WEKO3
アイテム
{"_buckets": {"deposit": "8e6a5278-3be0-4139-965f-2fa5afdb1fd5"}, "_deposit": {"created_by": 2, "id": "16137", "owners": [2], "pid": {"revision_id": 0, "type": "depid", "value": "16137"}, "status": "published"}, "_oai": {"id": "oai:nagasaki-u.repo.nii.ac.jp:00016137", "sets": ["11"]}, "author_link": ["60593", "60595", "60610", "60592", "60597", "60607", "60604", "60609", "60606", "60598", "60599", "60594", "60600", "60601", "60602", "60605", "60608", "60603", "60596"], "item_2_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2009-05", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "5", "bibliographicPageEnd": "309", "bibliographicPageStart": "304", "bibliographicVolumeNumber": "54", "bibliographic_titles": [{"bibliographic_title": "Journal of human genetics"}]}]}, "item_2_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "The Kabuki syndrome (KS, OMIM 147920), also known as the Niikawa-Kuroki syndrome, is a multiple congenital anomaly/mental retardation syndrome characterized by a distinct facial appearance. The cause of KS has been unidentified, even by whole-genome scan with array comparative genomic hybridization (CGH). In recent years, high-resolution oligonucleotide array technologies have enabled us to detect fine copy number alterations. In 17 patients with KS, molecular karyotyping was carried out with GeneChip 250K NspI array (Affymetrix) and Copy Number Analyser for GeneChip (CNAG). It showed seven copy number alterations, three deleted regions and four duplicated regions among the patients, with the exception of registered copy number variants (CNVs). Among the seven loci, only the region of 9q21.11-q21.12 ( approximately 1.27 Mb) involved coding genes, namely, transient receptor potential cation channel, subfamily M, member 3 (TRPM3), Kruppel-like factor 9 (KLF9), structural maintenance of chromosomes protein 5 (SMC5) and MAM domain containing 2 (MAMDC2). Mutation screening for the genes detected 10 base substitutions consisting of seven single-nucleotide polymorphisms (SNPs) and three silent mutations in 41 patients with KS. Our study could not show the causative genes for KS, but the locus of 9q21.11-q21.12, in association with a cleft palate, may contribute to the manifestation of KS in the patient. As various platforms on oligonucleotide arrays have been developed, higher resolution platforms will need to be applied to search tiny genomic rearrangements in patients with KS.Journal of Human Genetics (2009) 54, 304-309; doi:10.1038/jhg.2009.30; published online 03 April 2009.", "subitem_description_type": "Abstract"}]}, "item_2_description_63": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "Journal of Human Genetics (2009) 54, 304?309", "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": "19343044", "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": "10.1038/jhg.2009.30", "subitem_relation_type_select": "DOI"}}]}, "item_2_rights_13": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "c 2009 The Japan Society of Human Genetics"}]}, "item_2_source_id_10": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA11206160", "subitem_source_identifier_type": "NCID"}]}, "item_2_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "14345161", "subitem_source_identifier_type": "ISSN"}]}, "item_2_source_id_8": {"attribute_name": "EISSN", "attribute_value_mlt": [{"subitem_source_identifier": "1435-232X", "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": "60592", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yoshiura, Koh-Ichiro"}], "nameIdentifiers": [{"nameIdentifier": "60593", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kondoh, Tatsuro"}], "nameIdentifiers": [{"nameIdentifier": "60594", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Ohashi, Hirofumi"}], "nameIdentifiers": [{"nameIdentifier": "60595", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kurosawa, Kenji"}], "nameIdentifiers": [{"nameIdentifier": "60596", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Tonoki, Hidefumi"}], "nameIdentifiers": [{"nameIdentifier": "60597", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nagai, Toshiro"}], "nameIdentifiers": [{"nameIdentifier": "60598", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Okamoto, Nobuhiko"}], "nameIdentifiers": [{"nameIdentifier": "60599", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kato, Mitsuhiro"}], "nameIdentifiers": [{"nameIdentifier": "60600", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Fukushima, Yoshimitsu"}], "nameIdentifiers": [{"nameIdentifier": "60601", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kaname, Tadashi"}], "nameIdentifiers": [{"nameIdentifier": "60602", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Naritomi, Kenji"}], "nameIdentifiers": [{"nameIdentifier": "60603", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Matsumoto, Tadashi"}], "nameIdentifiers": [{"nameIdentifier": "60604", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Moriuchi, Hiroyuki"}], "nameIdentifiers": [{"nameIdentifier": "60605", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kishino, Tatsuya"}], "nameIdentifiers": [{"nameIdentifier": "60606", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kinoshita, Akira"}], "nameIdentifiers": [{"nameIdentifier": "60607", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Miyake, Noriko"}], "nameIdentifiers": [{"nameIdentifier": "60608", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Matsumoto, Naomichi"}], "nameIdentifiers": [{"nameIdentifier": "60609", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Niikawa, Norio"}], "nameIdentifiers": [{"nameIdentifier": "60610", "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": "2020-12-23"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "Kuniba_JHG54_304_Kabuki.pdf", "filesize": [{"value": "1.4 