The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database
The Human Cytochrome P450 (CYP) Allele Nomenclature Database, a critical resource for the pharmacogenetics and genomics communities, has transitioned to the Pharmacogene Variation (PharmVar) Consortium. In this report we provide a summary of the current database, provide an overview of the PharmVar...
Gespeichert in:
| Veröffentlicht in: | Clinical pharmacology and therapeutics 2018-03, Vol.103 (3), p.399-401 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 401 |
|---|---|
| container_issue | 3 |
| container_start_page | 399 |
| container_title | Clinical pharmacology and therapeutics |
| container_volume | 103 |
| creator | Gaedigk, Andrea Ingelman‐Sundberg, Magnus Miller, Neil A. Leeder, J. Steven Whirl‐Carrillo, Michelle Klein, Teri E. |
| description | The Human Cytochrome P450 (CYP) Allele Nomenclature Database, a critical resource for the pharmacogenetics and genomics communities, has transitioned to the Pharmacogene Variation (PharmVar) Consortium. In this report we provide a summary of the current database, provide an overview of the PharmVar consortium, and highlight the PharmVar database which will serve as the new home for pharmacogene nomenclature. |
| doi_str_mv | 10.1002/cpt.910 |
| format | Article |
| fullrecord | <record><control><sourceid>wiley_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_492612</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CPT910</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5090-4b59b4c1b8098501c168df2b134ccc70bb1807004915d16b0d9b18ec7692ec183</originalsourceid><addsrcrecordid>eNp1kV9PwjAUxRujEUTjNzB9E2KGbbeO1QcTMv9AQpQHNPGpaUuB6baSbpPw5Fe3OCTy4FN7zz33194cAM4x6mKEyLVall2G0QFoYuoTL6Q-PQRNhBDzGPHDBjgpindXBiyKjkGDMOwHIaFN8DVZaDheCJsJZeY61_BV2ESUiclh-0d3dQfGJi-MLZMqu4HDXBm7NLY2mRksHWJQZSKH8bo0amFN5pgBRbAdv407sJ-mOtXwycm5SkVZWQ3vRCmkKPQpOJqJtNBn27MFXh7uJ_HAGz0_DuP-yFMUMeQFkjIZKCwjxCKKsMJhNJ0R6dZQSvWQlDhCvc1-mE5xKNGUOUWrXsiIVjjyW8CrucVKLyvJlzbJhF1zIxK-lT7cTfOAkRAT57-t_a6T6anSeWlFuje238mTBZ-bT04jP3Q_dIDLGqCsKQqrZ7tZjPgmM-4y4y4z57z4-9TO9xuSM1zVhlWS6vV_HB6PJxvcN6eaoUU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>SWEPUB Freely available online</source><creator>Gaedigk, Andrea ; Ingelman‐Sundberg, Magnus ; Miller, Neil A. ; Leeder, J. Steven ; Whirl‐Carrillo, Michelle ; Klein, Teri E.</creator><creatorcontrib>Gaedigk, Andrea ; Ingelman‐Sundberg, Magnus ; Miller, Neil A. ; Leeder, J. Steven ; Whirl‐Carrillo, Michelle ; Klein, Teri E. ; PharmVar Steering Committee ; the PharmVar Steering Committee</creatorcontrib><description>The Human Cytochrome P450 (CYP) Allele Nomenclature Database, a critical resource for the pharmacogenetics and genomics communities, has transitioned to the Pharmacogene Variation (PharmVar) Consortium. In this report we provide a summary of the current database, provide an overview of the PharmVar consortium, and highlight the PharmVar database which will serve as the new home for pharmacogene nomenclature.