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科研项目国家重大科技计划专栏科研队伍发表论文研究成果专著专利
 

2017年发表论文

浏览:3750 来源:SKLMG
 

1.        Li, J., Wang, L., Yu, P., Shi, L., Zhang, K., Sun, Z. S. and Xia, K. (2017). Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet: doi: 10.1002/ajmg.b.32543.

2.        Yang, Z., Liu, Y., Qin, L., Wu, P., Xia, Z., Luo, M., Zeng, Y., Tsukamoto, H., Ju, Z., Su, D., Kang, H., Xiao, Z., Zheng, S., Duan, Z., Hu, R., Wang, Q., Pandol, S. J. and Han, Y. P. (2017). Cathepsin H-Mediated Degradation of HDAC4 for Matrix Metalloproteinase Expression in Hepatic Stellate Cells: Implications of Epigenetic Suppression of Matrix Metalloproteinases in Fibrosis through Stabilization of Class IIa Histone Deacetylases. Am J Pathol 187(4): 781-797.

3.        Yin, B., Zeng, Y., Wu, T., Yu, S., Xu, J., Liu, S., Diao, L., Zhao, Z., Liang, D. and Li, Y. (2017). Functional properties of peripheral CD8+ T cells in patients with repeated implantation failure. Am J Reprod Immunol: doi: 10.1111/aji.12704.

4.        Liu, J.-S., Fan, L.-L., Li, J.-J. and Xiang, R. (2017). Whole-Exome Sequencing Identifies a Novel Mutation of Desmocollin 2 in a Chinese Family With Arrhythmogenic Right Ventricular Cardiomyopathy. The American journal of cardiology 119(9): 1485-1489.

5.        Liu, H., Ma, C., Wang, J., Chen, H. and Wang, K. (2017). Label-free colorimetric assay for T4 polynucleotide kinase/phosphatase activity and its inhibitors based on G-quadruplex/hemin DNAzyme. Anal Biochem 517: 18-21.

6.        Mao, X., Qian, S., Peng, J., Cui, W., Lu, G. and Zhan, Y. (2017). Two patients with TNK2 mutations and late onset infantile spasm. Ann Neurol 81(1): 161.

7.        Xiang, R., Fan, L. L., Lin, M. J., Li, J. J., Shi, X. Y., Jin, J. Y., Liu, Y. X., Chen, Y. Q., Xia, K. and Zhao, S. P. (2017). The genetic spectrum of familial hypercholesterolemia in the central south region of China. Atherosclerosis 258: 84-88.

8.        Lijuan, C., Xing, Y., Minxi, W., Wenkai, L. and Le, D. (2017). Development of an aptamer-ampicillin conjugate for treating biofilms. Biochem Biophys Res Commun 483(2): 847-854.

9.        Wang, Y. J., Zhang, H. Q., Han, H. L., Zou, Y. Y., Gao, Q. L. and Yang, G. T. (2017). Taxifolin enhances osteogenic differentiation of human bone marrow mesenchymal stem cells partially via NF-kappaB pathway. Biochem Biophys Res Commun 490(1): 36-43.

10.     Ma, C., Lv, X., Wang, K., Jin, S., Liu, H., Wu, K. and Zeng, W. (2017). Simple fluorescence-based detection of protein kinase A activity using a molecular beacon probe. Bioengineered: doi: 10.1080/21655979.21652017.21338219.

11.     Li, L. Y., Xiao, J., Liu, Q. and Xia, K. (2017). Parecoxib inhibits glioblastoma cell proliferation, migration and invasion by upregulating miRNA-29c. Biol Open 6(3): 311-316.

12.     Li, H., Choesang, T., Bao, W., Chen, H., Feola, M., Garcia-Santos, D., Li, J., Sun, S., Follenzi, A., Pham, P., Liu, J., Zhang, J., Ponka, P., An, X., Mohandas, N., Fleming, R. E., Rivella, S., Li, G. and Ginzburg, Y. Z. (2017). Decreasing TfR1 expression reverses anemia and hepcidin suppression in beta-thalassemic mice. Blood 129(11): 1514-1526.

13.     Han, X., Zhang, J., Peng, Y., Peng, M., Chen, X., Chen, H., Song, J., Hu, X., Ye, M., Li, J., Sankaran, V. G., Hillyer, C. D., Mohandas, N., An, X. and Liu, J. (2017). Unexpected role for p19INK4d in posttranscriptional regulation of GATA1 and modulation of human terminal erythropoiesis. Blood 129(2): 226-237.

14.     Tian, Q., Li, Y., Kousar, R., Guo, H., Peng, F., Zheng, Y., Yang, X., Long, Z., Tian, R., Xia, K., Lin, H. and Pan, Q. (2017). A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family. Bmc Medical Genetics 18: 2.

15.     Xu, Q., Li, K., Sun, Q., Ding, D., Zhao, Y., Yang, N., Luo, Y., Liu, Z., Zhang, Y., Wang, C., Xia, K., Yan, X., Jiang, H., Shen, L., Tang, B. and Guo, J. (2017). Rare GCH1 heterozygous variants contributing to Parkinson's disease. Brain 140(7): e41.

