Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.
1 to 19 of 19  Show

Literature citations Results

Citation
Upregulation of miR-200b Inhibits Hepatocellular Carcinoma Cell Proliferation and Migration by Targeting HMGB3 Protein.

Wang L.K., Xie X.N., Song X.H., Su T., Chang X.L., Xu M., Liang B., Huang D.Y.

Technol. Cancer Res. Treat. 17:1533033818806475-1533033818806475(2018) · Mapped (3)

SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.

Li N.N., Mao X.Y., Chang X.L., Zhao D.M., Zhang J.H., Liao Q., Yu W.J., Tan E.K., Peng R.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 162B:452-456(2013) · Mapped (8)

[Role of connective tissue growth factor and alpha-smooth muscle actin in pulmonary fibrosis among acute paraquat poisoned rats].

Huang M., Qi X.J., Zhang P., Chang X.L., Wu Q., Zhou Z.J.

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 28:729-734(2010) · Mapped (7)

No association of four candidate genetic variants in MnSOD and SYNIII with Parkinson's disease in two Chinese populations.

Yu W.J., Li N.N., Tan E.K., Cheng L., Zhang J.H., Mao X.Y., Chang X.L., Zhao D.M., Liao Q., Peng R.

PLoS ONE 9:e88050-e88050(2014) · Mapped (21)

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.

Tan E.K., Peng R., Teo Y.Y., Tan L.C., Angeles D., Ho P., Chen M.L., Lin C.H., Mao X.Y., Chang X.L. et al.

Hum. Mutat. 31:561-568(2010) · Mapped (5)

MTHFR C677T variant reduces risk of sporadic Parkinson's disease in ethnic Chinese.

Liao Q., Li N.N., Mao X.Y., Chang X.L., Zhao D.M., Zhang J.H., Yu W.J., Tan E.K., Peng R.

Acta Neurol. Scand. 130:e30-4(2014) · Mapped (12)

Metallothionein 1 isoform gene expression induced by cadmium in human peripheral blood lymphocytes.

Chang X.L., Jin T.Y., Zhou Y.F.

Biomed. Environ. Sci. 19:104-109(2006)

MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese.

Li N.N., Tan E.K., Chang X.L., Mao X.Y., Zhao D.M., Zhang J.H., Liao Q., Peng R.

Acta Neurol. Scand. 128:136-139(2013) · Mapped (8)

GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.

Li N.N., Chang X.L., Mao X.Y., Zhang J.H., Zhao D.M., Tan E.K., Peng R.

Hum. Genet. 131:1089-1093(2012) · Mapped (10)

GSK3beta reduces risk of sporadic Parkinson's disease in ethnic Chinese.

Zhao D.M., Li N.N., Zhang J.H., Chang X.L., Mao X.Y., Liao Q., Tan E.K., Peng R.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 159B:718-721(2012) · Mapped (4)

Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease.

Li N.N., Tan E.K., Chang X.L., Mao X.Y., Zhang J.H., Zhao D.M., Liao Q., Yu W.J., Peng R.

PLoS ONE 8:e79211-e79211(2013) · Mapped (14)

Genetic analysis of LRRK2 A419V variant in ethnic Chinese.

Li N.N., Tan E.K., Chang X.L., Mao X.Y., Zhang J.H., Zhao D.M., Liao Q., Peng R.

Neurobiol. Aging 33:1849.e1-3(2012) · Mapped (5)

Functional parkin promoter polymorphism in Parkinson's disease: new data and meta-analysis.

Chang X.L., Mao X.Y., Li H.H., Zhang J.H., Li N.N., Burgunder J.M., Peng R., Tan E.K.

J. Neurol. Sci. 302:68-71(2011) · Mapped (11)

Distribution of EV71 receptors SCARB2 and PSGL-1 in human tissues.

Jiao X.Y., Guo L., Huang D.Y., Chang X.L., Qiu Q.C.

Virus Res. 190:40-52(2014) · Mapped (8)

[Changes of cytokine and nuclear factor-kappa B in acute paraquat poisoned rats].

Huang M., Zhang P., Chang X.L., Gu X.A., Wu Q., Zhou Z.J.

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 27:463-467(2009) · Mapped (2)

[Change of oxidative stress and nuclear factor-kappa B in acute paraquat poisoned rats].

Huang M., Zhang P., Chang X.L., Wu Q., Zhou Z.J.

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 27:457-462(2009) · Mapped (2)

ATP13A2 G2236A variant is rare in patients with early-onset Parkinson's disease and familial Parkinson's disease from Mainland China.

Mao X.Y., Burgunder J.M., Zhang Z.J., Chang X.L., Peng R., Burgunder J.M., Yang Y., Wang Y.C., Li T., Zhang Z.J.

Parkinsonism Relat. Disord. 16:235-236(2010) · Mapped (4)

Association of HMGCR polymorphism with late-onset Alzheimer's disease in Han Chinese.

Chang X.L., Tan L., Tan M.S., Wang H.F., Tan C.C., Zhang W., Zheng Z.J., Kong L.L., Wang Z.X., Jiang T. et al.

Oncotarget 7:22746-22751(2016) · Mapped (5)

Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China.

Mao X.Y., Burgunder J.M., Zhang Z.J., An X.K., Zhang J.H., Yang Y., Li T., Wang Y.C., Chang X.L., Peng R.

Neurosci. Lett. 469:256-259(2010) · Mapped (5)

1 to 19 of 19  Show
UniProt is an ELIXIR core data resource
Main funding by: National Institutes of Health

We'd like to inform you that we have updated our Privacy Notice to comply with Europe’s new General Data Protection Regulation (GDPR) that applies since 25 May 2018.

Do not show this banner again