Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 55

1.

Enhanced bonding strength between lithium disilicate ceramics and resin cement by multiple surface treatments after thermal cycling.

Li R, Ma SQ, Zang CC, Zhang WY, Liu ZH, Sun YC, Feng YY.

PLoS One. 2019 Jul 25;14(7):e0220466. doi: 10.1371/journal.pone.0220466. eCollection 2019.

2.

Genetic diversity and population structure analysis in Perilla crop and their weedy types from northern and southern areas of China based on simple sequence repeat (SSRs).

Ma SJ, Sa KJ, Hong TK, Lee JK.

Genes Genomics. 2019 Mar;41(3):267-281. doi: 10.1007/s13258-018-0756-3. Epub 2018 Nov 14.

PMID:
30426456
3.

[Analysis of NF1 gene mutations among eleven sporadic patients with neurofibromatosis type 1].

Peng C, Ma S, Tang X, Yang J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):480-483. doi: 10.3760/cma.j.issn.1003-9406.2018.04.004. Chinese.

PMID:
30098238
4.

Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.

Zhang L, Sun Z, Zhao P, Huang L, Xu M, Yang Y, Chen X, Lu F, Zhang X, Wang H, Zhang S, Liu W, Jiang Z, Ma S, Chen R, Zhao C, Yang Z, Sui R, Zhu X.

Hum Mol Genet. 2018 Dec 1;27(23):4157-4168. doi: 10.1093/hmg/ddy281.

PMID:
30085091
5.

A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridia.

Liu X, Wu Y, Miao Z, Zhang H, Gong B, Zhu X, Huang L, Shi Y, Hao F, Ma S, Lin H, Wang L, Yang Z.

Ophthalmic Genet. 2018 Aug;39(4):428-436. doi: 10.1080/13816810.2018.1466336. Epub 2018 Jun 14.

PMID:
29902091
6.

Accuracy and stability improvement for meat species identification using multiplicative scatter correction and laser-induced breakdown spectroscopy.

Chu YW, Tang SS, Ma SX, Ma YY, Hao ZQ, Guo YM, Guo LB, Lu YF, Zeng XY.

Opt Express. 2018 Apr 16;26(8):10119-10127. doi: 10.1364/OE.26.010119.

PMID:
29715952
7.

Amycolamycins A and B, Two Enediyne-Derived Compounds from a Locust-Associated Actinomycete.

Ma SY, Xiao YS, Zhang B, Shao FL, Guo ZK, Zhang JJ, Jiao RH, Sun Y, Xu Q, Tan RX, Ge HM.

Org Lett. 2017 Nov 17;19(22):6208-6211. doi: 10.1021/acs.orglett.7b03113. Epub 2017 Nov 1.

PMID:
29090939
8.

Association study of candidate genes for susceptibility to Kashin-Beck disease in a Tibetan population.

Tai Z, Huang L, Lu F, Shi Y, Ma S, Cheng J, Lin H, Liu X, Li Y, Yang Z.

BMC Med Genet. 2017 Jun 26;18(1):69. doi: 10.1186/s12881-017-0423-6.

9.

Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families.

Huang L, Zhang Q, Huang X, Qu C, Ma S, Mao Y, Yang J, Li Y, Li Y, Tan C, Zhao P, Yang Z.

Sci Rep. 2017 May 16;7(1):1948. doi: 10.1038/s41598-017-00963-6.

10.

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy.

Huang L, Zhang H, Cheng CY, Wen F, Tam PO, Zhao P, Chen H, Li Z, Chen L, Tai Z, Yamashiro K, Deng S, Zhu X, Chen W, Cai L, Lu F, Li Y, Cheung CM, Shi Y, Miyake M, Lin Y, Gong B, Liu X, Sim KS, Yang J, Mori K, Zhang X, Cackett PD, Tsujikawa M, Nishida K, Hao F, Ma S, Lin H, Cheng J, Fei P, Lai TY, Tang S, Laude A, Inoue S, Yeo IY, Sakurada Y, Zhou Y, Iijima H, Honda S, Lei C, Zhang L, Zheng H, Jiang D, Zhu X, Wong TY, Khor CC, Pang CP, Yoshimura N, Yang Z.

