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2015年发表论文

浏览:7691 来源:SKLMG
 

1.      Afrin, S., Huang, J. J. and Luo, Z. Y. (2015). JA-mediated transcriptional regulation of secondary metabolism in       medicinal plants. Chinese Sci Bull 60(12): 1062-1072.

2.      Chang, J., Zhao, L., Chen, C., Peng, Y., Xia, Y., Tang, G., Bai, T., Zhang, Y., Ma, R., Guo, R., Mei, L., Liang, D., Cao, Q. and Wu, L. (2015). Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23. Gene 569(1): 46-50.

3.      Che, X. Q., Tang, B. S., Wang, H. F., Yan, X. X., Jiang, H., Shen, L., Xu, Q., Wang, G. H., Zhang, H. N., Wang, C. Y. and Guo, J. F. (2015). The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80Q. Int J Neurosci 125(5): 390-394.

4.      Chen, S., Li, Z., He, Y., Zhang, F., Li, H., Liao, Y., Wei, Z., Wan, G., Xiang, X., Hu, M., Xia, K., Chen, X. and Tang, J. (2015). Elevated mitochondrial DNA copy number in peripheral blood cells is associated with childhood autism. BMC Psychiatry 15: 50.

5.      Chen, Y., Chen, C., Zhang, Z., Liu, C. C., Johnson, M. E., Espinoza, C. A., Edsall, L. E., Ren, B., Zhou, X. J., Grant, S. F., Wells, A. D. and Chen, L. (2015). DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions. Nucleic Acids Res 43(2): 1268-1282.

6.      Chen, Z., Ye, W., Long, Z., Ding, D., Peng, H., Hou, X., Qiu, R., Xia, K., Tang, B. and Jiang, H. (2015). Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective. PLoS One 10(10): e0139738.

7.      Du, R. F., Huang, H., Fan, L. L., Li, X. P., Xia, K. and Xiang, R. (2015). A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases. Ophthalmic Genet: 1-5.

8.      Edens, B. M., Ajroud-Driss, S., Ma, L. and Ma, Y. C. (2015). Molecular mechanisms and animal models of spinal muscular atrophy. BBA-Mol Basis Dis 1852(4): 685-692.

9.      Fan, L. L., Lin, M. J., Chen, Y. Q., Huang, H., Peng, D. Q., Xia, K., Zhao, S. P. and Xiang, R. (2015). Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia. Appl Biochem Biotechnol 176(1): 101-109.

10.   Gui, B., Yao, Z., Huang, Y., Mei, L., Li, Y., Liu, D., Liu, N., Xia, Y., Liang, D. and Wu, L. (2015). Morphometric analysis and developmental comparison of embryos from carriers with balanced chromosomal rearrangements in preimplantation genetic diagnosis cycles. Reprod Fertil Dev: doi: 10.1071/RD15093.

11.   Guo, H., Tong, P., Liu, Y., Xia, L., Wang, T., Tian, Q., Li, Y., Hu, Y., Zheng, Y., Jin, X., Xiong, W., Tang, B., Feng, Y., Li, J., Pan, Q., Hu, Z. and Xia, K. (2015). Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia. Genet Med 17(4): 300-306.

12.   Guo, J. F., Dong, X. L., Xu, Q., Li, N., Yan, X. X., Xia, K. and Tang, B. S. (2015). Exon dosage analysis of parkin gene in Chinese sporadic Parkinson's disease. Neurosci Lett 604: 47-51.

13.   Guo, J. F., He, S., Kang, J. F., Xu, Q., Hu, Y. C., Zhang, H. N., Wang, C. Y., Yan, X. X. and Tang, B. S. (2015). Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagiline. Int J Clin Exp Med 8(10): 18158-18164.

14.   Guo, J. F., Li, K., Yu, R. L., Sun, Q. Y., Wang, L., Yao, L. Y., Hu, Y. C., Lv, Z. Y., Luo, L. Z., Shen, L., Jiang, H., Yan, X. X., Pan, Q., Xia, K. and Tang, B. S. (2015). Polygenic determinants of Parkinson's disease in a Chinese population. Neurobiol Aging 36(4): 1765 e1761-1766.

15.   Guo, R., Zhu, G., Zhu, H., Ma, R., Peng, Y., Liang, D. and Wu, L. (2015). DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy. J Hum Genet 60(8): 435-442.

