Can noninvasive brain stimulation enhance function in the ageing brain?Ann-Maree Vallence, Mitchell R. Goldsworthy
doi: 10.1152/jn.00088.2013pmid: 24004526
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OpenUrl CrossRef Medline Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords noninvasive brain stimulation ageing skill acquisition consolidation Article Abstract DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Info 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 Can noninvasive brain stimulation enhance function in the ageing brain? 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 Can noninvasive brain stimulation enhance function in the ageing brain? Ann-Maree Vallence , Mitchell R. Goldsworthy Journal of Neurophysiology Jan 2014, 111 (1) 1-3; DOI: 10.1152/jn.00088.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Can noninvasive brain stimulation enhance function in the ageing brain? Can noninvasive brain stimulation enhance function in the ageing brain? Ann-Maree Vallence , Mitchell R. Goldsworthy Journal of Neurophysiology Jan 2014, 111 (1) 1-3; DOI: 10.1152/jn.00088.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Dopamine gates sensory representations in cortex The basis of orientation decoding in human primary visual cortex: fine- or coarse-scale biases? Explaining autism spectrum disorders: central coherence versus predictive coding theories. Show more Neuro Forum Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Energy-related optimal control accounts for gravitational load: comparing shoulder, elbow, and wrist rotationsJérémie Gaveau, Bastien Berret, Laurent Demougeot, Luciano Fadiga, Thierry Pozzo, Charalambos Papaxanthis
doi: 10.1152/jn.01029.2012pmid: 24133223
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OpenUrl CrossRef Medline Web of Science Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords sensorimotor control reaching movement gravity force optimal control proximal distal Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info 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 Energy-related optimal control accounts for gravitational load: comparing shoulder, elbow, and wrist rotations 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 Energy-related optimal control accounts for gravitational load: comparing shoulder, elbow, and wrist rotations Jérémie Gaveau , Bastien Berret , Laurent Demougeot , Luciano Fadiga , Thierry Pozzo , Charalambos Papaxanthis Journal of Neurophysiology Jan 2014, 111 (1) 4-16; DOI: 10.1152/jn.01029.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Energy-related optimal control accounts for gravitational load: comparing shoulder, elbow, and wrist rotations Energy-related optimal control accounts for gravitational load: comparing shoulder, elbow, and wrist rotations Jérémie Gaveau , Bastien Berret , Laurent Demougeot , Luciano Fadiga , Thierry Pozzo , Charalambos Papaxanthis Journal of Neurophysiology Jan 2014, 111 (1) 4-16; DOI: 10.1152/jn.01029.2012 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Combining d -cycloserine with motor training does not result in improved general motor learning in neurologically intact people or in people with stroke Localizing evoked cortical activity associated with balance reactions: does the anterior cingulate play a role? Visual and vestibular perceptual thresholds each demonstrate better precision at specific frequencies and also exhibit optimal integration Show more Articles Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Functional difference in short- and long-latency interhemispheric inhibitions from active to resting hemisphere during a unilateral muscle contractionKazumasa Uehara, Takuya Morishita, Shinji Kubota, Masato Hirano, Kozo Funase
doi: 10.1152/jn.00494.2013pmid: 24089401
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords transcranial magnetic stimulation interhemispheric inhibition voluntary muscle contraction Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info 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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Your Personal Message Print Citation Tools Functional difference in short- and long-latency interhemispheric inhibitions from active to resting hemisphere during a unilateral muscle contraction Kazumasa Uehara , Takuya Morishita , Shinji Kubota , Masato Hirano , Kozo Funase Journal of Neurophysiology Jan 2014, 111 (1) 17-25; DOI: 10.1152/jn.00494.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Functional difference in short- and long-latency interhemispheric inhibitions from active to resting hemisphere during a unilateral muscle contraction Functional difference in short- and long-latency interhemispheric inhibitions from active to resting hemisphere during a unilateral muscle contraction Kazumasa Uehara , Takuya Morishita , Shinji Kubota , Masato Hirano , Kozo Funase Journal of Neurophysiology Jan 2014, 111 (1) 17-25; DOI: 10.1152/jn.00494.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Synaptic excitation is regulated by the postsynaptic dSK channel at the Drosophila larval NMJ Motor cortical disinhibition with baroreceptor unloading induced by orthostatic stress Perturbation schedule does not alter retention of a locomotor adaptation across days Show more Articles Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Effects of the motor cortical quadripulse transcranial magnetic stimulation (QPS) on the contralateral motor cortex and interhemispheric interactionsRyosuke Tsutsumi, Ritsuko Hanajima, Yasuo Terao, Yuichiro Shirota, Shinya Ohminami, Takahiro Shimizu, Nobuyuki Tanaka, Yoshikazu Ugawa
