Li W - Search Results

1

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. Among authors: li w. 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.

2

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: li d, li w, li h. Ann Neurol. 2018 Nov;84(5):659-673. doi: 10.1002/ana.25338. Epub 2018 Oct 19. Ann Neurol. 2018. PMID: 30232818

3

"Myo-neuropathy" is commonly associated with mitochondrial tRNA^Lysine mutation.

Ji K, Zhao B, Lin Y, Wang W, Liu F, Li W, Zhao Y, Yan C. Ji K, et al. Among authors: li w. J Neurol. 2020 Nov;267(11):3319-3328. doi: 10.1007/s00415-020-10017-z. Epub 2020 Jun 23. J Neurol. 2020. PMID: 32577866

4

Anti-HMGCR myopathy overlaps with dermatomyositis-like rash: a distinct subtype of idiopathic inflammatory myopathy.

Hou Y, Shao K, Yan Y, Dai T, Li W, Zhao Y, Li D, Lu JQ, Norman GL, Yan C. Hou Y, et al. Among authors: li d, li w. J Neurol. 2022 Jan;269(1):280-293. doi: 10.1007/s00415-021-10621-7. Epub 2021 May 21. J Neurol. 2022. PMID: 34021410

5

[Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].

Ren SC, Yan CZ, Li MX, Liu SP, Wu JL, Zhao YY, Li W, Li DN. Ren SC, et al. Among authors: li w, li mx, li dn. Zhonghua Yi Xue Za Zhi. 2007 Jun 5;87(21):1486-90. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17785089 Chinese.

6

Idiopathic inflammatory myopathies with anti-mitochondrial antibodies: Clinical features and treatment outcomes in a Chinese cohort.

Hou Y, Liu M, Luo YB, Sun Y, Shao K, Dai T, Li W, Zhao Y, Yan C. Hou Y, et al. Among authors: li w. Neuromuscul Disord. 2019 Jan;29(1):5-13. doi: 10.1016/j.nmd.2018.11.004. Epub 2018 Nov 22. Neuromuscul Disord. 2019. PMID: 30579751 Free article.

7

Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy.

Liu M, Li L, Dai T, Hou Y, Li W, Zhao Y, Fang Q, Yan C. Liu M, et al. Among authors: li w, li l. J Neuropathol Exp Neurol. 2020 May 1;79(5):551-561. doi: 10.1093/jnen/nlaa023. J Neuropathol Exp Neurol. 2020. PMID: 32296846

8

A mitochondrial myopathy-associated tRNA^Ser(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function.

Lin Y, Xu X, Wang W, Liu F, Zhao D, Li D, Ji K, Li W, Zhao Y, Yan C. Lin Y, et al. Among authors: li d, li w. Mitochondrion. 2021 Mar;57:1-8. doi: 10.1016/j.mito.2020.11.015. Epub 2020 Dec 3. Mitochondrion. 2021. PMID: 33279600

9

Generation of a human induced pluripotent stem cell line (INNDSUi003-A) derived from patient with Becker muscular dystrophy (BMD).

Ji X, Wang Y, Sun P, Wang D, Sun X, Zhang R, Xu J, Li W, Liu F, Yan C. Ji X, et al. Among authors: li w. Stem Cell Res. 2022 Jul;62:102794. doi: 10.1016/j.scr.2022.102794. Epub 2022 Apr 27. Stem Cell Res. 2022. PMID: 35526387 Free article.

10

Accuracy of FGF-21 and GDF-15 for the diagnosis of mitochondrial disorders: A meta-analysis.

Lin Y, Ji K, Ma X, Liu S, Li W, Zhao Y, Yan C. Lin Y, et al. Among authors: li w. Ann Clin Transl Neurol. 2020 Jul;7(7):1204-1213. doi: 10.1002/acn3.51104. Epub 2020 Jun 25. Ann Clin Transl Neurol. 2020. PMID: 32585080 Free PMC article.

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