132076299 · Cited by 263 · see citing works
Seizures and recovery from experimental brain damage
Hernández, T. D., & Schallert, T. J. (1988) · Experimental Neurology · doi:10.1016/0014-4886(88)90226-9 · Cited by 215 · see citing works
Wiessner, C., Bareyre, F. M., Allegrini, P. R., Mir, A. K., Frentzel, S., Zurini, M., Schnell, L., Oertle, T., & Schwab, M. E. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200302000-00003 · Cited by 209 · see citing works
Transgenic labeling of the corticospinal tract for monitoring axonal responses to spinal cord injury
Bareyre, F. M., Kerschensteiner, M., Misgeld, T., & Sanes, J. R. (2005) · Nature Medicine · doi:10.1038/nm1331 · Cited by 201 · see citing works
Genomics of the Periinfarction Cortex after Focal Cerebral Ischemia
Lu, A., Tang, Y., Ran, R., Clark, J. F., Aronow, B. J., & Sharp, F. R. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000062340.80057.06 · Cited by 176 · see citing works
Banfield, B. W., Kaufman, J. D., Randall, J. A., & Pickard, G. E. (2003) · Journal of Virology · doi:10.1128/jvi.77.18.10106-10112.2003 · Cited by 141 · see citing works
Pickard, G. E., Smeraski, C. A., Tomlinson, C. C., Banfield, B. W., Kaufman, J. D., Wilcox, C. L., Enquist, L. W., & Sollars, P. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02701.2002 · Cited by 133 · see citing works
Schaechter, J. D., Perdue, K. L., & Wang, R. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.071 · Cited by 124 · see citing works
Liu, Z., Li, Y., Zhang, X., Savant-Bhonsale, S., & Chopp, M. (2008) · Stroke · doi:10.1161/strokeaha.107.511659 · Cited by 115 · see citing works
Self-citationFromm, C., & Evarts, E. V. (1982) · Brain Research · doi:10.1016/0006-8993(82)90781-8 · Cited by 104 · see citing works
New developments in tracing neural circuits with herpesviruses
Song, C. K., Enquist, L. W., & Bartness, T. J. (2005) · Virus Research · doi:10.1016/j.virusres.2005.04.012 · Cited by 83 · see citing works
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Xin, H., Li, Y., Buller, B., Katakowski, M., Zhang, Y., Wang, X., Shang, X., Zhang, Z. G., & Chopp, M. (2012) · Stem Cells · doi:10.1002/stem.1129 · Cited by 897 · see citing works
Self-citationMotor compensation and its effects on neural reorganization after stroke
Jones, T. A. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.26 · Cited by 380 · see citing works
Hermann, D. M., & Chopp, M. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70039-x · Cited by 333 · see citing works
Self-citationModulation of Neural Plasticity as a Basis for Stroke Rehabilitation
Pekna, M., Pekny, M., & Nilsson, M. (2012) · Stroke · doi:10.1161/strokeaha.112.654228 · Cited by 258 · see citing works
Vagus Nerve Stimulation Enhances Stable Plasticity and Generalization of Stroke Recovery
Meyers, E., Solorzano, B. R., James, J. T., Ganzer, P. D., Lai, E. S., Rennaker, R. L., Kilgard, M. P., & Hays, S. A. (2018) · Stroke · doi:10.1161/strokeaha.117.019202 · Cited by 222 · see citing works
Role of the Contralesional Hemisphere in Post-Stroke Recovery of Upper Extremity Motor Function
Buetefisch, C. M. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00214 · Cited by 197 · see citing works
van Velthoven, C. T. J., Kavelaars, A., van Bel, F., & Heijnen, C. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1835-10.2010 · Cited by 182 · see citing works
Lindvall, O., & Kokaia, Z. (2011) · Stroke · doi:10.1161/strokeaha.110.599654 · Cited by 176 · see citing works
Neurorestorative Therapy for Stroke
Chen, J., Venkat, P., Zacharek, A., & Chopp, M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00382 · Cited by 169 · see citing works
