{"_buckets": {"deposit": "e878d57e-d443-47c4-b2bc-b3372abfbe19"}, "_deposit": {"id": "3681", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "3681"}, "status": "published"}, "_oai": {"id": "oai:soar-ir.repo.nii.ac.jp:00003681", "sets": ["462"]}, "author_link": ["6279", "6280", "6281", "6282", "6283", "6284", "6285", "6286"], "item_1628147817048": {"attribute_name": "出版タイプ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_970fb48d4fbd8a85", "subitem_version_type": "VoR"}]}, "item_6_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2012-04", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "4", "bibliographicPageEnd": "384", "bibliographicPageStart": "377", "bibliographicVolumeNumber": "132", "bibliographic_titles": [{"bibliographic_title": "ACTA OTO-LARYNGOLOGICA"}]}]}, "item_6_description_20": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Conclusions: CDH23 mutations and the 1555A\u003eG mitochondrial mutation were identified among our series of electric acoustic stimulation (EAS) patients, confirming that these genes were important in hearing loss with involvement of high frequency. Successful hearing preservation as well as good outcomes from EAS indicated that patients with this combination of mutations are good candidates for EAS. Objectives: Screening for gene mutations that possibly cause hearing loss involving high frequency was performed to identify the responsible genes in patients with EAS. In addition to a review of the genetic background of the patients with residual hearing loss, the benefit of EAS for patients with particular gene mutations was evaluated. Methods: Eighteen patients (15 late-onset, 3 early-onset) with residual hearing who had received EAS were included in this study. Genetic analysis was performed to identify GJB2, CDH23, SLC26A4, and the 1555 mitochondrial mutations. Results: Three early-onset patients had CDH23 mutations. One late-onset patient had the 1555 A\u003eG mitochondrial mutation.", "subitem_description_type": "Abstract"}]}, "item_6_description_30": {"attribute_name": "資源タイプ（コンテンツの種類）", "attribute_value_mlt": [{"subitem_description": "Article", "subitem_description_type": "Other"}]}, "item_6_description_5": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "ACTA OTO-LARYNGOLOGICA. 132(4):377-384 (2012)", "subitem_description_type": "Other"}]}, "item_6_link_3": {"attribute_name": "信州大学研究者総覧へのリンク", "attribute_value_mlt": [{"subitem_link_text": "Usami, Shin-ichi", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.ZmAUHUSC.html"}, {"subitem_link_text": "Nishio, Shin-Ya", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.uCSmPpym.html"}, {"subitem_link_text": "Moteki, Hideaki", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.HNcauNkh.html"}, {"subitem_link_text": "Takumi, Yutaka", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.HNnNHhSC.html"}]}, "item_6_link_67": {"attribute_name": "WoS", "attribute_value_mlt": [{"subitem_link_text": "Web of Science", "subitem_link_url": "http://gateway.isiknowledge.com/gateway/Gateway.cgi?\u0026GWVersion=2\u0026SrcAuth=ShinshuUniv\u0026SrcApp=ShinshuUniv\u0026DestLinkType=FullRecord\u0026DestApp=WOS\u0026KeyUT=000302068700006"}]}, "item_6_publisher_4": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "INFORMA HEALTHCARE"}]}, "item_6_relation_47": {"attribute_name": "PubMed", "attribute_value_mlt": [{"subitem_relation_name": [{"subitem_relation_name_text": "22443853"}], "subitem_relation_type_id": {"subitem_relation_type_id_text": "https://pubmed.ncbi.nlm.nih.gov/22443853", "subitem_relation_type_select": "PMID"}}]}, "item_6_relation_48": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_name": [{"subitem_relation_name_text": "10.3109/00016489.2011.649493"}], "subitem_relation_type_id": {"subitem_relation_type_id_text": "https://doi.org/10.3109/00016489.2011.649493", "subitem_relation_type_select": "DOI"}}]}, "item_6_rights_62": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "Copyright© 2012 Informa Healthcare"}]}, "item_6_select_64": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "publisher"}]}, "item_6_source_id_35": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0001-6489", "subitem_source_identifier_type": "PISSN"}]}, "item_6_source_id_39": {"attribute_name": "NII ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0001-6489", "subitem_source_identifier_type": "PISSN"}]}, "item_6_source_id_40": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA0050923X", "subitem_source_identifier_type": "NCID"}]}, "item_6_text_69": {"attribute_name": "wosonly