doi: 10.1152/jn.00515.2013pmid: 24108795
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OpenUrl Abstract / FREE Full Text Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords corpus callosum interhemispheric inhibition interhemispheric facilitation plasticity repetitive transcranial magnetic stimulation Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info 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 Effects of the motor cortical quadripulse transcranial magnetic stimulation (QPS) on the contralateral motor cortex and interhemispheric interactions 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 Effects of the motor cortical quadripulse transcranial magnetic stimulation (QPS) on the contralateral motor cortex and interhemispheric interactions Ryosuke Tsutsumi , Ritsuko Hanajima , Yasuo Terao , Yuichiro Shirota , Shinya Ohminami , Takahiro Shimizu , Nobuyuki Tanaka , Yoshikazu Ugawa Journal of Neurophysiology Jan 2014, 111 (1) 26-35; DOI: 10.1152/jn.00515.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Effects of the motor cortical quadripulse transcranial magnetic stimulation (QPS) on the contralateral motor cortex and interhemispheric interactions Effects of the motor cortical quadripulse transcranial magnetic stimulation (QPS) on the contralateral motor cortex and interhemispheric interactions Ryosuke Tsutsumi , Ritsuko Hanajima , Yasuo Terao , Yuichiro Shirota , Shinya Ohminami , Takahiro Shimizu , Nobuyuki Tanaka , Yoshikazu Ugawa Journal of Neurophysiology Jan 2014, 111 (1) 26-35; DOI: 10.1152/jn.00515.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Thalamostriatal projections from the medial posterior and parafascicular nuclei have distinct topographic and physiologic propertiesKevin D. Alloway, Jared B. Smith, Glenn D. R. Watson
doi: 10.1152/jn.00399.2013pmid: 24108793
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OpenUrl Abstract / FREE Full Text Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords basal ganglia habituation neuronal latency neuronal tracing whisker stimulation Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info 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 Thalamostriatal projections from the medial posterior and parafascicular nuclei have distinct topographic and physiologic properties 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 Thalamostriatal projections from the medial posterior and parafascicular nuclei have distinct topographic and physiologic properties Kevin D. Alloway , Jared B. Smith , Glenn D. R. Watson Journal of Neurophysiology Jan 2014, 111 (1) 36-50; DOI: 10.1152/jn.00399.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Thalamostriatal projections from the medial posterior and parafascicular nuclei have distinct topographic and physiologic properties Thalamostriatal projections from the medial posterior and parafascicular nuclei have distinct topographic and physiologic properties Kevin D. Alloway , Jared B. Smith , Glenn D. R. Watson Journal of Neurophysiology Jan 2014, 111 (1) 36-50; DOI: 10.1152/jn.00399.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science Scopus PubMed Google Scholar Cited By... No citing articles found. Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Reflex responses of human masseter motor units to mechanical stimulation of the teethP. Uginčius, E. S. Atiş, K. S. Türker
doi: 10.1152/jn.00478.2013pmid: 24133225
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords masseter reflex periodontal mechanoreceptor muscle spindle Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info 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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Türker Journal of Neurophysiology Jan 2014, 111 (1) 51-61; DOI: 10.1152/jn.00478.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Central complex neurons exhibit behaviorally gated responses to visual motion in DrosophilaPeter T. Weir, Bettina Schnell, Michael H. Dickinson
doi: 10.1152/jn.00593.2013pmid: 24108792
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords context task dependent flight fan-shaped body optic flow Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS Footnotes REFERENCES Figures & Data Info 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 Central complex neurons exhibit behaviorally gated responses to visual motion in Drosophila 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 Central complex neurons exhibit behaviorally gated responses to visual motion in Drosophila Peter T. Weir , Bettina Schnell , Michael H. Dickinson Journal of Neurophysiology Jan 2014, 111 (1) 62-71; DOI: 10.1152/jn.00593.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Central complex neurons exhibit behaviorally gated responses to visual motion in Drosophila Central complex neurons exhibit behaviorally gated responses to visual motion in Drosophila Peter T. Weir , Bettina Schnell , Michael H. Dickinson Journal of Neurophysiology Jan 2014, 111 (1) 62-71; DOI: 10.1152/jn.00593.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science Scopus PubMed Google Scholar Cited By... Cellular mechanisms for integral feedback in visually guided behavior Abstract Fulltext PDF Web of Science (1) Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect 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 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 © 2014 The American Physiological Society | Print ISSN: 0022-3077 | Online ISSN: 1522-1598
Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleepKimiya Narikiyo, Hiroyuki Manabe, Kensaku Mori
