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2016年发表论文

浏览:7169 来源:SKLMG
 

1.       Nuruzzaman, M., Cao, H., Xiu, H., Luo, T., Li, J., Chen, X., Luo, J. and Luo, Z. (2016). Transcriptomics-based identification of WRKY genes and characterization of a salt and hormone-responsive PgWRKY1 gene in Panax ginseng. Acta Biochim Biophys Sin (Shanghai) 48(2): 117-131.

2.       Huang, J., Peng, K., Wang, L., Wen, B., Zhou, L., Luo, T., Su, M., Li, J. and Luo, Z. (2016). Ginsenoside Rh2 inhibits proliferation and induces apoptosis in human leukemia cells via TNF-alpha signaling pathway. Acta Biochim Et Biophys Sin 48(8): 750-755.

3.       Luo, X., Zhu, L.-j., Cai, N.-f., Zheng, L.-y. and Cheng, Z.-n. (2016). Prediction of tacrolimus metabolism and dosage requirements based on CYP3A4 phenotype and CYP3A5*3 genotype in Chinese renal transplant recipients. Acta Pharmacologica Sinica 37(4): 555-560.

4.       Zhan, X. Q., Peng, F. and Cheng, T. T. (2016). Insights into tyrosine nitration in an astrocytoma proteome. ADV IMMUNOL 1: e1177. doi: 1110.14800/ia.11177.

5.       Stessman, H. A., Willemsen, M. H., Fenckova, M., Penn, O., Hoischen, A., Xiong, B., Wang, T., Hoekzema, K., Vives, L., Vogel, I., Brunner, H. G., van der Burgt, I., Ockeloen, C. W., Schuurs-Hoeijmakers, J. H., Klein Wassink-Ruiter, J. S., Stumpel, C., Stevens, S. J., Vles, H. S., Marcelis, C. M., van Bokhoven, H., Cantagrel, V., Colleaux, L., Nicouleau, M., Lyonnet, S., Bernier, R. A., Gerdts, J., Coe, B. P., Romano, C., Alberti, A., Grillo, L., Scuderi, C., Nordenskjold, M., Kvarnung, M., Guo, H., Xia, K., Piton, A., Gerard, B., Genevieve, D., Delobel, B., Lehalle, D., Perrin, L., Prieur, F., Thevenon, J., Gecz, J., Shaw, M., Pfundt, R., Keren, B., Jacquette, A., Schenck, A., Eichler, E. E. and Kleefstra, T. (2016). Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders. Am J Hum Genet 98(3): 541-552.

6.       Yang, P., Tan, H., Xia, Y., Yu, Q., Wei, X., Guo, R., Peng, Y., Chen, C., Li, H., Mei, L., Huang, Y., Liang, D. and Wu, L. (2016). De novo exonic deletion of KDM6A in a Chinese girl with Kabuki syndrome: A case report and brief literature review. Am J Med Genet A 170(6): 1613-1621.

7.       Zhang, W., Zhou, X., Zhang, H., Yao, Q., Liu, Y. and Dong, Z. (2016). Extracellular vesicles in diagnosis and therapy of kidney diseases. Am J Physiol Renal Physiol 311(5): F844-F851.

8.       Chen, X., Yin, B., Lian, R. C., Zhang, T., Zhang, H. Z., Diao, L. H., Li, Y. Y., Huang, C. Y., Liang, D. S. and Zeng, Y. (2016). Modulatory effects of vitamin D on peripheral cellular immunity in patients with recurrent miscarriage. Am J Reprod Immunol 76(6): 432-438.

9.       Ma, C., Liu, H., Wang, J., Jin, S. and Wang, K. (2016). Label-free molecular beacon for real-time monitoring of DNA polymerase activity. Anal Bioanal Chem 408(12): 3275-3280.

10.    Liu, H., Ma, C., Zhou, M., Chen, H., He, H. and Wang, K. (2016). Quencher-free fluorescence strategy for detection of DNA methyltransferase activity based on exonuclease III-assisted signal amplification. Anal Bioanal Chem 408(28): 8111-8116.

11.    Liu, H., Ma, C., Wang, J., Chen, H. and Wang, K. (2016). Label-free colorimetric assay for T4 polynucleotide kinase/phosphatase activity and its inhibitors based on G-quadruplex/hemin DNAzyme. Anal Biochem: doi:10.1016/j.ab.2016.1010.1022.

12.    Ma, C., Liu, H., Du, J., Chen, H., He, H., Jin, S., Wang, K. and Wang, J. (2016). Quencher-free hairpin probes for real-time detection of T4 polynucleotide kinase activity. Anal Biochem 494: 1-3.

13.    Ma, C., Jin, S., Wang, J., Wang, K., Liu, H. and Wu, K. (2016). A fluorescence-based assay for T4 polynucleotide kinase/phosphatase activity based on a terminal transferase-aided photoinduced electron transfer strategy. Analytical Methods 8(9): 1989-1994.

14.    Du, J., Xiong, L., Ma, C., Liu, H., Wang, J. and Wang, K. (2016). Label-free DNA hairpin probe for real-time monitoring of alkaline phosphatase activity. Analytical Methods 8(25): 5095-5100.

15.    Tang, Y., Zhao, X., Antoine, D., Xiao, X., Wang, H., Andersson, U., Billiar, T. R., Tracey, K. J. and Lu, B. (2016). Regulation of Posttranslational Modifications of HMGB1 During Immune Responses. Antioxid Redox Signal 24(12): 620-634.

16.    Yang, L., Qiao, G., Hassan, Y., Li, Z., Zhang, X., Kong, H., Zeng, W., Yin, F. and Zhang, J. (2016). Program Death-1 Suppresses Autoimmune Arthritis by Inhibiting Th17 Response. Archivum Immunologiae Et Therapiae Experimentalis 64(5): 417-423.

17.    Hu, X. L., Zhou, J. P., Kuang, D. B., Qi, H., Peng, L. M., Yang, T. L., Li, X., Zhang, W., Zhou, H. H. and Chen, X. P. (2016). Considerable impacts of AGXT2 V140I polymorphism on chronic heart failure in the Chinese population. Atherosclerosis 251: 255-262.

18.    Guo, W., Liu, F., Chen, J., Wu, R., Zhang, Z., Yu, M., Xue, Z. and Zhao, J. (2016). Decreased long- and short-range functional connectivity at rest in drug-naive major depressive disorder. Australian and New Zealand Journal of Psychiatry 50(8): 763-769.

19.    Shen, Y., Xun, G., Guo, H., He, Y., Ou, J., Dong, H., Xia, K. and Zhao, J. (2016). Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population. Autism Research 9(4): 436-442.

20.    Gao, J., Li, M., Qin, S., Zhang, T., Jiang, S., Hu, Y., Deng, Y., Zhang, C., You, D., Li, H., Mu, D., Zhang, Z. and Jiang, C. (2016). Cytosolic PINK1 promotes the targeting of ubiquitinated proteins to the aggresome-autophagy pathway during proteasomal stress. Autophagy 12(4): 632-647.

21.    Livingston, M. J., Ding, H. F., Huang, S., Hill, J. A., Yin, X. M. and Dong, Z. (2016). Persistent activation of autophagy in kidney tubular cells promotes renal interstitial fibrosis during unilateral ureteral obstruction. Autophagy 12(6): 976-998.

22.    Song, J., Li, J., Liu, H. D., Liu, W., Feng, Y., Zhou, X. T. and Li, J. D. (2016). Snapin interacts with G-protein coupled receptor PKR2. Biochem Biophys Res Commun 469(3): 501-506.

23.    Pang, J., Wu, Y., Li, Z., Hu, Z., Wang, X., Hu, X., Wang, X., Liu, X., Zhou, M., Liu, B., Wang, Y., Feng, M. and Liang, D. (2016). Targeting of the human F8 at the multicopy rDNA locus in Hemophilia a patient-derived iPSCs using TALENickases. Biochem Biophys Res Commun 472(1): 144-149.

24.    Li, L. Y., Xiao, J., Liu, Q. and Xia, K. (2016). Parecoxib inhibits glioblastoma cell proliferation, migration and invasion by up-regulating miRNA-29c. Biol Open: doi: 10.1242/bio.021410.

25.    Wu, B., Xiao, K., Zhang, Z. and Ma, L. (2016). Altered Expression of EPO Might Underlie Hepatic Hemangiomas in LRRK2 Knockout Mice. Biomed Res Int 2016: 7681259.

26.    Tan, H., Mei, L., Huang, Y., Yang, P., Li, H., Peng, Y., Chen, C., Wei, X., Pan, Q., Liang, D. and Wu, L. (2016). Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome. BMC Med Genet 17(1): 77.

27.    Ding, D., Li, K., Wang, C., Chen, Z., Long, Z., Peng, Y., Zhou, X., Peng, H., Qiu, R., Xia, K., Tang, B. and Jiang, H. (2016). ATXN2 polymorphism modulates age at onset in Machado-Joseph disease. Brain: doi: 10.1093/brain/aww1176.