authkey", "attribute_value_mlt": [{"subitem_text_value": "Residual hearing; hearing preservation; gene; mitochondria; 12S rRNA"}]}, "item_6_text_70": {"attribute_name": "wosonly keywords", "attribute_value_mlt": [{"subitem_text_value": "SYNDROMIC HEARING-LOSS; COCHLEAR IMPLANTATION; USHER-SYNDROME; DEAFNESS; INDIVIDUALS; JAPANESE; CHILDREN"}]}, "item_6_textarea_68": {"attribute_name": "wosonly abstract", "attribute_value_mlt": [{"subitem_textarea_value": "Conclusions: CDH23 mutations and the 1555A\u003eG mitochondrial mutation were identified among our series of electric acoustic stimulation (EAS) patients, confirming that these genes were important in hearing loss with involvement of high frequency. Successful hearing preservation as well as good outcomes from EAS indicated that patients with this combination of mutations are good candidates for EAS. Objectives: Screening for gene mutations that possibly cause hearing loss involving high frequency was performed to identify the responsible genes in patients with EAS. In addition to a review of the genetic background of the patients with residual hearing loss, the benefit of EAS for patients with particular gene mutations was evaluated. Methods: Eighteen patients (15 late-onset, 3 early-onset) with residual hearing who had received EAS were included in this study. Genetic analysis was performed to identify GJB2, CDH23, SLC26A4, and the 1555 mitochondrial mutations. Results: Three early-onset patients had CDH23 mutations. One late-onset patient had the 1555 A\u003eG mitochondrial mutation."}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Usami,  Shin-ichi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6279", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Miyagawa,  Maiko", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6280", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nishio,  Shin-Ya", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6281", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Moteki,  Hideaki", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6282", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Takumi,  Yutaka", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6283", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Suzuki,  Mika", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6284", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kitano,  Yoko", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6285", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Iwasaki,  Satoshi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "6286", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2015-09-24"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "Patients_CDH23_mutations_1555AG_mitochondrial.pdf", "filesize": [{"value": "476.9 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_note", "mimetype": "application/pdf", "size": 476900.0, "url": {"label": "Patients_CDH23_mutations_1555AG_mitochondrial.pdf", "url": "https://soar-ir.repo.nii.ac.jp/record/3681/files/Patients_CDH23_mutations_1555AG_mitochondrial.pdf"}, "version_id": "48c4cb56-05ad-4e66-83b1-2808e77ad32b"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Residual hearing", "subitem_subject_scheme": "Other"}, {"subitem_subject": "hearing preservation", "subitem_subject_scheme": "Other"}, {"subitem_subject": "gene", "subitem_subject_scheme": "Other"}, {"subitem_subject": "mitochondria", "subitem_subject_scheme": "Other"}, {"subitem_subject": "12S rRNA", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "journal article", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "Patients with CDH23 mutations and the 1555A \u003e G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Patients with CDH23 mutations and the 1555A \u003e G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)", "subitem_title_language": "en"}]}, "item_type_id": "6", "owner": "1", "path": ["462"], "permalink_uri": "http://hdl.handle.net/10091/17788", "pubdate": {"attribute_name": "PubDate", "attribute_value": "2014-07-25"}, "publish_date": "2014-07-25", "publish_status": "0", "recid": "3681", "relation": {}, "relation_version_is_last": true, "title": ["Patients with CDH23 mutations and the 1555A \u003e G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)"], "weko_shared_id": -1}