Jiang L - Search Results

1

Analysis of LDLR variants from homozygous FH patients carrying multiple mutations in the LDLR gene.

Jiang L, Benito-Vicente A, Tang L, Etxebarria A, Cui W, Uribe KB, Pan XD, Ostolaza H, Yang SW, Zhou YJ, Martin C, Wang LY. Jiang L, et al. Atherosclerosis. 2017 Aug;263:163-170. doi: 10.1016/j.atherosclerosis.2017.06.014. Epub 2017 Jun 8. Atherosclerosis. 2017. PMID: 28645073

2

Characterization of the unique Chinese W483X mutation in the low-density lipoprotein-receptor gene in young patients with homozygous familial hypercholesterolemia.

Jiang L, Sun LY, Pan XD, Chen PP, Tang L, Wang W, Zhao LM, Yang SW, Wang LY. Jiang L, et al. J Clin Lipidol. 2016 May-Jun;10(3):538-546.e5. doi: 10.1016/j.jacl.2015.12.016. Epub 2015 Dec 23. J Clin Lipidol. 2016. PMID: 27206941

3

The use of targeted exome sequencing in genetic diagnosis of young patients with severe hypercholesterolemia.

Jiang L, Wu WF, Sun LY, Chen PP, Wang W, Benito-Vicente A, Zhang F, Pan XD, Cui W, Yang SW, Zhou YJ, Martin C, Wang LY. Jiang L, et al. Sci Rep. 2016 Nov 10;6:36823. doi: 10.1038/srep36823. Sci Rep. 2016. PMID: 27830735 Free PMC article.

4

Novel Approaches for the Treatment of Familial Hypercholesterolemia: Current Status and Future Challenges.

Jiang L, Wang LY, Cheng XS. Jiang L, et al. J Atheroscler Thromb. 2018 Aug 1;25(8):665-673. doi: 10.5551/jat.43372. Epub 2018 Jun 13. J Atheroscler Thromb. 2018. PMID: 29899171 Free PMC article. Review.

5

Extremely severe aortic stenosis developed in a young female patient with underdiagnosis of homozygous familial hypercholesterolemia: An 8-year follow-up.

Tang L, Jiang L, Pan XD, Chen PP, Wang W, Jiao J, Yang Y, Chen J, Wang LY. Tang L, et al. Among authors: jiang l. Int J Cardiol. 2016 Mar 15;207:372-4. doi: 10.1016/j.ijcard.2016.01.087. Epub 2016 Jan 9. Int J Cardiol. 2016. PMID: 26820372 No abstract available.

6

Role of sEH R287Q in LDLR expression, LDL binding to LDLR and LDL internalization in BEL-7402 cells.

Tang L, Wang G, Jiang L, Chen P, Wang W, Chen J, Wang L. Tang L, et al. Among authors: jiang l. Gene. 2018 Aug 15;667:95-100. doi: 10.1016/j.gene.2018.04.038. Epub 2018 Apr 14. Gene. 2018. PMID: 29665449

7

Seven-year clinical follow-up of a Chinese homozygous familial hypercholesterolemia child with premature xanthomas and coronary artery disease--a need for early diagnosis and aggressive treatment.

Jiang L, Gao F, Hu LB, Sun LY, Pan XD, Lin J, Zhang HB, Yong Q, Wang Q, Yang Y, Wang CM, Yang SW, Zhang F, Wang LY. Jiang L, et al. Int J Cardiol. 2014 Nov 15;177(1):188-91. doi: 10.1016/j.ijcard.2014.09.058. Epub 2014 Sep 28. Int J Cardiol. 2014. PMID: 25499375 No abstract available.

8

Identification of the gene defect responsible for severe hypercholesterolaemia using whole-exome sequencing.

Sun LY, Zhang YB, Jiang L, Wan N, Wu WF, Pan XD, Yu J, Zhang F, Wang LY. Sun LY, et al. Among authors: jiang l. Sci Rep. 2015 Jun 16;5:11380. doi: 10.1038/srep11380. Sci Rep. 2015. PMID: 26077743 Free PMC article.

9

The distribution and characteristics of LDL receptor mutations in China: A systematic review.

Jiang L, Sun LY, Dai YF, Yang SW, Zhang F, Wang LY. Jiang L, et al. Sci Rep. 2015 Nov 26;5:17272. doi: 10.1038/srep17272. Sci Rep. 2015. PMID: 26608663 Free PMC article. Review.

10

A case of sitosterolemia misdiagnosed as familial hypercholesterolemia: A 4-year follow-up.

Wang W, Jiang L, Chen PP, Wu Y, Su PY, Wang LY. Wang W, et al. Among authors: jiang l. J Clin Lipidol. 2018 Jan-Feb;12(1):236-239. doi: 10.1016/j.jacl.2017.10.008. Epub 2017 Nov 11. J Clin Lipidol. 2018. PMID: 29246730

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