Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes.
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| Title: | Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes. |
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| Authors: | Zhao, Weixin1,2,3 (AUTHOR), Song, Ailing4 (AUTHOR), Xu, Yang5 (AUTHOR), Wu, Qian5 (AUTHOR), Liu, Cuicui5 (AUTHOR), Yin, Jiani C.5 (AUTHOR), Ou, Qiuxiang5 (AUTHOR), Wu, Xue5 (AUTHOR), Shao, Yang5,6 (AUTHOR), Zhao, Xinmin2,7 (AUTHOR) mizuyiaaa@163.com |
| Source: | BMC Medicine. 2/24/2023, Vol. 21 Issue 1, p1-16. 16p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 162076103 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zhao%2C+Weixin%22">Zhao, Weixin</searchLink><relatesTo>1,2,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Song%2C+Ailing%22">Song, Ailing</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Yang%22">Xu, Yang</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Qian%22">Wu, Qian</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Cuicui%22">Liu, Cuicui</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yin%2C+Jiani+C%2E%22">Yin, Jiani C.</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ou%2C+Qiuxiang%22">Ou, Qiuxiang</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Xue%22">Wu, Xue</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shao%2C+Yang%22">Shao, Yang</searchLink><relatesTo>5,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhao%2C+Xinmin%22">Zhao, Xinmin</searchLink><relatesTo>2,7</relatesTo> (AUTHOR)<i> mizuyiaaa@163.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22BMC+Medicine%22">BMC Medicine</searchLink>. 2/24/2023, Vol. 21 Issue 1, p1-16. 16p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=162076103 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12916-023-02768-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 16 StartPage: 1 Titles: – TitleFull: Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zhao, Weixin – PersonEntity: Name: NameFull: Song, Ailing – PersonEntity: Name: NameFull: Xu, Yang – PersonEntity: Name: NameFull: Wu, Qian – PersonEntity: Name: NameFull: Liu, Cuicui – PersonEntity: Name: NameFull: Yin, Jiani C. – PersonEntity: Name: NameFull: Ou, Qiuxiang – PersonEntity: Name: NameFull: Wu, Xue – PersonEntity: Name: NameFull: Shao, Yang – PersonEntity: Name: NameFull: Zhao, Xinmin IsPartOfRelationships: – BibEntity: Dates: – D: 24 M: 02 Text: 2/24/2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 17417015 Numbering: – Type: volume Value: 21 – Type: issue Value: 1 Titles: – TitleFull: BMC Medicine Type: main |
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