WEKO3
アイテム
{"_buckets": {"deposit": "71a8fea0-a45e-4508-a7e2-f7eb06b39922"}, "_deposit": {"created_by": 2, "id": "26263", "owners": [2], "pid": {"revision_id": 0, "type": "depid", "value": "26263"}, "status": "published"}, "_oai": {"id": "oai:nagasaki-u.repo.nii.ac.jp:00026263", "sets": ["11"]}, "author_link": ["112077", "112074", "112071", "112076", "112078", "112082", "112072", "112073", "112081", "112084", "112083", "112080", "112075", "112079"], "item_2_alternative_title_19": {"attribute_name": "その他のタイトル", "attribute_value_mlt": [{"subitem_alternative_title": "No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome."}]}, "item_2_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2008-07-15", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "14", "bibliographicPageEnd": "1896", "bibliographicPageStart": "1893", "bibliographicVolumeNumber": "146A", "bibliographic_titles": [{"bibliographic_title": "American journal of medical genetics. Part A"}]}]}, "item_2_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Kabuki (Niikawa-Kuroki) syndrome (KS) is a multiple congenital anomaly/mental retardation (MCA/MR) syndrome characterized by long palpebral fissures with eversion of the lower eyelids, skeletal anomalies, persistence of fingerpads, short stature, joint laxity, and occasional immune abnormalities. Previous molecular cytogenetic approaches including fluorescence in situ hybridization and whole-genome CGH microarray analysis failed to find copy-number changes in the genome of KS patients. Recently, germline mutations in PTPN11/KRAS/SOS1/RAF1, HRAS, and KRAS/BRAF/MEK1/MEK2 were shown to be causes of Noonan syndrome, Costello syndrome and cardio-facio-cutaneous syndrome, respectively. Since KS patients share some phenotypical manifestations with the syndromes above, we hypothesized that KS may be associated with mutations in genes involving the RAS-MAPK pathway. Sixteen genes (PTPN11, GRB2, SOS1, HRAS, ERAS, NRAS, KRAS, ARAF, BRAF, RAF1, MEK1, MEK2, RASA1, RASA2, RASA3, and RASA4) in the pathway were screened for mutations. DNA from 30 KS patients (14 females and 16 males) was sequenced for entire coding regions and splice junctions of the 16 genes. We identified 29 base substitutions in the genes, including 9 nonsynonymous changes, 18 synonymous changes, one in 5’ untranslated region and one at position “-4” in splice acceptor site. But they were almost all confirmed as SNPs listed in the NCBI database or found in 82-89 normal Japanese individuals, while two of them were rare variants with nonsynonymous changes.", "subitem_description_type": "Abstract"}]}, "item_2_description_63": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "American journal of medical genetics. Part A, 146A(14), pp.1893-1896; 2009", "subitem_description_type": "Other"}]}, "item_2_relation_11": {"attribute_name": "PubMed番号", "attribute_value_mlt": [{"subitem_relation_type": "isVersionOf", "subitem_relation_type_id": {"subitem_relation_type_id_text": "18553519", "subitem_relation_type_select": "PMID"}}]}, "item_2_relation_12": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isVersionOf", "subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1002/ajmg.a.32382", "subitem_relation_type_select": "DOI"}}]}, "item_2_rights_13": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "Copyright c 2009 Wiley-Liss, Inc., A Wiley Company"}, {"subitem_rights": "This is the pre-peer reviewed version of the following article: Kuniba H, Sato D, Yoshiura K, Ohashi H, Kurosawa K, Miyake N, Kondoh T, Matsumoto T, Nagai T, Okamoto N, Fukushima Y, Naritomi K, Matsumoto N, Niikawa N. 2008. No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome. Am J Med Genet Part A 146A:1893-1896., which has been published in final form at http://dx.doi.org/10.1002/ajmg.a.32382."}]}, "item_2_source_id_10": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA11815067", "subitem_source_identifier_type": "NCID"}]}, "item_2_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "15524825", "subitem_source_identifier_type": "ISSN"}]}, "item_2_source_id_8": {"attribute_name": "EISSN", "attribute_value_mlt": [{"subitem_source_identifier": "15524833", "subitem_source_identifier_type": "ISSN"}]}, "item_2_version_type_16": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_ab4af688f83e57aa", "subitem_version_type": "AM"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Kuniba, Hideo"}], "nameIdentifiers": [{"nameIdentifier": "112071", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Sato, Daisuke"}], "nameIdentifiers": [{"nameIdentifier": "112072", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yoshiura, Koh-ichiro"}], "nameIdentifiers": [{"nameIdentifier": "112073", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Ohashi, Hirofumi"}], "nameIdentifiers": [{"nameIdentifier": "112074", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kurosawa, Kenji"}], "nameIdentifiers": [{"nameIdentifier": "112075", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Miyake, Noriko"}], "nameIdentifiers": [{"nameIdentifier": "112076", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kondoh, Tasturo"}], "nameIdentifiers": [{"nameIdentifier": "112077", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Matsumoto, Tadashi"}], "nameIdentifiers": [{"nameIdentifier": "112078", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nagai, Toshiro"}], "nameIdentifiers": [{"nameIdentifier": "112079", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Okamoto, Nobuhiko"}], "nameIdentifiers": [{"nameIdentifier": "112080", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Fukushima, Yoshimitsu"}], "nameIdentifiers": [{"nameIdentifier": "112081", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Naritomi, Kenji"}], "nameIdentifiers": [{"nameIdentifier": "112082", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Matsumoto, Naomichi"}], "nameIdentifiers": [{"nameIdentifier": "112083", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Niikawa, Norio"}], "nameIdentifiers": [{"nameIdentifier": "112084", "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": "2020-12-25"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "Preprint_Kuniba_AJMG146A_1893_Kabuki.pdf", "filesize": [{"value": "422.3 