16.     Chen, Z., Wang, C., Zheng, C., Long, Z., Cao, L., Li, X., Shang, H., Yin, X., Zhang, B., Liu, J., Ding, D., Peng, Y., Peng, H., Ye, W., Qiu, R., Pan, Q., Xia, K., Chen, S., Sequeiros, J., Ashizawa, T., Tang, B., Jiang, H. and Chinese Clinical Research Cooperative Group for Spinocerebellar, A. (2017). Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease. Brain 140(4): e25.

17.     Liu, J.-S., Fan, L.-L., Zhang, H., Liu, X., Huang, H., Li, J., Xia, K. and Xiang, R. (2017). Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated Cardiomyopathy. Cardiology 136(1): 10-14.

18.     Xie, H. F., Liu, Y. Z., Du, R., Wang, B., Chen, M. T., Zhang, Y. Y., Deng, Z. L. and Li, J. (2017). miR-377 induces senescence in human skin fibroblasts by targeting DNA methyltransferase 1. Cell Death Dis 8(3): e2663.

19.     Sun, Y., Cao, L., Sheng, X., Chen, J., Zhou, Y., Yang, C., Deng, T., Ma, H., Feng, P., Liu, J., Tan, W. and Ye, M. (2017). WDR79 promotes the proliferation of non-small cell lung cancer cells via USP7-mediated regulation of the Mdm2-p53 pathway. Cell Death Dis 8(4): e2743.

20.     Qiu, W., Lin, J., Zhu, Y., Zhang, J., Zeng, L., Su, M. and Tian, Y. (2017). Kaempferol Modulates DNA Methylation and Downregulates DNMT3B in Bladder Cancer. Cell Physiol Biochem 41(4): 1325-1335.

21.     Chen, J., Zhao, J., Chen, X., Ding, C., Lee, K., Jia, Z., Zhang, Y., Zhou, Y., Wei, C., He, J., Xia, Z. and Peng, J. (2017). Hyper activation of beta-catenin signalling induced by IKKepsilon inhibition thwarts colorectal cancer cell proliferation. Cell Prolif: doi: 10.1111/cpr.12350.

22.     Chen, T., Dong, B., Chen, K., Zhao, F., Cheng, X., Ma, C., Lee, S., Zhang, P., Kang, S. H., Ha, J. W., Xu, W. and Fang, N. (2017). Optical Super-Resolution Imaging of Surface Reactions. Chem Rev 117(11): 7510-7537.

23.     Han, X. and Liu, J. (2017). Cell cycle-independent roles of p19INK4d in human terminal erythropoiesis. Chin J Cancer 36(1): 22.

24.     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. (2017). Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIII. Clin Chim Acta 464: 170-175.

25.     Jiang, C., Gai, N., Zou, Y., Zheng, Y., Ma, R., Wei, X., Liang, D. and Wu, L. (2017). WDR73 missense mutation causes infantile onset intellectual disability and cerebellar hypoplasia in a consanguineous family. Clin Chim Acta 464: 24-29.

26.     Liu, L., Li, X. B., Hu, Z. H. M., Zi, X. H., Zhao, X., Xie, Y. Z., Huang, S. H. X., Xia, K., Tang, B. S. and Zhang, R. X. (2017). Phenotypes and cellular effects of GJB1 mutations causing CMT1X in a cohort of 226 Chinese CMT families. Clin Genet 91(6): 881-891.

27.     Cheng, T. and Zhan, X. (2017). Pattern recognition for predictive, preventive, and personalized medicine in cancer. EPMA J 8(1): 51-60.

28.     Wang, Y., Guo, Z., Shu, Y., Zhou, H., Wang, H. and Zhang, W. (2017). BART miRNAs: an unimaginable force in the development of nasopharyngeal carcinoma. Eur J Cancer Prev 26(2): 144-150.

29.     Wang, C., Fang, Z., Zhu, Z., Liu, J. and Chen, H. (2017). Reciprocal regulation between hepcidin and erythropoiesis and its therapeutic application in erythroid disorders. Exp Hematol: doi: 10.1016/j.exphem.2017.1005.1002.

30.     Li, H., Zhou, H., Luo, J. and Huang, J. (2017). MicroRNA-17-5p inhibits proliferation and triggers apoptosis in non-small cell lung cancer by targeting transforming growth factor beta receptor 2. Exp Ther Med 13(6): 2715-2722.

31.     Zhang, R., Linpeng, S., Wei, X., Li, H., Huang, Y., Guo, J., Wu, Q., Liang, D. and Wu, L. (2017). Novel variants in PAX6 gene caused congenital aniridia in two Chinese families. Eye (Lond) 31(6): 956-961.

32.     Tan, H., Wei, X., Yang, P., Huang, Y., Li, H., Liang, D. and Wu, L. (2017). A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report. Fam Cancer 16(3): 417-422.

33.     Kong, H. E., Zhao, J., Xu, S., Jin, P. and Jin, Y. (2017). Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics. Front Cell Neurosci 11: 128.

