Growth-associated gene expression after stroke: evidence for a growth-promoting region in peri-infarct cortex

A new mathematical model for relative quantification in real-time RT-PCR

Pfaffl, M. W. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.9.e45 · Cited by 34,610

Relative expression software tool (REST(C)) for group-wise comparison and statistical analysis of relative expression results in real-time PCR

Pfaffl, M. W. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.9.e36 · Cited by 7,377

Regeneration beyond the glial scar

Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151

Chondroitinase ABC promotes functional recovery after spinal cord injury

Bradbury, E. J., Moon, L. D. F., Popat, R. J., King, V. R., Bennett, G. S., Patel, P. N., Fawcett, J. W., & McMahon, S. B. (2002) · Nature · doi:10.1038/416636a · Cited by 2,357

The glial scar and central nervous system repair

Fawcett, J. W., & Asher, R. A. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00072-6 · Cited by 1,808

Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex

Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679

GAP-43: an intrinsic determinant of neuronal development and plasticity

Benowitz, L. I., & Routtenberg, A. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10072-2 · Cited by 1,329

Quantitative RT-PCR: Pitfalls and Potential

Freeman, W. M., Walker, S. J., & Vrana, K. E. (1999) · BioTechniques · doi:10.2144/99261rv01 · Cited by 1,149

In situ Hybridization

Langdale, J. A. (1994) · Springer eBooks · doi:10.1007/978-1-4612-2694-9_18 · Cited by 869

Matrix metalloproteinases in neuroinflammation

Rosenberg, G. A. (2002) · Glia · doi:10.1002/glia.10108 · Cited by 868

Associations Between Time After Stroke and Exercise Training Outcomes: A Meta‐Regression Analysis

Marzolini, S., Wu, C., Hussein, R., Xiong, L. Y., Kangatharan, S., Peni, A., Cooper, C. R., Lau, K. S. K., Mahdoum, G. N., Pakosh, M. T., et al. (2021) · Journal of the American Heart Association · doi:10.1161/jaha.121.022588 · Cited by 28

Cortical Reorganization after Experimental Traumatic Brain Injury: A Functional Autoradiography Study

Harris, N. G., Chen, S., & Pickard, J. D. (2013) · Journal of Neurotrauma · doi:10.1089/neu.2012.2785 · Cited by 25

Gene Expression Suggests Spontaneously Hypertensive Rats May Have Altered Metabolism and Reduced Hypoxic Tolerance

Ritz, M., Grond‐Ginsbach, C., Engelter, S. T., & Lyrer, P. A. (2012) · Current Neurovascular Research · doi:10.2174/156720212799297074 · Cited by 25

The effects of ceftriaxone on skill learning and motor functional outcome after ischemic cortical damage in rats

Kim, S. Y., & Jones, T. A. (2013) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2012-120245 · Cited by 24

Biology-driven material design for ischaemic stroke repair

Phan, N. V., Rathbun, E. M., Ouyang, Y., Carmichael, S. T., & Segura, T. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-023-00117-6 · Cited by 26

Suppression of neurocan and enhancement of axonal density in rats after treatment of traumatic brain injury with scaffolds impregnated with bone marrow stromal cells

Mahmood, A., Wu, H., Qu, C., Mahmood, S., Xiong, Y., Kaplan, D. L., & Chopp, M. (2014) · Journal of neurosurgery · doi:10.3171/2013.12.jns131362 · Cited by 23

Modifications of perineuronal nets and remodelling of excitatory and inhibitory afferents during vestibular compensation in the adult mouse

Faralli, A., Dagna, F., Albera, A., Bekku, Y., Oohashi, T., Albera, R., Rossi, F., & Carulli, D. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1095-7 · Cited by 24

Imaging motor recovery after stroke

Yozbatıran, N., & Cramer, S. C. (2006) · NeuroRx · doi:10.1016/j.nurx.2006.07.003 · Cited by 23

Gene expression changes of interconnected spared cortical neurons 7 days after ischemic infarct of the primary motor cortex in the rat

Urban, E. T. R., Bury, S. D., Barbay, H. S., Guggenmos, D. J., Dong, Y.-F., & Nudo, R. J. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1390-z · Cited by 25

A view of the genetic and proteomic profile of extracellular matrix molecules in aging and stroke

