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Ma, C., Tang, Z., Wang, K., Yang, X., and Tan, W. (2013). A novel sensitive and selective ligation-based ATP assay using a molecular beacon. Analyst. [Epub ahead of print]


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 Wu, G., Ouyang, X., Yang, B., Li, L., Wang, Z., Yi, W., Liu, C., Wang, P., Chiu, H.F.K., Lee, E., Xue, Z., Rosenheck, R., and Liu, Z. (2013). Long- and short-term inpatients with schizophrenia in China: Implications for community-based service development. Asia-Pacific Psychiatry, 5: E39-E46.


 Ma, Y.T., Luo, H., Guan, W.J., Zhang, H., Chen, C., Wang, Z., and Li, J.D. (2013). O-GlcNAcylation of BMAL1 regulates circadian rhythms in NIH3T3 fibroblasts. Biochem Biophys Res Commun, 431: 382-7.


Guan, W.J., Wang, J.L., Liu, Y.T., Ma, Y.T., Zhou, Y., Jiang, H., Shen, L., Guo, J.F., Xia, K., Li, J.D., and Tang, B.S. (2013). Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis. Biochem Biophys Res Commun, 430: 780-6.


Chen, G., Wang, J., Xu, X., Wu, X., Piao, R., and Siu, C.H. (2013). TgrC1 mediates cell-cell adhesion by interacting with TgrB1 via mutual IPT/TIG domains during development of Dictyostelium discoideum. Biochem J. [Epub ahead of print]


Hu, J., Liu, J., Xue, F., Halverson, G., Reid, M., Guo, A., Chen, L., Raza, A., Galili, N., Jaffray, J., Lane, J., Chasis, J.A., Taylor, N., Mohandas, N., and An, X. (2013). Isolation and functional characterization of human erythroblasts at distinct stages: implications for understanding of normal and disordered erythropoiesis in vivo.Blood. [Epub ahead of print]


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 Xu, X., Han, L., Duan, L., Zhao, Y., Yang, H., Zhou, B., Ma, R., Yuan, R., Zhou, H., and Liu, Z. (2013). Association between eIF3alpha polymorphism and severe toxicity caused by platinum-based chemotherapy in non-small cell lung cancer patients. Br J Clin Pharmacol, 75: 516-23.


 Xie, W., Xie, H., Liu, F., Li, W., Dan, J., Mei, Y., Dan, L., Xiao, X., Li, J., and Chen, X. (2013). Propranolol induces apoptosis of human umbilical vein endothelial cells through downregulation of CD147. Br J Dermatol, 168: 739-48.


 Yin, J.Y., Dong, Z.Z., Liu, R.Y., Chen, J., Liu, Z.Q., and Zhang, J.T. (2013). Translational regulation of RPA2 via internal ribosomal entry site and by eIF3a. Carcinogenesis. [Epub ahead of print]


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Peng, L., Wang, C., Chen, Z., Wang, J.L., Tang, B.S., and Jiang, H. (2013). Spinocerebellar Ataxia Type 13 is an Uncommon SCA Subtype in the Chinese Han Population. Int J Neurosci. [Epub ahead of print]


Huang, F., Tang, B., and Jiang, H. (2013). Optogenetic investigation of neuropsychiatric diseases. Int J Neurosci, 123: 7-16.


Lv, Z., Tang, B., Sun, Q., Yan, X., and Guo, J. (2013). Association study between vitamin d receptor gene polymorphisms and patients with Parkinson disease in Chinese Han population. Int J Neurosci, 123: 60-4.


Sun, Q.Y., Guo, J.F., Han, W.W., Zuo, X., Wang, L., Yao, L.Y., Pan, Q., Xia, K., Yan, X.X., and Tang, B.S. (2013). Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China. J Clin Neurosci, 20: 217-9.


 Liu, H., Wu, X., Dong, Z., Luo, Z., Zhao, Z., Xu, Y., and Zhang, J.T. (2013). Fatty acid synthase causes drug resistance by inhibiting TNF-alpha and ceramide production. J Lipid Res, 54: 776-85.


