Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons
Highlights • Immunocytochemistry was used to detect torsinA in presynaptic structures. • Neurons from the striatum, cerebral motor cortex and hippocampus were assessed. • ΔE-torsinA knock-in mice and wild-type littermates were studied. • TorsinA was not detected in presynaptic nerve terminals or axo...
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Veröffentlicht in: | Neuroscience 2013-12, Vol.253, p.316-329 |
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description | Highlights • Immunocytochemistry was used to detect torsinA in presynaptic structures. • Neurons from the striatum, cerebral motor cortex and hippocampus were assessed. • ΔE-torsinA knock-in mice and wild-type littermates were studied. • TorsinA was not detected in presynaptic nerve terminals or axonal shafts. • This morphological study narrows down the possible actions of torsinA. |
doi_str_mv | 10.1016/j.neuroscience.2013.08.060 |
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Psychology ; Hippocampus - cytology ; immunocytochemistry ; Mice ; Mice, Inbred BALB C ; Molecular Chaperones - metabolism ; Nerve Endings - metabolism ; nerve terminals ; Neurology ; Neurons - cytology ; Neurons - drug effects ; omega-Agatoxin IVA - pharmacology ; omega-Conotoxin GVIA - pharmacology ; Potassium - pharmacology ; torsinA ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2013-12, Vol.253, p.316-329</ispartof><rights>IBRO</rights><rights>2013 IBRO</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-4093c187e24ede2c39e12cdd1aa956e7ae7f65253e7dab6f6632b65fdc5f48d43</citedby><cites>FETCH-LOGICAL-c498t-4093c187e24ede2c39e12cdd1aa956e7ae7f65253e7dab6f6632b65fdc5f48d43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuroscience.2013.08.060$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28010085$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24025868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koh, J.-Y</creatorcontrib><creatorcontrib>Iwabuchi, S</creatorcontrib><creatorcontrib>Harata, N.C</creatorcontrib><title>Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Highlights • Immunocytochemistry was used to detect torsinA in presynaptic structures. • Neurons from the striatum, cerebral motor cortex and hippocampus were assessed. • ΔE-torsinA knock-in mice and wild-type littermates were studied. • TorsinA was not detected in presynaptic nerve terminals or axonal shafts. • This morphological study narrows down the possible actions of torsinA.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cadmium Chloride - pharmacology</subject><subject>Calcium Channel Blockers - pharmacology</subject><subject>Cells, Cultured</subject><subject>central neurons</subject><subject>confocal and widefield fluorescence microscopy</subject><subject>Dose-Response Relationship, Drug</subject><subject>dystonia</subject><subject>Embryo, Mammalian</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hippocampus - cytology</subject><subject>immunocytochemistry</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Molecular Chaperones - metabolism</subject><subject>Nerve Endings - metabolism</subject><subject>nerve terminals</subject><subject>Neurology</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>omega-Agatoxin IVA - pharmacology</subject><subject>omega-Conotoxin GVIA - pharmacology</subject><subject>Potassium - pharmacology</subject><subject>torsinA</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkstuFDEQRS1ERIbALyALCSmb7vjdHhZIUcIjUiQWwNry2NXCQ48dbHek-XvczPAQm-BNLXyq6ureQuglJT0lVF1s-whzTsUFiA56Rijvie6JIo_QiuqBd4MU4jFaEU5UJyRjp-hpKVvSnhT8CTplgjCplV4hc70vNcVgO1tKcsFW8Pgupwoh4ppyCfESh4JjqthDBVftZgJsK65fAUfI94Ar5F2Idio4jdhBrNlO-KfEWJ6hk7H9wPNjPUNf3r39fPWhu_34_ubq8rZzYq1rJ8iauyYdmAAPzPE1UOa8p9aupYLBwjAqySSHwduNGpXibKPk6J0chfaCn6Hzw9ym_fsMpZpdKA6myUZIczFUcUk45c2rB1EhNKNMiwV9fUBds7tkGM1dDjub94YSs2RhtubvLMyShSHatCxa84vjnnmzA_-79Zf5DXh1BGxxdhqzjS6UP5wmlBAtG3d94KAZeB8gm-M6H3ILxPgU_k_Pm3_GuCnE0DZ_gz2UbZrzEqKhpjBDzKflepbjaaaRQSrGfwC8AcR6</recordid><startdate>20131203</startdate><enddate>20131203</enddate><creator>Koh, J.-Y</creator><creator>Iwabuchi, S</creator><creator>Harata, N.C</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20131203</creationdate><title>Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons</title><author>Koh, J.-Y ; Iwabuchi, S ; Harata, N.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-4093c187e24ede2c39e12cdd1aa956e7ae7f65253e7dab6f6632b65fdc5f48d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cadmium Chloride - pharmacology</topic><topic>Calcium Channel Blockers - pharmacology</topic><topic>Cells, Cultured</topic><topic>central neurons</topic><topic>confocal and widefield fluorescence microscopy</topic><topic>Dose-Response Relationship, Drug</topic><topic>dystonia</topic><topic>Embryo, Mammalian</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hippocampus - cytology</topic><topic>immunocytochemistry</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Molecular Chaperones - metabolism</topic><topic>Nerve Endings - metabolism</topic><topic>nerve terminals</topic><topic>Neurology</topic><topic>Neurons - cytology</topic><topic>Neurons - drug effects</topic><topic>omega-Agatoxin IVA - pharmacology</topic><topic>omega-Conotoxin GVIA - pharmacology</topic><topic>Potassium - pharmacology</topic><topic>torsinA</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koh, J.-Y</creatorcontrib><creatorcontrib>Iwabuchi, S</creatorcontrib><creatorcontrib>Harata, N.C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koh, J.-Y</au><au>Iwabuchi, S</au><au>Harata, N.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2013-12-03</date><risdate>2013</risdate><volume>253</volume><spage>316</spage><epage>329</epage><pages>316-329</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Highlights • Immunocytochemistry was used to detect torsinA in presynaptic structures. • Neurons from the striatum, cerebral motor cortex and hippocampus were assessed. • ΔE-torsinA knock-in mice and wild-type littermates were studied. • TorsinA was not detected in presynaptic nerve terminals or axonal shafts. • This morphological study narrows down the possible actions of torsinA.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>24025868</pmid><doi>10.1016/j.neuroscience.2013.08.060</doi><tpages>14</tpages></addata></record> |
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subjects | Analysis of Variance Animals Biological and medical sciences Cadmium Chloride - pharmacology Calcium Channel Blockers - pharmacology Cells, Cultured central neurons confocal and widefield fluorescence microscopy Dose-Response Relationship, Drug dystonia Embryo, Mammalian Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Hippocampus - cytology immunocytochemistry Mice Mice, Inbred BALB C Molecular Chaperones - metabolism Nerve Endings - metabolism nerve terminals Neurology Neurons - cytology Neurons - drug effects omega-Agatoxin IVA - pharmacology omega-Conotoxin GVIA - pharmacology Potassium - pharmacology torsinA Vertebrates: nervous system and sense organs |
title | Dystonia-associated protein torsinA is not detectable at the nerve terminals of central neurons |
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