28.    Chen, Z., Zheng, C., Long, Z., Cao, L., Li, X., Shang, H., Yin, X., Zhang, B., Liu, J., Ding, D., Peng, Y., Wang, C., Peng, H., Ye, W., Qiu, R., Pan, Q., Xia, K., Chen, S., Sequeiros, J., Ashizawa, T., Klockgether, T., Tang, B., Jiang, H. and Chinese Clinical Research Cooperative Group for Spinocerebellar, A. (2016). (CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China. Brain 139(Pt 8): e41.

29.    Jiao, B., Xiao, T., Hou, L., Gu, X., Zhou, Y., Zhou, L., Tang, B., Xu, J. and Shen, L. (2016). High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China. Brain 139(Pt 4): e21.

30.    Zhao, X., Li, X., Hu, Z., Liu, L., Xie, Y., Tian, T., Man, J., Wang, J., Zi, X., Xia, K., Tang, B., Wei, X. and Zhang, R. (2016). MORC2 mutations in a cohort of Chinese patients with Charcot-Marie-Tooth disease type 2. Brain 139(Pt 10): e56.

31.    Li, Z., Heng, J., Yan, J., Guo, X., Tang, L., Chen, M., Peng, L., Wu, Y., Wang, S., Xiao, Z., Deng, Z., Dai, L. and Wang, J. (2016). Integrated analysis of gene expression and methylation profiles of 48 candidate genes in breast cancer patients. Breast Cancer Res Treat 160(2): 371-383.

32.    Lu, Q., Tu, M. L., Li, C. J., Zhang, L., Jiang, T. J., Liu, T. and Luo, X. H. (2016). GDF11 Inhibits Bone Formation by Activating Smad2/3 in Bone Marrow Mesenchymal Stem Cells. Calcif Tissue Int 99(5): 500-509.

33.    Tian, X., Hu, Y., Li, M., Xia, K., Yin, J., Chen, J. and Liu, Z. (2016). Carnosic acid attenuates acute ethanol-induced liver injury via a SIRT1/p66Shc-mediated mitochondrial pathway. Can J Physiol Pharmacol 94(4): 416-425.

34.    Zou, T., Yin, J., Zheng, W., Xiao, L., Tan, L., Chen, J., Wang, Y., Li, X., Qian, C., Cui, J., Zhang, W., Zhou, H. and Liu, Z. (2016). Rho GTPases: RAC1 polymorphisms affected platinum-based chemotherapy toxicity in lung cancer patients. Cancer Chemother Pharmacol 78(2): 249-258.

35.    Mao, X. Y., Li, Q. Q., Gao, Y. F., Zhou, H. H., Liu, Z. Q. and Jin, W. L. (2016). Gap junction as an intercellular glue: Emerging roles in cancer EMT and metastasis. Cancer Lett 381(1): 133-137.

36.    Yin, J. Y., Li, X., Li, X. P., Xiao, L., Zheng, W., Chen, J., Mao, C. X., Fang, C., Cui, J. J., Guo, C. X., Zhang, W., Gao, Y., Zhang, C. F., Chen, Z. H., Zhou, H., Zhou, H. H. and Liu, Z. Q. (2016). Prediction models for platinum-based chemotherapy response and toxicity in advanced NSCLC patients. Cancer Lett 377(1): 65-73.

37.    Zhao, J., Zeng, Y., Xu, S., Chen, J., Shen, G., Yu, C., Knipe, D., Yuan, W., Peng, J., Xu, W., Zhang, C., Xia, Z. and Feng, P. (2016). A Viral Deamidase Targets the Helicase Domain of RIG-I to Block RNA-Induced Activation. Cell Host Microbe 20(6): 770-784.

38.    Zhang, S., Qiu, D., Liu, J. and Li, Z. (2016). Active Components of Fungus Shiraia bambusiscola Can Specifically Induce BGC823 Gastric Cancer Cell Apoptosis. Cell journal 18(2): 149-158.

39.    Tang, B. S. (2016). Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants. Chin Med J (Engl) 129(9): 1009-1010.

40.    Zhang, Z. L., Li, H. L., Wen, Z. P., Yang, G. P., Zhang, W. and Chen, X. P. (2016). Influence of G-protein beta-Polypeptide 3 C825T Polymorphism on Antihypertensive Response to Telmisartan and Amlodipine in Chinese Patients. Chin Med J (Engl) 129(1): 8-14.

41.    Zhang, Y., Li, H., Ma, R., Mei, L., Wei, X., Liang, D. and Wu, L. (2016). Clinical and molecular investigation in Chinese patients with glutaric aciduria type I. Clin Chim Acta 453: 75-79.

42.    Xue, J., Gao, Q., Huang, Y., Zhang, X., Yang, P., Cram, D. S., Liang, D. and Wu, L. (2016). A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree. Clin Chim Acta 461: 135-140.

43.    Gai, N., Jiang, C., Zou, Y. Y., Zheng, Y., Liang, D. S. and Wu, L. Q. (2016). Novel SIL1 nonstop mutation in a Chinese consanguineous family with Marinesco-Sjogren syndrome and Dandy-Walker syndrome. Clin Chim Acta 458: 1-4.

44.    Huang, Y., Mei, L., Lv, W., Li, H., Zhang, R., Pan, Q., Tan, H., Guo, J., Luo, X., Chen, C., Liang, D. and Wu, L. (2016). Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIII. Clin Chim Acta 464: 170-175.

45.    Ma, Y., Chen, C., Wang, Y., Wu, L., He, F., Chen, C., Zhang, C., Deng, X., Yang, L., Chen, Y., Wu, L., Yin, F. and Peng, J. (2016). Analysis copy number variation of Chinese children in early-onset epileptic encephalopathies with unknown cause. Clin Genet 90(5): 428-436.

46.    Zeng, S., Zeng, J., He, M., Zeng, X., Zhou, Y., Liu, Z., Xia, K., Pan, Q., Jiang, H., Shen, L., Yan, X., Tang, B. and Wang, J. (2016). Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China. Clin Genet 90(2): 141-148.

47.    Sun, B., Hu, L., Luo, Z. Y., Chen, X. P., Zhou, H. H. and Zhang, W. (2016). DNA methylation perspectives in the pathogenesis of autoimmune diseases. Clin Immunol 164: 21-27.

48.    Xiao, T., Jiao, B., Zhang, W., Tang, B. and Shen, L. (2016). Effect of the CYP2D6 and APOE Polymorphisms on the Efficacy of Donepezil in Patients with Alzheimer's Disease: A Systematic Review and Meta-Analysis. CNS Drugs 30(10): 899-907.

49.    Yin, J. Y., Qu, J., Mao, C. X., Li, X., Mao, X. Y., Xiao, B., Xiao, L., Zheng, W., Zhou, H. H. and Liu, Z. Q. (2016). Establishing Prediction Model of Antiepileptic Drugs Response using Data Mining Approach. CNS Neurosci Ther 22(10): 860-862.

50.    Sun, S., Wang, Y., Chen, H., Fang, L., Cui, Y., Han, X., Wu, D., Li, H., Ye, M., Zhao, X. and Liu, J. (2016). STIP Regulates ERK1/2 Signaling Pathway Involved in Interaction with PP1gamma in Lymphoblastic Leukemia. Curr Mol Med 16(8): 767-775.

51.    Ren, Q., Xiao, D., Han, X., Edwards, S. L., Wang, H., Tang, Y., Zhang, S., Li, X., Zhang, X., Cai, X., Liu, Z., Paul, S. K. and Ji, L. (2016). Genetic and Clinical Predictive Factors of Sulfonylurea Failure in Patients with Type 2 Diabetes. Diabetes Technol Ther 18(9): 586-593.

52.    Li, B., Liu, Y., Liu, Y., Guo, H., Hu, Z., Xia, K. and Jin, X. (2016). Identification of a GJA3 Mutation in a Large Family with Bilateral Congenital Cataract. DNA Cell Biol 35(3): 135-139.

53.    He, F., Liu, M., Chen, Z., Liu, G., Wang, Z., Liu, R., Luo, J., Tang, J., Wang, X., Liu, X., Zhou, H., Chen, X., Liu, Z. and Zhang, W. (2016). Assessment of Human Tribbles Homolog 3 Genetic Variation (rs2295490) Effects on Type 2 Diabetes Patients with Glucose Control and Blood Pressure Lowering Treatment. EBioMedicine 13: 181-189.

54.    Wu, Y. H., Li, X. W., Li, W. Q., Li, X. H., Li, Y. J., Hu, G. Y., Liu, Z. Q. and Li, D. (2016). Fluorofenidone attenuates bleomycin-induced pulmonary fibrosis by inhibiting eukaryotic translation initiation factor 3a (eIF3a) in rats. Eur J Pharmacol 773: 42-50.

55.    Ou, J., Lyu, H., Hu, M., Li, J., Guo, W., Guo, X., Li, L., Zheng, J., Wei, Q., Liu, F., He, Z., Wang, J., Liu, F., Wu, R., Chen, J., Li, L., Hu, B., Chen, H. and Zhao, J. (2016). Decreased white matter FA values in the left inferior frontal gyrus is a possible intermediate phenotype of schizophrenia: evidences from a novel group strategy. European archives of psychiatry and clinical neuroscience: doi: 10.1007/s00406-00016-00752-z.

56.    Zhang, Q., Guo, X. M. and Li, Y. (2016). Optimal polar bodies angle for higher subsequent embryo viability: a pilot study. Fertil Steril 105(3): 670-675 e672.