Chmelová, M., Androvic, P., Kirdajová, D., Turečková, J., Kriška, J., Valihrach, L., Anděrová, M., & Vargová, L. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1296455 · Cited by 24

Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis

Rué, L., Oeckl, P., Timmers, M., Lenaerts, A., van der Vos, J., Smolders, S., Poppe, L., de Boer, A., Bosch, L. V. D., Damme, P. V., et al. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0759-6 · Cited by 23

Hyaluronidase inhibition accelerates functional recovery from stroke in the mouse brain

Gręda, A., & Nowicka, D. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15279 · Cited by 24

PDE2A Inhibition Enhances Axonal Sprouting, Functional Connectivity, and Recovery after Stroke

Bechay, K., Abduljawad, N., Latifi, S., Suzuki, K., Iwashita, H., & Carmichael, S. T. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0730-22.2022 · Cited by 21

Management of patients with stroke: Is it time to expand treatment options?

Adams, H. P., & Nudo, R. J. (2013) · Annals of Neurology · doi:10.1002/ana.23948 · Cited by 23

Protein-Energy Malnutrition Developing after Global Brain Ischemia Induces an Atypical Acute-Phase Response and Hinders Expression of GAP-43

Smith, S., Figley, S. A., Schreyer, D. J., & Paterson, P. G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107570 · Cited by 23

Functions of subventricular zone neural precursor cells in stroke recovery

Williamson, M. R., Jones, T. A., & Drew, M. R. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112209 · Cited by 24

The Neuroprotective Effect of the HDAC2/3 Inhibitor MI192 on the Penumbra After Photothrombotic Stroke in the Mouse Brain

Demyanenko, S. V., Nikul, V. V., & Uzdensky, A. B. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01773-9 · Cited by 23

Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice

Jan, T. A., Lu, L., Li, C., Williams, R. W., & Waters, R. S. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-3 · Cited by 23

Venlafaxine treatment after endothelin-1-induced cortical stroke modulates growth factor expression and reduces tissue damage in rats

Zepeda, R., Contreras, V., Pissani, C., Stack, K., Vargas, M., Owen, G. I., Lazo, O. M., & Bronfman, F. C. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.011 · Cited by 22

Clinical trial design for stem cell therapies in stroke: What have we learned?

Muir, K. W. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.09.011 · Cited by 22

Ketone bodies promote stroke recovery via GAT-1-dependent cortical network remodeling

Lin, Y., Yang, D., Ni, H., Xu, X.-M., Wu, F., Lin, L., Chen, J., Sun, Y. H., Huang, Z., Li, S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112294 · Cited by 24

Early Poststroke Experience Differentially Alters Periinfarct Layer II and III Cortex

Clarke, J., Langdon, K. D., & Corbett, D. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.237 · Cited by 22

Diffusion tensor and volumetric magnetic resonance imaging using an MR-compatible hand-induced robotic device suggests training-induced neuroplasticity in patients with chronic stroke

Lazaridou, A., Astrakas, L. G., Mintzopoulos, D., Khanicheh, A., Singhal, A. B., Moskowitz, M. A., Rosen, B. R., & Tzika, A. A. (2013) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2013.1476 · Cited by 22

Intraparenchymal treatment with bone marrow mesenchymal stem cell-conditioned medium exerts neuroprotection following intracerebral hemorrhage

Cui, C., Cui, Y., Gao, J., Li, R., Jiang, X., Tian, Y., Wang, R. C., & Cui, J. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6223 · Cited by 22

Volumetric effects of motor cortex injury on recovery of ipsilesional dexterous movements

Darling, W. G., Pizzimenti, M. A., Hynes, S. M., Rotella, D. L., Headley, G., Ge, J., Stilwell‐Morecraft, K. S., McNeal, D. W., Solon, K., & Morecraft, R. J. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.015 · Cited by 23

Neurophysiological and Anatomical Plasticity in the Adult Sensorimotor Cortex

Dancause, N. (2006) · Reviews in the Neurosciences · doi:10.1515/revneuro.2006.17.6.561 · Cited by 22

The Effect of Diabetes on Cortical Function in Stroke: Implications for Poststroke Plasticity

