OXA1L deficiency causes mitochondrial myopathy via reactive oxygen species regulated nuclear factor kappa B signalling pathway.
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| Title: | OXA1L deficiency causes mitochondrial myopathy via reactive oxygen species regulated nuclear factor kappa B signalling pathway. |
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| Authors: | Zhan, Yongkun1 (AUTHOR) zhanyongkun@xinhuamed.com.cn, Wang, Qian2 (AUTHOR), Wang, Ya3 (AUTHOR), Fan, Yanjie1 (AUTHOR), Yan, Dan1 (AUTHOR), Lin, Xianlong3 (AUTHOR), Chen, Yaoting1 (AUTHOR), Hu, Tingting1 (AUTHOR), Li, Nan1 (AUTHOR), Dai, Weiqian1 (AUTHOR), Fang, Hezhi2,4 (AUTHOR) fangh@wmu.edu.cn, Yu, Yongguo1,5 (AUTHOR) yuyongguo@shsmu.edu.cn |
| Source: | Clinical & Translational Medicine. Jun2025, Vol. 15 Issue 6, p1-28. 28p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 186162711 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: OXA1L deficiency causes mitochondrial myopathy via reactive oxygen species regulated nuclear factor kappa B signalling pathway. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zhan%2C+Yongkun%22">Zhan, Yongkun</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> zhanyongkun@xinhuamed.com.cn</i><br /><searchLink fieldCode="AR" term="%22Wang%2C+Qian%22">Wang, Qian</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Ya%22">Wang, Ya</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fan%2C+Yanjie%22">Fan, Yanjie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yan%2C+Dan%22">Yan, Dan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Xianlong%22">Lin, Xianlong</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Yaoting%22">Chen, Yaoting</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hu%2C+Tingting%22">Hu, Tingting</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Nan%22">Li, Nan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Dai%2C+Weiqian%22">Dai, Weiqian</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fang%2C+Hezhi%22">Fang, Hezhi</searchLink><relatesTo>2,4</relatesTo> (AUTHOR)<i> fangh@wmu.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Yu%2C+Yongguo%22">Yu, Yongguo</searchLink><relatesTo>1,5</relatesTo> (AUTHOR)<i> yuyongguo@shsmu.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Clinical+%26+Translational+Medicine%22">Clinical & Translational Medicine</searchLink>. Jun2025, Vol. 15 Issue 6, p1-28. 28p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186162711 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ctm2.70385 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 28 StartPage: 1 Titles: – TitleFull: OXA1L deficiency causes mitochondrial myopathy via reactive oxygen species regulated nuclear factor kappa B signalling pathway. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zhan, Yongkun – PersonEntity: Name: NameFull: Wang, Qian – PersonEntity: Name: NameFull: Wang, Ya – PersonEntity: Name: NameFull: Fan, Yanjie – PersonEntity: Name: NameFull: Yan, Dan – PersonEntity: Name: NameFull: Lin, Xianlong – PersonEntity: Name: NameFull: Chen, Yaoting – PersonEntity: Name: NameFull: Hu, Tingting – PersonEntity: Name: NameFull: Li, Nan – PersonEntity: Name: NameFull: Dai, Weiqian – PersonEntity: Name: NameFull: Fang, Hezhi – PersonEntity: Name: NameFull: Yu, Yongguo IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 20011326 Numbering: – Type: volume Value: 15 – Type: issue Value: 6 Titles: – TitleFull: Clinical & Translational Medicine Type: main |
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