Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.
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| Title: | Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. |
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| Authors: | Khan Z; Genentech, 1 DNA Way, South San Francisco, 94080, USA. khanz12@gene.com., Jung M; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Crow M; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Mohindra R; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland., Maiya V; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Kaminker JS; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Hackos DH; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Chandler GS; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland., McCarthy MI; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Bhangale T; Genentech, 1 DNA Way, South San Francisco, 94080, USA. tusharb@gene.com. |
| Source: | Genome medicine [Genome Med] 2023 Jun 21; Vol. 15 (1), pp. 45. Date of Electronic Publication: 2023 Jun 21. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 37344884 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Khan+Z%22">Khan Z</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA. khanz12@gene.com.<br /><searchLink fieldCode="AU" term="%22Jung+M%22">Jung M</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Crow+M%22">Crow M</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Mohindra+R%22">Mohindra R</searchLink>; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland.<br /><searchLink fieldCode="AU" term="%22Maiya+V%22">Maiya V</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Kaminker+JS%22">Kaminker JS</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Hackos+DH%22">Hackos DH</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Chandler+GS%22">Chandler GS</searchLink>; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland.<br /><searchLink fieldCode="AU" term="%22McCarthy+MI%22">McCarthy MI</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA.<br /><searchLink fieldCode="AU" term="%22Bhangale+T%22">Bhangale T</searchLink>; Genentech, 1 DNA Way, South San Francisco, 94080, USA. tusharb@gene.com. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101475844%22">Genome medicine</searchLink> [Genome Med] 2023 Jun 21; Vol. 15 (1), pp. 45. <i>Date of Electronic Publication: </i>2023 Jun 21. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101475844 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1756-994X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221756994X%22">1756994X </searchLink><i>NLM ISO Abbreviation: </i>Genome Med <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37344884 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13073-023-01193-4 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 45 Titles: – TitleFull: Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Khan Z – PersonEntity: Name: NameFull: Jung M – PersonEntity: Name: NameFull: Crow M – PersonEntity: Name: NameFull: Mohindra R – PersonEntity: Name: NameFull: Maiya V – PersonEntity: Name: NameFull: Kaminker JS – PersonEntity: Name: NameFull: Hackos DH – PersonEntity: Name: NameFull: Chandler GS – PersonEntity: Name: NameFull: McCarthy MI – PersonEntity: Name: NameFull: Bhangale T IsPartOfRelationships: – BibEntity: Dates: – D: 21 M: 06 Text: 2023 Jun 21 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 1756-994X Numbering: – Type: volume Value: 15 – Type: issue Value: 1 Titles: – TitleFull: Genome medicine Type: main |
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