{"created":"2025-02-21T04:02:30.817588+00:00","id":2007772,"links":{},"metadata":{"_buckets":{"deposit":"02ffd659-7964-4715-84ce-e990afcc0c13"},"_deposit":{"created_by":41,"id":"2007772","owners":[41],"pid":{"revision_id":0,"type":"depid","value":"2007772"},"status":"published"},"_oai":{"id":"oai:hiroshima.repo.nii.ac.jp:02007772","sets":["1730444907710"]},"author_link":[],"item_1617186331708":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_title":"Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population","subitem_title_language":"en"}]},"item_1617186419668":{"attribute_name":"Creator","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Sugihara, Katsunobu","creatorNameLang":"en"}],"familyNames":[{"familyName":"Sugihara","familyNameLang":"en"}],"givenNames":[{"givenName":"Katsunobu","givenNameLang":"en"}]},{"creatorNames":[{"creatorName":"Maruyama, Hirofumi","creatorNameLang":"en"}],"familyNames":[{"familyName":"Maruyama","familyNameLang":"en"}],"givenNames":[{"givenName":"Hirofumi","givenNameLang":"en"}]},{"creatorNames":[{"creatorName":"Kamada, Masaki","creatorNameLang":"en"}],"familyNames":[{"familyName":"Kamada","familyNameLang":"en"}],"givenNames":[{"givenName":"Masaki","givenNameLang":"en"}]},{"creatorNames":[{"creatorName":"Morino, Hiroyuki","creatorNameLang":"en"}],"familyNames":[{"familyName":"Morino","familyNameLang":"en"}],"givenNames":[{"givenName":"Hiroyuki","givenNameLang":"en"}]},{"creatorNames":[{"creatorName":"Kawakami, Hideshi","creatorNameLang":"en"}],"familyNames":[{"familyName":"Kawakami","familyNameLang":"en"}],"givenNames":[{"givenName":"Hideshi","givenNameLang":"en"}]}]},"item_1617186476635":{"attribute_name":"Access Rights","attribute_value_mlt":[{"subitem_access_right":"open access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_abf2"}]},"item_1617186499011":{"attribute_name":"Rights","attribute_value_mlt":[{"subitem_rights":"(c) 2011 Elsevier Inc. All rights reserved."}]},"item_1617186609386":{"attribute_name":"Subject","attribute_value_mlt":[{"subitem_subject":"ALS","subitem_subject_scheme":"Other"},{"subitem_subject":"amyotrophic lateral sclerosis","subitem_subject_scheme":"Other"},{"subitem_subject":"Polymorphism","subitem_subject_scheme":"Other"},{"subitem_subject":"Optineurin","subitem_subject_scheme":"Other"},{"subitem_subject":"OPTN","subitem_subject_scheme":"Other"},{"subitem_subject":"490","subitem_subject_scheme":"NDC"}]},"item_1617186626617":{"attribute_name":"Description","attribute_value_mlt":[{"subitem_description":"Mutations in the optineurin (OPTN) gene cause amyotrophic lateral sclerosis (ALS). We previously reported 3 types of OPTN mutation in Japanese ALS subjects. Here, to identify the OPTN mutations in individuals of different ethnicity, we screened 563 sporadic ALS (SALS) subjects and 124 familial ALS (FALS) subjects who were mainly Caucasian. We found a c. 964T>C synonymous variation in exon 8. However, we could not find the meaningful OPTN mutations. The results indicate that OPTN mutations causing ALS are rare, especially in mainly Caucasian ALS subjects.","subitem_description_language":"en"}]},"item_1617186643794":{"attribute_name":"Publisher","attribute_value_mlt":[{"subitem_publisher":"Elsevier Science Inc"}]},"item_1617186702042":{"attribute_name":"Language","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_1617186920753":{"attribute_name":"Source Identifier","attribute_value_mlt":[{"subitem_source_identifier":"0197-4580","subitem_source_identifier_type":"ISSN"},{"subitem_source_identifier":"AA10618297","subitem_source_identifier_type":"NCID"}]},"item_1617187024783":{"attribute_name":"Page Start","attribute_value_mlt":[{"subitem_start_page":"1923.e9"}]},"item_1617187056579":{"attribute_name":"Bibliographic Information","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2011","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"10","bibliographicPageEnd":"1923.e10","bibliographicPageStart":"1923.e9","bibliographicVolumeNumber":"32","bibliographic_titles":[{"bibliographic_title":"Neurobiology of Aging"},{"bibliographic_title":"Neurobiology of Aging"}]}]},"item_1617258105262":{"attribute_name":"Resource Type","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_1617265215918":{"attribute_name":"Version Type","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_b1a7d7d4d402bcce","subitem_version_type":"AO"}]},"item_1617353299429":{"attribute_name":"Relation","attribute_value_mlt":[{"subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1016/j.neurobiolaging.2011.03.024","subitem_relation_type_select":"DOI"}},{"subitem_relation_type_id":{"subitem_relation_type_id_text":"http://dx.doi.org/10.1016/j.neurobiolaging.2011.03.024","subitem_relation_type_select":"DOI"}}]},"item_1617605131499":{"attribute_name":"File","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_access","date":[{"dateType":"Available","dateValue":"2023-03-18"}],"displaytype":"simple","filename":"NeurobioAging_32_1923e9.pdf","filesize":[{"value":"71.7 KB"}],"mimetype":"application/pdf","url":{"objectType":"fulltext","url":"https://hiroshima.repo.nii.ac.jp/record/2007772/files/NeurobioAging_32_1923e9.pdf"},"version_id":"de1d1559-3638-4510-8312-e3025c5ca7e6"}]},"item_1732771732025":{"attribute_name":"旧ID","attribute_value":"34789"},"item_title":"Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population","item_type_id":"40003","owner":"41","path":["1730444907710"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2023-03-18"},"publish_date":"2023-03-18","publish_status":"0","recid":"2007772","relation_version_is_last":true,"title":["Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population"],"weko_creator_id":"41","weko_shared_id":-1},"updated":"2025-02-21T10:57:00.321003+00:00"}