Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism

Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hypertension research 2021-07, Vol.44 (7), p.891-893
Hauptverfasser: Nakano, Yasuhiro, Iwata, Nahoko, Ogura-Ochi, Kanako, Hasegawa, Kosei, Hirasawa, Akira, Otsuka, Fumio
Format: Artikel
Sprache:eng
Schlagworte:
Child
Cytochrome P-450 CYP11B2 - genetics
Humans
Hyperaldosteronism - diagnosis
Hyperaldosteronism - genetics
Japan
Steroid 11-beta-Hydroxylase - genetics
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 893
container_issue 7
container_start_page 891
container_title Hypertension research
container_volume 44
creator Nakano, Yasuhiro
Iwata, Nahoko
Ogura-Ochi, Kanako
Hasegawa, Kosei
Hirasawa, Akira
Otsuka, Fumio
description
doi_str_mv 10.1038/s41440-021-00633-1
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2494879598</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2494879598</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-822dbc0d6964c017c94ca0407e27763868c6c3ce8dfbecf78bdc2f5e59ecbe133</originalsourceid><addsrcrecordid>eNpdkc1u1DAUhS0EokPhBVggS2zYhPovjrOEUaFFlegCFqws5-ZmxlViD7ajqi_Ec-JhCgtWd-HvHB35I-Q1Z-85k-YiK64Ua5jgDWNayoY_IRsulWmU4Oop2bCe66bXUp-RFznfMSZM2_Pn5ExKrUSruw35dZsQZh88uJmO3u1CzD5TF0bqRwzFT_Wl-BhonGjZI4W9XzB5oNsft5x_5BenK-gOA1IfaLmP9IC1qhwpcBnzMevoF3dwATPSyS1-fqD3vuzpbl4hQkzFQ_Rjk3A5RocZqZvHmAumGHxeXpJnk5szvnq85-T7p8tv26vm5uvn6-2HmwYk06UxQowDsFH3WgHjHfQKHFOsQ9F1WhptQIMENOM0IEydGUYQU4ttjzAgl_KcvDv1HlL8uWIudvEZcJ7r8rhmK1SvTNe3vano2__Qu7imUNdZ0Soj6gTNKiVOFKSYc8LJHpJfXHqwnNmjRXuyaKtF-8ei5TX05rF6Hep__Iv81SZ_A_remdQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2548296460</pqid></control><display><type>article</type><title>Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Nakano, Yasuhiro ; Iwata, Nahoko ; Ogura-Ochi, Kanako ; Hasegawa, Kosei ; Hirasawa, Akira ; Otsuka, Fumio</creator><creatorcontrib>Nakano, Yasuhiro ; Iwata, Nahoko ; Ogura-Ochi, Kanako ; Hasegawa, Kosei ; Hirasawa, Akira ; Otsuka, Fumio</creatorcontrib><identifier>ISSN: 0916-9636</identifier><identifier>EISSN: 1348-4214</identifier><identifier>DOI: 10.1038/s41440-021-00633-1</identifier><identifier>PMID: 33642567</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Child ; Cytochrome P-450 CYP11B2 - genetics ; Humans ; Hyperaldosteronism - diagnosis ; Hyperaldosteronism - genetics ; Japan ; Steroid 11-beta-Hydroxylase - genetics</subject><ispartof>Hypertension research, 2021-07, Vol.44 (7), p.891-893</ispartof><rights>The Author(s), under exclusive licence to The Japanese Society of Hypertension 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c306t-822dbc0d6964c017c94ca0407e27763868c6c3ce8dfbecf78bdc2f5e59ecbe133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33642567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakano, Yasuhiro</creatorcontrib><creatorcontrib>Iwata, Nahoko</creatorcontrib><creatorcontrib>Ogura-Ochi, Kanako</creatorcontrib><creatorcontrib>Hasegawa, Kosei</creatorcontrib><creatorcontrib>Hirasawa, Akira</creatorcontrib><creatorcontrib>Otsuka, Fumio</creatorcontrib><title>Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism</title><title>Hypertension research</title><addtitle>Hypertens Res</addtitle><subject>Child</subject><subject>Cytochrome P-450 CYP11B2 - genetics</subject><subject>Humans</subject><subject>Hyperaldosteronism - diagnosis</subject><subject>Hyperaldosteronism - genetics</subject><subject>Japan</subject><subject>Steroid 11-beta-Hydroxylase - genetics</subject><issn>0916-9636</issn><issn>1348-4214</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkc1u1DAUhS0EokPhBVggS2zYhPovjrOEUaFFlegCFqws5-ZmxlViD7ajqi_Ec-JhCgtWd-HvHB35I-Q1Z-85k-YiK64Ua5jgDWNayoY_IRsulWmU4Oop2bCe66bXUp-RFznfMSZM2_Pn5ExKrUSruw35dZsQZh88uJmO3u1CzD5TF0bqRwzFT_Wl-BhonGjZI4W9XzB5oNsft5x_5BenK-gOA1IfaLmP9IC1qhwpcBnzMevoF3dwATPSyS1-fqD3vuzpbl4hQkzFQ_Rjk3A5RocZqZvHmAumGHxeXpJnk5szvnq85-T7p8tv26vm5uvn6-2HmwYk06UxQowDsFH3WgHjHfQKHFOsQ9F1WhptQIMENOM0IEydGUYQU4ttjzAgl_KcvDv1HlL8uWIudvEZcJ7r8rhmK1SvTNe3vano2__Qu7imUNdZ0Soj6gTNKiVOFKSYc8LJHpJfXHqwnNmjRXuyaKtF-8ei5TX05rF6Hep__Iv81SZ_A_remdQ</recordid><startdate>20210701</startdate><enddate>20210701</enddate><creator>Nakano, Yasuhiro</creator><creator>Iwata, Nahoko</creator><creator>Ogura-Ochi, Kanako</creator><creator>Hasegawa, Kosei</creator><creator>Hirasawa, Akira</creator><creator>Otsuka, Fumio</creator><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20210701</creationdate><title>Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism</title><author>Nakano, Yasuhiro ; Iwata, Nahoko ; Ogura-Ochi, Kanako ; Hasegawa, Kosei ; Hirasawa, Akira ; Otsuka, Fumio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-822dbc0d6964c017c94ca0407e27763868c6c3ce8dfbecf78bdc2f5e59ecbe133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Child</topic><topic>Cytochrome P-450 CYP11B2 - genetics</topic><topic>Humans</topic><topic>Hyperaldosteronism - diagnosis</topic><topic>Hyperaldosteronism - genetics</topic><topic>Japan</topic><topic>Steroid 11-beta-Hydroxylase - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakano, Yasuhiro</creatorcontrib><creatorcontrib>Iwata, Nahoko</creatorcontrib><creatorcontrib>Ogura-Ochi, Kanako</creatorcontrib><creatorcontrib>Hasegawa, Kosei</creatorcontrib><creatorcontrib>Hirasawa, Akira</creatorcontrib><creatorcontrib>Otsuka, Fumio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Hypertension research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakano, Yasuhiro</au><au>Iwata, Nahoko</au><au>Ogura-Ochi, Kanako</au><au>Hasegawa, Kosei</au><au>Hirasawa, Akira</au><au>Otsuka, Fumio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism</atitle><jtitle>Hypertension research</jtitle><addtitle>Hypertens Res</addtitle><date>2021-07-01</date><risdate>2021</risdate><volume>44</volume><issue>7</issue><spage>891</spage><epage>893</epage><pages>891-893</pages><issn>0916-9636</issn><eissn>1348-4214</eissn><cop>England</cop><pub>Nature Publishing Group</pub><pmid>33642567</pmid><doi>10.1038/s41440-021-00633-1</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0916-9636
ispartof Hypertension research, 2021-07, Vol.44 (7), p.891-893
issn 0916-9636
1348-4214
language eng
recordid cdi_proquest_miscellaneous_2494879598
source MEDLINE; Alma/SFX Local Collection
subjects Child
Cytochrome P-450 CYP11B2 - genetics
Humans
Hyperaldosteronism - diagnosis
Hyperaldosteronism - genetics
Japan
Steroid 11-beta-Hydroxylase - genetics
title Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A38%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preclinical%20diagnosis%20and%20identification%20of%20the%20chimeric%20CYP11B1/CYP11B2%20gene%20in%20two%20pediatric%20cases%20of%20a%20Japanese%20family%20with%20glucocorticoid-remediable%20aldosteronism&rft.jtitle=Hypertension%20research&rft.au=Nakano,%20Yasuhiro&rft.date=2021-07-01&rft.volume=44&rft.issue=7&rft.spage=891&rft.epage=893&rft.pages=891-893&rft.issn=0916-9636&rft.eissn=1348-4214&rft_id=info:doi/10.1038/s41440-021-00633-1&rft_dat=%3Cproquest_cross%3E2494879598%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2548296460&rft_id=info:pmid/33642567&rfr_iscdi=true