Nat Genet. 2016 Jun;48(6):640-7. doi: 10.1038/ng.3546. Epub 2016 Apr 18.

PMID:
27089177
11.

Breast Tumor Kinase (Brk/PTK6) Is Induced by HIF, Glucocorticoid Receptor, and PELP1-Mediated Stress Signaling in Triple-Negative Breast Cancer.

Regan Anderson TM, Ma SH, Raj GV, Cidlowski JA, Helle TM, Knutson TP, Krutilina RI, Seagroves TN, Lange CA.

Cancer Res. 2016 Mar 15;76(6):1653-63. doi: 10.1158/0008-5472.CAN-15-2510. Epub 2016 Jan 29.

12.

Association study of polymorphisms in FOXO3, AKT1 and IGF-2R genes with human longevity in a Han Chinese population.

Li N, Luo H, Liu X, Ma S, Lin H, Chen R, Hao F, Zhang D.

Oncotarget. 2016 Jan 5;7(1):23-32. doi: 10.18632/oncotarget.6627.

13.

Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy.

Fei P, Zhu X, Jiang Z, Ma S, Li J, Zhang Q, Zhou Y, Xu Y, Tai Z, Zhang L, Huang L, Yang Z, Zhao P, Zhu X.

Sci Rep. 2015 Nov 4;5:16120. doi: 10.1038/srep16120.

14.

KDM4/JMJD2 Histone Demethylase Inhibitors Block Prostate Tumor Growth by Suppressing the Expression of AR and BMYB-Regulated Genes.

Duan L, Rai G, Roggero C, Zhang QJ, Wei Q, Ma SH, Zhou Y, Santoyo J, Martinez ED, Xiao G, Raj GV, Jadhav A, Simeonov A, Maloney DJ, Rizo J, Hsieh JT, Liu ZP.

Chem Biol. 2015 Sep 17;22(9):1185-96. doi: 10.1016/j.chembiol.2015.08.007. Epub 2015 Sep 10.

15.

Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter.

Wang J, Sun C, Gerdes N, Liu C, Liao M, Liu J, Shi MA, He A, Zhou Y, Sukhova GK, Chen H, Cheng XW, Kuzuya M, Murohara T, Zhang J, Cheng X, Jiang M, Shull GE, Rogers S, Yang CL, Ke Q, Jelen S, Bindels R, Ellison DH, Jarolim P, Libby P, Shi GP.

Nat Med. 2015 Jul;21(7):820-6. doi: 10.1038/nm.3890. Epub 2015 Jun 22.

16.

Altered intrinsic brain activity in patients with familial cortical myoclonic tremor and epilepsy: an amplitude of low-frequency fluctuation study.

Wang P, Luo C, Dong L, Bin Y, Ma S, Yao D, Guo F, Yang Z.

J Neurol Sci. 2015 Apr 15;351(1-2):133-139. doi: 10.1016/j.jns.2015.03.005. Epub 2015 Mar 10.

PMID:
25796300
17.

Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.

Xu Y, Huang L, Li J, Zhang Q, Fei P, Zhu X, Tai Z, Ma S, Gong B, Li Y, Zang W, Zhu X, Zhao P, Yang Z.

Mol Vis. 2014 Sep 20;20:1296-306. eCollection 2014.

18.

Genetic association study between INSULIN pathway related genes and high myopia in a Han Chinese population.

Liu X, Wang P, Qu C, Zheng H, Gong B, Ma S, Lin H, Cheng J, Yang Z, Lu F, Shi Y.

Mol Biol Rep. 2015 Jan;42(1):303-10. doi: 10.1007/s11033-014-3773-6. Epub 2014 Sep 30.

PMID:
25266237
19.

IgE actions on CD4+ T cells, mast cells, and macrophages participate in the pathogenesis of experimental abdominal aortic aneurysms.

Wang J, Lindholt JS, Sukhova GK, Shi MA, Xia M, Chen H, Xiang M, He A, Wang Y, Xiong N, Libby P, Wang JA, Shi GP.

EMBO Mol Med. 2014 Jul;6(7):952-69. doi: 10.15252/emmm.201303811.