16.   Guo, T., Wang, X., Li, M., Yang, H., Li, L., Peng, F. and Zhan, X. (2015). Identification of Glioblastoma Phosphotyrosine-Containing Proteins with Two-Dimensional Western Blotting and Tandem Mass Spectrometry. Biomed Res Int 2015: 134050.

17.   He, F., Wang, X., Cai, X., Peng, H., Zhang, L., Zhu, T., Xia, K., Pan, Q. and Hu, Z. (2015). Novel missense mutation in the COL3A1 gene caused vascular Ehlers-Danlos syndrome in a Chinese family. J Dermatol 42(1): 95-96.

18.   Hou, X., Xu, J., Chen, Z., Li, G. and Jiang, H. (2015). Posterior reversible encephalopathy syndrome with involvement of the cervical cord and medulla: a case report. J Clin Diagn Res 9(1): CD01-02.

19.   Huang, F., Long, Z., Chen, Z., Li, J., Hu, Z., Qiu, R., Zhuang, W., Tang, B., Xia, K. and Jiang, H. (2015). Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China. PLoS One 10(6): e0129052.

20.   Huang, W., Xia, Q. P., Luo, S. Y., He, H., Zhu, T., Du, Q. and Duan, R. H. (2015). Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population. Mol Genet Genomic Med 3(3): 172-181.

21.   Huang, Y., Mei, L., Pan, Q., Tan, H., Quan, Y., Gui, B., Chang, J., Ma, R., Peng, Y., Yang, P., Liang, D. and Wu, L. (2015). Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets. Gene 565(1): 150-154.

22.   Kang, J., Tang, B., Li, K., Liu, Z., Yan, X. and Guo, J. (2015). Genetic analysis of P387L mutation in SLC18A2 gene in sporadic Parkinson's disease in Chinese Han population. 中南大学学报(医学版) 40(8): 825-828.

23.   Li, B., Liu, Y., Liu, Y., Guo, H., Hu, Z., Xia, K. and Jin, X. (2015). Identification of a GJA3 Mutation in a Large Family with Bilateral Congenital Cataract. DNA Cell Biol.

24.   Li, H., Zhang, Y., Wei, X., Peng, Y., Yang, P., Tan, H., Chen, C., Pan, Q., Liang, D. and Wu, L. (2015). Rare intracranial cholesterol deposition and a homozygous mutation of LDLR in a familial hypercholesterolemia patient. Gene 569(2): 313-317.

25.   Li, J., Cai, T., Jiang, Y., Chen, H., He, X., Chen, C., Li, X., Shao, Q., Ran, X., Li, Z., Xia, K., Liu, C., Sun, Z. S. and Wu, J. (2015). Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database. Mol Psychiatry: doi: 10.1038/mp.2015.1040.

26.   Li, J., Jiang, Y., Wang, T., Chen, H., Xie, Q., Shao, Q., Ran, X., Xia, K., Sun, Z. S. and Wu, J. (2015). mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing. J Med Genet 52(4): 275-281.

27.   Li, K., Tang, B. S., Liu, Z. H., Kang, J. F., Zhang, Y., Shen, L., Li, N., Yan, X. X., Xia, K. and Guo, J. F. (2015). LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population. Neurobiol Aging 36(10): 2908 e2911-2905.

28.   Li, K., Tang, B. S., Yang, N. N., Kang, J. F., Liu, Z. H., Liu, R. Q., Yan, X. X., Shen, L. and Guo, J. F. (2015). Association study between SMPD1 p.L302P and sporadic Parkinson's disease in ethnic Chinese population. Int J Clin Exp Med 8(8): 13869-13873.

29.   Li, X., Hu, Z., Liu, L., Xie, Y., Zhan, Y., Zi, X., Wang, J., Wu, L., Xia, K., Tang, B. and Zhang, R. (2015). A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy. Neurology 84(24): 2430-2437.

30.   Li, Z., Guo, X., Wu, Y., Li, S., Yan, J., Peng, L., Xiao, Z., Wang, S., Deng, Z., Dai, L., Yi, W., Xia, K., Tang, L. and Wang, J. (2015). Methylation profiling of 48 candidate genes in tumor and matched normal tissues from breast cancer patients. Breast Cancer Res Treat 149(3): 767-779.

31.   Li, Z., He, Y., Tang, J., Zong, X., Hu, M. and Chen, X. (2015). Molecular imaging of striatal dopamine transporters in major depression--a meta-analysis. J Affect Disord 174: 137-143.