Self-citationOrtega, S. B., Torres, V. O., Latchney, S. E., Whoolery, C. W., Noorbhai, I., Poinsatte, K., Selvaraj, U. M., Benson, M. A., Meeuwissen, A., Plautz, E. J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913292117 · Cited by 137 · see citing works
Xin, H., Liu, Z., Buller, B., Li, Y., Golembieski, W., Gan, X., Wang, F., Lü, M., Ali, M. M., Zhang, Z. G., et al. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20950489 · Cited by 132 · see citing works
Self-citationMotor System Reorganization After Stroke: Stimulating and Training Toward Perfection
Jones, T. A., & Adkins, D. L. (2015) · Physiology · doi:10.1152/physiol.00014.2015 · Cited by 130 · see citing works
Ueno, M., Hayano, Y., Nakagawa, H., & Yamashita, T. (2012) · Brain · doi:10.1093/brain/aws053 · Cited by 124 · see citing works
Enhancing plasticity in central networks improves motor and sensory recovery after nerve damage
Meyers, E., Kasliwal, N., Solorzano, B. R., Lai, E., Bendale, G. S., Berry, A., Ganzer, P. D., Romero‐Ortega, M. I., Rennaker, R. L., Kilgard, M. P., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13695-0 · Cited by 115 · see citing works
Liu, Z., Li, Y., Zhang, Z. G., Cui, X., Cui, Y., Lu, M., Savant-Bhonsale, S., & Chopp, M. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.8 · Cited by 111 · see citing works
Self-citationCell-based and pharmacological neurorestorative therapies for ischemic stroke
Venkat, P., Shen, Y., Chopp, M., & Chen, J. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.08.036 · Cited by 99 · see citing works
Self-citationPromoting neuroplasticity and recovery after stroke
Bowden, M. G., Woodbury, M. L., & Duncan, P. W. (2012) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32835c5ba0 · Cited by 86 · see citing works
Slow Waves Promote Sleep-Dependent Plasticity and Functional Recovery after Stroke
Facchin, L., Schöne, C., Mensen, A., Bandarabadi, M., Pilotto, F., Saxena, S., Libourel, P., Bassetti, C. L., & Adamantidis, A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0373-20.2020 · Cited by 75 · see citing works
Sada, N., Fujita, Y., Mizuta, N., Ueno, M., Furukawa, T., & Yamashita, T. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02897-w · Cited by 74 · see citing works
Liu, Z., Li, Y., Zhang, R. L., Cui, Y., & Chopp, M. (2011) · Stroke · doi:10.1161/strokeaha.110.607226 · Cited by 75 · see citing works
Self-citationMesenchymal stem cells restore cortical rewiring after neonatal ischemia in mice
van Velthoven, C. T. J., van de Looij, Y., Kavelaars, A., Zijlstra, J., van Bel, F., Hüppi, P. S., Sizonenko, S. V., & Heijnen, C. J. (2012) · Annals of Neurology · doi:10.1002/ana.23543 · Cited by 70 · see citing works
Stem cells and stroke: opportunities, challenges and strategies
Burns, T. C., & Steinberg, G. K. (2011) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2011.552883 · Cited by 67 · see citing works
Xiong, Y., Zhang, Y., Mahmood, A., Meng, Y., Qu, C., & Chopp, M. (2011) · Translational Stroke Research · doi:10.1007/s12975-011-0120-2 · Cited by 66 · see citing works
Self-citationDegree of corticospinal tract damage correlates with motor function after stroke
Maraka, S., Jiang, Q., Jafari‐Khouzani, K., Li, L., Malik, S., Hamidian, H., Zhang, T., Lü, M., Hamid Soltanian-zadeh, A., Chopp, M., et al. (2014) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.132 · Cited by 65 · see citing works
Self-citationSist, B., Fouad, K., & Winship, I. R. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.11.019 · Cited by 64 · see citing works
Alawieh, A. M., Tomlinson, S., Adkins, D. L., Kautz, S. A., & Feng, W. (2017) · Translational Stroke Research · doi:10.1007/s12975-017-0551-5 · Cited by 59 · see citing works