20.

Genetic variants in PVRL2-TOMM40-APOE region are associated with human longevity in a Han Chinese population.

Lu F, Guan H, Gong B, Liu X, Zhu R, Wang Y, Qian J, Zhou T, Lan X, Wang P, Lin Y, Ma S, Lin H, Zhu X, Chen R, Zhu X, Shi Y, Yang Z.

PLoS One. 2014 Jun 12;9(6):e99580. doi: 10.1371/journal.pone.0099580. eCollection 2014.

21.

Identification of two novel LRP5 mutations in families with familial exudative vitreoretinopathy.

Fei P, Zhang Q, Huang L, Xu Y, Zhu X, Tai Z, Gong B, Ma S, Yao Q, Li J, Zhao P, Yang Z.

Mol Vis. 2014 Mar 29;20:395-409. eCollection 2014.

22.

Estrogen receptor-positive breast cancer molecular signatures and therapeutic potentials (Review).

Zhang MH, Man HT, Zhao XD, Dong N, Ma SL.

Biomed Rep. 2014 Jan;2(1):41-52. Epub 2013 Oct 25.

23.

A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degeneration.

Lu F, Huang L, Lei C, Sha G, Zheng H, Liu X, Yang J, Shi Y, Lin Y, Gong B, Zhu X, Ma S, Qiao L, Lin H, Cheng J, Yang Z.

PLoS One. 2013 Nov 11;8(11):e78274. doi: 10.1371/journal.pone.0078274. eCollection 2013.

24.

Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan population.

Huang L, Shi Y, Lu F, Zheng H, Liu X, Gong B, Yang J, Lin Y, Cheng J, Ma S, Lin H, Yang Z.

PLoS One. 2013 Aug 23;8(8):e71411. doi: 10.1371/journal.pone.0071411. eCollection 2013.

25.

A genetic variant in the SKIV2L gene is significantly associated with age-related macular degeneration in a Han Chinese population.

Lu F, Shi Y, Qu C, Zhao P, Liu X, Gong B, Ma S, Zhou Y, Zhang Q, Fei P, Xu Y, Hu J, Fan Y, Lin Y, Zhu X, Yang Z.

Invest Ophthalmol Vis Sci. 2013 Apr 26;54(4):2911-7. doi: 10.1167/iovs.12-11381.

PMID:
23557739
26.

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Shi Y, Gong B, Chen L, Zuo X, Liu X, Tam PO, Zhou X, Zhao P, Lu F, Qu J, Sun L, Zhao F, Chen H, Zhang Y, Zhang D, Lin Y, Lin H, Ma S, Cheng J, Yang J, Huang L, Zhang M, Zhang X, Pang CP, Yang Z.

Hum Mol Genet. 2013 Jun 1;22(11):2325-33. doi: 10.1093/hmg/ddt066. Epub 2013 Feb 12.

PMID:
23406873
27.

Evaluation of MMP2 as a candidate gene for high myopia.

Gong B, Liu X, Zhang D, Wang P, Huang L, Lin Y, Lu F, Ma S, Cheng J, Chen R, Li X, Lin H, Zeng G, Zhu X, Hu J, Yang Z, Shi Y.

Mol Vis. 2013;19:121-7. Epub 2013 Jan 28.

28.

Chemokine (C-C motif) receptor 2 mediates mast cell migration to abdominal aortic aneurysm lesions in mice.

Zhang J, Chen H, Liu L, Sun J, Shi MA, Sukhova GK, Shi GP.

Cardiovasc Res. 2012 Dec 1;96(3):543-51. doi: 10.1093/cvr/cvs262. Epub 2012 Aug 7.

29.

Alternative surgical strategies in patients with sporadic medullary thyroid carcinoma: Long-term follow-up.

Ma SH, Liu QJ, Zhang YC, Yang R.

Oncol Lett. 2011 Sep 1;2(5):975-980. Epub 2011 Jul 5.

30.

The genetic variants at the HLA-DRB1 gene are associated with primary IgA nephropathy in Han Chinese.

