{"created":"2023-05-15T16:40:49.519184+00:00","id":15239,"links":{},"metadata":{"_buckets":{"deposit":"19a35814-1359-441a-90c6-3a3b2accc87e"},"_deposit":{"created_by":2,"id":"15239","owners":[2],"pid":{"revision_id":0,"type":"depid","value":"15239"},"status":"published"},"_oai":{"id":"oai:nagasaki-u.repo.nii.ac.jp:00015239","sets":["29:30:1713167819629:1231"]},"author_link":["56153","56145","56150","56152","56148","56144","56146","56149","56147","56151"],"item_3_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2010-03","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"3","bibliographicPageEnd":"71","bibliographicPageStart":"67","bibliographicVolumeNumber":"54","bibliographic_titles":[{"bibliographic_title":"Acta medica Nagasakiensia"}]}]},"item_3_description_4":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"Objective: Sporadic Parkinson's disease (PD) is thought to be a complex multifactorial, age-related neurodegenerative disease caused by theinteraction between genetic and environmental factors. Whether PARK2, a major responsible gene causing familial PD, affects to the diseasesusceptibility or the phenotypic variability in sporadic PD remains controversial. In this study, we perform the sequence analysis of PARK2 andassess the correlation between clinical features of sporadic PD patients and the detected variants. Materials and Methods: A total of 92 sporadicPD patients were sequenced and underwent the clinical examinations. MIBG scintigraphy was performed in 61 patients and the cardiacuptake was measured as the heart/mediastinum (H/M) ratio. Results: We only detected two novel variants (R51R, L272I) in 3 patients andthree common polymorphisms, S167N, V380L, and R366W, which had the allele frequencies of 38.6%, 7% and 0.5%, respectively. There wereno significant difference of the allele frequencies between patients and controls. On the evaluation of clinical features, the patients with S167Nhad the younger onsets of age and the tendency of preserved cardiac uptake of MIBG in the early Hoehn and Yahr (HY) stage compared tothe patients without S167N. Conclusions: These results suggest the common polymorphisms of PARK2 might affect the phenotype of sporadicPD without altered susceptibility to PD.","subitem_description_type":"Abstract"}]},"item_3_description_64":{"attribute_name":"引用","attribute_value_mlt":[{"subitem_description":"Acta medica Nagasakiensia, 54(3), pp.67-71 ; 2010","subitem_description_type":"Other"}]},"item_3_publisher_33":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Nagasaki University School of Medicine"}]},"item_3_relation_42":{"attribute_name":"関係URI","attribute_value_mlt":[{"subitem_relation_name":[{"subitem_relation_name_text":"http://joi.jlc.jst.go.jp/JST.JSTAGE/amn/54.67"}]}]},"item_3_source_id_10":{"attribute_name":"書誌レコードID","attribute_value_mlt":[{"subitem_source_identifier":"AA00508432","subitem_source_identifier_type":"NCID"}]},"item_3_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0001-6055","subitem_source_identifier_type":"ISSN"}]},"item_3_version_type_16":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Sakai, Muniko"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Tsujino, Akira"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Eguchi, Hiroto"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Sato, Katsuya"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Shirabe, Susumu"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Tateishi, Yohei"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Sato, Akira"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Tsujihata, Mitsuhiro"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Yoshimura, Toshiro"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Eguchi, Katsumi"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2020-12-23"}],"displaytype":"detail","filename":"acta_54_3_67.pdf","filesize":[{"value":"102.7 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"acta_54_3_67.pdf","url":"https://nagasaki-u.repo.nii.ac.jp/record/15239/files/acta_54_3_67.pdf"},"version_id":"f31e64f5-bf10-4f17-a7ed-bdbb3f554c2d"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"PARK2","subitem_subject_scheme":"Other"},{"subitem_subject":"Polymorphism","subitem_subject_scheme":"Other"},{"subitem_subject":"MIBG scintigraphy","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":"departmental bulletin paper","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"A Single-Nucleotide Polymorphism of PARK2 Affects the Phenotype in Sporadic Parkinson Disease","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"A Single-Nucleotide Polymorphism of PARK2 Affects the Phenotype in Sporadic Parkinson Disease"}]},"item_type_id":"3","owner":"2","path":["1231"],"pubdate":{"attribute_name":"公開日","attribute_value":"2010-04-16"},"publish_date":"2010-04-16","publish_status":"0","recid":"15239","relation_version_is_last":true,"title":["A Single-Nucleotide Polymorphism of PARK2 Affects the Phenotype in Sporadic Parkinson Disease"],"weko_creator_id":"2","weko_shared_id":-1},"updated":"2024-04-16T05:32:17.824584+00:00"}