Huynh, W., Kwai, N. C. G., Arnold, R., Krishnan, A. V., Lin, C. S.-Y., Vucic, S., & Kiernan, M. C. (2017) · Diabetes · doi:10.2337/db16-0961 · Cited by 22

Effect of Tetramethylpyrazine on Neuroplasticity after Transient Focal Cerebral Ischemia Reperfusion in Rats

Lin, J., Hao, C., Gong, Y. L., Zhang, Y., Li, Y., Feng, Z.-H., Xu, X., Huang, H., & Liao, W. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/1587241 · Cited by 21

A Review on Preclinical Models of Ischemic Stroke: Insights Into the Pathomechanisms and New Treatment Strategies

Singh, A. A., Kharwar, A. K., & Dandekar, M. P. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210907092928 · Cited by 21

The factors affecting neurogenesis after stroke and the role of acupuncture

Mu, J.-D., Ma, L., Zhang, Z., Xu, Q., Zhang, Q., Ma, L.-H., & Sun, T. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1082625 · Cited by 22

Neovascularization in retinopathy of prematurity: opposing actions of neuronal factors GPR91 and semaphorins 3A

Joyal, J., Omri, S., Sitaras, N., Rivera, J., Sapieha, P. S., & Chemtob, S. (2012) · Acta Paediatrica · doi:10.1111/j.1651-2227.2012.02692.x · Cited by 21

Corticospinal responses of quadriceps are abnormally coupled with hip adductors in chronic stroke survivors

Krishnan, C., & Dhaher, Y. Y. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.11.007 · Cited by 21

An optimized dosing regimen of cimaglermin (neuregulin 1β3, glial growth factor 2) enhances molecular markers of neuroplasticity and functional recovery after permanent ischemic stroke in rats

Iaci, J. F., Parry, T. J., Huang, Z., Pavlopoulos, E., Finklestein, S. P., Ren, J., & Caggiano, A. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23699 · Cited by 21

Role of microRNAs in stroke recovery

Bansal, A., Prathap, R., Gupta, S., Chaurasia, A., & Chaudhary, P. (2019) · Journal of Family Medicine and Primary Care · doi:10.4103/jfmpc.jfmpc_296_19 · Cited by 21

Disrupted mitochondrial genes and inflammation following stroke

Gibbs, W. S., Weber, R. A., Schnellmann, R. G., & Adkins, D. L. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.09.021 · Cited by 21

Spatiotemporal microstructural white matter changes in diffusion tensor imaging after transient focal ischemic stroke in rats

Jung, W., Han, Y. H., Chung, J. J., Chae, S. Y., Lee, S. H., Im, G. H., Cha, J., & Lee, J. H. (2017) · NMR in Biomedicine · doi:10.1002/nbm.3704 · Cited by 19

Recovery of fine motor performance after ischemic damage to motor cortex is facilitated by cell therapy in the rhesus monkey

Moore, T. L., Pessina, M. A., Finklestein, S. P., Kramer, B. C., Killiany, R., & Rosene, D. L. (2013) · Somatosensory & Motor Research · doi:10.3109/08990220.2013.790806 · Cited by 20

Inhibition of Nkcc1 promotes axonal growth and motor recovery in ischemic rats

Mu, X., Wang, H. B., Cheng, X., Yang, L., Sun, X. Y., Qu, H., Zhao, S., Zhou, Z., Liu, T. T., Xiao, T., et al. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.036 · Cited by 20

Bone Marrow Cell Transplantation Time-Dependently Abolishes Efficacy of Granulocyte Colony-Stimulating Factor After Stroke in Hypertensive Rats

Pösel, C., Scheibe, J., Kranz, A., Bothe, V., Quente, E., Fröhlich, W., Lange, F., Schäbitz, W., Minnerup, J., Boltze, J., et al. (2014) · Stroke · doi:10.1161/strokeaha.113.004460 · Cited by 20

Thinking outside the brain: Structural plasticity in the spinal cord promotes recovery from cortical stroke

Tennant, K. A. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.02.003 · Cited by 19

Transcriptional changes in sensory ganglia associated with primary afferent axon collateral sprouting in spared dermatome model

Harrison, B. J., Venkat, G., Hutson, T. H., Rau, K. K., Bunge, M. B., Mendell, L. M., Gage, F. H., Johnson, R. D., Hill, C. E., Rouchka, E. C., et al. (2015) · Genomics Data · doi:10.1016/j.gdata.2015.10.005 · Cited by 19

