14
results
for author:"Chen R.-S."
in Literature Citations
| Emodin enhances gefitinib-induced cytotoxicity via Rad51 downregulation and ERK1/2 inactivation. Chen R.S., Jhan J.Y., Su Y.J., Lee W.T., Cheng C.M., Ciou S.C., Lin S.T., Chuang S.M., Ko J.C., Lin Y.W. Exp. Cell Res. 315:2658-2672(2009) · Mapped (13) |
| A longitudinal study of Taiwanese sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndrome. Lai S.C., Chen R.S., Wu Chou Y.H., Chang H.C., Kao L.Y., Huang Y.Z., Weng Y.H., Chen J.K., Hwu W.L., Lu C.S. Eur. J. Neurol. 16:912-919(2009) · Mapped (8) |
| Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese. Tan E.K., Lu C.S., Peng R., Teo Y.Y., Wu-Chou Y.H., Chen R.S., Weng Y.H., Chen C.M., Fung H.C., Tan L.C. et al. Neurobiol. Aging 0:0-0(2009) · Mapped (4) |
| Disruption of xCT inhibits cancer cell metastasis via the caveolin-1/beta-catenin pathway. Chen R.S., Song Y.M., Zhou Z.Y., Tong T., Li Y., Fu M., Guo X.L., Dong L.J., He X., Qiao H.X. et al. Oncogene 28:599-609(2009) · Mapped (15) |
| The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population. Lu C.S., Wu-Chou Y.H., van Doeselaar M., Simons E.J., Chang H.C., Breedveld G.J., Di Fonzo A., Chen R.S., Weng Y.H., Lai S.C. et al. Neurogenetics 9:271-276(2008) · Mapped (4) |
| Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan. Lu C.S., Chang H.C., Weng Y.H., Chen R.S., Bonifati V., Wu-Chou Y.H. Parkinsonism Relat. Disord. 14:393-396(2008) · Mapped (4) |
| JNK activation mediates the apoptosis of xCT-deficient cells. Qiao H.X., Hao C.J., Li Y., He X., Chen R.S., Cui J., Xu Z.H., Li W. Biochem. Biophys. Res. Commun. 370:584-588(2008) · Mapped (9) |
| PINK1 mutation in Taiwanese early-onset parkinsonism : clinical, genetic, and dopamine transporter studies. Weng Y.H., Chou Y.H., Wu W.S., Lin K.J., Chang H.C., Yen T.C., Chen R.S., Wey S.P., Lu C.S. J. Neurol. 254:1347-1355(2007) · Mapped (1) |
| A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Di Fonzo A., Wu-Chou Y.H., Lu C.S., van Doeselaar M., Simons E.J., Rohe C.F., Chang H.C., Chen R.S., Weng Y.H., Vanacore N. et al. Neurogenetics 7:133-138(2006) · Mapped (4) |
| DYT1 mutation in a cohort of Taiwanese primary dystonias. Lin Y.W., Chang H.C., Chou Y.H., Chen R.S., Hsu W.C., Wu W.S., Weng Y.H., Lu C.S. Parkinsonism Relat. Disord. 12:15-19(2006) · Mapped (3) |
| Taiwanese cases of SCA2 are derived from a single founder. Momeni P., Lu C.S., Chou Y.H., Chang H.C., Chen R.S., Chen C.C., Hsu J.T., Singleton A., Hardy J. Mov. Disord. 20:1633-1636(2005) · Mapped (4) |
| Genome-based analysis of virulence genes in a non-biofilm-forming Staphylococcus epidermidis strain (ATCC 12228). Zhang Y.-Q., Ren S.-X., Li H.-L., Wang Y.-X., Fu G., Yang J., Qin Z.-Q., Miao Y.-G., Wang W.-Y., Chen R.-S. et al. Mol. Microbiol. 49:1577-1593(2003) · UniProtKB (2,461) |
| Molecular cloning, characterization, chromosomal assignment, genomic organization and verification of SFRS12(SRrp508), a novel member of human SR protein superfamily and a human homolog of rat SRrp86. Zhang D.L., Sun X.J., Ling L.J., Chen R.S., Ma D.L. Yi Chuan Xue Bao 29:377-383(2002) · UniProtKB (1) |
| Specificity and efficiency of Cre-mediated recombination in Emx1-Cre knock-in mice. Guo H., Hong S., Jin X.L., Chen R.S., Avasthi P.P., Tu Y.T., Ivanco T.L., Li Y. Biochem. Biophys. Res. Commun. 273:661-665(2000) · Mapped (1) |
