Cellular-resolution monitoring of ischemic stroke pathologies in the rat cortex
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Aniruddha Das | A. Machado | H. Dana | K. Baker | H. Chan | John K. Hermann | S. Chornyy | Thomas C. Jaramillo | Julie A. Borovicka | Davina Patel | Hugh H. N. Chan
[1] Kenneth D. Harris,et al. Neuropixels 2.0: A miniaturized high-density probe for stable, long-term brain recordings , 2020, Science.
[2] M. Rowan,et al. Hippocampal hyperactivity in a rat model of Alzheimer’s disease , 2020, bioRxiv.
[3] Damian J. Wallace,et al. Three-photon head-mounted microscope for imaging deep cortical layers in freely moving rats , 2020, Nature Methods.
[4] Francesca N. Delling,et al. Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association , 2020, Circulation.
[5] S. Rossi,et al. Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS): An update (2014–2018) , 2019, Clinical Neurophysiology.
[6] Aniruddha Das,et al. Reversible Loss of Hippocampal Function in a Mouse Model of Demyelination/Remyelination , 2019, bioRxiv.
[7] S. Johnstone,et al. Predicting functional outcomes after stroke: an observational study of acute single-channel EEG , 2019, Topics in stroke rehabilitation.
[8] Christof Koch,et al. Relationship between simultaneously recorded spiking activity and fluorescence signal in GCaMP6 transgenic mice , 2019, eLife.
[9] Felipe Fregni,et al. Searching for the optimal tDCS target for motor rehabilitation , 2019, Journal of NeuroEngineering and Rehabilitation.
[10] J. J. Macklin,et al. High-performance calcium sensors for imaging activity in neuronal populations and microcompartments , 2019, Nature Methods.
[11] K. Deisseroth,et al. Rational Engineering of XCaMPs, a Multicolor GECI Suite for In Vivo Imaging of Complex Brain Circuit Dynamics , 2019, Cell.
[12] D. Corbett,et al. Characterizing Spontaneous Motor Recovery Following Cortical and Subcortical Stroke in the Rat , 2018, Neurorehabilitation and neural repair.
[13] D. Tank,et al. Imaging Cortical Dynamics in GCaMP Transgenic Rats with a Head-Mounted Widefield Macroscope , 2018, Neuron.
[14] A. Machado,et al. Lateral cerebellar nucleus stimulation promotes motor recovery and suppresses neuroinflammation in a fluid percussion injury rodent model , 2018, Brain Stimulation.
[15] A. Machado,et al. Lateral Cerebellar Nucleus Stimulation has Selective Effects on Glutamatergic and GABAergic Perilesional Neurogenesis After Cortical Ischemia in the Rodent Model , 2018, Neurosurgery.
[16] F. Hummel,et al. Non-invasive Cerebellar Stimulation: a Promising Approach for Stroke Recovery? , 2018, The Cerebellum.
[17] Andreas Luft,et al. Global Burden of Stroke , 2018, Seminars in Neurology.
[18] Zachary B. Loris,et al. Beneficial Effects of Delayed P7C3-A20 Treatment After Transient MCAO in Rats , 2017, Translational Stroke Research.
[19] Amy Hu,et al. Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo , 2018, bioRxiv.
[20] John W. Krakauer,et al. Broken Movement: The Neurobiology of Motor Recovery after Stroke , 2017 .
[21] Kelly A. Tennant,et al. Optogenetic rewiring of thalamocortical circuits to restore function in the stroke injured brain , 2017, Nature Communications.
[22] S. Kuang,et al. Evaluation of Muscle Performance in Mice by Treadmill Exhaustion Test and Whole-limb Grip Strength Assay. , 2017, Bio-protocol.
[23] Julien Vermot,et al. Faculty Opinions recommendation of Neural circuits. Labeling of active neural circuits in vivo with designed calcium integrators. , 2017 .
[24] Andreas S Tolias,et al. In vivo three-photon imaging of activity of GCaMP6-labeled neurons deep in intact mouse brain , 2017, Nature Methods.
[25] A. Machado,et al. Crossed Cerebellar Atrophy of the Lateral Cerebellar Nucleus in an Endothelin-1-Induced, Rodent Model of Ischemic Stroke , 2017, Front. Aging Neurosci..