32.   Li, Z., Hu, M., Zong, X., He, Y., Wang, D., Dai, L., Dong, M., Zhou, J., Cao, H., Lv, L., Chen, X. and Tang, J. (2015). Association of telomere length and mitochondrial DNA copy number with risperidone treatment response in first-episode antipsychotic-naive schizophrenia. Sci Rep 5: 18553.

33.   Liao, X., Luo, Y., Zhan, Z., Du, J., Hu, Z., Wang, J., Guo, J., Yan, X., Pan, Q., Xia, K., Tang, B. and Shen, L. (2015). SPG35 contributes to the second common subtype of AR-HSP in China: frequency analysis and functional characterization of FA2H gene mutations. Clin Genet 87(1): 85-89.

34.   Lin, Y., He, H., Luo, Y., Zhu, T. and Duan, R. (2015). Inhibition of transglutaminase exacerbates polyglutamine-induced neurotoxicity by increasing the aggregation of mutant ataxin-3 in an SCA3 Drosophila model. Neurotox Res 27(3): 1-9.

35.   Liu, C. and Chung, M. (2015). Genetics and epigenetics of circadian rhythms and their potential roles in neuropsychiatric disorders. Neurosci Bull 31(1): 141-159.

36.   Liu, C., Saffen, D., Schulze, T. G., Burmeister, M., Sham, P. C., Yao, Y. G., Kuo, P. H., Chen, C., An, Y., Dai, J., Yue, W., Li, M. X., Xue, H., Su, B., Chen, L., Shi, Y., Qiao, M., Liu, T., Xia, K. and Chan, R. C. (2015). Psychiatric genetics in China: achievements and challenges. Mol Psychiatry: doi: 10.1038/mp.2015.1095.

37.   Liu, J., Han, X. and An, X. (2015). Novel methods for studying normal and disordered erythropoiesis. Sci China Life Sci 58(12): 1270-1275.

38.   Liu, Q., Wan, W., Liu, Y., Liu, Y., Hu, Z., Guo, H., Xia, K. and Jin, X. (2015). A novel PAX6 deletion in a Chinese family with congenital aniridia. Gene 563(1): 41-44.

39.   Liu, R., Xie, H., Luo, C., Chen, Z., Zhou, X., Xia, K., Chen, X., Zhou, M., Cao, P., Cao, K. and Zhou, J. (2015). Identification of FLOT2 as a novel target for microRNA-34a in melanoma. J Cancer Res Clin Oncol 141(6): 993-1006.

40.   Liu, X. S., Genet, M. D., Haines, J. E., Mehanna, E. K., Wu, S., Chen, H. I., Chen, Y., Qureshi, A. A., Han, J., Chen, X., Fisher, D. E., Pandolfi, P. P. and Yuan, Z. M. (2015). ZBTB7A Suppresses Melanoma Metastasis by Transcriptionally Repressing MCAM. Mol Cancer Res 13(8): 1206-1217.

41.   Liu, Z., Guo, J., Li, K., Qin, L., Kang, J., Shu, L., Zhang, Y., Wei, Y., Yang, N., Luo, Y., Sun, Q., Xu, Q., Yan, X. and Tang, B. (2015). Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease. Neurobiol Aging 36(11): 3117 e3117-3118.

42.   Liu, Z., Zeng, S., Zeng, J., Zhou, Y., Zeng, X., Jiang, H., Shen, L., Tang, B. and Wang, J. (2015). SCA38 is rare in mainland China. J Neurol Sci 358(1-2): 333-334.

43.   Liu, Z. H., Guo, J. F., Li, K., Wang, Y. Q., Kang, J. F., Wei, Y., Sun, Q. Y., Xu, Q., Wang, D. L., Xia, K., Yan, X. X., Xu, C. S. and Tang, B. S. (2015). Analysis of several loci from genome-wide association studies in Parkinson's disease in mainland China. Neurosci Lett 587: 68-71.

44.   Liu, Z. H., Guo, J. F., Wang, Y. Q., Li, K., Sun, Q. Y., Xu, Q., Yan, X. X., Xu, C. S. and Tang, B. S. (2015). Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China. Neurobiol Aging 36(3): 1600 e1609-1611.

45.   Long, Z., Chen, Z., Wang, C., Huang, F., Peng, H., Hou, X., Ding, D., Ye, W., Wang, J., Pan, Q., Li, J., Xia, K., Tang, B., Ashizawa, T. and Jiang, H. (2015). Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients. PLoS One 10(2): e0117488.

46.   Lu, L., Su, J., Chen, X. and Chen, M. (2015). A giant mass on the left shin: report of a case. Int J Clin Exp Pathol 8(2): 2180-2182.