Okabe, N., Shiromoto, T., Himi, N., Feng, L., Nakamura‐Maruyama, E., Narita, K., Iwachidou, N., Yagita, Y., & Miyamoto, O. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.008 · Cited by 55 · see citing works
AdipoRon Attenuates Neuroinflammation After Intracerebral Hemorrhage Through AdipoR1-AMPK Pathway
Zheng, J., Sun, Z., Liang, F., Xu, W., Lü, J., Shi, L., Shao, A., Yu, J., & Zhang, J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.060 · Cited by 56 · see citing works
Niaspan increases axonal remodeling after stroke in type 1 diabetes rats
Yan, T., Chopp, M., Ye, X., Liu, Z., Zacharek, A., Cui, Y., Roberts, C. J., Buller, B., & Chen, J. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.01.001 · Cited by 55 · see citing works
Self-citationShen, L. H., Xin, H., Li, Y., Zhang, R. L., Cui, Y., Zhang, L., Lu, M., Zhang, Z. G., & Chopp, M. (2011) · Stroke · doi:10.1161/strokeaha.110.593863 · Cited by 51 · see citing works
Self-citationJiang, Q., Zhang, Z. G., & Chopp, M. (2009) · Stroke · doi:10.1161/strokeaha.109.568048 · Cited by 50 · see citing works
Self-citationAxonal remodeling of the corticospinal tract during neurological recovery after stroke
Liu, Z., Xin, H., & Chopp, M. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.297060 · Cited by 48 · see citing works
Self-citationCell-based therapy for ischemic stroke
Zhang, J., & Chopp, M. (2013) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2013.804507 · Cited by 46 · see citing works
Self-citationUmarova, R. M., Reisert, M., Beier, T., Kiselev, V. G., Klöppel, S., Kaller, C. P., Glauche, V., Mader, I., Beume, L.-A., Hennig, J., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22503 · Cited by 44 · see citing works
Automated measurement of nerve fiber density using line intensity scan analysis
Sathyanesan, A. G., Ogura, T., & Lin, W. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.02.019 · Cited by 44 · see citing works
Class IIa histone deacetylases affect neuronal remodeling and functional outcome after stroke
Kassis, H., Shehadah, A., Li, C., Zhang, Y., Cui, Y., Roberts, C. J., Sadry, N., Liu, X., Chopp, M., & Zhang, Z. G. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.04.006 · Cited by 40 · see citing works
Self-citationYu, J., Zheng, J., Lü, J., Sun, Z., Wang, Z., & Zhang, J. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02794-5 · Cited by 40 · see citing works
Liu, Z., Chopp, M., Ding, X., Cui, Y., & Li, Y. (2013) · Stroke · doi:10.1161/strokeaha.113.001162 · Cited by 38 · see citing works
Self-citationPreclinical Studies of Neuroplasticity Following Experimental Brain Injury
Bundy, D. T., & Nudo, R. J. (2019) · Stroke · doi:10.1161/strokeaha.119.023550 · Cited by 39 · see citing works
Zolkefley, M. K. I., Firwana, Y. M. S., Hatta, H. Z. M., Rowbin, C., Nassir, C. M. N. C. M., Hanafi, M. H., Abdullah, M. S., & Mustapha, M. (2021) · Journal of Physical Therapy Science · doi:10.1589/jpts.33.75 · Cited by 39 · see citing works
Motor System Plasticity in Stroke Models
Jones, T. A., Allred, R. P., Jefferson, S. C., Kerr, A. L., Woodie, D. A., Cheng, S.-Y., & Adkins, D. L. (2013) · Stroke · doi:10.1161/strokeaha.111.000037 · Cited by 37 · see citing works
Lulic, D., Burns, J., Bae, E., van Loveren, H. V., & Borlongan, C. (2011) · Neurosurgery · doi:10.1227/neu.0b013e31820c6cdc · Cited by 38 · see citing works
Xu, G., Huo, C., Yin, J., Li, W., Xie, H., Li, X., Li, Z., Wang, Y., & Wang, D. (2022) · Medical Physics · doi:10.1002/mp.15570 · Cited by 32 · see citing works
Stroke Induces Nuclear Shuttling of Histone Deacetylase 4
