Journal of Neurophysiology

Hjalmar K. Turesson, Olga E. Rodríguez-Sierra, Denis Pare

doi: 10.1152/jn.00004.2013pmid: 23446692

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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords bed nucleus of the stria terminalis glutamate uncaging fear anxiety Article Abstract MATERIALS AND 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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Alex H. Williams, Molly A. Kwiatkowski, Adam L. Mortimer, Eve Marder, Mary Lou Zeeman, Patsy S. Dickinson

doi: 10.1152/jn.01010.2012pmid: 23446690

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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 neuronal oscillators central pattern generator morris-lecar model phase relationships 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. You are going to email the following Animal-to-animal variability in the phasing of the crustacean cardiac motor pattern: an experimental and computational analysis 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 Animal-to-animal variability in the phasing of the crustacean cardiac motor pattern: an experimental and computational analysis Alex H. Williams , Molly A. Kwiatkowski , Adam L. Mortimer , Eve Marder , Mary Lou Zeeman , Patsy S. Dickinson Journal of Neurophysiology May 2013, 109 (10) 2451-2465; DOI: 10.1152/jn.01010.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Animal-to-animal variability in the phasing of the crustacean cardiac motor pattern: an experimental and computational analysis Animal-to-animal variability in the phasing of the crustacean cardiac motor pattern: an experimental and computational analysis Alex H. Williams , Molly A. Kwiatkowski , Adam L. Mortimer , Eve Marder , Mary Lou Zeeman , Patsy S. Dickinson Journal of Neurophysiology May 2013, 109 (10) 2451-2465; DOI: 10.1152/jn.01010.2012 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Sensory convergence in the parieto-insular vestibular cortex 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 Show more Articles Related Articles Corrigendum Web of Science Scopus PubMed Google Scholar Cited By... Ionic Current Variability and Functional Stability in the Nervous System Abstract Fulltext PDF The Neuromuscular Transform of the Lobster Cardiac System Explains the Opposing Effects of a Neuromodulator on Muscle Output 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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Gary C. Sing, Simon P. Orozco, Maurice A. Smith

doi: 10.1152/jn.00497.2011pmid: 23365184

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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords motor adaptation force pulse motor primitives force-field adaptation Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION GRANTS DISCLOSURES AUTHOR CONTRIBUTIONS 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 Limb motion dictates how motor learning arises from arbitrary environmental dynamics 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 Limb motion dictates how motor learning arises from arbitrary environmental dynamics Gary C. Sing , Simon P. Orozco , Maurice A. Smith Journal of Neurophysiology May 2013, 109 (10) 2466-2482; DOI: 10.1152/jn.00497.2011 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Limb motion dictates how motor learning arises from arbitrary environmental dynamics Limb motion dictates how motor learning arises from arbitrary environmental dynamics Gary C. Sing , Simon P. Orozco , Maurice A. Smith Journal of Neurophysiology May 2013, 109 (10) 2466-2482; DOI: 10.1152/jn.00497.2011 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Sensory convergence in the parieto-insular vestibular cortex 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 Show more Articles Related Articles Web of Science Scopus PubMed Google Scholar Cited By... The training schedule affects the stability, not the magnitude, of the interlimb transfer of learned dynamics Abstract Fulltext PDF The Generalization of Visuomotor Learning to Untrained Movements and Movement Sequences Based on Movement Vector and Goal Location Remapping 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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Charles A. Hass, Gregory D. Horwitz

doi: 10.1152/jn.00671.2012pmid: 23446689

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OpenUrl Medline Web of Science ↵ Webster MA , Mollon JD . The influence of contrast adaptation on color appearance . Vision Res 34 : 1993 – 2020 , 1994 . 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 color vision visual cortex detection psychophysics electrophysiology 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 V1 mechanisms underlying chromatic contrast detection 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 V1 mechanisms underlying chromatic contrast detection Charles A. Hass , Gregory D. Horwitz Journal of Neurophysiology May 2013, 109 (10) 2483-2494; DOI: 10.1152/jn.00671.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share V1 mechanisms underlying chromatic contrast detection V1 mechanisms underlying chromatic contrast detection Charles A. Hass , Gregory D. Horwitz Journal of Neurophysiology May 2013, 109 (10) 2483-2494; DOI: 10.1152/jn.00671.2012 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. 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M. Scott Alexander, Brent W. G. Flodin, Daniel S. Marigold

doi: 10.1152/jn.00810.2012pmid: 23446691

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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords vision locomotion transfer of learning visuomotor adaptation fear 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. You are going to email the following Changes in task parameters during walking prism adaptation influence the subsequent generalization pattern 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 Changes in task parameters during walking prism adaptation influence the subsequent generalization pattern M. Scott Alexander , Brent W. G. Flodin , Daniel S. Marigold Journal of Neurophysiology May 2013, 109 (10) 2495-2504; DOI: 10.1152/jn.00810.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Changes in task parameters during walking prism adaptation influence the subsequent generalization pattern Changes in task parameters during walking prism adaptation influence the subsequent generalization pattern M. Scott Alexander , Brent W. G. Flodin , Daniel S. Marigold Journal of Neurophysiology May 2013, 109 (10) 2495-2504; DOI: 10.1152/jn.00810.2012 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Sensory convergence in the parieto-insular vestibular cortex 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 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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Fu-Zen Shaw, Yi-Fang Liao, Ruei-Feng Chen, Yu-Hsing Huang, Rick C. S. Lin

