Journal of Neurophysiology

Jack Brooks, Anne Thaler

doi: 10.1152/jn.00232.2017pmid: 28424295

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Nat Neurosci 18 : 1152 – 1158 , 2015 . doi: 10.1038/nn.4055 . pmid: 26120962 OpenUrl CrossRef PubMed View Abstract Previous Next Back to top View this article with LENS What is LENS? About the Cover About the Cover Cover image Cover : Presence of sodium voltage-gated channel isoform 1.6 (NaV1.6) at the heminode and sensory terminals of a Ia afferent branch supplying innervation to a cat muscle spindle stained with antibodies targeting neurofilament H (green) and NaV1.6 (red). In the lower left corner are action potentials and instantaneous firing rates evoked by ramp-hold-release stretches recorded from a cat Ia afferent. From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords motor control uncertainty Bayesian inference predictive control object lifting Article Abstract DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following The sensorimotor system minimizes prediction error for object lifting when the object’s weight is uncertain Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools The sensorimotor system minimizes prediction error for object lifting when the object’s weight is uncertain Jack Brooks , Anne Thaler Journal of Neurophysiology Aug 2017, 118 (2) 649-651; DOI: 10.1152/jn.00232.2017 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share The sensorimotor system minimizes prediction error for object lifting when the object’s weight is uncertain Jack Brooks , Anne Thaler Journal of Neurophysiology Aug 2017, 118 (2) 649-651; DOI: 10.1152/jn.00232.2017 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Optimal motor synergy extraction for novel actions and virtual environments EEG oscillations: how are they modulated during different phases of repetitive movements? Show more Neuro Forum Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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Arran T. Reader

doi: 10.1152/jn.00165.2017pmid: 28539395

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Kinematics and muscle activity of reach-to-grasp movements are influenced by the action goal, but observers do not detect these differences . Exp Brain Res 225 : 261 – 275 , 2013 . doi: 10.1007/s00221-012-3367-2 . pmid: 23247469 OpenUrl CrossRef PubMed Web of Science ↵ Paulignan Y , Frak VG , Toni I , Jeannerod M . Influence of object position and size on human prehension movements . Exp Brain Res 114 : 226 – 234 , 1997 . doi: 10.1007/PL00005631 . pmid: 9166912 OpenUrl CrossRef PubMed Web of Science ↵ Steele KM , Tresch MC , Perreault EJ . Consequences of biomechanically constrained tasks in the design and interpretation of synergy analyses . J Neurophysiol 113 : 2102 – 2113 , 2015 . doi: 10.1152/jn.00769.2013 . pmid: 25589591 OpenUrl Abstract / FREE Full Text ↵ Vinjamuri R , Patel V , Powell M , Mao Z , Crone NE . Candidates for synergies: linear discriminants versus principal components . Comput Intell Neurosci 2014 : 373957 , 2014 . doi: 10.1155/2014/373957 . OpenUrl CrossRef ↵ Wang J , Stelmach GE . Spatial and temporal control of trunk-assisted prehensile actions . Exp Brain Res 136 : 231 – 240 , 2001 . doi: 10.1007/s002210000572 . pmid: 11206285 OpenUrl CrossRef PubMed Web of Science View Abstract Previous Next Back to top View this article with LENS What is LENS? About the Cover About the Cover Cover image Cover : Presence of sodium voltage-gated channel isoform 1.6 (NaV1.6) at the heminode and sensory terminals of a Ia afferent branch supplying innervation to a cat muscle spindle stained with antibodies targeting neurofilament H (green) and NaV1.6 (red). In the lower left corner are action potentials and instantaneous firing rates evoked by ramp-hold-release stretches recorded from a cat Ia afferent. From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords motor synergies dimensionality reduction virtual environments novel actions Article Abstract DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following Optimal motor synergy extraction for novel actions and virtual environments Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools Optimal motor synergy extraction for novel actions and virtual environments Arran T. Reader Journal of Neurophysiology Aug 2017, 118 (2) 652-654; DOI: 10.1152/jn.00165.2017 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share Optimal motor synergy extraction for novel actions and virtual environments Arran T. Reader Journal of Neurophysiology Aug 2017, 118 (2) 652-654; DOI: 10.1152/jn.00165.2017 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section The sensorimotor system minimizes prediction error for object lifting when the object’s weight is uncertain EEG oscillations: how are they modulated during different phases of repetitive movements? Show more Neuro Forum Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... GA_googleFillSlot("JN_tower_right_160x600"); Navigate Current Issue Articles in Press Archives Feedback Submit Subscribe Personal Alerts More Information About this Journal Information for Authors Submit a Manuscript Press Advertising AuthorChoice Calls for Papers Ethics Policy PubMed Central Policy Reprints and Permissions Institutional Administrators APS Publications News Follow APS Publications on Twitter American Physiological Society Journals Cell Physiology Advances in Physiology Education Comprehensive Physiology Endocrinology and Metabolism Gastrointestinal and Liver Physiology Heart and Circulatory Physiology Journal of Applied Physiology Journal of Neurophysiology Lung Cellular and Molecular Physiology Physiological Genomics Physiological Reviews Physiology Regulatory, Integrative and Comparative Physiology Renal Physiology Physiological Reports Legacy Content APS Select www.physiology.org Copyright © 2017 The American Physiological Society | Print ISSN: 0022-3077 | Online ISSN: 1522-1598