Low-intensity contralesional electrical theta burst stimulation modulates ipsilesional excitability and enhances stroke recovery

Boddington, L. J., Gray, J. P., Schulz, J. M., & Reynolds, J. N. J. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113071 · Cited by 19

Engraftment, migration and differentiation of neural stem cells in the rat spinal cord following contusion injury

McMahon, S. S., Albermann, S., Rooney, G. E., Shaw, G., Garcia, Y., Sweeney, E. M., Hynes, J. B., Dockery, P., O’Brien, T., Windebank, A. J., et al. (2010) · Cytotherapy · doi:10.3109/14653241003695018 · Cited by 19

Model System for Live Imaging of Neuronal Responses to Injury and Repair

Gravel, M., Weng, Y.-C., & Križ, J. (2011) · Molecular Imaging · doi:10.2310/7290.2011.00013 · Cited by 18

Inosine enhances recovery of grasp following cortical injury to the primary motor cortex of the rhesus monkey

Moore, T. L., Pessina, M. A., Finklestein, S. P., Killiany, R., Bowley, B. G. E., Benowitz, L. I., & Rosene, D. L. (2016) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-160661 · Cited by 20

Future directions of stroke rehabilitation

Kakuda, W. (2020) · Rinsho Shinkeigaku · doi:10.5692/clinicalneurol.cn-001399 · Cited by 18

Stroke research at the crossroads – where are we heading?

Roth, S., & Liesz, A. (2016) · Swiss Medical Weekly · doi:10.4414/smw.2016.14329 · Cited by 17

Leveraging Social Networks for the Assessment and Management of Neurological Patients

Dhand, A., Podury, A., Choudhry, N. K., Narayanan, S. S., Shin, M. C., & Mehl, M. R. (2022) · Seminars in Neurology · doi:10.1055/s-0042-1744532 · Cited by 18

Stroke-Related Translational Research

Caplan, L. R., Arenillas, J. F., Cramer, S. C., Joutel, A., Lo, E. H., Meschia, J. F., Savitz, S. I., & Tournier‐Lasserve, E. (2011) · Archives of Neurology · doi:10.1001/archneurol.2011.99 · Cited by 17

Long-term gene expression changes in the cortex following cortical ischemia revealed by transcriptional profiling

Krüger, C., Cira, D. K., Sommer, C., Fischer, A., Schäbitz, W., & Schneider, A. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.01.025 · Cited by 17

Semaphorin 6A Improves Functional Recovery in Conjunction with Motor Training after Cerebral Ischemia

Rogalewski, A., Dittgen, T., Klugmann, M., Kirsch, F., Krüger, C., Pitzer, C., Minnerup, J., Schäbitz, W., & Schneider, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010737 · Cited by 17

Neuroplasticity and Cellular Therapy in Cerebral Infarction

Rodríguez‐González, R., Hurtado, O., Sobrino, T., & Castillo, J. (2007) · Cerebrovascular Diseases · doi:10.1159/000107393 · Cited by 17

Characterization of Cortical Glial Scars in the Diisopropylfluorophosphate (DFP) Rat Model of Epilepsy

Gage, M., Gard, M., & Thippeswamy, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.867949 · Cited by 18

Animal models of post-ischemic forced use rehabilitation: methods, considerations, and limitations

Livingston‐Thomas, J. M., & Tasker, R. A. (2013) · Experimental & Translational Stroke Medicine · doi:10.1186/2040-7378-5-2 · Cited by 16

Optogenetic modulation in stroke recovery

Pendharkar, A. V., Levy, S. L., Ho, A. L., Sussman, E. S., Cheng, M., & Steinberg, G. K. (2016) · Neurosurgical FOCUS · doi:10.3171/2016.2.focus163 · Cited by 16

Aberrant cortical activity, functional connectivity, and neural assembly architecture after photothrombotic stroke in mice

Bandet, M. V., & Winship, I. R. (2023) · eLife · doi:10.7554/elife.90080 · Cited by 20

Marcks and Marcks-like 1 proteins promote spinal cord development and regeneration in Xenopus

