Zheng J - Search Results

1

Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a Chinese population.

Shan J, Chen B, Lin P, Li D, Luo Y, Ji K, Zheng J, Yuan Y, Yan C. Shan J, et al. Among authors: zheng j. Neuromolecular Med. 2014 Dec;16(4):782-6. doi: 10.1007/s12017-014-8327-5. Epub 2014 Oct 5. Neuromolecular Med. 2014. PMID: 25283883

2

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: zheng j. 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

3

Novel PANK2 gene mutations in two Chinese siblings with atypical pantothenate kinase-associated neurodegeneration.

Shan J, Wen B, Zhu J, Lin P, Zheng J, Yan C. Shan J, et al. Among authors: zheng j. Neurol Sci. 2013 Apr;34(4):561-3. doi: 10.1007/s10072-012-1177-8. Epub 2012 Aug 29. Neurol Sci. 2013. PMID: 22930366

4

Increased muscle coenzyme Q10 in riboflavin responsive MADD with ETFDH gene mutations due to secondary mitochondrial proliferation.

Wen B, Li D, Shan J, Liu S, Li W, Zhao Y, Lin P, Zheng J, Li D, Gong Y, Yan C. Wen B, et al. Among authors: zheng j. Mol Genet Metab. 2013 Jun;109(2):154-60. doi: 10.1016/j.ymgme.2013.04.007. Epub 2013 Apr 11. Mol Genet Metab. 2013. PMID: 23628458

5

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

6

[Study of mutations of presenilin 1 gene in early-onset familial Alzheimers disease].

Cao L, Qiu X, Zheng J, Lin P, Wang S. Cao L, et al. Among authors: zheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):298-301. doi: 10.3760/cma.j.issn.1003-9406.2014.03.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928006 Chinese.

7

Skeletal muscle increases FGF21 expression in mitochondrial disorders to compensate for energy metabolic insufficiency by activating the mTOR-YY1-PGC1α pathway.

Ji K, Zheng J, Lv J, Xu J, Ji X, Luo YB, Li W, Zhao Y, Yan C. Ji K, et al. Among authors: zheng j. Free Radic Biol Med. 2015 Jul;84:161-170. doi: 10.1016/j.freeradbiomed.2015.03.020. Epub 2015 Apr 3. Free Radic Biol Med. 2015. PMID: 25843656

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. 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

Clinical and diagnostic features of anti-neurofascin-155 antibody-positive neuropathy in Han Chinese.

Wang W, Liu C, Li W, Zhang D, Shan Y, Zheng J, Shan J, Zhao Y, Yan C, Wang Q. Wang W, et al. Among authors: zheng j. Ann Clin Transl Neurol. 2022 May;9(5):695-706. doi: 10.1002/acn3.51550. Epub 2022 Mar 21. Ann Clin Transl Neurol. 2022. PMID: 35313093 Free PMC article.

10

Design and Preparation of NiFe₂O₄@FeOOH Composite Electrocatalyst for Highly Efficient and Stable Oxygen Evolution Reaction.

Li TT, Shi BY, Jiang LW, Zheng JF, Wang JJ. Li TT, et al. Molecules. 2022 Nov 1;27(21):7438. doi: 10.3390/molecules27217438. Molecules. 2022. PMID: 36364265 Free PMC article.

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