57.    Qin, J. B., Wang, H., Sheng, X., Xie, Q. and Gao, S. (2016). Assisted reproductive technology and risk of adverse obstetric outcomes in dichorionic twin pregnancies: a systematic review and meta-analysis. Fertility and Sterility 105(5): 1180-1192.

58.    Zhan, X. and Desiderio, D. M. (2016). Editorial: Systems Biological Aspects of Pituitary Tumors. Front Endocrinol (Lausanne) 7: 86.

59.    Zhan, X. and Long, Y. (2016). Exploration of Molecular network Variations in Different Subtypes of Human non-functional pituitary Adenomas. Front Endocrinol (Lausanne) 7: 13.

60.    Zhan, X., Wang, X. and Cheng, T. (2016). Human Pituitary Adenoma Proteomics: New Progresses and Perspectives. Front Endocrinol (Lausanne) 7: 54.

61.    Terrando, N., Yang, T., Wang, X., Fang, J., Cao, M., Andersson, U., Erlandsson, H. H., Ouyang, W. and Tong, J. (2016). Systemic HMGB1 Neutralization Prevents Postoperative Neurocognitive Dysfunction in Aged Rats. Front Immunol 7: 441.

62.    Fu, Y., Zhu, Z., Chang, H., Liu, Z., Liu, J. and Chen, H. (2016). Comparative transcriptome analyses indicate enhanced cellular protection against FMDV in PK15 cells pretreated with IFN-gamma. Gene 586(2): 206-215.

63.    Peng, H., Xu, X., Zhang, L., Zhang, X., Peng, H., Zheng, Y., Luo, S., Guo, H., Xia, K., Li, J., Yao, H. and Hu, Z. (2016). GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing. Gene 575: 363-367.

64.    Zhang, S., Qin, H., Lv, W., Luo, S., Wang, J., Fu, C., Ma, R., Shen, Y., Chen, S. and Wu, L. (2016). Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis. Gene 577(2): 187-192.

65.    Chen, J., Qi, B., Zhao, J., Liu, W., Duan, R. and Zhang, M. (2016). A novel mutation of GATA4 (K300T) associated with familial atrial septal defect. Gene 575(2): 473-477.

66.    Huang, S. (2016). Editorial: Special issue on the comprehensive functionality of genomic DNAs. Genomics 108(1): 1-2.

67.    Luo, D. and Huang, S. (2016). The genetic equidistance phenomenon at the proteomic level. Genomics 108(1): 25-30.

68.    Huang, S. (2016). New thoughts on an old riddle: What determines genetic diversity within and between species? Genomics 108(1): 3-10.

69.    Li, X., Lin, M., Xie, Z., Huang, R., Chen, A. F. and Jiang, W. (2016). Establishing a low-expression renalase gene model in cardiac tissue of Sprague–Dawley rats. Herz 41(4): 326-330.

70.    Tsang, S. Y., Ahmad, T., Mat, F. W., Zhao, C., Xiao, S., Xia, K. and Xue, H. (2016). Variation of global DNA methylation levels with age and in autistic children. Hum Genomics 10(1): 31.

71.    Bernstein, A. I., Lin, Y., Street, R. C., Lin, L., Dai, Q., Yu, L., Bao, H., Gearing, M., Lah, J. J., Nelson, P. T., He, C., Levey, A. I., Mulle, J. G., Duan, R. and Jin, P. (2016). 5-Hydroxymethylation-associated epigenetic modifiers of Alzheimer's disease modulate Tau-induced neurotoxicity. Hum Mol Genet 25(12): 2437-2450.

72.    Han, W.-Q., Chen, W.-D., Zhang, K., Liu, J.-J., Wu, Y.-J. and Gao, P.-J. (2016). Ca2+-regulated lysosome fusion mediates angiotensin II-induced lipid raft clustering in mesenteric endothelial cells. Hypertension Research 39(4): 227-236.

73.    Li, F., Tang, C. and Dong, Z. (2016). Therapeutic potential of FGF21 in cardiorenal syndrome. Int J Cardiol 214: 70-71.

74.    Xiang, R., Fan, L. L., Huang, H., Zhao, S. P. and Chen, Y. Q. (2016). Whole-exome sequencing identifies a novel mutation of DSG2 (Y198C) in a Chinese arrhythmogenic right ventricular cardiomyopathy patient. Int J Cardiol 214: 1-3.

75.    Xiao, D., Guo, Y., Li, X., Yin, J. Y., Zheng, W., Qiu, X. W., Xiao, L., Liu, R. R., Wang, S. Y., Gong, W. J., Zhou, H. H. and Liu, Z. Q. (2016). The Impacts of SLC22A1 rs594709 and SLC47A1 rs2289669 Polymorphisms on Metformin Therapeutic Efficacy in Chinese Type 2 Diabetes Patients. Int J Endocrinol 2016: 4350712.

76.    Xiu, H., Nuruzzaman, M., Guo, X., Cao, H., Huang, J., Chen, X., Wu, K., Zhang, R., Huang, Y., Luo, J. and Luo, Z. (2016). Molecular Cloning and Expression Analysis of Eight PgWRKY Genes in Panax ginseng Responsive to Salt and Hormones. Int J Mol Sci 17(3): 319.

77.    Li, L., Zhu, T., Gao, Y. F., Zheng, W., Wang, C. J., Xiao, L., Huang, M. S., Yin, J. Y., Zhou, H. H. and Liu, Z. Q. (2016). Targeting DNA Damage Response in the Radio(Chemo)therapy of Non-Small Cell Lung Cancer. Int J Mol Sci 17(6): 839.

78.    Quan, H., Fang, L., Pan, H., Deng, Z., Gao, S., Liu, O., Wang, Y., Hu, Y., Fang, X., Yao, Z., Guo, F., Lu, R., Xia, K. and Tang, Z. (2016). An adaptive immune response driven by mature, antigen-experienced T and B cells within the microenvironment of oral squamous cell carcinoma. International Journal of Cancer 138(12): 2952-2962.

79.    Ou, J., Wang, G., Hu, M., Liu, F., He, Z., Wang, J., Wu, R., Chen, J., Li, L., Zhao, J. and Guo, W. (2016). Differences among first-episode schizophrenia patients, healthy siblings, and controls at the individual level. International Journal of Psychophysiology 104: 24-32.

80.    Zou, Y. and Huang, J. (2016). Comment on Qian et al.: Outcomes of radical debridement versus no debridement for the treatment of thoracic and lumbar spinal tuberculosis. International Orthopaedics 40(10): 2089-2089.

81.    Lv, D., Lin, W., Xue, Z., Pu, W., Yang, Q., Huang, X., Zhou, L., Yang, L. and Liu, Z. (2016). Decreased functional connectivity in the language regions in bipolar patients during depressive episodes but not remission. J Affect Disord 197: 116-124.

82.    Wei, Q., Liu, Y., Liu, P., Hao, J., Liang, M., Mi, Q. S., Chen, J. K. and Dong, Z. (2016). MicroRNA-489 Induction by Hypoxia-Inducible Factor-1 Protects against Ischemic Kidney Injury. J Am Soc Nephrol 27(9): 2784-2796.

83.    Tang, C. and Dong, Z. (2016). Mitochondria in Kidney Injury: When the Power Plant Fails. J Am Soc Nephrol 27(7): 1869-1872.

84.    Zhang, D., Pan, J., Xiang, X., Liu, Y., Dong, G., Livingston, M. J., Chen, J. K., Yin, X. M. and Dong, Z. (2016). Protein Kinase Cdelta Suppresses Autophagy to Induce Kidney Cell Apoptosis in Cisplatin Nephrotoxicity. J Am Soc Nephrol 28: doi: 10.1681/ASN.201603033.

85.    Zhang, T., Xue, L., Li, L., Tang, C., Wan, Z., Wang, R., Tan, J., Tan, Y., Han, H., Tian, R., Billiar, T. R., Tao, W. A. and Zhang, Z. (2016). BNIP3 Protein Suppresses PINK1 Kinase Proteolytic Cleavage to Promote Mitophagy. J Biol Chem 291(41): 21616-21629.

86.    Park, G., Tan, J., Garcia, G., Kang, Y., Salvesen, G. and Zhang, Z. (2016). Regulation of Histone Acetylation by Autophagy in Parkinson Disease. J Biol Chem 291(7): 3531-3540.

87.    Zeng, L. P., Hu, Z. M., Li, K. and Xia, K. (2016). miR-222 attenuates cisplatin-induced cell death by targeting the PPP2R2A/Akt/mTOR Axis in bladder cancer cells. J Cell Mol Med 20(3): 559-567.

88.    Sun, Y., Yang, C., Chen, J., Song, X., Li, Z., Duan, M., Li, J., Hu, X., Wu, K., Yan, G., Yang, C., Liu, J., Tan, W. and Ye, M. (2016). Overexpression of WDR79 in non-small cell lung cancer is linked to tumour progression. J Cell Mol Med 20(4): 698-709.