doi: 10.1152/jn.00750.2011pmid: 23446687

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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords zona incerta absence seizure spike-wave discharge tremor deep brain stimulation Article Abstract MATERIALS AND 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 The zona incerta modulates spontaneous spike-wave discharges in the rat 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 zona incerta modulates spontaneous spike-wave discharges in the rat Fu-Zen Shaw , Yi-Fang Liao , Ruei-Feng Chen , Yu-Hsing Huang , Rick C. S. Lin Journal of Neurophysiology May 2013, 109 (10) 2505-2516; DOI: 10.1152/jn.00750.2011 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share The zona incerta modulates spontaneous spike-wave discharges in the rat The zona incerta modulates spontaneous spike-wave discharges in the rat Fu-Zen Shaw , Yi-Fang Liao , Ruei-Feng Chen , Yu-Hsing Huang , Rick C. S. Lin Journal of Neurophysiology May 2013, 109 (10) 2505-2516; DOI: 10.1152/jn.00750.2011 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. 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... 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Masayuki Kurose, Ian D. Meng

doi: 10.1152/jn.00889.2012pmid: 23446686

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OpenUrl CrossRef Medline Web of Science ↵ Hirata H , Meng ID . Cold-sensitive corneal afferents respond to a variety of ocular stimuli central to tear production: implications for dry eye disease . Invest Ophthalmol Vis Sci 51 : 3969 – 3976 , 2010 . OpenUrl Abstract / FREE Full Text ↵ Hirata H , Okamoto K , Tashiro A , Bereiter DA . A novel class of neurons at the trigeminal subnucleus interpolaris/caudalis transition region monitors ocular surface fluid status and modulates tear production . J Neurosci 24 : 4224 – 4232 , 2004 . OpenUrl Abstract / FREE Full Text ↵ Hirata H , Takeshita S , Hu JW , Bereiter DA . Cornea-responsive medullary dorsal horn neurons: modulation by local opioids and projections to thalamus and brain stem . J Neurophysiol 84 : 1050 – 1061 , 2000 . OpenUrl Abstract / FREE Full Text ↵ Madrid R , Donovan-Rodriguez T , Meseguer V , Acosta MC , Belmonte C , Viana F . Contribution of TRPM8 channels to cold transduction in primary sensory neurons and peripheral nerve terminals . J Neurosci 26 : 12512 – 12525 , 2006 . OpenUrl Abstract / FREE Full Text ↵ Marfurt CF , Del Toro DR . Corneal sensory pathway in the rat: a horseradish peroxidase tracing study . J Comp Neurol 261 : 450 – 459 , 1987 . OpenUrl CrossRef Medline Web of Science ↵ McCoy DD , Knowlton WM , McKemy DD . Scraping through the ice: uncovering the role of TRPM8 in cold transduction . Am J Physiol Regul Integr Comp Physiol 300 : R1278 – R1287 , 2011 . OpenUrl Abstract / FREE Full Text ↵ McKemy DD , Neuhausser WM , Julius D . Identification of a cold receptor reveals a general role for TRP channels in thermosensation . Nature 416 : 52 – 58 , 2002 . OpenUrl CrossRef Medline ↵ Meng ID , Bereiter DA . Differential distribution of Fos-like immunoreactivity in the spinal trigeminal nucleus after noxious and innocuous thermal and chemical stimulation of rat cornea . 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OpenUrl Abstract / FREE Full Text ↵ Parra A , Madrid R , Echevarria D , del Olmo S , Morenilla-Palao C , Acosta MC , Gallar J , Dhaka A , Viana F , Belmonte C . Ocular surface wetness is regulated by TRPM8-dependent cold thermoreceptors of the cornea . Nat Med 16 : 1396 – 1399 , 2010 . OpenUrl CrossRef Medline Web of Science ↵ Peier AM , Moqrich A , Hergarden AC , Reeve AJ , Andersson DA , Story GM , Earley TJ , Dragoni I , McIntyre P , Bevan S , Patapoutian A . A TRP channel that senses cold stimuli and menthol . Cell 108 : 705 – 715 , 2002 . OpenUrl CrossRef Medline Web of Science ↵ Robbins A , Kurose M , Winterson BJ , Meng ID . Menthol activation of corneal cool cells induces TRPM8-mediated lacrimation but not nociceptive responses in rodents . Invest Ophthalmol Vis Sci 53 : 7034 – 7042 , 2012 . OpenUrl Abstract / FREE Full Text ↵ Strassman AM , Vos BP . Somatotopic and laminar organization of fos-like immunoreactivity in the medullary and upper cervical dorsal horn induced by noxious facial stimulation in the rat . J Comp Neurol 331 : 495 – 516 , 1993 . OpenUrl CrossRef Medline Web of Science ↵ Tanelian DL , Beuerman RW . Responses of rabbit corneal nociceptors to mechanical and thermal stimulation . Exp Neurol 84 : 165 – 178 , 1984 . OpenUrl CrossRef Medline Web of Science ↵ Tashiro A , Okamoto K , Chang Z , Bereiter DA . Behavioral and neurophysiological correlates of nociception in an animal model of photokeratitis . Neuroscience 169 : 455 – 462 , 2010 . OpenUrl CrossRef Medline Web of Science ↵ Thut PD , Wrigley D , Gold MS . Cold transduction in rat trigeminal ganglia neurons in vitro . Neuroscience 119 : 1071 – 1083 , 2003 . OpenUrl CrossRef Medline Web of Science ↵ Toth IE , Boldogkoi Z , Medveczky I , Palkovits M . Lacrimal preganglionic neurons form a subdivision of the superior salivatory nucleus of rat: transneuronal labelling by pseudorabies virus . J Auton Nerv Syst 77 : 45 – 54 , 1999 . OpenUrl CrossRef Medline Web of Science ↵ Zanotto KL , Merrill AW , Carstens MI , Carstens E . Neurons in superficial trigeminal subnucleus caudalis responsive to oral cooling, menthol, and other irritant stimuli . J Neurophysiol 97 : 966 – 978 , 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 trigeminal cornea nociception eye Article Abstract MATERIALS AND 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 Corneal dry-responsive neurons in the spinal trigeminal nucleus respond to innocuous cooling in the rat 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 Corneal dry-responsive neurons in the spinal trigeminal nucleus respond to innocuous cooling in the rat Masayuki Kurose , Ian D. Meng Journal of Neurophysiology May 2013, 109 (10) 2517-2522; DOI: 10.1152/jn.00889.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Corneal dry-responsive neurons in the spinal trigeminal nucleus respond to innocuous cooling in the rat Corneal dry-responsive neurons in the spinal trigeminal nucleus respond to innocuous cooling in the rat Masayuki Kurose , Ian D. Meng Journal of Neurophysiology May 2013, 109 (10) 2517-2522; DOI: 10.1152/jn.00889.2012 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... The TFOS International Workshop on Contact Lens Discomfort: Report of the Subcommittee on Neurobiology Abstract Fulltext PDF Dry eye modifies the thermal and menthol responses in rat corneal primary afferent cool cells Abstract Fulltext PDF Web of Science (3) 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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N. Peter Reeves, Pramod Pathak, John M. Popovich, Jr, Vilok Vijayanagar