</description><identifier>ISSN: 0009-9236</identifier><identifier>EISSN: 1532-6535</identifier><identifier>DOI: 10.1002/cpt.910</identifier><identifier>PMID: 29134625</identifier><language>eng</language><publisher>United States: John Wiley and Sons Inc</publisher><subject>Alleles ; Cytochrome P-450 Enzyme System - drug effects ; Cytochrome P-450 Enzyme System - genetics ; Databases, Factual ; Databases, Genetic ; Development ; Discovery & Development ; Genetic Variation ; Humans ; Pharmacogenetics ; Terminology as Topic</subject><ispartof>Clinical pharmacology and therapeutics, 2018-03, Vol.103 (3), p.399-401</ispartof><rights>2017 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics</rights><rights>2017 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5090-4b59b4c1b8098501c168df2b134ccc70bb1807004915d16b0d9b18ec7692ec183</citedby><cites>FETCH-LOGICAL-c5090-4b59b4c1b8098501c168df2b134ccc70bb1807004915d16b0d9b18ec7692ec183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcpt.910$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcpt.910$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29134625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:137692080$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Gaedigk, Andrea</creatorcontrib><creatorcontrib>Ingelman‐Sundberg, Magnus</creatorcontrib><creatorcontrib>Miller, Neil A.</creatorcontrib><creatorcontrib>Leeder, J. Steven</creatorcontrib><creatorcontrib>Whirl‐Carrillo, Michelle</creatorcontrib><creatorcontrib>Klein, Teri E.</creatorcontrib><creatorcontrib>PharmVar Steering Committee</creatorcontrib><creatorcontrib>the PharmVar Steering Committee</creatorcontrib><title>The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database</title><title>Clinical pharmacology and therapeutics</title><addtitle>Clin Pharmacol Ther</addtitle><description>The Human Cytochrome P450 (CYP) Allele Nomenclature Database, a critical resource for the pharmacogenetics and genomics communities, has transitioned to the Pharmacogene Variation (PharmVar) Consortium. In this report we provide a summary of the current database, provide an overview of the PharmVar consortium, and highlight the PharmVar database which will serve as the new home for pharmacogene nomenclature.</description><subject>Alleles</subject><subject>Cytochrome P-450 Enzyme System - drug effects</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>Databases, Factual</subject><subject>Databases, Genetic</subject><subject>Development</subject><subject>Discovery & Development</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>Pharmacogenetics</subject><subject>Terminology as Topic</subject><issn>0009-9236</issn><issn>1532-6535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNp1kV9PwjAUxRujEUTjNzB9E2KGbbeO1QcTMv9AQpQHNPGpaUuB6baSbpPw5Fe3OCTy4FN7zz33194cAM4x6mKEyLVall2G0QFoYuoTL6Q-PQRNhBDzGPHDBjgpindXBiyKjkGDMOwHIaFN8DVZaDheCJsJZeY61_BV2ESUiclh-0d3dQfGJi-MLZMqu4HDXBm7NLY2mRksHWJQZSKH8bo0amFN5pgBRbAdv407sJ-mOtXwycm5SkVZWQ3vRCmkKPQpOJqJtNBn27MFXh7uJ_HAGz0_DuP-yFMUMeQFkjIZKCwjxCKKsMJhNJ0R6dZQSvWQlDhCvc1-mE5xKNGUOUWrXsiIVjjyW8CrucVKLyvJlzbJhF1zIxK-lT7cTfOAkRAT57-t_a6T6anSeWlFuje238mTBZ-bT04jP3Q_dIDLGqCsKQqrZ7tZjPgmM-4y4y4z57z4-9TO9xuSM1zVhlWS6vV_HB6PJxvcN6eaoUU</recordid><startdate>201803</startdate><enddate>201803</enddate><creator>Gaedigk, Andrea</creator><creator>Ingelman‐Sundberg, Magnus</creator><creator>Miller, Neil A.</creator><creator>Leeder, J. Steven</creator><creator>Whirl‐Carrillo, Michelle</creator><creator>Klein, Teri E.