89.    Wei, X., Tan, H., Yang, P., Zhang, R., Tan, B., Zhang, Y., Mei, L., Liang, D. and Wu, L. (2016). Notable Carrier Risks for Individuals Having Two Copies of SMN1 in Spinal Muscular Atrophy Families with 2-copy Alleles: Estimation Based on Chinese Meta-analysis Data. J Genet Couns 26(1): 72-78.

90.    Gui, B., Yang, P., Yao, Z., Li, Y., Liu, D., Liu, N., Lu, S., Liang, D. and Wu, L. (2016). A New Next-Generation Sequencing-Based Assay for Concurrent Preimplantation Genetic Diagnosis of Charcot-Marie-Tooth Disease Type 1A and Aneuploidy Screening. J Genet Genomics 43(3): 155-159.

91.    Zhang, L., Deng, J., Pan, Q., Zhan, Y., Fan, J. B., Zhang, K. and Zhang, Z. (2016). Targeted methylation sequencing reveals dysregulated Wnt signaling in Parkinson disease. J Genet Genomics 43(10): 587-592.

92.    Tan, B., Zou, Y., Zhang, Y., Zhang, R., Ou, J., Shen, Y., Zhao, J., Luo, X., Guo, J., Zeng, L., Hu, Y., Zheng, Y., Pan, Q., Liang, D. and Wu, L. (2016). A novel de novo POGZ mutation in a patient with intellectual disability. J Hum Genet 61(4): 357-359.

93.    Zhou, L., Li, Y., Li, X., Chen, G., Liang, H., Wu, Y., Tong, J. and Ouyang, W. (2016). Propranolol Attenuates Surgical Stress-Induced Elevation of the Regulatory T Cell Response in Patients Undergoing Radical Mastectomy. J Immunol 196(8): 3460-3469.

94.    Zhang, Y., Jieqiong, T., Long, M., Yang, H., Shuwen, Y., Tang, A., Chang, S. and Hu, Y. (2016). An emerging dual collaborative strategy for high-performance tumor therapy by mesoporous silica nanotubes loading Mn3O4. J Mater Chem B 4(46): 7406-7414.

95.    Li, W., Li, Y., Zhang, L., Guo, H., Tian, D., Li, Y., Peng, Y., Zheng, Y., Dai, Y., Xia, K., Lan, X., Wang, B. and Hu, Z. (2016). AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis. J Med Genet 53(7): 488-493.

96.    Zhang, X., Yu, H., Zhao, J., Li, X., Li, J., He, J., Xia, Z. and Zhao, J. (2016). IKK negatively regulates RIG-I via direct phosphorylation. J Med Virol 88(4): 712-718.

97.    Yan, W., Zhao, C., Sun, L. and Tang, B. (2016). Association between polymorphism of COMT gene (Val158Met) with Alzheimer's disease: An updated analysis. J Neurol Sci 361: 250-255.

98.    He, M., Yan, W. Q., Zeng, S., Liu, Z., Zhou, Y., Zeng, X. F., Zeng, J. S., Jiang, H., Shen, L., Tang, B. S. and Wang, J. L. (2016). C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China. J Neurol Sci 361: 181-183.

99.    Wei, Y., Yang, N., Xu, Q., Sun, Q., Guo, J., Li, K., Liu, Z., Yan, X., Zhu, X. and Tang, B. (2016). The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han population. J Neurol Sci 367: 11-14.

100.Xie, Y., Li, X., Liu, L., Hu, Z., Huang, S., Zhan, Y., Zi, X., Xia, K., Tang, B. and Zhang, R. (2016). MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patients. J Peripher Nerv Syst 21(1): 38-44.

101.Liu, G., Wen, J., Guo, D., Wang, Z., Hu, X., Tang, J., Liu, Z., Zhou, H. and Zhang, W. (2016). The effects of rabeprazole on metformin pharmacokinetics and pharmacodynamics in Chinese healthy volunteers. J Pharmacol Sci 132(4): 244-248.

102.Wang, Y., Qu, J., Ba, Q., Dong, J., Zhang, L., Zhang, H., Wu, A., Wang, D., Xia, Z., Peng, D., Shu, Y., Cao, B. and Jiang, T. (2016). Detection and typing of human-infecting influenza viruses in China by using a multiplex DNA biochip assay. J Virol Methods 234: 178-185.

103.Li, Y.-M., Ou, J.-J., Liu, L., Zhang, D., Zhao, J.-P. and Tang, S.-Y. (2016). Association Between Maternal Obesity and Autism Spectrum Disorder in Offspring: A Meta-analysis. Journal of Autism and Developmental Disorders 46(1): 95-102.

104.Wang, Y. and Yin, F. (2016). A Review of X-linked Charcot-Marie-Tooth Disease. Journal of Child Neurology 31(6): 761-772.

105.Tang, C., Cai, J. and Dong, Z. (2016). Mitochondrial dysfunction in obesity-related kidney disease: a novel therapeutic target. Kidney Int 90(5): 930-933.

106.He, F., Liu, M., Wang, X., Liu, X., Zhou, H., Chen, X. and Zhang, W. (2016). Relation between the TRIB3 Gln84Arg genetic variation and vascular complications in type 2 diabetes: an analysis of a 2 × 2 factorial randomised controlled trial. The Lancet Diabetes & Endocrinology 4: S4.

107.Wu, C., Liu, D., Yang, X., Wu, R., Zhang, J., Huang, J. and He, H. (2016). Improving Production of Protease from Pseudoalteromonas sp. CSN423 by Random Mutagenesis. Marine biotechnology (New York, N.Y.) 18(5): 610-618.

108.Wang, H., Guo, W., Liu, F., Chen, J., Wu, R., Zhang, Z., Yu, M., Li, L. and Zhao, J. (2016). Clinical significance of increased cerebellar default-mode network connectivity in resting-state patients with drug-naive somatization disorder. Medicine 95(28): 1-6.

109.Yuan, X. Q., Peng, L., Zeng, W. J., Jiang, B. Y., Li, G. C. and Chen, X. P. (2016). DNMT3A R882 Mutations Predict a Poor Prognosis in AML: A Meta-Analysis From 4474 Patients. Medicine (Baltimore) 95(18): e3519.

110.Ding, X., Liu, R., Li, W., Ni, H., Liu, Y., Wu, D., Yang, S., Liu, J., Xiao, B. and Liu, S. (2016). A metabonomic investigation on the biochemical perturbation in post-stroke patients with depressive disorder (PSD). Metab Brain Dis 31(2): 279-287.

111.Tang, T., Ouyang, J., Hu, L., Guo, L., Yang, M. and Chen, X. (2016). Synthesis of peptide templated copper nanoclusters for fluorometric determination of Fe(III) in human serum. Microchimica Acta 183(10): 0026-3672

112.2831-2836 (electronic).

113.Wu, L., Peng, J., Ma, Y., He, F., Deng, X., Wang, G., Lifen, Y. and Yin, F. (2016). Leukodystrophy associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFAF1 gene. Mitochondrial DNA Part A 27(2): 1034-1037.

114.Wang, Z., Zhang, J., Zeng, Y., Sun, S., Zhang, J., Zhang, B., Zhu, M., Ouyang, R., Ma, B., Ye, M., An, X. and Liu, J. (2016). Knockout of 4.1B triggers malignant transformation in SV40T-immortalized mouse embryo fibroblast cells. Mol Carcinog 56(2): 538-549.

115.Jin, S., Liu, H., Xia, K., Ma, C., He, H. and Wang, K. (2016). Real-time monitoring of DNA methyltransferase activity using a hemimethylated smart probe. Mol Cell Probes 30(3): 185-187.

116.Wu, T., Yin, B., Zhu, Y., Li, G., Ye, L., Chen, C., Zeng, Y. and Liang, D. (2016). Molecular cytogenetic analysis of early spontaneous abortions conceived from varying assisted reproductive technology procedures. Mol Cytogenet 9: 79.

117.Guo, Z., Shu, Y., Zhou, H. and Zhang, W. (2016). Identification of diagnostic and prognostic biomarkers for cancer: Focusing on genetic variations in microRNA regulatory pathways (Review). Mol Med Rep 13(3): 1943-1952.

118.Wei, X., Gao, H., Zou, J., Liu, X., Chen, D., Liao, J., Xu, Y., Ma, L., Tang, B., Zhang, Z., Cai, X., Jin, K., Xia, Y. and Wang, Q. (2016). Contra-directional Coupling of Nur77 and Nurr1 in Neurodegeneration: A Novel Mechanism for Memantine-Induced Anti-inflammation and Anti-mitochondrial Impairment. Mol Neurobiol 53(9): 5876-5892.

119.Xiao, T., Jiao, B., Zhang, W., Pan, C., Wei, J., Liu, X., Zhou, Y., Zhou, L., Tang, B. and Shen, L. (2016). Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease. Mol Neurobiol: doi: 10.1007/s12035-12016-10056-12033.

120.Li, H., Bi, R., Fan, Y., Wu, Y., Tang, Y., Li, Z., He, Y., Zhou, J., Tang, J., Chen, X. and Yao, Y. G. (2016). mtDNA Heteroplasmy in Monozygotic Twins Discordant for Schizophrenia. Mol Neurobiol: doi: 10.1007/s12035-12016-19996-x.

121.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. (2016). Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database. Mol Psychiatry 21(2): 298.