Amri, M. E., Pandit, A. S., & Schlosser, G. (2024) · eLife · doi:10.7554/elife.98277 · Cited by 14

Motor Improvement of Skilled Forelimb Use Induced by Treatment with Growth Hormone and Rehabilitation Is Dependent on the Onset of the Treatment after Cortical Ablation

Heredia, M., Palomero, J., de la Fuente, A., Criado, J. M., Yajeya, J., Devesa, J., Devesa, P., Villardón, J. L. V., & Riolobos, A. S. (2018) · Neural Plasticity · doi:10.1155/2018/6125901 · Cited by 15

Searching for differentially expressed proteins in spinal cord injury based on the proteomics analysis

Ding, H. D., Yu, J. H., Chang, W., Liu, F., & He, Z. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.117235 · Cited by 15

Experience‐dependent brain plasticity after stroke: effect of ibuprofen and poststroke delay

Jablonka, J., Kossut, M. M., Witte, O. W., & Liguz‐Lecznar, M. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08174.x · Cited by 15

Therapeutic potential of amniotic fluid-derived cells for treating the injured nervous system

Rennie, K., Haukenfrers, J., Ribecco‐Lutkiewicz, M., Ly, D., Jezierski, A., Smith, B., Zurakowski, B., Martina, M., Gruslin, A., & Bani‐Yaghoub, M. (2013) · Biochemistry and Cell Biology · doi:10.1139/bcb-2013-0019 · Cited by 15

Abolished perineuronal nets and altered parvalbumin-immunoreactivity in the nucleus reticularis thalami of wildtype and 3xTg mice after experimental stroke

Härtig, W., Appel, S., Suttkus, A., Grosche, J., & Michalski, D. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.09.004 · Cited by 15

Localization and Expression of Sirtuins 1, 2, 6 and Plasticity-Related Proteins in the Recovery Period after a Photothrombotic Stroke in Mice

Demyanenko, S. V., Ганцгорн, Е. В., Rodkin, S., & Sharifulina, S. (2020) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2020.105152 · Cited by 15

Phosphacan and receptor protein tyrosine phosphatase β expression mediates deafferentation‐induced synaptogenesis

Harris, J. L., Reeves, T. M., & Phillips, L. L. (2009) · Hippocampus · doi:10.1002/hipo.20725 · Cited by 15

Epicortical Brevetoxin Treatment Promotes Neural Repair and Functional Recovery after Ischemic Stroke

Sequeira, E., Pierce, M. L., Akasheh, D., Sellers, S., Gerwick, W. H., Baden, D. G., & Murray, T. F. (2020) · Marine Drugs · doi:10.3390/md18070374 · Cited by 15

Harnessing Plasticity for the Treatment of Neurosurgical Disorders: An Overview

Chen, H. I., Attiah, M. A., Baltuch, G. H., Smith, D. H., Hamilton, R. H., & Lucas, T. H. (2014) · World Neurosurgery · doi:10.1016/j.wneu.2014.02.003 · Cited by 15

Enhanced serotonin signaling increases intestinal neuroplasticity

Greig, C. J., Gandotra, N., Tackett, J. J., Bamdad, M. C., & Cowles, R. A. (2016) · Journal of Surgical Research · doi:10.1016/j.jss.2016.07.021 · Cited by 14

Structural changes of CA1 pyramidal neurons after stroke in the contralesional hippocampus

Merino‐Serrais, P., Plaza‐Alonso, S., Hellal, F., Valero-Freitag, S., Kastanauskaite, A., Plesnila, N., & DeFelipe, J. (2023) · Brain Pathology · doi:10.1111/bpa.13222 · Cited by 12

Suppression of PTBP1 in hippocampal astrocytes promotes neurogenesis and ameliorates recognition memory in mice with cerebral ischemia

Fukui, Y., Morihara, R., Hu, X., Nakano, Y., Yunoki, T., Takemoto, M., Abe, K., & Yamashita, T. (2024) · Scientific Reports · doi:10.1038/s41598-024-71212-w · Cited by 13

Influencing neuroplasticity in stroke treatment with advanced biomaterials-based approaches

Obermeyer, J. M., Ho, E., Gracias, A., & Shoichet, M. S. (2018) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.12.012 · Cited by 13

Assessing neuronal density in peri‐infarct cortex with PET: Effects of cortical topology and partial volume correction