Kassis, H., Shehadah, A., Chopp, M., Roberts, C. J., & Zhang, Z. G. (2015) · Stroke · doi:10.1161/strokeaha.115.009046 · Cited by 31 · see citing works
Self-citationBeker, M., Çağlayan, A. B., Beker, M. Ç., Altunay, S., Karaçay, R., Dalay, A., Altıntaş, M. Ö., Köse, G. T., Hermann, D. M., & Kılıç, E. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113364 · Cited by 30 · see citing works
Nagahama, H., Nakazaki, M., Sasaki, M., Kataoka-Sasaki, Y., Namioka, T., Namioka, A., Oka, S., Onodera, R., Suzuki, J., Sasaki, Y., et al. (2018) · Brain Research · doi:10.1016/j.brainres.2018.05.033 · Cited by 30 · see citing works
Heat shock protein 72 (Hsp72) improves long term recovery after focal cerebral ischemia in mice
Xu, L., Xiong, X., Ouyang, Y., Barreto, G. E., & Giffard, R. G. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.11.047 · Cited by 23 · see citing works
Poinsatte, K., Betz, D., Torres, V. O., Ajay, A. D., Mirza, S., Selvaraj, U. M., Plautz, E. J., Kong, X., Gokhale, S., Meeks, J. P., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01055 · Cited by 22 · see citing works
Advanced non-invasive MRI of neuroplasticity in ischemic stroke: Techniques and applications
Sun, C., Liu, X., Bao, C., Wei, F., Gong, Y., Li, Y., & Liu, J. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118365 · Cited by 22 · see citing works
Self-citationWang, J., Cai, Y., Sun, J., Feng, H., Zhu, X., Chen, Q., Gao, F., Ni, Q., Mao, L., Yang, M., et al. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114236 · Cited by 20 · see citing works
Tennant, K. A. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.02.003 · Cited by 19 · see citing works
Empl, L., Chovsepian, A., Chahin, M., Kan, W. Y. V., Fourneau, J., Steenbergen, V. V., Weidinger, S., Marcantoni, M., Ghanem, A., Bradley, P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29992-0 · Cited by 15 · see citing works
Chen, N., Chopp, M., Xiong, Y., Qian, J.-Y., Lü, M., Zhou, D., He, L., & Liu, Z. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.03.001 · Cited by 14 · see citing works
Self-citationNekanti, U., Sakthivel, P. S., Zahedi, A., Creasman, D. A., Nishi, R. A., Dumont, C. M., Piltti, K. M., Guardamondo, G. L., Hernandez, N., Chen, X., et al. (2024) · npj Regenerative Medicine · doi:10.1038/s41536-024-00356-0 · Cited by 13 · see citing works
Liu, Z., Li, Y., Qian, J.-Y., Cui, Y., & Chopp, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094505 · Cited by 13 · see citing works
Self-citationInterrogating autonomic peripheral nervous system neurons with viruses – A literature review
Feng, M., Xiang, B., Li, F., Wang, Q., Xu, W., & Xiang, H. (2020) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2020.108958 · Cited by 11 · see citing works
Targeted tPA overexpression in denervated spinal motor neurons promotes stroke recovery in mice
Gan, X., Chopp, M., Xin, H., Wang, F., Golembieski, W., Lü, M., He, L., & Liu, Z. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20901686 · Cited by 11 · see citing works
Self-citationWillenberg, R., & Steward, O. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23809 · Cited by 10 · see citing works
Diaschisis, Degeneration, and Adaptive Plasticity After Focal Ischemic Stroke
Sist, B., Jesudasan, S. J. B., & Ian, R. (2012) · InTech eBooks · doi:10.5772/28577 · Cited by 9 · see citing works
Yoshikawa, A., Nakamachi, T., Shibato, J., Rakwal, R., & Shioda, S. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151222492 · Cited by 9 · see citing works
Neural Stem Cells in Stroke: Intracerebral Approaches
Manley, N. C., Azevedo-Pereira, R. L., Bliss, T. M., & Steinberg, G. K. (2015) · Springer eBooks · doi:10.1007/978-3-319-15063-5_7 · Cited by 7 · see citing works