Jiyun Y, Guisen L, Li Z, Yi S, Jicheng L, Fang L, Xiaoqi L, Shi M, Cheng J, Ying L, Haiyan W, Li W, Hong Z, Zhenglin Y.

BMC Med Genet. 2012 May 14;13:33. doi: 10.1186/1471-2350-13-33.

31.

Different roles of mast cells in obesity and diabetes: lessons from experimental animals and humans.

Shi MA, Shi GP.

Front Immunol. 2012 Jan 25;3:7. doi: 10.3389/fimmu.2012.00007. eCollection 2012.

32.

An association study of the COL1A1 gene and high myopia in a Han Chinese population.

Zhang D, Shi Y, Gong B, He F, Lu F, Lin H, Wu Z, Cheng J, Chen B, Liao S, Ma S, Hu J, Yang Z.

Mol Vis. 2011;17:3379-83. Epub 2011 Dec 24.

33.

miRNAs in breast cancer tumorigenesis (Review).

Zhang ZJ, Ma SL.

Oncol Rep. 2012 Apr;27(4):903-10. doi: 10.3892/or.2011.1611. Epub 2011 Dec 23. Review.

34.

Genetic variants in the HLA-DRB1 gene are associated with Kashin-Beck disease in the Tibetan population.

Shi Y, Lu F, Liu X, Wang Y, Huang L, Liu X, Long W, Lv B, Zhang K, Ma S, Lin H, Cheng J, Zhou B, Hu M, Deng J, Zhu J, Hao P, Yang X, Zeng M, Wang X, Shen S, Yang Z.

Arthritis Rheum. 2011 Nov;63(11):3408-16. doi: 10.1002/art.30526.

35.

Exome sequencing identifies ZNF644 mutations in high myopia.

Shi Y, Li Y, Zhang D, Zhang H, Li Y, Lu F, Liu X, He F, Gong B, Cai L, Li R, Liao S, Ma S, Lin H, Cheng J, Zheng H, Shan Y, Chen B, Hu J, Jin X, Zhao P, Chen Y, Zhang Y, Lin Y, Li X, Fan Y, Yang H, Wang J, Yang Z.

PLoS Genet. 2011 Jun;7(6):e1002084. doi: 10.1371/journal.pgen.1002084. Epub 2011 Jun 9.

36.

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Shi Y, Qu J, Zhang D, Zhao P, Zhang Q, Tam POS, Sun L, Zuo X, Zhou X, Xiao X, Hu J, Li Y, Cai L, Liu X, Lu F, Liao S, Chen B, He F, Gong B, Lin H, Ma S, Cheng J, Zhang J, Chen Y, Zhao F, Yang X, Chen Y, Yang C, Lam DSC, Li X, Shi F, Wu Z, Lin Y, Yang J, Li S, Ren Y, Xue A, Fan Y, Li D, Pang CP, Zhang X, Yang Z.

Am J Hum Genet. 2011 Jun 10;88(6):805-813. doi: 10.1016/j.ajhg.2011.04.022. Epub 2011 Jun 6.

37.

Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.

Zhu J, Zhang D, Wu F, He F, Liu X, Wu L, Zhou B, Liu J, Lu F, Liu J, Luo R, Long W, Yang M, Ma S, Wu X, Shi Y, Wu T, Lin Y, Yang J, Yuan G, Yang Z.

BMC Med Genet. 2011 Apr 14;12:53. doi: 10.1186/1471-2350-12-53.

38.

Cystatin C deficiency promotes epidermal dysplasia in K14-HPV16 transgenic mice.

Yu W, Liu J, Shi MA, Wang J, Xiang M, Kitamoto S, Wang B, Sukhova GK, Murphy GF, Orasanu G, Grubb A, Shi GP.

PLoS One. 2010 Nov 15;5(11):e13973. doi: 10.1371/journal.pone.0013973.

39.

Intracellular delivery strategies for microRNAs and potential therapies for human cardiovascular diseases.

Shi MA, Shi GP.

Sci Signal. 2010 Nov 2;3(146):pe40. doi: 10.1126/scisignal.3146pe40.

40.

Infection control and the burden of tuberculosis infection and disease in health care workers in china: a cross-sectional study.