doi: 10.1152/jn.00429.2012pmid: 23446693

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Mathematical Statistics and Data Analysis . Belmont, CA : Thomson/Brooks/Cole , 2007 . ↵ Selen LPJ , Beek PJ , Dieën JHV . Can co-activation reduce kinematic variability? A simulation study . Biol Cybern 93 : 373 – 381 , 2005 . OpenUrl CrossRef Medline Web of Science ↵ Van Dieen JH , Pijnappels M . Falls in older people . J Electromyogr Kinesiol 18 : 169 – 171 , 2008 . 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 motor control biological stability feedback delay electromechanical delay muscle coactivation Article Abstract MATERIALS AND METHODS RESULTS DISCUSSION DISCLOSURES AUTHOR CONTRIBUTIONS ACKNOWLEDGMENTS APPENDIX 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 Limits in motor control bandwidth during stick balancing 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 Limits in motor control bandwidth during stick balancing N. Peter Reeves , Pramod Pathak , John M. Popovich , Vilok Vijayanagar Journal of Neurophysiology May 2013, 109 (10) 2523-2527; DOI: 10.1152/jn.00429.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Limits in motor control bandwidth during stick balancing Limits in motor control bandwidth during stick balancing N. Peter Reeves , Pramod Pathak , John M. Popovich , Vilok Vijayanagar Journal of Neurophysiology May 2013, 109 (10) 2523-2527; DOI: 10.1152/jn.00429.2012 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Temporal scaling of neural responses to compressed and dilated natural speech Corticospinal excitability underlying digit force planning for grasping in humans Sensory convergence in the parieto-insular vestibular cortex 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... 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

Mark D. Benton, Amanda H. Lewis, Jason S. Bant, Indira M. Raman

doi: 10.1152/jn.00127.2012pmid: 23446695

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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords cerebellum calcium-activated potassium Kca action potential voltage-clamp SK EBIO Article Abstract MATERIALS AND 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 Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata 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 Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata Mark D. Benton , Amanda H. Lewis , Jason S. Bant , Indira M. Raman Journal of Neurophysiology May 2013, 109 (10) 2528-2541; DOI: 10.1152/jn.00127.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata Iberiotoxin-sensitive and -insensitive BK currents in Purkinje neuron somata Mark D. Benton , Amanda H. Lewis , Jason S. Bant , Indira M. Raman Journal of Neurophysiology May 2013, 109 (10) 2528-2541; DOI: 10.1152/jn.00127.2012 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 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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