122.Ma, C., Liu, H., Li, W., Chen, H., Jin, S., Wang, J. and Wang, J. (2016). Label-free monitoring of DNA methyltransferase activity based on terminal deoxynucleotidyl transferase using a thioflavin T probe. Molecular and Cellular Probes 30(2): 118-121.

123.Wu, R. R., Zhang, F. Y., Gao, K. M., Ou, J. J., Shao, P., Jin, H., Guo, W. B., Chan, P. K. and Zhao, J. P. (2016). Metformin treatment of antipsychotic-induced dyslipidemia: an analysis of two randomized, placebo-controlled trials. Molecular Psychiatry 21(11): 1537-1544.

124.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. K. (2016). Psychiatric genetics in China: achievements and challenges. Molecular Psychiatry 21(1): 4-9.

125.Wang, T., Guo, H., Xiong, B., Stessman, H. A., Wu, H., Coe, B. P., Turner, T. N., Liu, Y., Zhao, W., Hoekzema, K., Vives, L., Xia, L., Tang, M., Ou, J., Chen, B., Shen, Y., Xun, G., Long, M., Lin, J., Kronenberg, Z. N., Peng, Y., Bai, T., Li, H., Ke, X., Hu, Z., Zhao, J., Zou, X., Xia, K. and Eichler, E. E. (2016). De novo genic mutations among a Chinese autism spectrum disorder cohort. Nat Commun 7: 13316.

126.Deng, H. X., Shi, Y., Yang, Y., Ahmeti, K. B., Miller, N., Huang, C., Cheng, L., Zhai, H., Deng, S., Nuytemans, K., Corbett, N. J., Kim, M. J., Deng, H., Tang, B., Yang, Z., Xu, Y., Chan, P., Huang, B., Gao, X. P., Song, Z., Liu, Z., Fecto, F., Siddique, N., Foroud, T., Jankovic, J., Ghetti, B., Nicholson, D. A., Krainc, D., Melen, O., Vance, J. M., Pericak-Vance, M. A., Ma, Y. C., Rajput, A. H. and Siddique, T. (2016). Identification of TMEM230 mutations in familial Parkinson's disease. Nat Genet 48(7): 733-739.

127.Liu, Z., Wang, S., Mi, Q. S. and Dong, Z. (2016). MicroRNAs in Pathogenesis of Acute Kidney Injury. Nephron Clin Pract 134(3): 149-153.

128.Tang, M., Gu, X., Wei, J., Jiao, B., Zhou, L., Zhou, Y., Weng, L., Yan, X., Tang, B., Xu, J. and Shen, L. (2016). Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia. Neurobiol Aging 46: 235 e211-235.

129.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. (2016). 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 39: 217 e219-211.

130.Fan, K., Tang, B. S., Wang, Y. Q., Kang, J. F., Li, K., Liu, Z. H., Sun, Q. Y., Xu, Q., Yan, X. X. and Guo, J. F. (2016). The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients. Neurosci Lett 621: 133-136.

131.Kuang, D. B., Zhou, J. P., Yu, L. Y., Zeng, W. J., Xiao, J., Zhu, G. Z., Zhang, Z. L. and Chen, X. P. (2016). DDAH1-V3 transcript might act as miR-21 sponge to maintain balance of DDAH1-V1 in cultured HUVECs. Nitric Oxide 60: 59-68.

132.Xie, X., Man, X., Zhu, Z., Yuan, D. and Huang, S. (2016). Tumor suppressor RIZ1 in obesity and the PI3K/AKT/mTOR pathway. Obesity (Silver Spring) 24(2): 389-397.

133.Peng, C., Zeng, W., Su, J., Kuang, Y., He, Y., Zhao, S., Zhang, J., Ma, W., Bode, A. M., Dong, Z. and Chen, X. (2016). Cyclin-dependent kinase 2 (CDK2) is a key mediator for EGF-induced cell transformation mediated through the ELK4/c-Fos signaling pathway. Oncogene 35(9): 1170-1179.

134.Cheng, Y., Ren, X., Yuan, Y., Shan, Y., Li, L., Chen, X., Zhang, L., Takahashi, Y., Yang, J. W., Han, B., Liao, J., Li, Y., Harvey, H., Ryazanov, A., Robertson, G. P., Wan, G., Liu, D., Chen, A. F., Tao, Y. and Yang, J. M. (2016). eEF-2 kinase is a critical regulator of Warburg effect through controlling PP2A-A synthesis. Oncogene 35(49): 6293-6308.

135.Yan, H., Wen, L., Tan, D., Xie, P., Pang, F. M., Zhou, H. H., Zhang, W., Liu, Z. Q., Tang, J., Li, X. and Chen, X. P. (2016). Association of a cytarabine chemosensitivity related gene expression signature with survival in cytogenetically normal acute myeloid leukemia. Oncotarget 8(1): 1529-1540.

136.Mao, X. Y., Dai, J. X., Zhou, H. H., Liu, Z. Q. and Jin, W. L. (2016). Brain tumor modeling using the CRISPR/Cas9 system: state of the art and view to the future. Oncotarget 7(22): 33461-33471.

137.Su, J., Gao, T., Jiang, M., Wu, L., Zeng, W., Zhao, S., Peng, C. and Chen, X. (2016). CD147 silencing inhibits tumor growth by suppressing glucose transport in melanoma. Oncotarget 7(40): 64778-64784.

138.Zhang, S., Zhang, J., Deng, Z., Liu, H., Mao, W., Jiang, F., Xia, Z. and Li, J. D. (2016). Circadian clock components RORalpha and Bmal1 mediate the anti-proliferative effect of MLN4924 in osteosarcoma cells. Oncotarget 7(40): 66087-66099.

139.Gong, W. J., Zheng, W., Xiao, L., Tan, L. M., Song, J., Li, X. P., Xiao, D., Cui, J. J., Li, X., Zhou, H. H., Yin, J. Y. and Liu, Z. Q. (2016). Circulating resistin levels and obesity-related cancer risk: A meta-analysis. Oncotarget 7(36): 57694-57704.

140.Zhang, J., Lei, Z., Huang, Z., Zhang, X., Zhou, Y., Luo, Z., Zeng, W., Su, J., Peng, C. and Chen, X. (2016). Epigallocatechin-3-gallate(EGCG) suppresses melanoma cell growth and metastasis by targeting TRAF6 activity. Oncotarget 7(48): 79557-79571.

141.Yuan, X. Q., Zhang, D. Y., Yan, H., Yang, Y. L., Zhu, K. W., Chen, Y. H., Li, X., Yin, J. Y., Li, X. L., Zeng, H. and Chen, X. P. (2016). Evaluation of DNMT3A genetic polymorphisms as outcome predictors in AML patients. Oncotarget 7(37): 60555-60574.

142.Liu, R., Zhang, W., Liu, Z. Q. and Zhou, H. H. (2016). Gene modules associated with breast cancer distant metastasis-free survival in the PAM50 molecular subtypes. Oncotarget 7(16): 21686-21698.

143.Xie, B., Cao, K., Li, J., Chen, J., Tang, J., Chen, X., Xia, K., Zhou, X., Cheng, Y., Zhou, J. and Xie, H. (2016). Hmgb1 inhibits Klotho expression and malignant phenotype in melanoma cells by activating NF-kappaB. Oncotarget 7(49): 80765-80782.

144.Xiao, L., Zhou, H., Li, X. P., Chen, J., Fang, C., Mao, C. X., Cui, J. J., Zhang, W., Zhou, H. H., Yin, J. Y. and Liu, Z. Q. (2016). MicroRNA-138 acts as a tumor suppressor in non small cell lung cancer via targeting YAP1. Oncotarget 7(26): 40038-40046.

145.Chen, J., Wang, Z., Zou, T., Cui, J., Yin, J., Zheng, W., Jiang, W., Zhou, H. and Liu, Z. (2016). Pharmacogenomics of platinum-based chemotherapy response in NSCLC: a genotyping study and a pooled analysis. Oncotarget 7(34): 55741-55756.

146.Zhou, C., Chen, X., Zeng, W., Peng, C., Huang, G., Li, X., Ouyang, Z., Luo, Y., Xu, X., Xu, B., Wang, W., He, R., Zhang, X., Zhang, L., Liu, J., Knepper, T. C., He, Y. and McLeod, H. L. (2016). Propranolol induced G0/G1/S phase arrest and apoptosis in melanoma cells via AKT/MAPK pathway. Oncotarget 7(42): 68314-68327.

147.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. (2016). Protein 4.1N acts as a potential tumor suppressor linking PP1 to JNK-c-Jun pathway regulation in NSCLC. Oncotarget 7(1): 509-523.

148.Su, F., Chen, Y., Zhu, S., Li, F., Zhao, S., Wu, L., Chen, X. and Su, J. (2016). RAB22A overexpression promotes the tumor growth of melanoma. Oncotarget 7(44): 71744-71753.

149.Duan, M., Long, Y., Yang, C., Wu, X., Sun, Y., Li, J., Hu, X., Lin, W., Han, D., Zhao, Y., Liu, J., Ye, M. and Tan, W. (2016). Selection and characterization of DNA aptamer for metastatic prostate cancer recognition and tissue imaging. Oncotarget 7(24): 36436-36446.

