Lin J - Search Results

1

[The pathological changes of abdominal and peripheral arteries in familial hypercholesterolemia--the result of high-resolution color Doppler ultrasonography].

Yong Q, Sun H, Li ZA, Lin J, Wang LY. Yong Q, et al. Among authors: lin j. Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Apr;33(4):340-2. Zhonghua Xin Xue Guan Bing Za Zhi. 2005. PMID: 15932665 Chinese.

2

Analysis of low-density lipoprotein receptor gene mutations in a Chinese patient with clinically homozygous familial hypercholesterolemia.

Cao S, Wang L, Qin Y, Lin J, Wu B, Liu S, Pan X, Du L, Chen B. Cao S, et al. Among authors: lin j. Chin Med J (Engl). 2003 Oct;116(10):1535-8. Chin Med J (Engl). 2003. PMID: 14570618

3

[Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].

Lin J, Wang LY, Liu S, Pan XD, Du LP, Shi FR, Qin YW, Zhao Q, Guo HY. Lin J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):14-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767901 Chinese.

4

[Molecular basis of familial hypercholesterolemia-like phenotype heterogeneity].

Wang LY, Lin J, Liu S, Chen BS. Wang LY, et al. Among authors: lin j. Yi Chuan Xue Bao. 2005 Jul;32(7):770-7. Yi Chuan Xue Bao. 2005. PMID: 16078748 Review. Chinese.

5

TSC-36/FRP inhibits vascular smooth muscle cell proliferation and migration.

Liu S, Wang L, Wang W, Lin J, Han J, Sun H, Guo H, Sun R, Wu Q. Liu S, et al. Among authors: lin j. Exp Mol Pathol. 2006 Apr;80(2):132-40. doi: 10.1016/j.yexmp.2005.07.005. Epub 2005 Oct 26. Exp Mol Pathol. 2006. PMID: 16256108

6

Functional analysis of low-density lipoprotein receptor in homozygous familial hypercholesterolemia patients with novel 1439 C-->T mutation of low-density lipoprotein receptor gene.

Lin J, Wang LY, Liu S, Xia JH, Yong Q, Du LP, Pan XD, Xue H, Chen BS, Jiang ZS. Lin J, et al. Chin Med J (Engl). 2008 May 5;121(9):776-81. Chin Med J (Engl). 2008. PMID: 18701038

7

A novel mutation in proprotein convertase subtilisin/kexin type 9 gene leads to familial hypercholesterolemia in a Chinese family.

Lin J, Wang LY, Liu S, Wang XM, Yong Q, Yang Y, DU LP, Pan XD, Wang X, Jiang ZS. Lin J, et al. Chin Med J (Engl). 2010 May 5;123(9):1133-8. Chin Med J (Engl). 2010. PMID: 20529551

8

Evaluation of coronary flow velocity reserve in homozygous familial hypercholesterolemia by transthoracic Doppler echocardiography and dual-source computed tomography.

Yang Y, Zhang X, Li R, Ren H, Wang Z, Li Z, Lin J, Wang L, Yu W, Zhang Z. Yang Y, et al. Among authors: lin j. Ultrasound Med Biol. 2010 Oct;36(10):1756-61. doi: 10.1016/j.ultrasmedbio.2010.05.013. Ultrasound Med Biol. 2010. PMID: 20800956

9

Noninvasive evaluation of coronary flow velocity reserve in homozygous familial hypercholesterolemia by transthoracic Doppler echocardiography.

Zhang X, Yang Y, Li Z, Ren H, Lin J, Wang L. Zhang X, et al. Among authors: lin j. Echocardiography. 2010 Sep;27(8):985-9. doi: 10.1111/j.1540-8175.2010.01169.x. Echocardiography. 2010. PMID: 20849486

10

Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22.

Wang X, Li X, Zhang YB, Zhang F, Sun L, Lin J, Wang DM, Wang LY. Wang X, et al. Among authors: lin j. PLoS One. 2011;6(10):e24838. doi: 10.1371/journal.pone.0024838. Epub 2011 Oct 14. PLoS One. 2011. PMID: 22022364 Free PMC article.

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