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These findings provide evidence that ganglion cytoskeletal genes play key roles in determining mechanosensory properties, which may contribute to altered pain sensitivity in Rett syndrome and other painful conditions.<\/jats:p>","DOI":"10.1073\/pnas.1618210114","type":"journal-article","created":{"date-parts":[[2017,7,31]],"date-time":"2017-07-31T20:50:22Z","timestamp":1501534222000},"update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":65,"title":["Neuronal cytoskeletal gene dysregulation and mechanical hypersensitivity in a rat model of Rett syndrome"],"prefix":"10.1073","volume":"114","author":[{"given":"Aritra","family":"Bhattacherjee","sequence":"first","affiliation":[{"name":"Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160;"},{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ying","family":"Mu","sequence":"additional","affiliation":[{"name":"Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michelle K.","family":"Winter","sequence":"additional","affiliation":[{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer R.","family":"Knapp","sequence":"additional","affiliation":[{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Linda S.","family":"Eggimann","sequence":"additional","affiliation":[{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sumedha S.","family":"Gunewardena","sequence":"additional","affiliation":[{"name":"Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160;"},{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kazuto","family":"Kobayashi","sequence":"additional","affiliation":[{"name":"Department of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima 9601295, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shigeki","family":"Kato","sequence":"additional","affiliation":[{"name":"Department of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima 9601295, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dora","family":"Krizsan-Agbas","sequence":"additional","affiliation":[{"name":"Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1931-7660","authenticated-orcid":false,"given":"Peter G.","family":"Smith","sequence":"additional","affiliation":[{"name":"Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160;"},{"name":"Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160;"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"341","published-online":{"date-parts":[[2017,7,31]]},"reference":[{"key":"e_1_3_4_1_2","doi-asserted-by":"crossref","first-page":"736","DOI":"10.1177\/08830738050200090701","article-title":"MeCP2 dysfunction in humans and mice","volume":"20","author":"Zoghbi HY","year":"2005","unstructured":"HY Zoghbi, MeCP2 dysfunction in humans and mice. 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