doi: 10.1152/jn.00535.2013pmid: 24108798
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords olfactory tubercle sleep sharp wave Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info 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 Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleep 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 Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleep Kimiya Narikiyo , Hiroyuki Manabe , Kensaku Mori Journal of Neurophysiology Jan 2014, 111 (1) 72-81; DOI: 10.1152/jn.00535.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleep Sharp wave-associated synchronized inputs from the piriform cortex activate olfactory tubercle neurons during slow-wave sleep Kimiya Narikiyo , Hiroyuki Manabe , Kensaku Mori Journal of Neurophysiology Jan 2014, 111 (1) 72-81; DOI: 10.1152/jn.00535.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science Scopus PubMed Google Scholar Cited By... Odor- and state-dependent olfactory tubercle local field potential dynamics in awake rats Abstract Fulltext PDF Thalamic olfaction: characterizing odor processing in the mediodorsal thalamus of the rat Abstract Fulltext PDF Web of Science (2) Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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Whole person-evoked fMRI activity patterns in human fusiform gyrus are accurately modeled by a linear combination of face- and body-evoked activity patternsDaniel Kaiser, Lukas Strnad, Katharina N. Seidl, Sabine Kastner, Marius V. Peelen
doi: 10.1152/jn.00371.2013pmid: 24108794
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J Neurosci 27 : 12292 – 12307 , 2007 . OpenUrl Abstract / FREE Full Text Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords fusiform face area fusiform body area extrastriate body area object perception category selectivity Article Abstract METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS REFERENCES Figures & Data Info 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 Whole person-evoked fMRI activity patterns in human fusiform gyrus are accurately modeled by a linear combination of face- and body-evoked activity patterns 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 Whole person-evoked fMRI activity patterns in human fusiform gyrus are accurately modeled by a linear combination of face- and body-evoked activity patterns Daniel Kaiser , Lukas Strnad , Katharina N. Seidl , Sabine Kastner , Marius V. Peelen Journal of Neurophysiology Jan 2014, 111 (1) 82-90; DOI: 10.1152/jn.00371.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Whole person-evoked fMRI activity patterns in human fusiform gyrus are accurately modeled by a linear combination of face- and body-evoked activity patterns Whole person-evoked fMRI activity patterns in human fusiform gyrus are accurately modeled by a linear combination of face- and body-evoked activity patterns Daniel Kaiser , Lukas Strnad , Katharina N. Seidl , Sabine Kastner , Marius V. Peelen Journal of Neurophysiology Jan 2014, 111 (1) 82-90; DOI: 10.1152/jn.00371.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Unilateral electrical stimulation of rat locus coeruleus elicits bilateral response of norepinephrine neurons and sustained activation of medial prefrontal cortex Early vestibular processing does not discriminate active from passive self-motion if there is a discrepancy between predicted and actual proprioceptive feedback Organization of local horizontal functional interactions between neurons in the inferior temporal cortex of macaque monkeys Show more Articles Related Articles Web of Science PubMed Google Scholar Most Read Most Cited Recruitment in Retractor Bulbi Muscle During Eyeblink Conditioning: EMG Analysis and Common-Drive Model Predictive Reward Signal of Dopamine Neurons Somatic calcium level reports integrated spiking activity of cerebellar interneurons in vitro and in vivo Fast Functional Imaging of Single Neurons Using Random-Access Multiphoton (RAMP) Microscopy Inaudible High-Frequency Sounds Affect Brain Activity: Hypersonic Effect More... 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The dynamics of invariant object recognition in the human visual systemLeyla Isik, Ethan M. Meyers, Joel Z. Leibo, Tomaso Poggio
doi: 10.1152/jn.00394.2013pmid: 24089402
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OpenUrl Abstract / FREE Full Text Previous Next Back to top About the Cover About the Cover Cover image Cover : From Lerner Y, Honey CJ, Katkov M, Hasson U. Temporal scaling of neural responses to compressed and dilated natural speech. J Neurophysiol ; published ahead of print March 19, 2014, doi: 10.1152/jn.00497.2013 . Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords vision decoding magnetoencephalography object recognition invariance Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS REFERENCES Figures & Data Info 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. 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Leibo , Tomaso Poggio Journal of Neurophysiology Jan 2014, 111 (1) 91-102; DOI: 10.1152/jn.00394.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Simultaneous adaptation of the thumb and index finger of the same hand to opposite prism displacements Visuomotor adaptation in Parkinson's disease: effects of perturbation type and medication state Temporal scaling of neural responses to compressed and dilated natural speech Show more Articles Related Articles Web of Science Scopus PubMed Google Scholar Cited By... 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