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2020 | 1 |
2022 | 2 |
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Page 1
CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model.
Proc Natl Acad Sci U S A. 2022 Oct 11;119(41):e2208649119. doi: 10.1073/pnas.2208649119. Epub 2022 Oct 3.
Proc Natl Acad Sci U S A. 2022.
PMID: 36191230
Free PMC article.
The polyG diseases: a new disease entity.
Liufu T, Zheng Y, Yu J, Yuan Y, Wang Z, Deng J, Hong D.
Liufu T, et al.
Acta Neuropathol Commun. 2022 May 31;10(1):79. doi: 10.1186/s40478-022-01383-y.
Acta Neuropathol Commun. 2022.
PMID: 35642014
Free PMC article.
Review.
Item in Clipboard
Treatment for mitochondrial diseases.
Liufu T, Wang Z.
Liufu T, et al.
Rev Neurosci. 2020 Sep 9:/j/revneuro.ahead-of-print/revneuro-2020-0034/revneuro-2020-0034.xml. doi: 10.1515/revneuro-2020-0034. Online ahead of print.
Rev Neurosci. 2020.
PMID: 32903211
Free article.
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COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy.
Zheng Y, Liufu T, Wen B, Zhou C, Liu L, Qiu Y, Zou W, Zhang W, Li Y, Pei J, Zeng Y, Chen W, Zhang C, Yuan Y, Wang G, Yan C, Lu X, Deng J, Wang Z, Hong D.
Zheng Y, et al. Among authors: liufu t.
Cell Discov. 2024 Feb 27;10(1):25. doi: 10.1038/s41421-023-00641-0.
Cell Discov. 2024.
PMID: 38413569
Free PMC article.
No abstract available.
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Diazo-carboxyl Click Derivatization Enables Sensitive Analysis of Carboxylic Acid Metabolites in Biosamples.
Li C, Cheng K, Zhao Q, Jin L, Wang X, Liufu T, Zhao X, Li X, Wang X, Lyu J, Huang D, Li P, Chen XW, Wang Z, Hu X, Quan L, Chen Z.
Li C, et al. Among authors: liufu t.
Anal Chem. 2023 Nov 21;95(46):16976-16986. doi: 10.1021/acs.analchem.3c03277. Epub 2023 Nov 9.
Anal Chem. 2023.
PMID: 37943785
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Complex I deficiency in m.3243A>G fibroblasts is alleviated by reducing NADH accumulation.
Liufu T, Yu H, Yu J, Yu M, Tian Y, Ou Y, Deng J, Xing G, Wang Z.
Liufu T, et al.
Front Physiol. 2023 Aug 15;14:1164287. doi: 10.3389/fphys.2023.1164287. eCollection 2023.
Front Physiol. 2023.
PMID: 37650111
Free PMC article.
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The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
Zhao Y, et al. Among authors: liufu t.
Mol Genet Genomic Med. 2024 Jan;12(1):e2328. doi: 10.1002/mgg3.2328. Epub 2023 Nov 28.
Mol Genet Genomic Med. 2024.
PMID: 38018320
Free PMC article.
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