Neuronal responses to target onset in oculomotor and somatomotor parietal circuits differ markedly in a choice taskJ. Kubanek, C. Wang, L. H. Snyder
doi: 10.1152/jn.00968.2012pmid: 23966670
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Modulated discharge of Purkinje and stellate cells persists after unilateral loss of vestibular primary afferent mossy fibers in miceN. H. Barmack, V. Yakhnitsa
doi: 10.1152/jn.00352.2013pmid: 23966673
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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 cerebellum Purkinje cell Golgi cell stellate cell labyrinthectomy complex spike simple spike 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 Modulated discharge of Purkinje and stellate cells persists after unilateral loss of vestibular primary afferent mossy fibers in mice 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 Modulated discharge of Purkinje and stellate cells persists after unilateral loss of vestibular primary afferent mossy fibers in mice N. H. Barmack , V. Yakhnitsa Journal of Neurophysiology Nov 2013, 110 (10) 2257-2274; DOI: 10.1152/jn.00352.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Modulated discharge of Purkinje and stellate cells persists after unilateral loss of vestibular primary afferent mossy fibers in mice Modulated discharge of Purkinje and stellate cells persists after unilateral loss of vestibular primary afferent mossy fibers in mice N. H. Barmack , V. Yakhnitsa Journal of Neurophysiology Nov 2013, 110 (10) 2257-2274; DOI: 10.1152/jn.00352.2013 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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Role of synaptic dynamics and heterogeneity in neuronal learning of temporal codeZiv Rotman, Vitaly A. Klyachko
doi: 10.1152/jn.00454.2013pmid: 23926043
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords neural learning short-term plasticity synapse synaptic dynamics temporal code 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 Role of synaptic dynamics and heterogeneity in neuronal learning of temporal code 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 Role of synaptic dynamics and heterogeneity in neuronal learning of temporal code Ziv Rotman , Vitaly A. Klyachko Journal of Neurophysiology Nov 2013, 110 (10) 2275-2286; DOI: 10.1152/jn.00454.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Role of synaptic dynamics and heterogeneity in neuronal learning of temporal code Role of synaptic dynamics and heterogeneity in neuronal learning of temporal code Ziv Rotman , Vitaly A. Klyachko Journal of Neurophysiology Nov 2013, 110 (10) 2275-2286; DOI: 10.1152/jn.00454.2013 Permalink: Copy View Full Page PDF Tweet Widget Facebook Like Google Plus One Reddit CiteULike Mendeley StumbleUpon More in this TOC Section Self-motion improves head direction cell tuning Phase maintenance in a rhythmic motor pattern during temperature changes in vivo Depressed GABA and glutamate synaptic signaling by 5-HT 1A receptors in the nucleus tractus solitarii and their role in cardiorespiratory function 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 lateral mesopontine tegmentum regulates both tonic and phasic activity of VTA dopamine neuronsLi Chen, Daniel J. Lodge
doi: 10.1152/jn.00307.2013pmid: 24004527
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OpenUrl CrossRef Medline Web of Science ↵ Woolf NJ , Butcher LL . Cholinergic systems in the rat brain: III. Projections from the pontomesencephalic tegmentum to the thalamus, tectum, basal ganglia, and basal forebrain . Brain Res Bul 16 : 603 – 637 , 1986 . 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 dopamine mesopontine tegmentum extracellular recording afferent input burst firing 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 lateral mesopontine tegmentum regulates both tonic and phasic activity of VTA dopamine neurons 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 lateral mesopontine tegmentum regulates both tonic and phasic activity of VTA dopamine neurons Li Chen , Daniel J. Lodge Journal of Neurophysiology Nov 2013, 110 (10) 2287-2294; DOI: 10.1152/jn.00307.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share The lateral mesopontine tegmentum regulates both tonic and phasic activity of VTA dopamine neurons The lateral mesopontine tegmentum regulates both tonic and phasic activity of VTA dopamine neurons Li Chen , Daniel J. Lodge Journal of Neurophysiology Nov 2013, 110 (10) 2287-2294; DOI: 10.1152/jn.00307.2013 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... 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Detection of submillisecond spike timing differences based on delay-line anticoincidence detectionAriel M. Lyons-Warren, Tsunehiko Kohashi, Steven Mennerick, Bruce A. Carlson
doi: 10.1152/jn.00444.2013pmid: 23966672
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords temporal coding electric fish calyx sound localization interaural time difference 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 Detection of submillisecond spike timing differences based on delay-line anticoincidence 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 Detection of submillisecond spike timing differences based on delay-line anticoincidence detection Ariel M. Lyons-Warren , Tsunehiko Kohashi , Steven Mennerick , Bruce A. Carlson Journal of Neurophysiology Nov 2013, 110 (10) 2295-2311; DOI: 10.1152/jn.00444.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Detection of submillisecond spike timing differences based on delay-line anticoincidence detection Detection of submillisecond spike timing differences based on delay-line anticoincidence detection Ariel M. Lyons-Warren , Tsunehiko Kohashi , Steven Mennerick , Bruce A. Carlson Journal of Neurophysiology Nov 2013, 110 (10) 2295-2311; DOI: 10.1152/jn.00444.2013 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