[26] C. Neuper,et al. Upper Alpha Based Neurofeedback Training in Chronic Stroke: Brain Plasticity Processes and Cognitive Effects , 2017, Applied psychophysiology and biofeedback.
[27] Geoffroy Saussez,et al. Rehabilitation of Motor Function after Stroke: A Multiple Systematic Review Focused on Techniques to Stimulate Upper Extremity Recovery , 2016, Front. Hum. Neurosci..
[28] Amiram Grinvald,et al. Accurate spike estimation from noisy calcium signals for ultrafast three-dimensional imaging of large neuronal populations in vivo , 2016, Nature Communications.
[29] Fritjof Helmchen,et al. Functional Imaging of Dentate Granule Cells in the Adult Mouse Hippocampus , 2016, The Journal of Neuroscience.
[30] Chaejeong Heo,et al. A soft, transparent, freely accessible cranial window for chronic imaging and electrophysiology , 2016, Scientific Reports.
[31] G. Katona,et al. Microglia protect against brain injury and their selective elimination dysregulates neuronal network activity after stroke , 2016, Nature Communications.
[32] A. Gordus,et al. Sensitive red protein calcium indicators for imaging neural activity , 2016, bioRxiv.
[33] C. Kleinschnitz,et al. Animal models of ischemic stroke and their application in clinical research , 2015, Drug design, development and therapy.
[34] K. Svoboda,et al. A Cellular Resolution Map of Barrel Cortex Activity during Tactile Behavior , 2015, Neuron.
[35] Nathan C. Klapoetke,et al. Transgenic Mice for Intersectional Targeting of Neural Sensors and Effectors with High Specificity and Performance , 2015, Neuron.
[36] Misha B. Ahrens,et al. Labeling of active neural circuits in vivo with designed calcium integrators , 2015, Science.
[37] Brenda C. Shields,et al. Thy1-GCaMP6 Transgenic Mice for Neuronal Population Imaging In Vivo , 2014, PloS one.
[38] A. Machado,et al. Chronic Deep Cerebellar Stimulation Promotes Long-Term Potentiation, Microstructural Plasticity, and Reorganization of Perilesional Cortical Representation in a Rodent Model , 2014, The Journal of Neuroscience.
[39] A. Machado,et al. Chronic 30-Hz deep cerebellar stimulation coupled with training enhances post-ischemia motor recovery and peri-infarct synaptophysin expression in rodents. , 2013, Neurosurgery.
[40] Stefan R. Pulver,et al. Ultra-sensitive fluorescent proteins for imaging neuronal activity , 2013, Nature.
[41] John T. Gale,et al. Semi-automated method for estimating lesion volumes , 2013, Journal of Neuroscience Methods.
[42] Kenneth B. Baker,et al. Integrative Neuroscience Original Research Article Upside down Crossed Cerebellar Diaschisis: Proposing Chronic Stimulation of the Dentatothalamocortical Pathway for Post-stroke Motor Recovery , 2022 .
[43] J. Simon Wiegert,et al. Multiple dynamic representations in the motor cortex during sensorimotor learning , 2012, Nature.
[44] Demetris K. Roumis,et al. Functional Specialization of Mouse Higher Visual Cortical Areas , 2011, Neuron.
[45] Sten Orrenius,et al. Calcium and cell death mechanisms: a perspective from the cell death community. , 2011, Cell calcium.
[46] T. Murphy,et al. In Vivo 2-Photon Imaging of Fine Structure in the Rodent Brain: Before, During, and After Stroke , 2010, Stroke.
[47] Liang Wang,et al. Dynamic functional reorganization of the motor execution network after stroke. , 2010, Brain : a journal of neurology.
[48] T. Murphy,et al. Plasticity during stroke recovery: from synapse to behaviour , 2009, Nature Reviews Neuroscience.
[49] Sreekanth H. Chalasani,et al. Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators , 2009, Nature Methods.
[50] Manoel Jacobsen Teixeira,et al. Functional mapping of the motor cortex of the rat using transdural electrical stimulation , 2009, Behavioural Brain Research.
[51] Alvaro Pascual-Leone,et al. Invasive cortical stimulation to promote recovery of function after stroke: a critical appraisal. , 2009, Stroke.
