Liu F - Search Results

1

Advances in the Differentiation of hiPSCs into Cerebellar Neuronal Cells.

Wang Y, Liu W, Jiao Y, Yang Y, Shan D, Ji X, Zhang R, Zhan Z, Tang Y, Guo D, Yan C, Liu F. Wang Y, et al. Among authors: liu w, liu f. Stem Cell Rev Rep. 2024 Oct;20(7):1782-1794. doi: 10.1007/s12015-024-10763-x. Epub 2024 Jul 18. Stem Cell Rev Rep. 2024. PMID: 39023738 Review.

2

Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles.

Li H, Chen Q, Liu F, Zhang X, Liu T, Li W, Liu S, Zhao Y, Wen B, Dai T, Lin P, Gong Y, Yan C. Li H, et al. Among authors: liu s, liu f, liu t. J Hum Genet. 2011 Apr;56(4):335-8. doi: 10.1038/jhg.2011.15. Epub 2011 Feb 10. J Hum Genet. 2011. PMID: 21307865

3

Unfolded protein response and activated degradative pathways regulation in GNE myopathy.

Li H, Chen Q, Liu F, Zhang X, Li W, Liu S, Zhao Y, Gong Y, Yan C. Li H, et al. Among authors: liu s, liu f. PLoS One. 2013;8(3):e58116. doi: 10.1371/journal.pone.0058116. Epub 2013 Mar 5. PLoS One. 2013. PMID: 23472144 Free PMC article.

4

Novel mitochondrial C15620A variant may modulate the phenotype of mitochondrial G11778A mutation in a Chinese family with Leigh syndrome.

Ji K, Zheng J, Sun B, Liu F, Shan J, Li D, Luo YB, Zhao Y, Yan C. Ji K, et al. Among authors: liu f. Neuromolecular Med. 2014 Mar;16(1):119-26. doi: 10.1007/s12017-013-8264-8. Epub 2013 Sep 24. Neuromolecular Med. 2014. PMID: 24062162

5

Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle.

Liu F, Lou J, Zhao D, Li W, Zhao Y, Sun X, Yan C. Liu F, et al. Int J Neurosci. 2016 Jun;126(6):499-509. doi: 10.3109/00207454.2015.1034801. Epub 2015 Jul 14. Int J Neurosci. 2016. PMID: 26000923

6

Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap.

Liu F, Zhang D, Yan C. Liu F, et al. Neurol India. 2016 Mar-Apr;64(2):336-8. doi: 10.4103/0028-3886.177607. Neurol India. 2016. PMID: 26954819 Free article. No abstract available.

7

Activation of the wnt/β-Catenin Signaling Pathway in Polymyositis, Dermatomyositis and Duchenne Muscular Dystrophy.

Liu F, Liang Z, Xu J, Li W, Zhao D, Zhao Y, Yan C. Liu F, et al. J Clin Neurol. 2016 Jul;12(3):351-60. doi: 10.3988/jcn.2016.12.3.351. Epub 2016 May 10. J Clin Neurol. 2016. PMID: 27165423 Free PMC article.

8

A novel Kir2.6 mutation associated with hypokalemic periodic paralysis.

Zheng J, Liang Z, Hou Y, Liu F, Hu Y, Lin P, Yan C. Zheng J, et al. Among authors: liu f. Clin Neurophysiol. 2016 Jun;127(6):2503-8. doi: 10.1016/j.clinph.2016.03.008. Epub 2016 Mar 17. Clin Neurophysiol. 2016. PMID: 27178871

9

ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.

Xu J, Li D, Lv J, Xu X, Wen B, Lin P, Liu F, Ji K, Shan J, Li H, Li W, Zhao Y, Zhao D, Pok JY, Yan C. Xu J, et al. Among authors: liu f. Ann Neurol. 2018 Nov;84(5):659-673. doi: 10.1002/ana.25338. Epub 2018 Oct 19. Ann Neurol. 2018. PMID: 30232818

10

Idebenone Protects against Atherosclerosis in Apolipoprotein E-Deficient Mice Via Activation of the SIRT3-SOD2-mtROS Pathway.

Jiang W, Geng H, Lv X, Ma J, Liu F, Lin P, Yan C. Jiang W, et al. Among authors: liu f. Cardiovasc Drugs Ther. 2021 Dec;35(6):1129-1145. doi: 10.1007/s10557-020-07018-5. Cardiovasc Drugs Ther. 2021. PMID: 32557012

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