</creator><general>John Wiley and Sons Inc</general><scope>24P</scope><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>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>201803</creationdate><title>The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database</title><author>Gaedigk, Andrea ; Ingelman‐Sundberg, Magnus ; Miller, Neil A. ; Leeder, J. Steven ; Whirl‐Carrillo, Michelle ; Klein, Teri E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5090-4b59b4c1b8098501c168df2b134ccc70bb1807004915d16b0d9b18ec7692ec183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alleles</topic><topic>Cytochrome P-450 Enzyme System - drug effects</topic><topic>Cytochrome P-450 Enzyme System - genetics</topic><topic>Databases, Factual</topic><topic>Databases, Genetic</topic><topic>Development</topic><topic>Discovery & Development</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>Pharmacogenetics</topic><topic>Terminology as Topic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gaedigk, Andrea</creatorcontrib><creatorcontrib>Ingelman‐Sundberg, Magnus</creatorcontrib><creatorcontrib>Miller, Neil A.</creatorcontrib><creatorcontrib>Leeder, J. Steven</creatorcontrib><creatorcontrib>Whirl‐Carrillo, Michelle</creatorcontrib><creatorcontrib>Klein, Teri E.</creatorcontrib><creatorcontrib>PharmVar Steering Committee</creatorcontrib><creatorcontrib>the PharmVar Steering Committee</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Clinical pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaedigk, Andrea</au><au>Ingelman‐Sundberg, Magnus</au><au>Miller, Neil A.</au><au>Leeder, J. Steven</au><au>Whirl‐Carrillo, Michelle</au><au>Klein, Teri E.</au><aucorp>PharmVar Steering Committee</aucorp><aucorp>the PharmVar Steering Committee</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database</atitle><jtitle>Clinical pharmacology and therapeutics</jtitle><addtitle>Clin Pharmacol Ther</addtitle><date>2018-03</date><risdate>2018</risdate><volume>103</volume><issue>3</issue><spage>399</spage><epage>401</epage><pages>399-401</pages><issn>0009-9236</issn><eissn>1532-6535</eissn><abstract>The Human Cytochrome P450 (CYP) Allele Nomenclature Database, a critical resource for the pharmacogenetics and genomics communities, has transitioned to the Pharmacogene Variation (PharmVar) Consortium. In this report we provide a summary of the current database, provide an overview of the PharmVar consortium, and highlight the PharmVar database which will serve as the new home for pharmacogene nomenclature.</abstract><cop>United States</cop><pub>John Wiley and Sons Inc</pub><pmid>29134625</pmid><doi>10.1002/cpt.910</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0009-9236 |
| ispartof | Clinical pharmacology and therapeutics, 2018-03, Vol.103 (3), p.399-401 |
| issn | 0009-9236 1532-6535 |
| language | eng |
| recordid | cdi_swepub_primary_oai_swepub_ki_se_492612 |
| source | MEDLINE; Wiley Online Library Journals Frontfile Complete; SWEPUB Freely available online |
| subjects | Alleles Cytochrome P-450 Enzyme System - drug effects Cytochrome P-450 Enzyme System - genetics Databases, Factual Databases, Genetic Development Discovery & Development Genetic Variation Humans Pharmacogenetics Terminology as Topic |
| title | The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP) Allele Nomenclature Database |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T22%3A58%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Pharmacogene%20Variation%20(PharmVar)%20Consortium:%20Incorporation%20of%20the%20Human%20Cytochrome%20P450%20(CYP)%20Allele%20Nomenclature%20Database&rft.jtitle=Clinical%20pharmacology%20and%20therapeutics&rft.au=Gaedigk,%20Andrea&rft.aucorp=PharmVar%20Steering%20Committee&rft.date=2018-03&rft.volume=103&rft.issue=3&rft.spage=399&rft.epage=401&rft.pages=399-401&rft.issn=0009-9236&rft.eissn=1532-6535&rft_id=info:doi/10.1002/cpt.910&rft_dat=%3Cwiley_swepu%3ECPT910%3C/wiley_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/29134625&rfr_iscdi=true |