Yan C - Search Results

1

Shedding Light on Lysosomal Malondialdehyde Affecting Vitamin B₁₂ Transport during Cerebral Ischemia/Reperfusion Injury.

Su D, Zhang R, Wang X, Ding Q, Che F, Liu Z, Xu J, Zhao Y, Ji K, Wu W, Yan C, Li P, Tang B. Su D, et al. Among authors: yan c. J Am Chem Soc. 2023 Oct 18;145(41):22609-22619. doi: 10.1021/jacs.3c07809. Epub 2023 Oct 6. J Am Chem Soc. 2023. PMID: 37803879

2

[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. Zhonghua Yi Xue Za Zhi. 2007 Jun 5;87(21):1486-90. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17785089 Chinese.

3

[Clinical and pathological features and prognosis of Chinese patients with distal myopathy with rimmed vacuoles: study of 17 cases].

Chen Q, Yan CZ, Liu SP, Zhao YY, Li W, Wu JL, Li DN. Chen Q, et al. Zhonghua Yi Xue Za Zhi. 2008 May 20;88(19):1313-7. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18956699 Chinese.

4

[Clinical and biopsy-based myopathological features of 5 cases with centronuclear myopathy].

Li HH, Liu SP, Li W, Zhao YY, Wu JL, Li DN, Yan CZ. Li HH, et al. Zhonghua Er Ke Za Zhi. 2008 Nov;46(11):856-9. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099905 Chinese.

5

Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.

Wen B, Dai T, Li W, Zhao Y, Liu S, Zhang C, Li H, Wu J, Li D, Yan C. Wen B, et al. Among authors: yan c. J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):231-6. doi: 10.1136/jnnp.2009.176404. Epub 2009 Sep 15. J Neurol Neurosurg Psychiatry. 2010. PMID: 19758981

6

Muscle injury induced by different types of contractions in dystrophic mdx mice.

Lou J, Bi W, Li W, Zhao Y, Liu S, Zheng J, Yan C. Lou J, et al. Among authors: yan c. J Muscle Res Cell Motil. 2012 Mar;32(6):411-9. doi: 10.1007/s10974-012-9284-y. Epub 2012 Feb 11. J Muscle Res Cell Motil. 2012. PMID: 22327507

7

Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.

Lin P, Li W, Wen B, Zhao Y, Fenster DS, Wang Y, Gong Y, Yan C. Lin P, et al. Among authors: yan c. J Hum Genet. 2012 Oct;57(10):679-81. doi: 10.1038/jhg.2012.84. Epub 2012 Jul 26. J Hum Genet. 2012. PMID: 22832386

8

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: yan c. PLoS One. 2013;8(3):e58116. doi: 10.1371/journal.pone.0058116. Epub 2013 Mar 5. PLoS One. 2013. PMID: 23472144 Free PMC article.

9

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: yan c. Neuromolecular Med. 2014 Mar;16(1):119-26. doi: 10.1007/s12017-013-8264-8. Epub 2013 Sep 24. Neuromolecular Med. 2014. PMID: 24062162

10

Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia.

Ji K, Liu K, Lin P, Wen B, Luo YB, Zhao Y, Yan C. Ji K, et al. Among authors: yan c. Neurol Sci. 2014 Mar;35(3):443-8. doi: 10.1007/s10072-013-1557-8. Epub 2013 Oct 4. Neurol Sci. 2014. PMID: 24091712

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