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 1400000.0, "url": {"label": "Kuniba_JHG54_304_Kabuki.pdf", "url": "https://nagasaki-u.repo.nii.ac.jp/record/16137/files/Kuniba_JHG54_304_Kabuki.pdf"}, "version_id": "4efcbf76-385d-44c4-8c01-97955e922b0e"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Kabuki syndrome", "subitem_subject_scheme": "Other"}, {"subitem_subject": "microdeletion", "subitem_subject_scheme": "Other"}, {"subitem_subject": "molecular karyotyping", "subitem_subject_scheme": "Other"}, {"subitem_subject": "mutation screening", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Niikawa?Kuroki syndrome", "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": "Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome.", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome."}]}, "item_type_id": "2", "owner": "2", "path": ["11"], "permalink_uri": "http://hdl.handle.net/10069/22018", "pubdate": {"attribute_name": "公開日", "attribute_value": "2009-07-06"}, "publish_date": "2009-07-06", "publish_status": "0", "recid": "16137", "relation": {}, "relation_version_is_last": true, "title": ["Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome."], "weko_shared_id": -1}
Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome.
http://hdl.handle.net/10069/22018
http://hdl.handle.net/10069/22018c61c3a45-bb0d-431b-931a-66bb25b347b9
名前 / ファイル | ライセンス | アクション |
---|---|---|
Kuniba_JHG54_304_Kabuki.pdf (1.4 MB)
|
|
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 | Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome. | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Kabuki syndrome | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | microdeletion | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | molecular karyotyping | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | mutation screening | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Niikawa?Kuroki syndrome | |||||
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× Yoshiura, Koh-Ichiro× Kondoh, Tatsuro× Ohashi, Hirofumi× Kurosawa, Kenji× Tonoki, Hidefumi× Nagai, Toshiro× Okamoto, Nobuhiko× Kato, Mitsuhiro× Fukushima, Yoshimitsu× Kaname, Tadashi× Naritomi, Kenji× Matsumoto, Tadashi× Moriuchi, Hiroyuki× Kishino, Tatsuya× Kinoshita, Akira× Miyake, Noriko× Matsumoto, Naomichi× Niikawa, Norio |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The Kabuki syndrome (KS, OMIM 147920), also known as the Niikawa-Kuroki syndrome, is a multiple congenital anomaly/mental retardation syndrome characterized by a distinct facial appearance. The cause of KS has been unidentified, even by whole-genome scan with array comparative genomic hybridization (CGH). In recent years, high-resolution oligonucleotide array technologies have enabled us to detect fine copy number alterations. In 17 patients with KS, molecular karyotyping was carried out with GeneChip 250K NspI array (Affymetrix) and Copy Number Analyser for GeneChip (CNAG). It showed seven copy number alterations, three deleted regions and four duplicated regions among the patients, with the exception of registered copy number variants (CNVs). Among the seven loci, only the region of 9q21.11-q21.12 ( approximately 1.27 Mb) involved coding genes, namely, transient receptor potential cation channel, subfamily M, member 3 (TRPM3), Kruppel-like factor 9 (KLF9), structural maintenance of chromosomes protein 5 (SMC5) and MAM domain containing 2 (MAMDC2). Mutation screening for the genes detected 10 base substitutions consisting of seven single-nucleotide polymorphisms (SNPs) and three silent mutations in 41 patients with KS. Our study could not show the causative genes for KS, but the locus of 9q21.11-q21.12, in association with a cleft palate, may contribute to the manifestation of KS in the patient. As various platforms on oligonucleotide arrays have been developed, higher resolution platforms will need to be applied to search tiny genomic rearrangements in patients with KS.Journal of Human Genetics (2009) 54, 304-309; doi:10.1038/jhg.2009.30; published online 03 April 2009. | |||||
書誌情報 |
Journal of human genetics 巻 54, 号 5, p. 304-309, 発行日 2009-05 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 14345161 | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1435-232X | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA11206160 | |||||
PubMed番号 | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | PMID | |||||
関連識別子 | 19343044 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1038/jhg.2009.30 | |||||
権利 | ||||||
権利情報 | c 2009 The Japan Society of Human Genetics | |||||
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 | Journal of Human Genetics (2009) 54, 304?309 |