Yang, J., Liu, L., Li, T., & Li, C. (2016) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2016.11.009 · Cited by 7 · see citing works
Chopp, M., & Li, Y. (2011) · European Neurological Review · doi:10.17925/enr.2011.06.02.97 · Cited by 6 · see citing works
Self-citationTongxinluo promotes axonal plasticity and functional recovery after stroke
Wang, X., Huang, X., Yang, M., Pan, X., Duan, M., Cai, H., Jiang, G., Wen, X., Zou, D., & Chen, L. (2020) · Translational Neuroscience · doi:10.1515/tnsci-2020-0127 · Cited by 5 · see citing works
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Shin, M., Kim, S. H., Lee, C.-H., & Shin, Y. (2014) · Brain & Neurorehabilitation · doi:10.12786/bn.2014.7.1.21 · Cited by 5 · see citing works
Liu, Y., Chen, L., Zeng, J., Li, W., Zeng, S., Ye, B., & Liang, Z. (2018) · Medical Science Monitor · doi:10.12659/msm.909071 · Cited by 5 · see citing works
Mitchell, E. J., Dewar, D., & Maxwell, D. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152176 · Cited by 5 · see citing works
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Jones, T. A., Nemchek, V., & Fracassi, M. (2024) · The Journal of Physiology · doi:10.1113/jp285565 · Cited by 4 · see citing works
Alionte, C., Notte, C., & Strubakos, C. D. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.120161 · Cited by 4 · see citing works
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Fait, B. W., Cotto, B., Murakami, T. C., Hagemann-Jensen, M., Zhan, H., Freivald, C., Turbek, I., Gao, Y., Yao, Z., Way, S. W., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.09.612115 · Cited by 4 · see citing works
Chu, J., Glinsky, J. V., Liu, H., Ben, M., Spooren, A. I. F., Roberts, S., Chen, L. W., Natal, F. D., Tamburella, F., Jørgensen, V., et al. (2023) · BMJ Open · doi:10.1136/bmjopen-2023-072219 · Cited by 3 · see citing works
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Liu, S. J., Liu, M., Wang, B., Sun, M., Yang, H., Qu, M., Ma, L., Shi, L., Song, Y., Li, P., et al. (2026) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.70830 · Cited by 1 · see citing works
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- Authors
- Liu, Z., Zhang, R. L., Li, Y., Cui, Y., & Chopp, M.
- Affiliations
- Oakland University (US)
- ORCID
- Chopp, Michael
- Venue
- Stroke
- Published
- 2009-07
- Volume
- 40
- Issue
- 7
- Pages
- 2546-2551
- ISSN
- 0039-2499 (ISSN-L)
- 1524-4628
- PMC
- PMC2704262
- OpenAlex
- W2117753971
- Cited by
- 81
- References
- 24
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 5 · 2023: 1 · 2022: 3 · 2021: 2 · 2020: 10 · 2019: 6 · 2018: 4 · 2017: 5 · 2016: 4 · 2015: 5 · 2014: 8 · 2013: 5 · 2012: 9
- FWCI
- 7.13
- Type
- journal article
- Language
- en
- Update notices
- correction (2009-12-01)
- Open access
- bronze
- doi.org
- Locations
- Stroke (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Princeton University
- National Institute of Neurological Disorders and Stroke (P01NS42345, P01NS042345)
- Topics
- Health Sciences › Medicine › Rehabilitation › Stroke Rehabilitation and Recovery
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Health Sciences › Medicine › Epidemiology › Acute Ischemic Stroke Management
- Keywords
- corticospinal tract, ischemic stroke, motor reorganization, axon density, pyramidal neurons, middle cerebral artery occlusion, cervical spinal cord
- MeSH terms
- Animals, Axons, Behavior, Animal, Cerebral Cortex, Disease Models, Animal, Fluorescent Antibody Technique, Luminescent Proteins, Male, Mice, Transgenic, Herpesvirus 1, Suid, Pyramidal Tracts, Synapses, Pyramidal Cells, Recovery of Function, Stroke, Mice
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