Unmasking the obligatory components of nociceptive event-related brain potentialsA. Mouraux, A. L. De Paepe, E. Marot, L. Plaghki, G. D. Iannetti, V. Legrain
doi: 10.1152/jn.00137.2013pmid: 23966678
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords pain nociception event-related potentials primary somatosensory cortex laser-evoked potentials intraepidermal stimulation 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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Regulation of dendritic calcium release in striatal spiny projection neuronsJoshua L. Plotkin, Weixing Shen, Igor Rafalovich, Luke E. Sebel, Michelle Day, C. Savio Chan, D. James Surmeier
doi: 10.1152/jn.00422.2013pmid: 23966676
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Growth hormone promotes Ca 2+ -induced Ca 2+ release in insulin-secreting cells by ryanodine receptor tyrosine phosphorylation . Mol Endocrinol 18 : 1658 – 1669 , 2004 . 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 two-photon imaging calcium long-term depression plasticity striatum 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. 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James Surmeier Journal of Neurophysiology Nov 2013, 110 (10) 2325-2336; DOI: 10.1152/jn.00422.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Regulation of dendritic calcium release in striatal spiny projection neurons Regulation of dendritic calcium release in striatal spiny projection neurons Joshua L. Plotkin , Weixing Shen , Igor Rafalovich , Luke E. Sebel , Michelle Day , C. Savio Chan , D. James Surmeier Journal of Neurophysiology Nov 2013, 110 (10) 2325-2336; DOI: 10.1152/jn.00422.2013 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 Cited By... Contrasting actions of group I metabotropic glutamate receptors in distinct mouse striatal neurones Abstract 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 cerebellar lesions on working memory interacting with motor tasks of different complexitiesWinfried Ilg, Andrea Christensen, Oliver M. Mueller, Sophia L. Goericke, Martin A. Giese, Dagmar Timmann
doi: 10.1152/jn.00062.2013pmid: 23966680
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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 cerebellum lesion-symptom mapping dual task working memory gait Article Abstract METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS Appendix Appendix Appendix Appendix 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 Effects of cerebellar lesions on working memory interacting with motor tasks of different complexities 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 cerebellar lesions on working memory interacting with motor tasks of different complexities Winfried Ilg , Andrea Christensen , Oliver M. Mueller , Sophia L. Goericke , Martin A. Giese , Dagmar Timmann Journal of Neurophysiology Nov 2013, 110 (10) 2337-2349; DOI: 10.1152/jn.00062.2013 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share Effects of cerebellar lesions on working memory interacting with motor tasks of different complexities Effects of cerebellar lesions on working memory interacting with motor tasks of different complexities Winfried Ilg , Andrea Christensen , Oliver M. Mueller , Sophia L. Goericke , Martin A. Giese , Dagmar Timmann Journal of Neurophysiology Nov 2013, 110 (10) 2337-2349; DOI: 10.1152/jn.00062.2013 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... 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Short- and long-term plasticity in CA1 neurons from mice lacking h-channel auxiliary subunit TRIP8bDarrin H. Brager, Alan S. Lewis, Dane M. Chetkovich, Daniel Johnston
doi: 10.1152/jn.00218.2013pmid: 23966674
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords hippocampus IH intrinsic plasticity Schaffer collateral perforant path 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. 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α7-Containing nicotinic acetylcholine receptors on interneurons of the basolateral amygdala and their role in the regulation of the network excitabilityVolodymyr I. Pidoplichko, Eric M. Prager, Vassiliki Aroniadou-Anderjaska, Maria F. M. Braga
doi: 10.1152/jn.01030.2012pmid: 24004528
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Table of Contents Back Matter (PDF) Ed Board (PDF) Front Matter (PDF) Keywords α7-nAChR GABAA receptor inhibition basolateral amygdala 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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Braga Journal of Neurophysiology Nov 2013, 110 (10) 2358-2369; DOI: 10.1152/jn.01030.2012 Citation Manager Formats BibTeX EndNote (tagged) EndNote 8 (xml) RefWorks Tagged RIS Medlars Bookends Mendeley Request Permissions Share α 7 -Containing nicotinic acetylcholine receptors on interneurons of the basolateral amygdala and their role in the regulation of the network excitability α 7 -Containing nicotinic acetylcholine receptors on interneurons of the basolateral amygdala and their role in the regulation of the network excitability Volodymyr I. Pidoplichko , Eric M. Prager , Vassiliki Aroniadou-Anderjaska , Maria F. M. 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