47.   Luo, J., Xu, Z., Tan, Z., Zhang, Z. and Ma, L. (2015). Neuropeptide Receptors NPR-1 and NPR-2 Regulate Caenorhabditis elegans Avoidance Response to the Plant Stress Hormone Methyl Salicylate. Genetics 199(2): 523-531.

48.   Luo, S., Huang, W., Xia, Q., Du, Q., Wu, L. and Duan, R. (2015). Mutational analyses of the FMR1 gene in Chinese pediatric population of fragile x suspects: low tolerance for point mutation. J Child Neurol 30(6): 803-806.

49.   Luo, Y., Roy, M., Xiao, X., Sun, S., Liang, L., Chen, H., Fu, Y., Sun, Y., Zhu, M., Ye, M. and Liu, J. (2015). Lycorine induces programmed necrosis in the multiple myeloma cell line ARH-77. Tumour Biol 36(4): 2937-2945.

50.   Lv, W., Wei, X., Guo, R., Liu, Q., Zheng, Y., Chang, J., Bai, T., Li, H., Zhang, J., Song, Z., Cram, D. S., Liang, D. and Wu, L. (2015). Non-invasive Prenatal Testing for Wilson Disease by Use of Circulating Single-Molecule Amplification and Resequencing Technology (cSMART). Clin Chem 61(1): 172-181.

51.   Ma, C., Jin, S., Liu, H., Xia, K., Tang, J., Wang, K. and Wang, J. (2015). Thioflavin T as a fluorescence probe for label-free detection of T4 polynucleotide kinase/phosphatase and its inhibitors. Mol Cell Probes 29(6): 500-502.

52.   Ma, R., Peng, Y., Zhang, Y., Xia, Y., Tang, G., Chang, J., Guo, R., Gui, B., Huang, Y., Chen, C., Liang, D. and Wu, L. (2015). Partial trisomy 2q33.3-q37.3 in a patient with an inverted duplicated neocentric marker chromosome. Mol Cytogenet 8: 10.

53.   Mei, L., Huang, Y., Pan, Q., Su, W., Quan, Y., Liang, D. and Wu, L. (2015). Targeted next-generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, type III. Clin Chim Acta 447: 47-51.

54.   Mei, L., Liang, D., Huang, Y., Pan, Q. and Wu, L. (2015). Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndrome. Gene 555(2): 476-480.

55.   Miller, N., Feng, Z., Edens, B. M., Yang, B., Shi, H., Sze, C. C., Hong, B. T., Su, S. C., Cantu, J. A., Topczewski, J., Crawford, T. O., Ko, C. P., Sumner, C. J., Ma, L. and Ma, Y. C. (2015). Non-aggregating tau phosphorylation by cyclin-dependent kinase 5 contributes to motor neuron degeneration in spinal muscular atrophy. J Neurosci 35(15): 6038-6050.

56.   Pan, Y., Chen, J., Guo, H., Ou, J., Peng, Y., Liu, Q., Shen, Y., Shi, L., Liu, Y., Xiong, Z., Zhu, T., Luo, S., Hu, Z., Zhao, J. and Xia, K. (2015). Association of genetic variants of GRIN2B with autism. Sci Rep 5: 8296.

57.   Park, G., Tan, J., Garcia, G., Kang, Y., Salvesen, G. and Zhang, Z. (2015). Regulation of Histone Acetylation by Autophagy in Parkinson Disease. J Biol Chem: doi: 10.1074/jbc.M1115.675488.

58.   Peng, C., Su, J., Zeng, W., Zhang, X. and Chen, X. (2015). TNFR1 Regulates Ovarian Cancer Cell Tumorigenicity Through PIK3CB-p110Beta. Curr Mol Med 15(5): 487-496.

59.   Peng, F., Li, J., Guo, T., Yang, H., Li, M., Sang, S., Li, X., Desiderio, D. M. and Zhan, X. (2015). Nitroproteins in Human Astrocytomas Discovered by Gel Electrophoresis and Tandem Mass Spectrometry. J Am Soc Mass Spectrom 26(12): 2062-2076.

60.   Peng, Y., Ma, R., Zhou, Y., Xia, Y., Wen, J., Zhang, Y., Guo, R., Li, H., Pan, Q., Zhang, R., Tang, C., Liang, D. and Wu, L. (2015). De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease. Mol Cytogenet 8: 88.