[52] F. J. Carod-Artal,et al. Quality of Life after Stroke: The Importance of a Good Recovery , 2009, Cerebrovascular Diseases.
[53] W. M. Keck,et al. Highly Selective Receptive Fields in Mouse Visual Cortex , 2008, The Journal of Neuroscience.
[54] David S. Greenberg,et al. Population imaging of ongoing neuronal activity in the visual cortex of awake rats , 2008, Nature Neuroscience.
[55] T. Murphy,et al. In Vivo Calcium Imaging Reveals Functional Rewiring of Single Somatosensory Neurons after Stroke , 2008, The Journal of Neuroscience.
[56] Steven C. Cramer. Repairing the human brain after stroke: I. Mechanisms of spontaneous recovery , 2008, Annals of neurology.
[57] J. Krakauer,et al. Neurorehabilitation and Neural Repair Inter-individual Variability in the Capacity for Motor Recovery after Ischemic Stroke Neurorehabilitation and Neural Repair Additional Services and Information for Inter-individual Variability in the Capacity for Motor Recovery after Ischemic Stroke , 2022 .
[58] M. Guanci,et al. Acute Ischemic Stroke Review , 2007, The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses.
[59] Gert Kwakkel,et al. Impact of Time on Improvement of Outcome After Stroke , 2006, Stroke.
[60] Steven C Cramer,et al. Motor Cortex Stimulation for the Enhancement of Recovery from Stroke: A Prospective, Multicenter Safety Study , 2006, Neurosurgery.
[61] Timothy H Murphy,et al. Rapid Reversible Changes in Dendritic Spine Structure In Vivo Gated by the Degree of Ischemia , 2005, The Journal of Neuroscience.
[62] M. Hommel,et al. Vicarious function within the human primary motor cortex? A longitudinal fMRI stroke study. , 2005, Brain : a journal of neurology.
[63] Sooyoung Chung,et al. Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex , 2005, Nature.
[64] Geoffrey A. Donnan,et al. Quality of Life After Stroke: The North East Melbourne Stroke Incidence Study (NEMESIS) , 2004, Stroke.
[65] J. Schaechter. Motor rehabilitation and brain plasticity after hemiparetic stroke , 2004, Progress in Neurobiology.
[66] J. Kleim,et al. Motor cortex stimulation enhances motor recovery and reduces peri-infarct dysfunction following ischemic insult , 2003, Neurological research.
[67] K. Fuxe,et al. Endothelin‐1 induced lesions of the frontoparietal cortex of the rat. A possible model of focal cortical ischemia , 1997, Neuroreport.
[68] S Giaquinto,et al. EEG Recordings in the Course of Recovery From Stroke , 1994, Stroke.
[69] D. Graham,et al. Endothelin-1-Induced Reductions in Cerebral Blood Flow: Dose Dependency, Time Course, and Neuropathological Consequences , 1993, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[70] P. Slater,et al. Rat middle cerebral artery occlusion: use of evoked potentials and Tetrazolium staining to assess chronic ischaemia , 1987, Journal of Neuroscience Methods.
[71] G. Quirk,et al. The organization of the rat motor cortex: A microstimulation mapping study , 1986, Brain Research Reviews.
[72] B. Vogt,et al. Direct connections of rat visual cortex with sensory, motor, and association cortices , 1984, The Journal of comparative neurology.
[73] David J. Guggenmos,et al. Physiological basis of neuromotor recovery , 2018 .
[74] M. Gassmann,et al. Post-acute delivery of erythropoietin induces stroke recovery by promoting perilesional tissue remodelling and contralesional pyramidal tract plasticity. , 2011, Brain : a journal of neurology.
[75] Michael Unser,et al. A pyramid approach to subpixel registration based on intensity , 1998, IEEE Trans. Image Process..
[76] D G Pelli,et al. The VideoToolbox software for visual psychophysics: transforming numbers into movies. , 1997, Spatial vision.
[77] D H Brainard,et al. The Psychophysics Toolbox. , 1997, Spatial vision.
[78] W. Young,et al. Somatosensory evoked potentials in rat cerebral cortex before and after middle cerebral artery occlusion. , 1990, Stroke.
[79] G. Paxinos,et al. The Rat Brain in Stereotaxic Coordinates , 1983 .