Lu Y - Search Results

1

Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy.

Lu Y, Zhao D, Yao S, Wu S, Hong D, Wang Q, Liu J, Smeitink JAM, Yuan Y, Wang Z. Lu Y, et al. J Neurol Sci. 2017 Aug 15;379:137-143. doi: 10.1016/j.jns.2017.05.056. Epub 2017 May 30. J Neurol Sci. 2017. PMID: 28716227

2

In response to the letter to the editor regarding: Serious assessment of mtDNA variants is a prerequisite to confirm pathogenicity.

Lu Y, Wang Z. Lu Y, et al. J Neurol Sci. 2017 Oct 15;381:343-344. doi: 10.1016/j.jns.2017.08.3232. Epub 2017 Aug 26. J Neurol Sci. 2017. PMID: 28847435 No abstract available.

3

Patients with MELAS with negative myopathology for characteristic ragged-red fibers.

Lu Y, Deng J, Zhao Y, Zhang Z, Hong D, Yao S, Zhao D, Xie J, Fang H, Yuan Y, Wang Z. Lu Y, et al. J Neurol Sci. 2020 Jan 15;408:116499. doi: 10.1016/j.jns.2019.116499. Epub 2019 Oct 15. J Neurol Sci. 2020. PMID: 31726383

4

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.

Lu YY, Lyu H, Jin SQ, Zuo YH, Liu J, Wang ZX, Zhang W, Yuan Y. Lu YY, et al. Chin Med J (Engl). 2017 May 5;130(9):1049-1054. doi: 10.4103/0366-6999.204925. Chin Med J (Engl). 2017. PMID: 28469099 Free PMC article.

5

[The clinical and muscular pathological features of statin-induced myopathy].

Meng L, Lu Y, Zhang W, Wang Z, Lyu H, Yuan Y. Meng L, et al. Among authors: lu y. Zhonghua Nei Ke Za Zhi. 2015 Aug;54(8):716-20. Zhonghua Nei Ke Za Zhi. 2015. PMID: 26674629 Chinese.

6

Fu J, Dai S, Lu Y, Wu R, Wang Z, Yuan Y, Lv H. Fu J, et al. Among authors: lu y. Neuromuscul Disord. 2017 Aug;27(8):760-765. doi: 10.1016/j.nmd.2017.04.001. Epub 2017 Apr 20. Neuromuscul Disord. 2017. PMID: 28495047

7

RNA-seq profiling, and impaired autophagic process in skeletal muscle of MELAS.

Deng J, Lu Y, Xie Z, Liu J, Yuan Y, Wang Z. Deng J, et al. Among authors: lu y. Biochem Biophys Res Commun. 2020 Feb 26;523(1):91-97. doi: 10.1016/j.bbrc.2019.12.005. Epub 2019 Dec 10. Biochem Biophys Res Commun. 2020. PMID: 31836143

8

Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations.

Yu M, Zhu Y, Lu Y, Lv H, Zhang W, Yuan Y, Wang Z. Yu M, et al. Among authors: lu y. Orphanet J Rare Dis. 2020 Dec 9;15(1):344. doi: 10.1186/s13023-020-01626-y. Orphanet J Rare Dis. 2020. PMID: 33298082 Free PMC article.

9

HADHB mutations cause infantile-onset axonal Charcot-Marie-Tooth disease: A report of two cases.

Lu Y, Wu R, Meng L, Lv H, Liu J, Zuo Y, Zhang W, Yuan Y, Wang Z. Lu Y, et al. Clin Neuropathol. 2018 Sep/Oct;37(5):232-238. doi: 10.5414/NP301097. Clin Neuropathol. 2018. PMID: 29956646

10

Mast1 mediates radiation-induced gastric injury via the P38 MAPK pathway.

Ding W, Lu Y, Zhou A, Chen Y, Wang Z, Wang L, Tian Y. Ding W, et al. Among authors: lu y. Exp Cell Res. 2021 Dec 15;409(2):112913. doi: 10.1016/j.yexcr.2021.112913. Epub 2021 Nov 11. Exp Cell Res. 2021. PMID: 34774870 Free article.

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