Roya Jalali, R. Chris Miall, Joseph M. Galea

doi: 10.1152/jn.00896.2016pmid: 28298304

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Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords adaptation brain stimulation cerebellum motor learning tDCS Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following No consistent effect of cerebellar transcranial direct current stimulation on visuomotor adaptation Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools No consistent effect of cerebellar transcranial direct current stimulation on visuomotor adaptation Roya Jalali , R. Chris Miall , Joseph M. Galea Journal of Neurophysiology Aug 2017, 118 (2) 655-665; DOI: 10.1152/jn.00896.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share No consistent effect of cerebellar transcranial direct current stimulation on visuomotor adaptation Roya Jalali , R. Chris Miall , Joseph M. Galea Journal of Neurophysiology Aug 2017, 118 (2) 655-665; DOI: 10.1152/jn.00896.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. Show more Research Article Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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Jalali, Roya; Miall, R. Chris; Galea, Joseph M.

doi: 10.1152/jn.00896.2016pmid: 28298304

Cerebellar transcranial direct current stimulation (ctDCS) is known to enhance motor adaptation and thus holds promise as a therapeutic intervention. However, understanding the reliability of ctDCS across varying task parameters is crucial. To examine this, we investigated whether ctDCS enhanced visuomotor adaptation across a range of varying task parameters. We found ctDCS to have no consistent effect on visuomotor adaptation, questioning the validity of using ctDCS within a clinical context.

Li-Ann Leow, Reece Gunn, Welber Marinovic, Timothy J. Carroll

doi: 10.1152/jn.00834.2016pmid: 28356480

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From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords Implicit Learning Explicit Learning compensatory strategies motor learning visuomotor rotation Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following Estimating the implicit component of visuomotor rotation learning by constraining movement preparation time Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools Estimating the implicit component of visuomotor rotation learning by constraining movement preparation time Li-Ann Leow , Reece Gunn , Welber Marinovic , Timothy J. Carroll Journal of Neurophysiology Aug 2017, 118 (2) 666-676; DOI: 10.1152/jn.00834.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share Estimating the implicit component of visuomotor rotation learning by constraining movement preparation time Li-Ann Leow , Reece Gunn , Welber Marinovic , Timothy J. Carroll Journal of Neurophysiology Aug 2017, 118 (2) 666-676; DOI: 10.1152/jn.00834.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. Show more Research Article Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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Daniel Galvis, Wei Wu, Richard L. Hyson, Frank Johnson, Richard Bertram

doi: 10.1152/jn.00917.2016pmid: 28381490

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About the Cover About the Cover Cover image Cover : Presence of sodium voltage-gated channel isoform 1.6 (NaV1.6) at the heminode and sensory terminals of a Ia afferent branch supplying innervation to a cat muscle spindle stained with antibodies targeting neurofilament H (green) and NaV1.6 (red). In the lower left corner are action potentials and instantaneous firing rates evoked by ramp-hold-release stretches recorded from a cat Ia afferent. From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords computational model zebra finch birdsong neural network bursting Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following A distributed neural network model for the distinct roles of medial and lateral HVC in zebra finch song production Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools A distributed neural network model for the distinct roles of medial and lateral HVC in zebra finch song production Daniel Galvis , Wei Wu , Richard L. Hyson , Frank Johnson , Richard Bertram Journal of Neurophysiology Aug 2017, 118 (2) 677-692; DOI: 10.1152/jn.00917.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share A distributed neural network model for the distinct roles of medial and lateral HVC in zebra finch song production Daniel Galvis , Wei Wu , Richard L. Hyson , Frank Johnson , Richard Bertram Journal of Neurophysiology Aug 2017, 118 (2) 677-692; DOI: 10.1152/jn.00917.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. Show more Research Article Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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Heidi M. Weeks, Amanda S. Therrien, Amy J. Bastian