150.Qiao, A., Wang, K., Yuan, Y., Guan, Y., Ren, X., Li, L., Chen, X., Li, F., Chen, A. F., Zhou, J., Yang, J. M. and Cheng, Y. (2016). Sirt3-mediated mitophagy protects tumor cells against apoptosis under hypoxia. Oncotarget 7(28): 43390-43400.

151.Luo, Z., Zhang, X., Zeng, W., Su, J., Yang, K., Lu, L., Lim, C. B., Tang, W., Wu, L., Zhao, S., Jia, X., Peng, C. and Chen, X. (2016). TRAF6 regulates melanoma invasion and metastasis through ubiquitination of Basigin. Oncotarget 7(6): 7179-7192.

152.Su, M., Huang, J., Li, J., Qin, X., Tang, X., Jin, F., Chen, S., Jiang, C., Zou, Z., Peng, K., Nuruzzaman, M., Zhang, J., Luo, J., Liu, S. and Luo, Z. (2016). ZLM-7 exhibits anti-angiogenic effects via impaired endothelial cell function and blockade of VEGF/VEGFR-2 signaling. Oncotarget 7(14): 19018-19030.

153.Du, R. F., Huang, H., Fan, L. L., Li, X. P., Xia, K. and Xiang, R. (2016). A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases. Ophthalmic Genet 37(1): 111-115.

154.Tang, J., Hu, Z., Tan, J., Yang, S. and Zeng, L. (2016). Parkin Protects against Oxygen-Glucose Deprivation/Reperfusion Insult by Promoting Drp1 Degradation. Oxid Med Cell Longev 2016: 8474303.

155.Lei, L. F., Yang, G. P., Wang, J. L., Chuang, D. M., Song, W. H., Tang, B. S. and Jiang, H. (2016). Safety and efficacy of valproic acid treatment in SCA3/MJD patients. Parkinsonism Relat Disord 26: 55-61.

156.Shu, L., Sun, Q., Zhang, Y., Xu, Q., Guo, J., Yan, X. and Tang, B. (2016). The Association between C9orf72 Repeats and Risk of Alzheimer's Disease and Amyotrophic Lateral Sclerosis: A Meta-Analysis. Parkinsons Dis 2016: 5731734.

157.Zhang, D. Y., Yuan, X. Q., Yan, H., Cao, S., Zhang, W., Li, X. L., Zeng, H. and Chen, X. P. (2016). Association between DCK 35708 T>C variation and clinical outcomes of acute myeloid leukemia in South Chinese patients. Pharmacogenomics 17(14): 1519-1531.

158.Wen, Z. P., Fan, S. S., Du, C., Yin, T., Zhou, B. T., Peng, Z. F., Xie, Y. Y., Zhang, W., Chen, Y., Tang, J., Xiao, J. and Chen, X. P. (2016). Influence of acylpeptide hydrolase polymorphisms on valproic acid level in Chinese epilepsy patients. Pharmacogenomics 17(11): 1219-1225.

159.Yin, J. Y., Li, X., Zhou, H. H. and Liu, Z. Q. (2016). Pharmacogenomics of platinum-based chemotherapy sensitivity in NSCLC: toward precision medicine. Pharmacogenomics 17(12): 1365-1378.

160.Yang, Y., Song, M., Liu, Y., Liu, H., Sun, L., Peng, Y., Liu, F., Venkatachalam, M. A. and Dong, Z. (2016). Renoprotective approaches and strategies in acute kidney injury. Pharmacol Ther 163: 58-73.

161.Chen, G., Le, Y., Zhou, L., Gong, L., Li, X., Li, Y., Liao, Q., Duan, K., Tong, J. and Ouyang, W. (2016). Dexmedetomidine Inhibits Maturation and Function of Human Cord Blood-Derived Dendritic Cells by Interfering with Synthesis and Secretion of IL-12 and IL-23. PLoS One 11(4): e0153288.

162.Duan, R., Shi, Y., Yu, L., Zhang, G., Li, J., Lin, Y., Guo, J., Wang, J., Shen, L., Jiang, H., Wang, G. and Tang, B. (2016). UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia. PLoS One 11(2): e0149039.

163.Song, P., Li, S., Wu, H., Gao, R., Rao, G., Wang, D., Chen, Z., Ma, B., Wang, H., Sui, N., Deng, H., Zhang, Z., Tang, T., Tan, Z., Han, Z., Lu, T., Zhu, Y. and Chen, Q. (2016). Parkin promotes proteasomal degradation of p62: implication of selective vulnerability of neuronal cells in the pathogenesis of Parkinson's disease. Protein Cell 7(2): 114-129.

164.Shen, Y., Ou, J., Liu, M., Shi, L., Li, Y., Xiao, L., Dong, H., Zhang, F., Xia, K. and Zhao, J. (2016). Altered plasma levels of chemokines in autism and their association with social behaviors. Psychiatry Research 244: 300-305.

165.Pu, W., Luo, Q., Palaniyappan, L., Xue, Z., Yao, S., Feng, J. and Liu, Z. (2016). Failed cooperative, but not competitive, interaction between large-scale brain networks impairs working memory in schizophrenia. Psychol Med 46(6): 1211-1224.

166.Hu, M., Zong, X., Zheng, J., Mann, J. J., Li, Z., Pantazatos, S. P., Li, Y., Liao, Y., He, Y., Zhou, J., Sang, D., Zhao, H., Tang, J., Chen, H., Lv, L. and Chen, X. (2016). Risperidone-induced topological alterations of anatomical brain network in first-episode drug-naive schizophrenia patients: a longitudinal diffusion tensor imaging study. Psychol Med: 1-12.

167.Zhao, J., Xu, B., Xie, S., Zhang, Q. and Li, Y. P. (2016). Whether G-CSF administration has beneficial effect on the outcome after assisted reproductive technology? A systematic review and meta-analysis. Reprod Biol Endocrinol 14(1): 62.

168.Xie, S., Batnasan, E., Zhang, Q. and Li, Y. (2016). MicroRNA Expression is Altered in Granulosa Cells of Ovarian Hyperresponders. Reprod Sci 23(8): 1001-1010.

169.Gui, B., Yao, Z., Li, Y., Liu, D., Liu, N., Xia, Y., Huang, Y., Mei, L., Ma, R., Lu, S., Liang, D. and Wu, L. (2016). Chromosomal analysis of blastocysts from balanced chromosomal rearrangement carriers. Reproduction 151(4): 455-464.

170.Zhao, J., Xu, B., Zhang, Q. and Li, Y. P. (2016). Which one has a better obstetric and perinatal outcome in singleton pregnancy, IVF/ICSI or FET?: a systematic review and meta-analysis. Reproductive Biology and Endocrinology 14(1): 51.

171.Liu, C., Xue, Z., Palaniyappan, L., Zhou, L., Liu, H., Qi, C., Wu, G., Mwansisya, T. E., Tao, H., Chen, X., Huang, X., Liu, Z. and Pu, W. (2016). Abnormally increased and incoherent resting-state activity is shared between patients with schizophrenia and their unaffected siblings. Schizophr Res 171(1-3): 158-165.

172.Mei, S., Livingston, M., Hao, J., Li, L., Mei, C. and Dong, Z. (2016). Autophagy is activated to protect against endotoxic acute kidney injury. Sci Rep 6: 22171.

173.Chen, Y., Wu, Z., Zhao, S. and Xiang, R. (2016). Chemical chaperones reduce ER stress and adipose tissue inflammation in high fat diet-induced mouse model of obesity. Sci Rep 6: 27486.

174.Hu, H., Liu, J., Liao, X., Zhang, S., Li, H., Lu, R., Li, X., Lin, W., Liu, M., Xia, Z., Qing, G. and Li, J. D. (2016). Genetic and functional analysis of a Li Fraumeni syndrome family in China. Sci Rep 6: 20221.

175.Ding, D., Chen, Z., Li, K., Long, Z., Ye, W., Tang, Z., Xia, K., Qiu, R., Tang, B. and Jiang, H. (2016). Identification of a de novo DYNC1H1 mutation via WES according to published guidelines. Sci Rep 6: 20423.

176.Zhou, Z., Hu, Z., Zhang, L., Hu, Z., Liu, H., Liu, Z., Du, J., Zhao, J., Zhou, L., Xia, K., Tang, B. and Shen, L. (2016). Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia. Sci Rep 6: 24327.

177.Wu, Y., Hu, Z., Li, Z., Pang, J., Feng, M., Hu, X., Wang, X., Lin-Peng, S., Liu, B., Chen, F., Wu, L. and Liang, D. (2016). In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs. Sci Rep 6: 18865.

178.Zhou, L., Pu, W., Wang, J., Liu, H., Wu, G., Liu, C., Mwansisya, T. E., Tao, H., Chen, X., Huang, X., Lv, D., Xue, Z., Shan, B. and Liu, Z. (2016). Inefficient DMN Suppression in Schizophrenia Patients with Impaired Cognitive Function but not Patients with Preserved Cognitive Function. Sci Rep 6: 21657.

179.Pan, Y., Zhang, L., Liu, Q., Li, Y., Guo, H., Peng, Y., Peng, H., Tang, B., Hu, Z., Zhao, J., Xia, K. and Li, J. D. (2016). Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression. Sci Rep 6: 35970.