61.   Qin, J., Sheng, X., Wang, H., Liang, D., Tan, H. and Xia, J. (2015). Assisted reproductive technology and risk of congenital malformations: a meta-analysis based on cohort studies. Arch Gynecol Obstet 292(4): 777-798.

62.   Qin, J., Wang, H., Sheng, X., Liang, D., Tan, H. and Xia, J. (2015). Pregnancy-related complications and adverse pregnancy outcomes in multiple pregnancies resulting from assisted reproductive technology: a meta-analysis of cohort studies. Fertil Steril 103(6): 1492-1508 e1491-1497.

63.   Shen, Y., Xun, G., Guo, H., He, Y., Ou, J., Dong, H., Xia, K. and Zhao, J. (2015). Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population. Autism Res: doi: 10.1002/aur.1540.

64.   Shi, Y., Wang, C., Huang, F., Chen, Z., Sun, Z., Wang, J., Tang, B., Ashizawa, T., Klockgether, T. and Jiang, H. (2015). High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression. Cerebellum 14(6): 677-681.

65.   Sun, Z., Jiang, H., Jiao, B., Hou, X., Shen, L., Xia, K. and Tang, B. (2015). C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy. Parkinsonism Relat Disord 21(7): 811-812.

66.   Sun, Z., Wang, Y., Han, X., Zhao, X., Peng, Y., Li, Y., Peng, M., Song, J., Wu, K., Sun, S., Zhou, W., Qi, B., Zhou, C., Chen, H., An, X. and Liu, J. (2015). miR-150 inhibits terminal erythroid proliferation and differentiation. Oncotarget: doi: 10.18632/oncotarget.15824.

67.   Tan, H., Yang, P., Li, H. X., Pan, Q., Liang, D. S. and Wu, L. Q. (2015). A novel FOXL2 mutation in a Chinese family with blepharophimosis, ptosis, epicanthus inversus syndrome. Human Genome Variation 2: 15008; doi:15010.11038/hgv.12015.15008.

68.   Tang, C., Chen, X., Chi, J., Yang, D., Liu, S., Liu, M., Pan, Q., Fan, J., Wang, D. and Zhang, Z. (2015). Pathogenic Cx31 is un/misfolded to cause skin abnormality via a Fos/JunB-mediated mechanism. Hum Mol Genet 24(21): 6054-6065.

69.   Tang, J., Morgan, H. L., Liao, Y., Corlett, P. R., Wang, D., Li, H., Tang, Y., Chen, J., Liu, T., Hao, W., Fletcher, P. C. and Chen, X. (2015). Chronic administration of ketamine mimics the perturbed sense of body ownership associated with schizophrenia. Psychopharmacology (Berl) 232(9): 1515-1526.

70.   Tang, Y., Yan, G., Song, X., Wu, K., Li, Z., Yang, C., Deng, T., Sun, Y., Hu, X., Yang, C., Bai, H., Li, H., Tan, W., Ye, M. and Liu, J. (2015). STIP overexpression confers oncogenic potential to human non-small cell lung cancer cells by regulating cell cycle and apoptosis. J Cell Mol Med 19(12): 2806-2817.

71.   Tang, Z., Chen, Z., Tang, B. and Jiang, H. (2015). Primary erythromelalgia: a review. Orphanet J Rare Dis 10: 127.

72.   Wang, C., Chen, Z., Yang, F., Jiao, B., Peng, H., Shi, Y., Wang, Y., Huang, F., Wang, J., Shen, L., Xia, K., Tang, B., Ashizawa, T. and Jiang, H. (2015). Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China. PLoS One 10(6): e0130336.

73.   Wang, H., Wang, X., He, C., Li, H., Qing, J., Grati, M., Hu, Z., Li, J., Hu, Y., Xia, K., Mei, L., Wang, X., Yu, J., Chen, H., Jiang, L., Liu, Y., Men, M., Zhang, H., Guan, L., Xiao, J., Zhang, J., Liu, X. and Feng, Y. (2015). Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family. J Hum Genet 60(3): 119-126.

74.   Wang, J., Cao, H., Liao, Y., Liu, W., Tan, L., Tang, Y., Chen, J., Xu, X., Li, H., Luo, C., Liu, C., Ries Merikangas, K., Calhoun, V., Tang, J., Shugart, Y. Y. and Chen, X. (2015). Three dysconnectivity patterns in treatment-resistant schizophrenia patients and their unaffected siblings. Neuroimage Clin 8: 95-103.