He GX, van denHof S, van der Werf MJ, Wang GJ, Ma SW, Zhao DY, Hu YL, Yu SC, Borgdorff MW.

BMC Infect Dis. 2010 Oct 28;10:313. doi: 10.1186/1471-2334-10-313.

41.

Mutation in connexin 32 causes Charcot-Marie-Tooth disease in a large Chinese family.

Guo F, Shi Y, Lin Y, Liu X, Liu B, Liu Y, Yang Y, Lu F, Ma S, Yang Z.

Muscle Nerve. 2010 Nov;42(5):715-21. doi: 10.1002/mus.21756.

PMID:
20730878
42.

Renin-angiotensin system gene polymorphisms in children with Henoch-Schönlein purpura in West China.

Desong Liu, Fang Lu, Songhui Zhai, Liu Wei, Shi Ma, Xiuying Chen, Liqun Dong, Yannan Guo, Jin Wu, Zheng Wang.

J Renin Angiotensin Aldosterone Syst. 2010 Dec;11(4):248-55. doi: 10.1177/1470320310374214. Epub 2010 Aug 11.

PMID:
20702504
43.

Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.

Lin Y, Li P, Cai L, Zhang B, Tang X, Zhang X, Li Y, Xian Y, Yang Y, Wang L, Lu F, Liu X, Rao S, Chen M, Ma S, Shi Y, Bao M, Wu J, Yang Y, Yang J, Yang Z.

BMC Med Genet. 2010 Jun 15;11:97. doi: 10.1186/1471-2350-11-97.

44.

[Association study on single nucleotide polymorphisms in HTRA1 gene and rheumatoid arthritis].

Luo RJ, Zhang DD, Zhu J, Zhou B, Ma S, Lu F, Liu J, Long WB, Yang ZL, Zhang CJ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Jun;27(3):305-9. doi: 10.3760/cma.j.issn.1003-9406.2010.0.015. Chinese.

PMID:
20533271
45.

Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a Han Chinese population.

Liu X, Zhao P, Tang S, Lu F, Hu J, Lei C, Yang X, Lin Y, Ma S, Yang J, Zhang D, Shi Y, Li T, Chen Y, Fan Y, Yang Z.

Retina. 2010 Sep;30(8):1177-84. doi: 10.1097/IAE.0b013e3181cea676.

PMID:
20523265
46.

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population.

Lu F, Zhao P, Fan Y, Tang S, Hu J, Liu X, Yang X, Chen Y, Li T, Lei C, Yang J, Lin Y, Ma S, Li C, Shi Y, Yang Z.

Mol Vis. 2010 Jan 10;16:1-6.

47.

[Linkage analysis of a family with familial hypertriglyceridemia].

Tang X, Lin Y, Liu B, Ma S, Yang Y, Yang ZL.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):499-503. doi: 10.3760/cma.j.issn.1003-9406.2009.05.004. Chinese.

PMID:
19806567
48.

[Disease gene screening of known loci in a Chinese family with autosomal dominant retinitis pigmentosa].

Liu W, Lu F, Qia LF, Sha ZQ, Liu XO, Ma S, Tang X, Chang JX, Yang ZL, Ye B.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):70-3. doi: 10.3760/cma.j.issn.1003-9406.2009.01.016. Chinese.

PMID:
19199256
49.

Deficiency and inhibition of cathepsin K reduce body weight gain and increase glucose metabolism in mice.

Yang M, Sun J, Zhang T, Liu J, Zhang J, Shi MA, Darakhshan F, Guerre-Millo M, Clement K, Gelb BD, Dolgnov G, Shi GP.

Arterioscler Thromb Vasc Biol. 2008 Dec;28(12):2202-8. doi: 10.1161/ATVBAHA.108.172320. Epub 2008 Sep 25.

50.

[The trend of cancer mortality from 1988 to 2005 in Kaifeng county, China].

Cui YL, Fu L, Geng ZX, Li HB, Ma S, Lü QJ, Lu WQ, Yang WX.

Zhonghua Yu Fang Yi Xue Za Zhi. 2007 Jun;41 Suppl:62-5. Chinese.

PMID:
17767860

Supplemental Content

Loading ...
Support Center