doi: 10.1152/jn.00417.2016pmid: 28404825

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Exp Brain Res 233 : 2449 – 2459 , 2015 . doi: 10.1007/s00221-015-4315-8 . pmid: 25990821 OpenUrl CrossRef PubMed View Abstract Previous Next Back to top View this article with LENS What is LENS? About the Cover About the Cover Cover image Cover : Presence of sodium voltage-gated channel isoform 1.6 (NaV1.6) at the heminode and sensory terminals of a Ia afferent branch supplying innervation to a cat muscle spindle stained with antibodies targeting neurofilament H (green) and NaV1.6 (red). In the lower left corner are action potentials and instantaneous firing rates evoked by ramp-hold-release stretches recorded from a cat Ia afferent. From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords proprioception temporal spatial cerebellum ataxia Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following The cerebellum contributes to proprioception during motion Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools The cerebellum contributes to proprioception during motion Heidi M. Weeks , Amanda S. Therrien , Amy J. Bastian Journal of Neurophysiology Aug 2017, 118 (2) 693-702; DOI: 10.1152/jn.00417.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share The cerebellum contributes to proprioception during motion Heidi M. Weeks , Amanda S. Therrien , Amy J. Bastian Journal of Neurophysiology Aug 2017, 118 (2) 693-702; DOI: 10.1152/jn.00417.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. Show more Research Article Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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Alexandra Woolgar, Regine Zopf

doi: 10.1152/jn.00559.2016pmid: 28404826

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Your Personal Message Print Citation Tools Multisensory coding in the multiple-demand regions: vibrotactile task information is coded in frontoparietal cortex Alexandra Woolgar , Regine Zopf Journal of Neurophysiology Aug 2017, 118 (2) 703-716; DOI: 10.1152/jn.00559.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share Multisensory coding in the multiple-demand regions: vibrotactile task information is coded in frontoparietal cortex Alexandra Woolgar , Regine Zopf Journal of Neurophysiology Aug 2017, 118 (2) 703-716; DOI: 10.1152/jn.00559.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. 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Joshua D. Downer, Mamiko Niwa, Mitchell L. Sutter

doi: 10.1152/jn.00899.2016pmid: 28446588

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Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords amplitude modulation attention auditory cortex belt noise correlation Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES ENDNOTE AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. 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Thomas Hulst, Liane John, Michael Küper, Jos N. van der Geest, Sophia L. Göricke, Opher Donchin, Dagmar Timmann

doi: 10.1152/jn.00808.2016pmid: 28469001

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About the Cover About the Cover Cover image Cover : Presence of sodium voltage-gated channel isoform 1.6 (NaV1.6) at the heminode and sensory terminals of a Ia afferent branch supplying innervation to a cat muscle spindle stained with antibodies targeting neurofilament H (green) and NaV1.6 (red). In the lower left corner are action potentials and instantaneous firing rates evoked by ramp-hold-release stretches recorded from a cat Ia afferent. From Carrasco DI, Vincent JA, Cope TC. Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles. J Neurophysiol 117: 1690–1701, 2017; doi: 10.1152/jn.00889.2016 . Table of Contents Back Matter (PDF) Ed Board (PDF) Keywords tDCS cerebellar degeneration motor adaptation rehabilitation Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info E-letters PDF Alert me when this article is cited Alert me if a correction is posted Email Thank you for your interest in spreading the word on Journal of Neurophysiology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas. You are going to email the following Cerebellar patients do not benefit from cerebellar or M1 transcranial direct current stimulation during force-field reaching adaptation Message Subject (Your Name) has sent you a message from Journal of Neurophysiology Message Body (Your Name) thought you would like to see the Journal of Neurophysiology web site. Your Personal Message Print Citation Tools Cerebellar patients do not benefit from cerebellar or M1 transcranial direct current stimulation during force-field reaching adaptation Thomas Hulst , Liane John , Michael Küper , Jos N. van der Geest , Sophia L. Göricke , Opher Donchin , Dagmar Timmann Journal of Neurophysiology Aug 2017, 118 (2) 732-748; DOI: 10.1152/jn.00808.2016 Citation Manager Formats BibTeX Bookends EasyBib EndNote (tagged) EndNote 8 (xml) Medlars Mendeley Papers RefWorks Tagged Ref Manager RIS Zotero Share Cerebellar patients do not benefit from cerebellar or M1 transcranial direct current stimulation during force-field reaching adaptation Thomas Hulst , Liane John , Michael Küper , Jos N. van der Geest , Sophia L. Göricke , Opher Donchin , Dagmar Timmann Journal of Neurophysiology Aug 2017, 118 (2) 732-748; DOI: 10.1152/jn.00808.2016 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Muscle Proprioceptors in Adult Rat: Mechanosensory Signaling and Synapse Distribution in Spinal Cord Variance in exposed perturbations impairs retention of visuomotor adaptation Perception of the dynamic visual vertical during sinusoidal linear motion. Show more Research Article Related Articles Cited By... Most Read Most Cited Nonlinearity of two-photon Ca 2+ imaging yields distorted measurements of tuning for V1 neuronal populations Theories of pain: from specificity to gate control Reward, Addiction, and Emotion Regulation Systems Associated With Rejection in Love The organization of the human cerebral cortex estimated by intrinsic functional connectivity Motor recovery beginning 23 years after ischemic stroke More... 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