Leng JH - Search Results

1

Premature ovarian insufficiency may be associated with the mutations in mitochondrial tRNA genes.

Ding Y, Xia BH, Zhuo GC, Zhang CJ, Leng JH. Ding Y, et al. Among authors: leng jh. Endocr J. 2019 Jan 28;66(1):81-88. doi: 10.1507/endocrj.EJ18-0308. Epub 2018 Nov 6. Endocr J. 2019. PMID: 30404982 Free article.

2

[The expression and significance of costimulatory molecule in peripheral blood B lymphocytes in rheumatoid arthritis].

Leng JH, Hu ZY, Zhuo GC, Wang KY, Wang ZW, Peng L, Zhang YF. Leng JH, et al. Zhonghua Nei Ke Za Zhi. 2004 Jul;43(7):519-21. Zhonghua Nei Ke Za Zhi. 2004. PMID: 15312407 Chinese.

3

Co-expression of IL-18 binding protein and IL-4 regulates Th1/Th2 cytokine response in murine collagen-induced arthritis.

Leng J, Yao H, Shen J, Wang K, Zhuo G, Wang Z. Leng J, et al. Acta Biochim Biophys Sin (Shanghai). 2008 Feb;40(2):116-24. doi: 10.1111/j.1745-7270.2008.00384.x. Acta Biochim Biophys Sin (Shanghai). 2008. PMID: 18235973 Free article.

4

A 9-bp deletion homoplasmy in women with polycystic ovary syndrome revealed by mitochondrial genome-mutation screen.

Zhuo G, Feng G, Leng J, Yu L, Jiang Y. Zhuo G, et al. Biochem Genet. 2010 Feb;48(1-2):157-63. doi: 10.1007/s10528-009-9308-5. Epub 2009 Nov 22. Biochem Genet. 2010. PMID: 20094848

5

[Serum IL-18 levels in mice with collagen-induced arthritis treated by recombinant adenovirus containing mIL-18BP and mIL-4 fusion gene].

Leng JH, Yao HP, Shen JY, Wang KY, Wang ZW, Zhuo GC. Leng JH, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2011 Mar;40(2):195-9. doi: 10.3785/j.issn.1008-9292.2011.02.013. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21488217 Chinese.

6

Critical reassessment of a five-generation Chinese family carrying deafness-associated mitochondrial 1555A>G mutation.

Ding Y, Leng J, Zheng J. Ding Y, et al. Acta Otolaryngol. 2011 Nov;131(11):1239-40. doi: 10.3109/00016489.2011.602358. Epub 2011 Aug 15. Acta Otolaryngol. 2011. PMID: 21838605 No abstract available.

7

Is mitochondrial tRNA Leu(UUR) 3291T>C mutation pathogenic?

Ding Y, Leng J. Ding Y, et al. Mitochondrial DNA. 2012 Aug;23(4):323-6. doi: 10.3109/19401736.2012.674119. Epub 2012 Apr 3. Mitochondrial DNA. 2012. PMID: 22471645

8

Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension.

Teng L, Zheng J, Leng J, Ding Y. Teng L, et al. Mitochondrial DNA. 2012 Dec;23(6):461-5. doi: 10.3109/19401736.2012.710205. Epub 2012 Aug 24. Mitochondrial DNA. 2012. PMID: 22917175

9

The role of mitochondrial DNA mutations in hearing loss.

Ding Y, Leng J, Fan F, Xia B, Xu P. Ding Y, et al. Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528-013-9589-6. Epub 2013 Apr 21. Biochem Genet. 2013. PMID: 23605717 Review.

10

Mitochondrial DNA mutations and essential hypertension (Review).

Ding Y, Xia B, Yu J, Leng J, Huang J. Ding Y, et al. Int J Mol Med. 2013 Oct;32(4):768-74. doi: 10.3892/ijmm.2013.1459. Epub 2013 Jul 29. Int J Mol Med. 2013. PMID: 23900616 Review.

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