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 422300.0, "url": {"label": "Preprint_Kuniba_AJMG146A_1893_Kabuki.pdf", "url": "https://nagasaki-u.repo.nii.ac.jp/record/26263/files/Preprint_Kuniba_AJMG146A_1893_Kabuki.pdf"}, "version_id": "70f36ac9-81ab-4620-b09b-1ea57f438f16"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Kabuki (Niikawa-Kuroki) syndrome", "subitem_subject_scheme": "Other"}, {"subitem_subject": "candidate gene approach", "subitem_subject_scheme": "Other"}, {"subitem_subject": "RAS-MAPK pathway", "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": "Unsuccessful Identification of Mutations in Genes Involving the RAS-MAPK Pathway among 30 Patients with Kabuki Syndrome", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Unsuccessful Identification of Mutations in Genes Involving the RAS-MAPK Pathway among 30 Patients with Kabuki Syndrome"}]}, "item_type_id": "2", "owner": "2", "path": ["11"], "permalink_uri": "http://hdl.handle.net/10069/22019", "pubdate": {"attribute_name": "公開日", "attribute_value": "2009-07-06"}, "publish_date": "2009-07-06", "publish_status": "0", "recid": "26263", "relation": {}, "relation_version_is_last": true, "title": ["Unsuccessful Identification of Mutations in Genes Involving the RAS-MAPK Pathway among 30 Patients with Kabuki Syndrome"], "weko_shared_id": 2}
Unsuccessful Identification of Mutations in Genes Involving the RAS-MAPK Pathway among 30 Patients with Kabuki Syndrome
http://hdl.handle.net/10069/22019
http://hdl.handle.net/10069/220191e95cef0-2e16-4279-b9ec-027c6796a327
名前 / ファイル | ライセンス | アクション |
---|---|---|
Preprint_Kuniba_AJMG146A_1893_Kabuki.pdf (422.3 kB)
|
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2009-07-06 | |||||
タイトル | ||||||
タイトル | Unsuccessful Identification of Mutations in Genes Involving the RAS-MAPK Pathway among 30 Patients with Kabuki Syndrome | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Kabuki (Niikawa-Kuroki) syndrome | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | candidate gene approach | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | RAS-MAPK pathway | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Kuniba, Hideo
× Kuniba, Hideo× Sato, Daisuke× Yoshiura, Koh-ichiro× Ohashi, Hirofumi× Kurosawa, Kenji× Miyake, Noriko× Kondoh, Tasturo× Matsumoto, Tadashi× Nagai, Toshiro× Okamoto, Nobuhiko× Fukushima, Yoshimitsu× Naritomi, Kenji× Matsumoto, Naomichi× Niikawa, Norio |
|||||
その他のタイトル | ||||||
その他のタイトル | No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome. | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Kabuki (Niikawa-Kuroki) syndrome (KS) is a multiple congenital anomaly/mental retardation (MCA/MR) syndrome characterized by long palpebral fissures with eversion of the lower eyelids, skeletal anomalies, persistence of fingerpads, short stature, joint laxity, and occasional immune abnormalities. Previous molecular cytogenetic approaches including fluorescence in situ hybridization and whole-genome CGH microarray analysis failed to find copy-number changes in the genome of KS patients. Recently, germline mutations in PTPN11/KRAS/SOS1/RAF1, HRAS, and KRAS/BRAF/MEK1/MEK2 were shown to be causes of Noonan syndrome, Costello syndrome and cardio-facio-cutaneous syndrome, respectively. Since KS patients share some phenotypical manifestations with the syndromes above, we hypothesized that KS may be associated with mutations in genes involving the RAS-MAPK pathway. Sixteen genes (PTPN11, GRB2, SOS1, HRAS, ERAS, NRAS, KRAS, ARAF, BRAF, RAF1, MEK1, MEK2, RASA1, RASA2, RASA3, and RASA4) in the pathway were screened for mutations. DNA from 30 KS patients (14 females and 16 males) was sequenced for entire coding regions and splice junctions of the 16 genes. We identified 29 base substitutions in the genes, including 9 nonsynonymous changes, 18 synonymous changes, one in 5’ untranslated region and one at position “-4” in splice acceptor site. But they were almost all confirmed as SNPs listed in the NCBI database or found in 82-89 normal Japanese individuals, while two of them were rare variants with nonsynonymous changes. | |||||
書誌情報 |
American journal of medical genetics. Part A 巻 146A, 号 14, p. 1893-1896, 発行日 2008-07-15 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 15524825 | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 15524833 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA11815067 | |||||
PubMed番号 | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | PMID | |||||
関連識別子 | 18553519 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1002/ajmg.a.32382 | |||||
権利 | ||||||
権利情報 | Copyright c 2009 Wiley-Liss, Inc., A Wiley Company | |||||
権利 | ||||||
権利情報 | This is the pre-peer reviewed version of the following article: Kuniba H, Sato D, Yoshiura K, Ohashi H, Kurosawa K, Miyake N, Kondoh T, Matsumoto T, Nagai T, Okamoto N, Fukushima Y, Naritomi K, Matsumoto N, Niikawa N. 2008. No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome. Am J Med Genet Part A 146A:1893-1896., which has been published in final form at http://dx.doi.org/10.1002/ajmg.a.32382. | |||||
著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | American journal of medical genetics. Part A, 146A(14), pp.1893-1896; 2009 |