75.   Wang, X., Guo, T., Peng, F., Long, Y., Mu, Y., Yang, H., Ye, N., Li, X. and Zhan, X. (2015). Proteomic and functional profiles of a follicle-stimulating hormone positive human nonfunctional pituitary adenoma. Electrophoresis 36(11-12): 1289-1304.

76.   Wang, X., Liu, Y., Chen, H., Mei, L., He, C., Jiang, L., Niu, Z., Sun, J., Luo, H., Li, J. and Feng, Y. (2015). LEF-1 Regulates Tyrosinase Gene Transcription In Vitro. PLoS One 10(11): e0143142.

77.   Wang, Y. Q., Tang, B. S., Yan, X. X., Chen, Z. H., Xu, Q., Liu, Z. H., Li, K., Wang, K. and Guo, J. F. (2015). A neurophysiological profile in Parkinson's disease with mild cognitive impairment and dementia in China. J Clin Neurosci 22(6): 981-985.

78.   Wang, Y. Q., Tang, B. S., Yang, Y., Cui, Y. T., Kang, J. F., Liu, Z. H., Li, K., Sun, Q. Y., Xu, Q., Yan, X. X. and Guo, J. F. (2015). Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based study. Neurobiol Aging.

79.   Wang, Z., Ma, B., Li, H., Xiao, X., Zhou, W., Liu, F., Zhang, B., Zhu, M., Yang, Q., Zeng, Y., Sun, Y., Sun, S., Wang, Y., Zhang, Y., Weng, H., Chen, L., Ye, M., An, X. and Liu, J. (2015). Protein 4.1N acts as a potential tumor suppressor linking PP1 to JNK-c-Jun pathway regulation in NSCLC. Oncotarget: doi: 10.18632/oncotarget.16312.

80.   Xie, X., Man, X., Zhu, Z., Yuan, D. and Huang, S. (2015). Tumor suppressor RIZ1 in obesity and the PI3K/AKT/mTOR pathway. Obesity (Silver Spring).

81.   Xu, Z., Luo, J., Li, Y. and Ma, L. (2015). The BLI-3/TSP-15/DOXA-1 dual oxidase complex is required for iodide toxicity in Caenorhabditis elegans. G3 (Bethesda) 5(2): 195-203.

82.   Yang, Y., Tang, B. S., Weng, L., Li, N., Shen, L., Wang, J., Zuo, C. T., Yan, X. X., Xia, K. and Guo, J. F. (2015). Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism. PLoS One 10(8): e0136245.

83.   Yang, Y., Tian, D., Lee, J., Zeng, J., Zhang, H., Chen, S., Guo, H., Xiong, Z., Xia, K., Hu, Z. and Luo, J. (2015). Clinical and genetic identification of a large chinese family with autosomal dominant retinitis pigmentosa. Ophthalmic Genet 36(1): 64-69.

84.   Ye, M., Tang, Y., Tang, S., Liu, J., Wu, K., Yao, S., Sun, Y., Zhou, L., Deng, T., Chen, Y., Huang, C. and Tan, W. (2015). STIP is a critical nuclear scaffolding protein linking USP7 to p53-Mdm2 pathway regulation. Oncotarget 6(33): 34718-34731.

85.   Yu, B. L., Xiang, R., Hu, D. and Peng, D. Q. (2015). A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy. Eur Heart J 36(3): 178.

86.   Yu, H., Liu, R., Ma, B., Li, X., Yen, H. Y., Zhou, Y., Krasnoperov, V., Xia, Z., Zhang, X., Bove, A. M., Buscarini, M., Parekh, D., Gill, I. S., Liao, Q., Tretiakova, M., Quinn, D., Zhao, J. and Gill, P. S. (2015). Axl receptor tyrosine kinase is a potential therapeutic target in renal cell carcinoma. Br J Cancer 113(4): 616-625.

87.   Yu, R. L., Guo, J. F., Wang, Y. Q., Liu, Z. H., Sun, Z. F., Su, L., Zhang, Y., Yan, X. X. and Tang, B. S. (2015). The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population. J Clin Neurosci 22(6): 1002-1004.

88.   Zeng, J., Wang, J., Zeng, S., He, M., Zeng, X., Zhou, Y., Liu, Z., Jiang, H. and Tang, B. (2015). Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population. J Neurol Sci 351(1-2): 124-126.

89.   Zeng, S., Zeng, J., He, M., Zeng, X., Zhou, Y., Liu, Z., Jiang, H., Tang, B. and Wang, J. (2015). Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case report. J Hum Genet 60(3): 157-160.

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