Xiong, Z., Lu, Y., Xue, J., Luo, S., Xu, X., Zhang, L., Peng, H., Li, W., Chen, D., Hu, Z., and Xia, K. (2013). Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports. J Med Case Rep, 7: 63.


Peng, J., Omran, A., Ashhab, M.U., Kong, H., Gan, N., He, F., and Yin, F. (2013). Expression Patterns of miR-124, miR-134, miR-132, and miR-21 in an Immature Rat Model and Children with Mesial Temporal Lobe Epilepsy. J Mol Neurosci. [Epub ahead of print]


Xu, X., Han, L., Yang, H., Duan, L., Zhou, B., Zhao, Y., Qu, J., Ma, R., Zhou, H., and Liu, Z. (2013). The A/G allele of eIF3a rs3740556 predicts platinum-based chemotherapy resistance in lung cancer patients. Lung Cancer,79: 65-72.


 Li, J., Li, Q.L., Chen, M.L., Xie, H.F., Li, Y.P., and Chen, X. (2013). Comparison of three problem-based learning conditions (real patients, digital and paper) with lecture-based learning in a dermatology course: A prospective randomized study from China. Med Teach, 35: e963-70.


Yi, J., Zhang, L., Tang, B., Han, W., Zhou, Y., Chen, Z., Jia, D., and Jiang, H. (2013). Sodium valproate alleviates neurodegeneration in SCA3/MJD via suppressing apoptosis and rescuing the hypoacetylation levels of histone H3 and H4. PLoS One, 8: e54792.


Zhou, Y.F., Liao, S.S., Luo, Y.Y., Tang, J.G., Wang, J.L., Lei, L.F., Chi, J.W., Du, J., Jiang, H., Xia, K., Tang, B.S., and Shen, L. (2013). SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity. PLoS One, 8: e54214.


Liang, D., Lv, W., Wang, H., Xu, L., Liu, J., Li, H., Hu, L., Peng, Y., and Wu, L. (2013). Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing. Prenat Diagn, [Epub ahead of print].


Li, M., Wu, X., Pan, Y., and Wang, J. (2013). hF-measure: A new measurement for evaluating clusters in protein-protein interaction networks. Proteomics, 13: 291-300.


Ou, J.J., Xu, Y., Chen, H.H., Fan, X., Gao, K., Wang, J., Guo, X.F., Wu, R.R., and Zhao, J.P. (2013). Comparison of metabolic effects of ziprasidone versus olanzapine treatment in patients with first-episode schizophrenia.Psychopharmacology (Berl), 225: 627-35.


 Xu, A., Li, Y., Zhu, L., Tian, T., Hao, J., Zhao, J., and Zhang, Q. (2013). Inhibition of endometrial fundocervical wave by phloroglucinol and the outcome of in vitro fertilization. Reprod Biol, 13: 88-91.


Hu, T., Long, M., Yuan, D., Zhu, Z., Huang, Y., and Huang, S. (2013). The genetic equidistance result: misreading by the molecular clock and neutral theory and reinterpretation nearly half of a century later. Sci China Life Sci, 56: 254-61.


 Hu, Y.J., Liu, X.H., Long, P.P., Xiao, D., Cun, J.T., Li, Z., Xue, J.F., Wu, Y., Luo, S., Wu, L.Q., and Liang, D.S. (2013). Nonviral Gene Targeting at rDNA Locus of Human Mesenchymal Stem Cells. BioMed Res Int, 2013: 10, http://dx.doi.org/10.1155/2013/135189 .


Chen, Z., Wang, J.L., Tang, B.S., Sun, Z.F., Shi, Y.T., Shen, L., Lei, L.F., Wei, X.M., Xiao, J.J., Hu, Z.M., Pan, Q., Xia, K., Zhang, Q.Y., Dai, M.Z., Liu, Y., Ashizawa, T., and Jiang, H. (2013). Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders. Neurobiology of Aging, http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.029: (Epub ahead of Print).