180.Liu, Z., Guo, J., Wang, Y., Li, K., Kang, J., Wei, Y., Sun, Q., Xu, Q., Xu, C., Yan, X. and Tang, B. (2016). Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson's disease with cognitive impairment in a Chinese population. Sci Rep 6: 19021.

181.Li, H., Ouyang, R., Wang, Z., Zhou, W., Chen, H., Jiang, Y., Zhang, Y., Li, H., Liao, M., Wang, W., Ye, M., Ding, Z., Feng, X., Liu, J. and Zhang, B. (2016). MiR-150 promotes cellular metastasis in non-small cell lung cancer by targeting FOXO4. Sci Rep 6: 39001.

182.Zhang, W., Jiao, B., Xiao, T., Pan, C., Liu, X., Zhou, L., Tang, B. and Shen, L. (2016). Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China. Sci Rep 6: 38435.

183.Wang, H., Guo, W., Liu, F., Wang, G., Lyu, H., Wu, R., Chen, J., Wang, S., Li, L. and Zhao, J. (2016). Patients with first-episode, drug-naive schizophrenia and subjects at ultra-high risk of psychosis shared increased cerebellar-default mode network connectivity at rest. Sci Rep 6: 26124.

184.Sun, Z., Jia, D., Shi, Y., Hou, X., Yang, X., Guo, J., Li, N., Wang, J., Sun, Q., Zhang, H., Lei, L., Shen, L., Yan, X., Xia, K., Jiang, H. and Tang, B. (2016). Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease. Sci Rep 6: 21649.

185.Kang, J. F., Luo, Y., Tang, B. S., Wan, C. M., Yang, Y., Li, K., Liu, Z. H., Sun, Q. Y., Xu, Q., Yan, X. X. and Guo, J. F. (2016). RAB39B gene mutations are not linked to familial Parkinson's disease in China. Sci Rep 6: 34502.

186.Long, Y., Qin, Z., Duan, M., Li, S., Wu, X., Lin, W., Li, J., Zhao, Z., Liu, J., Xiong, D., Huang, Y., Hu, X., Yang, C., Ye, M. and Tan, W. (2016). Screening and identification of DNA aptamers toward Schistosoma japonicum eggs via SELEX. Sci Rep 6: 24986.

187.Hou, L., Jiao, B., Xiao, T., Zhou, L., Zhou, Z., Du, J., Yan, X., Wang, J., Tang, B. and Shen, L. (2016). Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. Sci Rep 6: 32478.

188.Hu, M. L., Zong, X. F., Zheng, J. J., Pantazatos, S. P., Miller, J. M., Li, Z. C., Liao, Y. H., He, Y., Zhou, J., Sang, D. E., Zhao, H. Z., Lv, L. X., Tang, J. S., Mann, J. J. and Chen, X. G. (2016). Short-term Effects of Risperidone Monotherapy on Spontaneous Brain Activity in First-episode Treatment-naive Schizophrenia Patients: A Longitudinal fMRI Study. Sci Rep 6: 34287.

189.Zeng, S., Zeng, J., He, M., Zeng, X., Zhou, Y., Liu, Z., Xia, K., Pan, Q., Jiang, H., Shen, L., Yan, X., Tang, B. and Wang, J. (2016). Spinocerebellar ataxia type 21 exists in the Chinese Han population. Sci Rep 6: 19897.

190.Wang, X., He, F., Yin, F., Chen, C., Wu, L., Yang, L. and Peng, J. (2016). The use of targeted genomic capture and massively parallel sequencing in diagnosis of Chinese Leukoencephalopathies. Sci Rep 6: 35936.

191.Wang, S., Wang, G., Lv, H., Wu, R., Zhao, J. and Guo, W. (2016). Abnormal regional homogeneity as potential imaging biomarker for psychosis risk syndrome: a resting-state fMRI study and support vector machine analysis. Scientific Reports 6: 27619.

192.Su, M., Huang, J., Liu, S., Xiao, Y., Qin, X., Liu, J., Pi, C., Luo, T., Li, J., Chen, X. and Luo, Z. (2016). The anti-angiogenic effect and novel mechanisms of action of Combretastatin A-4. Scientific Reports 6: 28139.

193.Havasi, A. and Dong, Z. (2016). Autophagy and Tubular Cell Death in the Kidney. Semin Nephrol 36(3): 174-188.

194.Liu, H., Ma, L., Ma, C., Du, J., Wang, M. and Wang, K. (2016). Quencher-Free Fluorescence Method for the Detection of Mercury(II) Based on Polymerase-Aided Photoinduced Electron Transfer Strategy. Sensors (Basel) 16(11): 1945; doi:1910.3390/s16111945.

195.Du, R., Fan, L.-L., Lin, M.-J., He, Z.-J., Huang, H., Chen, Y.-Q., Li, J.-J., Xia, K., Zhao, S.-P. and Xiang, R. (2016). Mutation detection in Chinese patients with familial hypercholesterolemia. SpringerPlus 5(1): 2095.

196.Kang, J. F., Tang, B. S. and Guo, J. F. (2016). The Progress of Induced Pluripotent Stem Cells as Models of Parkinson's Disease. Stem Cell Int 2016: 1-6.

197.Xie, N. and Tang, B. (2016). The Application of Human iPSCs in Neurological Diseases: From Bench to Bedside. Stem Cells Int 2016: 6484713.

198.Zhang, W., Jiao, B., Zhou, M., Zhou, T. and Shen, L. (2016). Modeling Alzheimer's Disease with Induced Pluripotent Stem Cells: Current Challenges and Future Concerns. Stem Cells Int 2016: 7828049.

199.Ouyang, J., Zang, Q., Chen, W., Wang, L., Li, S., Liu, R. Y., Deng, Y., Liu, Z. Q., Li, J., Deng, L. and Liu, Y. N. (2016). Bright and photostable fluorescent probe with aggregation-induced emission characteristics for specific lysosome imaging and tracking. Talanta 159: 255-261.

200.Ma, C., Wu, K., Liu, H., Xia, K., Wang, K. and Wang, J. (2016). Label-free fluorescence turn-on detection of uracil DNA glycosylase activity based on G-quadruplex formation. Talanta 160: 449-453.

201.Roy, M., Liang, L., Xiao, X., Peng, Y., Luo, Y., Zhou, W., Zhang, J., Qiu, L., Zhang, S., Liu, F., Ye, M., Zhou, W. and Liu, J. (2016). Lycorine Downregulates HMGB1 to Inhibit Autophagy and Enhances Bortezomib Activity in Multiple Myeloma. Theranostics 6(12): 2209-2224.

202.Yan, M., Tang, C., Ma, Z., Huang, S. and Dong, Z. (2016). DNA damage response in nephrotoxic and ischemic kidney injury. Toxicol Appl Pharmacol 313: 104-108.

203.Deng, M., Hu, Z., Cai, T., Liu, K., Wu, W., Luo, X., Jiang, L., Wang, M., Yang, J., Xiao, Y. and Liang, S. (2016). Characterization of ion channels on subesophageal ganglion neurons from Chinese tarantula Ornithoctonus huwena: Exploring the myth of the spider insensitive to its venom. Toxicon 120: 61-68.

204.Yang, Q., Zhu, M., Wang, Z., Li, H., Zhou, W., Xiao, X., Zhang, B., Hu, W. and Liu, J. (2016). 4.1N is involved in a flotillin-1/beta-catenin/Wnt pathway and suppresses cell proliferation and migration in non-small cell lung cancer cell lines. Tumor Biol 37(9): 12713-12723.

205.Chen, J., Wu, L., Wang, Y., Yin, J., Li, X., Wang, Z., Li, H., Zou, T., Qian, C., Li, C., Zhang, W., Zhou, H. and Liu, Z. (2016). Effect of transporter and DNA repair gene polymorphisms to lung cancer chemotherapy toxicity. Tumour Biol 37(2): 2275-2284.

206.Li, Z., Guo, X., Tang, L., Peng, L., Chen, M., Luo, X., Wang, S., Xiao, Z., Deng, Z., Dai, L., Xia, K. and Wang, J. (2016). Methylation analysis of plasma cell-free DNA for breast cancer early detection using bisulfite next-generation sequencing. Tumour Biol 37(10): 13111-13119.

207.Yu, X., Zhai, Z., Zhao, Y., Zhu, Z., Tong, J., Yan, J. and Ouyang, W. (2016). Performance of Lung Ultrasound in Detecting Peri-Operative Atelectasis after General Anesthesia. Ultrasound Med Biol 42(12): 2775-2784.

208.Junjie, Z., Mao, T., Zanxian, X. and Pinghui, F. (2016). Roles of IκB kinase ε in the innate immune defense and beyond. Virol Sin 31(6): 457-465.

209.Luo, S.-Y., Wu, L.-Q. and Duan, R.-H. (2016). Molecular medicine of fragile X syndrome: based on known molecular mechanisms. World J Pediatr 12(1): 19-27.

210.羊蠡#, 尹飞* (2016). 热性惊厥、GEFS+、Dravet综合征与疫苗接种的关系. 国际儿科学杂志 43(12): 916-919.