Funck, T., Alkuwaiti, M., Lepage, C., Zepper, P., Minuk, J., Schipper, H. M., Evans, A. C., & Thiel, A. (2016) · Human Brain Mapping · doi:10.1002/hbm.23363 · Cited by 13

Perineuronal nets: Role in normal brain physiology and aging, and pathology of various diseases

Zhu, K., Fu, Y., Zhao, Y., Niu, B., & Han, L. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102756 · Cited by 20

Three cooperative mechanisms required for recovery after brain damage

Berger, D., Varriale, E., van Kessenich, L. M., Herrmann, H. J., & de Arcangelis, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-50946-y · Cited by 13

Development of endothelial-targeted CD39 as a therapy for ischemic stroke

Lee, N. T., Savvidou, I., Selan, C., Calvello, I., Vuong, A., Wright, D. K., Brkljača, R., Willcox, A., Chia, J. S., Wang, X., et al. (2024) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2024.04.023 · Cited by 11

Investigating the Acute and Chronic Effects of Cardiovascular Exercise on Brain-Derived Neurotrophic Factor in Early Subacute Stroke

Heras, B. D. L., Rodrigues, L., Cristini, J., Yu, E., Gan‐Or, Z., Arbour, N., Thiel, A., Tang, A., Fung, J., Eng, J. J., et al. (2025) · Neurorehabilitation and neural repair · doi:10.1177/15459683251342150 · Cited by 13

Complement C3a: Shaping the Plasticity of the Post-stroke Brain

Stokowska, A., & Pekna, M. (2017) · Springer series in translational stroke research · doi:10.1007/978-3-319-66679-2_26 · Cited by 11

SARA regulates neuronal migration during neocortical development through L1 trafficking

Mestres, I., Chuang, J.-Z., Calegari, F., Conde, C. B., & Sung, C.-H. (2016) · Development · doi:10.1242/dev.129338 · Cited by 11

Deep Sequencing Reveals Uncharted Isoform Heterogeneity of the Protein-Coding Transcriptome in Cerebral Ischemia

Bhattarai, S., Aly, A., Garcia, K., Ruiz, D., Pontarelli, F., & Dharap, A. A. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1147-0 · Cited by 11

Behavioral Effect of Short- and Long-Term Exercise on Motor Functional Recovery after Intracerebral Hemorrhage in Rats

Tamakoshi, K., Ishida, K., Hayao, K., Takahashi, H. E., & Tamaki, H. (2018) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2018.08.038 · Cited by 11

Rehabilitation and Plasticity

Luft, A. R. (2013) · Monographs in clinical neuroscience/Frontiers of neurology and neuroscience/Monographs in neural sciences · doi:10.1159/000348879 · Cited by 11

Roadmap for Stroke: Challenging the Role of the Neuronal Extracellular Matrix

Luca, C. D., Virtuoso, A., Maggio, N., Izzo, S., Papa, M., & Colangelo, A. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207554 · Cited by 10

Identification of MicroRNAs as potential biomarkers for detecting ischemic stroke

Li, K., Li, S., Zheng, P., Wang, Y., Wang, L., Meng, X., Lv, Y., Xue, Z., Guo, X., Zhang, A., et al. (2021) · Genes & Genomics · doi:10.1007/s13258-021-01060-9 · Cited by 10

Microanatomical study of pyramidal neurons in the contralesional somatosensory cortex after experimental ischemic stroke

Merino‐Serrais, P., Plaza‐Alonso, S., Hellal, F., Valero-Freitag, S., Kastanauskaite, A., Muñoz, A., Plesnila, N., & DeFelipe, J. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac121 · Cited by 10

Effect of task-specific training on Eph/ephrin expression after stroke

Choi, D., Ahn, J., Choi, I.-A., Kim, J., Kim, B.-R., & Lee, J. (2016) · BMB Reports · doi:10.5483/bmbrep.2016.49.11.172 · Cited by 10

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Cao, W., Zhang, C., Chen, R., Wu, Q., Xu, R., Zhang, L., & Zhang, X. (2020) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s289990 · Cited by 10

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Andino, S. L. G., Herrera‐Rincon, C., Panetsos, F., & de Peralta, R. G. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00087 · Cited by 10

