Lu JY - Search Results

1

Association of a SLC30A8 genetic variant with monotherapy of repaglinide and rosiglitazone effect in newly diagnosed type 2 diabetes patients in China.

Jiang F, Li Q, Hu C, Zhang R, Wang CR, Yu WH, Lu JY, Tang SS, Bao YQ, Xiang KS, Jia WP. Jiang F, et al. Among authors: lu jy. Biomed Environ Sci. 2012 Feb;25(1):23-9. doi: 10.3967/0895-3988.2012.01.004. Biomed Environ Sci. 2012. PMID: 22424623 Free article. Clinical Trial.

2

Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.

Wang C, Hu C, Zhang R, Bao Y, Ma X, Lu J, Qin W, Shao X, Lu J, Xu J, Lu H, Xiang K, Jia W. Wang C, et al. Diabetes. 2009 Apr;58(4):1023-7. doi: 10.2337/db08-1064. Epub 2009 Jan 23. Diabetes. 2009. PMID: 19168595 Free PMC article.

3

Association of apelin genetic variants with type 2 diabetes and related clinical features in Chinese Hans.

Zhang R, Hu C, Wang CR, Ma XJ, Bao YQ, Xu J, Lu JY, Qin W, Xiang KS, Jia WP. Zhang R, et al. Among authors: lu jy. Chin Med J (Engl). 2009 Jun 5;122(11):1273-6. Chin Med J (Engl). 2009. PMID: 19567136

4

PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population.

Hu C, Zhang R, Wang C, Wang J, Ma X, Lu J, Qin W, Hou X, Wang C, Bao Y, Xiang K, Jia W. Hu C, et al. PLoS One. 2009 Oct 28;4(10):e7643. doi: 10.1371/journal.pone.0007643. PLoS One. 2009. PMID: 19862325 Free PMC article.

5

A variation in NOS1AP gene is associated with repaglinide efficacy on insulin resistance in type 2 diabetes of Chinese.

Qin W, Zhang R, Hu C, Wang CR, Lu JY, Yu WH, Bao YQ, Xiang KS; International Type 2 Diabetes 1q Consortium; Jia WP. Qin W, et al. Among authors: lu jy. Acta Pharmacol Sin. 2010 Apr;31(4):450-4. doi: 10.1038/aps.2010.25. Epub 2010 Mar 22. Acta Pharmacol Sin. 2010. PMID: 20305679 Free PMC article.

6

Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion.

Hu C, Zhang R, Wang C, Yu W, Lu J, Ma X, Wang J, Jiang F, Tang S, Bao Y, Xiang K, Jia W. Hu C, et al. PLoS One. 2010 Jul 23;5(7):e11761. doi: 10.1371/journal.pone.0011761. PLoS One. 2010. PMID: 20668700 Free PMC article.

7

Precise microdeletion detection of Prader-Willi Syndrome with array comparative genome hybridization.

Shao XY, Zhang R, Hu C, Wang CR, Lu JY, Qin W, Yu HY, Bao YQ, Cheng XB, Jia WP. Shao XY, et al. Among authors: lu jy. Biomed Environ Sci. 2010 Jun;23(3):194-8. doi: 10.1016/S0895-3988(10)60052-9. Biomed Environ Sci. 2010. PMID: 20708498

8

Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 are associated with glucose metabolism in the Chinese.

Hu C, Zhang R, Wang C, Wang J, Ma X, Hou X, Lu J, Yu W, Jiang F, Bao Y, Xiang K, Jia W. Hu C, et al. PLoS One. 2010 Nov 17;5(11):e15542. doi: 10.1371/journal.pone.0015542. PLoS One. 2010. PMID: 21103350 Free PMC article.

9

A common polymorphism of CYP4A11 is associated with blood pressure in a Chinese population.

Zhang R, Lu J, Hu C, Wang C, Yu W, Ma X, Bao Y, Xiang K, Guan Y, Jia W. Zhang R, et al. Hypertens Res. 2011 May;34(5):645-8. doi: 10.1038/hr.2011.8. Epub 2011 Feb 17. Hypertens Res. 2011. PMID: 21326303

10

Phenotypic heterogeneity in Chinese patients with hepatocyte nuclear factor-1β mutations.

Wang C, Zhang R, Lu J, Jiang F, Hu C, Zhou J, Liu F, Zhang F, Qin W, Li M, Ma X, Yan J, Bao Y, Xiang K, Jia W. Wang C, et al. Diabetes Res Clin Pract. 2012 Jan;95(1):119-24. doi: 10.1016/j.diabres.2011.10.007. Epub 2011 Nov 1. Diabetes Res Clin Pract. 2012. PMID: 22051731

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