211.苗圃#, 尹飞* (2016). 外显子测序在不明原因智力障碍病因学研究的应用进展. 国际儿科学杂志 43(7): 557-559.

212.武翠玲#, 刘丹, 杨兴昊, 吴日帮, 黄嘉丰, 张姜, 伦梓丰, 何海伦* (2016). Salinivibrio sp.YH4胞外蛋白酶EYH的分离纯化、酶学性质及基因克隆. 山东大学学报(理学版) 51(05): 36-42.

213.毕桃玲#, 孙金剑, 田雨子, 周叶方* (2016). 外泌体与乳腺癌关系的研究进展. 生理学报 68(03): 352-358.

214.武翠玲#, 吴日帮, 刘丹, 杨兴昊, 张姜, 黄嘉丰, 何海伦* (2016). 鲮鱼皮胶原肽的制备及其抗氧化活性的检测. 生物工程学报 32(12): 1727-1734.

215.胡睿#, 朱曙东* (2016). Src蛋白激酶活性的调节机制. 生物化学与生物物理进展 43(11): 1061-1069.

216.周晓涛#, 夏开德, 周文涛, 刘化蝶, 彭震, 汤勇, 李家大* (2016). 酵母表达质粒pGBKT7-hPROKR2-Ct的构建及hPROKR2C端蛋白的自激活鉴定. 生物技术通讯 27(04): 479-482.

217.谢诗#, 赵静, 李艳萍* (2016). 转基因治疗不孕相关疾病研究进展. 生殖与避孕 36(08): 678-682.

218.牛志杰#, 蒋璐#, 梅凌云*, 冯永*, 陈红胜, 贺楚峰, 刘亚兰, 王雪萍, 刘畅, 熊俊 (2016). 一个常染色体显性遗传非综合征型聋家系的听力学及遗传学特征分析. 听力学及言语疾病杂志 24(1): 5-9.

219.李善妮#, 何海伦*, 邓梅春, 马昌杯 (2016). 中南大学生命科学学科国际化综合改革探索和创新. 西北医学教育 24(04): 518-522.

220.谢诗#, 曾筠, 卢凤笛, 张静平, 王萍, 李艳萍* (2016). 辅助生殖技术多胎妊娠行减胎术对临床结局的影响. 现代妇产科进展 25(09): 689-690.

221.李辉#, 吴栋文, 单年春, 曹兰, 王永刚, 刘婧, 李艳萍* (2016). 甘氨双唑钠对宫颈癌放疗及同步放化疗增敏疗效的Meta分析. 现代妇产科进展 25(09): 661-666.

222.李元丰, 韩玉波, 曹鹏博, 孟金凤, 李海北, 秦庚, 张锋, 靳光付, 杨勇, 邬玲仟, 平杰, 周钢桥* (2016). 2015年中国医学遗传学研究领域若干重要进展. 遗传 38(05): 363-390.

223.吴天慧#, 尹飞, 彭镜*, 孔惠敏, 李琳红 (2016). MicroRNA-132拮抗剂两种不同注射方式在匹罗卡品诱导的幼年大鼠癫痫急性期的差异. 中风与神经疾病杂志 33(07): 600-603.

224.吴天慧#, 尹飞, 彭镜*, 孔惠敏, 李琳红 (2016). MicroRNA-132拮抗剂对匹罗卡品诱导的幼年大鼠癫癎持续状态的影响. 中国当代儿科杂志 18(10): 1030-1034.

225.邓小鹿#, 王霞*, 张慈柳, 唐幸, 尹飞 (2016). 学龄期男孩发热、全身疼痛并肺部多发结节. 中国当代儿科杂志 18(09): 857-861.

226.刘亚兰#, 汪俊程, 邓宇元, 冯永* (2016). 荧光PCR法在非综合征型遗传性耳聋基因诊断中的应用研究. 中国耳鼻咽喉颅底外科杂志 22(5): 345-348,352.

227.唐颂亚#, 安静, 周世杰* (2016). 早期创伤与反社会人格障碍的关系. 中国临床心理学杂志 24(01): 155-159.

228.钱晨月#, 周宏灏, 刘昭前* (2016). eIF3a的生物学功能及其对肿瘤化疗的影响. 中国临床药理学与治疗学 21(3): 328-334.

229.邹婷#, 刘昭前* (2016). RAC1与肺癌发生及临床治疗的研究进展. 中国临床药理学与治疗学 21(9): 1055-1060.

230.茆晨雪#, 周宏灏, 刘昭前* (2016). 弥漫性胶质瘤生物标志物的发现及研究进展. 中国临床药理学与治疗学 21(1): 93-98.

231.张晓钿, 曹娟, 阎青青, 郭少丽, 刘昭前* (2016). 电刺激对缺氧缺血性脑损伤新生大鼠脑组织bFGF的影响. 中国热带医学 16(1): 17-19.

232.毛小元#, 周宏灏, 刘昭前* (2016). MicroRNA与神经胶质瘤血管生成及替莫唑胺化疗耐药关系的研究进展. 中国生化药物杂志 36(3): 1-4.

233.刘畅#, 凡秀丽, 刘能辉*, 李艳萍, 刘冬娥, 姚仲元, 陈仙花 (2016). 新鲜周期和冻融周期胚胎移植术后发生异位妊娠的相关因素分析. 中国现代医学杂志 26(07): 88-92.

234.邓小鹿#, 何芳, 吴丽文, 尹飞, 彭镜* (2016). CHD2基因突变导致Dravet综合征1例病例报告. 中国循证儿科杂志 11(06): 473-474.

235.谭丹, 颜晗, 庞凤梅, 谢攀, 尹继业, 刘昭前, 李曦* (2016). IDH突变通过影响GNG基因表达而影响低级别脑胶质瘤患者预后. 中国药理学与毒理学杂志 30(10): 1064-1067.

236.茆晨雪#, 周宏灏, 刘昭前* (2016). 星形胶质细胞瘤甲基化和非编码RNA表观基因组学研究. 中国药理学与毒理学杂志 30(10): 1060-1061.

237.杨湘峰#*, 尹飞 (2016). 六岁以下癫痫患儿认知功能损害的影响因素探讨. 中国医师进修杂志 39(8): 721-723.

238.王小伟#, 慕云, 龙樱, 詹显全* (2016). 人垂体腺瘤蛋白质组研究进展与展望. 中国医师杂志 18(7): 1102-1108.

239.张锐#, 彭莹, 郭若兰, 郭婧, 夏艳, 邬玲仟* (2016). 6p22.3微缺失导致精神发育迟滞一例. 中华儿科杂志 54(11): 866-867.

240.邓小鹿#, 尹飞, 张慈柳, 马玉平, 何芳, 吴丽文, 彭镜* (2016). Dynamin-1基因新生突变导致婴儿痉挛症一例并文献复习. 中华儿科杂志 54(11): 856-859.

241.黄文#, 罗仕玉, 杜倩, 杨璞, 谭虎, 邬玲仟, 段然慧* (2016). 脆性X综合征二例CGG重复序列及甲基化分析. 中华儿科杂志 54(4): 287-289.

242.罗洋, 唐北沙, 郭纪锋* (2016). ATP1 A3基因与快发病性肌张力障碍-帕金森综合征和儿童交替性偏瘫. 中华神经科杂志 49(11): 892-896.

243.康纪峰#, 唐北沙, 郭纪锋* (2016). PLA2G6基因与帕金森病. 中华神经科杂志(2): 145-149.

244.Duan, R., Luo, S., Huang, W., Li, H., Peng, Y., Du, Q. and Wu, L. (2016). [Analysis of CGG repeat instability in germline cells from two male fetuses affected with fragile X syndrome]. 中华医学遗传学杂志 33(5): 606-609.

245.Peng, Y., Tang, G., Zhang, R., Zhang, Y., Xia, Y., Ma, R., Guo, R., Wu, L. (2016). [Genetic diagnosis, analysis for two cases of ring chromosome 22]. 中华医学遗传学杂志 33(4): 494-497.

246.张莉#, 张冬梅*, 郑莹莹, 胡正茂, 曾怡, 岳芳芝 (2016). NLRP3基因单核苷酸多态性与代谢综合征的关系研究. 中华医学遗传学杂志 33(4): 530-534.

247.Yang, N., Wei, Y., Xu, Q. and Tang, B. (2016). Progress in epigenetic research on Alzheimer disease. 中华医学遗传学杂志 33(2): 252-255.

248.Yang, F., Cao, P., Zhou, G. (2016). 常见拷贝数变异与疾病的关联研究. 中华医学遗传学杂志 33(3): 388-391.

249.杜然, 范亮亮, 黄皓, 项荣* (2016). 原发性厚皮性骨膜病的遗传学研究进展. 中华医学遗传学杂志 33(1): 105-107.

250.李小平*#, 郝朝亮, 郭辉 (2016). Shank3基因多态性与汉族儿童孤独症的病例对照研究. 重庆医学 45(04): 469-471.

251.赖允丽#, 陈筠, 易升, 周林, 易赏, 雷亚琴, 郑海洋, 林飞, 邬玲仟*, 韦红卫* (2016). 无创产前检测的临床应用及随访研究. 重庆医学 45(11): 1491-1495.


     
     
     
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