 Jia, D., Tang, B., Shi, Y., Wang, J., Sun, Z., Chen, Z., Zhang, L., Xia, K., and Jiang, H. (2013). A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease. J Clin Neurosci, 20: 842-7.


Shi, Y.T., Tang, B.S., and Jiang, H. (2013). Kleine-Levin syndrome with brain atrophy. J Clin Neurosci,10.1016/j.jocn.2012.07.019: [Epub ahead of print]


Sun, Z., Yang, X., Ye, H., Zhou, G., and Jiang, H. (2012). Delayed encephalopathy with movement disorder and catatonia: A rare combination after wasp stings. Clin Neurol Neurosurg, 10.1016/j.clineuro.2012.11.030: [Epub ahead of print]


Li, Z., Liu, J., Li, H., Peng, Y., Lv, W., Long, Z., Liang, D., and Wu, L. (2013). Phenotypic expansion of the interstitial 16p13.3 duplication: A case report and review of the literature. Gene. 2013 Sep 12. pii: S0378-1119(13)01180-3. doi: 10.1016/j.gene.2013.09.006. [Epub ahead of print]


Deng, M., He, W., Tan, Y., Han, H., Hu, X., Xia, K., Zhang, Z., and Yan, R. (2013). Increased expression of reticulon 3 in neurons leads to reduced axonal transport of beta-site amyloid precursor protein cleaving enzyme 1. J Biol Chem. 2013 Sep 4. [Epub ahead of print]


Yang, Y., Tian, D., Lee, J., Zeng, J., Zhang, H., Chen, S., Guo, H., Xiong, Z., Xia, K., Hu, Z., and Luo, J. (2013). Clinical and Genetic Identification of a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa.Ophthalmic Genet, 10.3109/13816810.2013.809458. 2013 Jul 8. [Epub ahead of print]


Guo, H., Tong, P., Peng, Y., Wang, T., Liu, Y., Chen, J., Li, Y., Tian, Q., Hu, Y., Zheng, Y., Xiao, L., Xiong, W., Pan, Q., Hu, Z., and Xia, K. (2013). Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract. Clin Genet, 10.1111/cge.12309. [Epub ahead of print]


Xia, K., Guo, H., Hu, Z., Xun, G., Zuo, L., Peng, Y., Wang, K., He, Y., Xiong, Z., Sun, L., Pan, Q., Long, Z., Zou, X., Li, X., Li, W., Xu, X., Lu, L., Liu, Y., Hu, Y., Tian, D., Long, L., Ou, J., Zhang, L., Pan, Y., Chen, J., Peng, H., Liu, Q., Luo, X., Su, W., Wu, L., Liang, D., Dai, H., Yan, X., Feng, Y., Tang, B., Li, J., Miedzybrodzka, Z., Xia, J., Zhang, Z., Zhang, X., St Clair, D., Zhao, J., and Zhang, F. (2013). Common genetic variants on 1p13.2 associate with risk of autism. Mol Psychiatry, 10.1038/mp.2013.146. [Epub ahead of print]


Ma, C., Fang, H., Wang, K., Xia, K., Chen, H., He, H., and Zeng, W. (2013). Simultaneous detection of kinase and phosphatase activities of polynucleotide kinase using molecular beacon probes. Analytical Biochemistry, 443: 166-168.


Jiang, Y., Zhang, M., He, H., Chen, J., Zeng, H., Li, J., and Duan, R. (2013). MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm. BMC Medical Genomics, 6: 36.


Li, J., Huang, W., Luo, S., Lin, Y., and Duan, R. (2013). Attitude of Medical School Students in China Towards Genetic Testing and Counseling Issues in FXS. J Genet Counsel, 22: 733-740.


 Lin, Y., Tang, C., He, H., and Duan, R. (2013). Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration. PLoS One, 8: e62572.


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