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Scaglione, A., Conti, E., Mascaro, A. L. A., & Pavone, F. S. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.840922 · Cited by 9

Expansion of plasma MicroRNAs over the first month following human stroke

Edwardson, M. A., Shivapurkar, N., Li, J., Khan, M., Smith, J., Giannetti, M. L., Fan, R., & Dromerick, A. W. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231196982 · Cited by 9

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Choi, I.-A., Yun, J. H., Lee, J., & Choi, D.-H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111580 · Cited by 10

Safety, Pharmacokinetics, and Pharmacodynamics of a 6‐h N , N ‐Dimethyltryptamine (DMT) Infusion in Healthy Volunteers: A Randomized, Double‐Blind, Placebo‐Controlled Trial

van der Heijden, K. V., Zuiker, R. G. J. A., Otto, M. E., Bryan, C. F., Stewart, N., Stillwell, C., de Kam, M. L., van Leuken, M. B., van Gerven, J., & Jacobs, G. E. (2025) · Clinical and Translational Science · doi:10.1111/cts.70234 · Cited by 9

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 10

Neuropilin 2 deficiency does not affect cortical neuronal viability in response to oxygen–glucose-deprivation and transient middle cerebral artery occlusion

Hou, S., Jiang, S. X., Slinn, J., O’Hare, M., & Karchewski, L. A. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.12.010 · Cited by 9

Epileptiform discharge upregulates p-ERK1/2, growth-associated protein 43 and synaptophysin in cultured rat hippocampal neurons

Xu, Z., Chen, Y., Xu, P., Liu, H., Yun-lan, X., & Zeng, K. (2009) · Seizure · doi:10.1016/j.seizure.2009.09.004 · Cited by 9

Increased expression of the growth-associated protein-43 gene after primary motor cortex lesion in macaque monkeys

Murata, Y., Higo, N., Oishi, T., & Isa, T. (2015) · Neuroscience Research · doi:10.1016/j.neures.2015.04.007 · Cited by 9

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Hryciw, T., Geremia, N. M., Walker, M. A., Xu, X., & Brown, A. M. (2018) · Journal of Neurotrauma · doi:10.1089/neu.2018.5928 · Cited by 9

Post-ischemic reorganization of sensory responses in cerebral cortex

Hayley, P., Tuchek, C. A., Dalla, S., Borrell, J. I., Murphy, M. D., Nudo, R. J., & Guggenmos, D. J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1151309 · Cited by 8

Basic Science and Animal Studies

Cramer, S. C., & Nudo, R. J. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511777547.002 · Cited by 9

Stroke Repair via Biomimicry of the Subventricular Zone

Matta, R., & Gonzalez, A. L. (2018) · Frontiers in Materials · doi:10.3389/fmats.2018.00015 · Cited by 8

Recovery from ischemic stroke: a translational research perspective for neurology

Seitz, R. J., & Buetefisch, C. M. (2006) · Future Neurology · doi:10.2217/14796708.1.5.571 · Cited by 8

State-of-the-Art Techniques to Causally Link Neural Plasticity to Functional Recovery in Experimental Stroke Research

Wahl, A.-S. (2018) · Neural Plasticity · doi:10.1155/2018/3846593 · Cited by 8

Kainic acid-induced activation of nuclear factor-κB in the glial cells

Matsuoka, Y., Okazaki, M., Kitamura, Y., & Taniguchi, T. (1998) · Neuroscience Research · doi:10.1016/s0168-0102(98)82049-x

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Li, S., & Carmichael, S. T. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.03.011 · Cited by 162

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Li, S., Overman, J. J., Katsman, D., Kozlov, S. V., Donnelly, C. J., Twiss, J. L., Giger, R. J., Coppola, G., Geschwind, D. H., & Carmichael, S. T. (2010) · Nature Neuroscience · doi:10.1038/nn.2674 · Cited by 329

Acute increase in expression of growth associated protein GAP-43 following cortical ischemia in rat

Stroemer, R. P., Kent, T. A., & Hulsebosch, C. E. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90557-2 · Cited by 76

Gene expression changes after focal stroke, traumatic brain and spinal cord injuries

Carmichael, S. T. (2003) · Current Opinion in Neurology · doi:10.1097/00019052-200312000-00009 · Cited by 92