Liu JS - Search Results

1

Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated Cardiomyopathy.

Liu JS, Fan LL, Zhang H, Liu X, Huang H, Tao LJ, Xia K, Xiang R. Liu JS, et al. Among authors: liu x. Cardiology. 2017;136(1):10-14. doi: 10.1159/000447422. Epub 2016 Aug 20. Cardiology. 2017. PMID: 27544385

2

[Expression of p27 and TGF-beta in rat kidney with unilateral ureteral obstruction and the relationship between TGF-beta and p27].

Sun J, Tao LJ, Ning WB, Jin O, Liu JS. Sun J, et al. Among authors: liu js. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2008 Aug;24(8):808-10. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2008. PMID: 18687224 Chinese.

3

[The effect of losartan on glomerular sclerosis in rats with diabetic nephropathy].

Xu JY, Tao LJ, Wang L, Ning WB, Liu JS. Xu JY, et al. Among authors: liu js. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2008 Sep;33(9):836-40. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2008. PMID: 18812664 Chinese.

4

Application of GC-MS coupled with chemometrics for scanning serum metabolic biomarkers from renal fibrosis rat.

Liu S, Liu JS, Luo RN, Xu H, Zhang WR, Meng J, Liang YZ, Tao LJ. Liu S, et al. Among authors: liu js. Biochem Biophys Res Commun. 2015 May 22;461(1):186-92. doi: 10.1016/j.bbrc.2015.04.031. Epub 2015 Apr 13. Biochem Biophys Res Commun. 2015. PMID: 25881503

5

Fluorofenidone protects against renal fibrosis by inhibiting STAT3 tyrosine phosphorylation.

Tang J, Liu CY, Lu MM, Zhang J, Mei WJ, Yang WJ, Xie YY, Huang L, Peng ZZ, Yuan QJ, Liu JS, Hu GY, Tao LJ. Tang J, et al. Among authors: liu cy, liu js. Mol Cell Biochem. 2015 Sep;407(1-2):77-87. doi: 10.1007/s11010-015-2456-5. Epub 2015 Jun 2. Mol Cell Biochem. 2015. PMID: 26033204

6

Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy.

Liu JS, Fan LL, Li JJ, Xiang R. Liu JS, et al. Am J Cardiol. 2017 May 1;119(9):1485-1489. doi: 10.1016/j.amjcard.2017.01.011. Epub 2017 Feb 10. Am J Cardiol. 2017. PMID: 28256248

7

Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis.

Fan LL, Liu JS, Huang H, Du R, Xiang R. Fan LL, et al. Among authors: liu js. J Gene Med. 2019 Feb;21(2-3):e3073. doi: 10.1002/jgm.3073. Epub 2019 Feb 11. J Gene Med. 2019. PMID: 30690801

8

Long-term follow-up of an Alport syndrome patient with a novel mutation of COL4A5.

Xiang R, Li JJ, Liu JS, Fan LL, Li L, Xia K, Zhang H. Xiang R, et al. Among authors: liu js. Int J Clin Exp Pathol. 2017 Aug 1;10(8):8709-8714. eCollection 2017. Int J Clin Exp Pathol. 2017. PMID: 31966729 Free PMC article.

9

Identification of a Novel Arginine Vasopressin Receptor 2 Mutation (p.V183M) in a Chinese Family with Nephrogenic Diabetes Insipidus.

Liu JS, Huang H, Jin JY, Du R, Wang CY, Fan LL. Liu JS, et al. Mol Syndromol. 2020 Jul;11(3):130-134. doi: 10.1159/000507035. Epub 2020 Mar 28. Mol Syndromol. 2020. PMID: 32903920 Free PMC article.

10

Use of whole-exome sequencing to identify a novel ADCY10 mutation in a patient with nephrolithiasis.

Wang C, Du R, Jin J, Dong Y, Liu J, Fan L, Xiang R. Wang C, et al. Am J Transl Res. 2020 Aug 15;12(8):4576-4581. eCollection 2020. Am J Transl Res. 2020. PMID: 32913531 Free PMC article.

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