34.     Luo, H., Zheng, R., Zhao, Y., Wu, J., Li, J., Jiang, F., Chen, D. N., Zhou, X. T. and Li, J. D. (2017). A dominant negative FGFR1 mutation identified in a Kallmann syndrome patient. Gene 621: 1-4.

35.     Zhu, Z., Lu, X., Yuan, D. and Huang, S. (2017). Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs. Genomics 109(1): 9-15.

36.     Yuan, D. and Huang, S. (2017). Genetic equidistance at nucleotide level. Genomics 109(3-4): 192-195.

37.     Chen, Y., Bartanus, J., Liang, D., Zhu, H., Breman, A. M., Smith, J. L., Wang, H., Ren, Z., Patel, A., Stankiewicz, P., Cram, D. S., Cheung, S. W., Wu, L. and Yu, F. (2017). Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development. Hum Mutat 38(6): 669-677.

38.     Yin, B., Zhu, Y., Wu, T., Shen, S., Zeng, Y. and Liang, D. (2017). Clinical outcomes for couples containing a reciprocal chromosome translocation carrier without preimplantation genetic diagnosis. Int J Gynaecol Obstet 136(3): 304-308.

39.     Zhou, M.-J., Chen, F.-Z., Chen, H.-C., Wan, X.-X., Zhou, X., Fang, Q. and Zhang, D.-Z. (2017). ISG15 inhibits cancer cell growth and promotes apoptosis. Int J Mol Medicine 39(2): 446-452.

40.     Che, X. Q., Sun, Z. F., Mao, X., Xia, K., Yan, X. X., Jiang, H., Shen, L., Li, N. and Tang, B. S. (2017). Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population. Int J Neurosci 127(1): 10-13.

41.     Guo, W., Liu, F., Chen, J., Wu, R., Li, L., Zhang, Z., Chen, H. and Zhao, J. (2017). Anatomical distance affects cortical-subcortical connectivity in first-episode, drug-naive somatization disorder. J affect disorders 217: 153-158.

42.     Li, J., Guo, A., Chen, W., Bin, L., He, Y., Zhu, W., Yan, S., Peng, C., Chen, M., Zhang, J., Su, J., Yi, M., Liu, Z., Zhang, W., Zeng, W., Leung, D. Y. and Chen, X. (2017). Association of ORAI1 Gene Polymorphisms with Chronic Spontaneous Urticaria and the Efficacy of the Nonsedating H1-antihistamine Desloratadine. J Allergy Clin Immunol 139(4): 1386-1388 e1389.

43.     Huang, J., Wu, C., Liu, D., Yang, X., Wu, R., Zhang, J., Ma, C. and He, H. (2017). C-terminal domains of bacterial proteases: structure, function and the biotechnological applications. J Appl Microbiol 122(1): 12-22.

44.     Lin, L., You, J., Qian, Y., Han, Y., Xiong, H., Zhu, T., Xia, K. and Su, T. (2017). The prognostic value of T Lymphoma Invasion and Metastasis 1 (TIAM1) expression in oral squamous cell carcinoma. J Biochem Mol Toxicol 31(4): doi: 10.1002/jbt.21875.

45.     Li, G., Guo, X., Tang, L., Chen, M., Luo, X., Peng, L., Xu, X., Wang, S., Xiao, Z., Yi, W., Dai, L. and Wang, J. (2017). Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing. J Cancer Res Clin Oncol: doi: 10.1007/s00432-00017-02465-00438.

46.     Wei, X., Tan, H., Yang, P., Zhang, R., Tan, B., Zhang, Y., Mei, L., Liang, D. and Wu, L. (2017). 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.

47.     Cai, X. Z., Li, Y., Xia, L., Peng, Y., He, C. F., Jiang, L., Feng, Y., Xia, K., Liu, X. Z., Mei, L. Y. and Hu, Z. M. (2017). Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss. J Hum Genet 62(2): 317-320.

48.     Sun, J., Hao, Z., Luo, H., He, C., Mei, L., Liu, Y., Wang, X., Niu, Z., Chen, H., Li, J. D. and Feng, Y. (2017). Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2. J Hum Genet 62(7): 703-709.

49.     Luo, X., Zou, Y., Tan, B., Zhang, Y., Guo, J., Zeng, L., Zhang, R., Tan, H., Wei, X., Hu, Y., Zheng, Y., Liang, D. and Wu, L. (2017). Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases. J Hum Genet 62(4): 513-516.

50.     Huang, X., Liu, Z., Mwansisya, T. E., Pu, W., Zhou, L., Liu, C., Chen, X., Rohrbaugh, R., Marienfeld, C., Xue, Z. and Liu, H. (2017). Betel quid chewing alters functional connectivity in frontal and default networks: A resting-state fMRI study. J Magn Reson Imaging 45(1): 157-166.

51.     de Polo, A., Luo, Z., Gerarduzzi, C., Chen, X., Little, J. B. and Yuan, Z. M. (2017). AXL receptor signalling suppresses p53 in melanoma through stabilization of the MDMX-MDM2 complex. J Mol Cell Biol 9(2): 154-165.

52.     Luo, Z., Li, X., Zhu, M., Tang, J., Li, Z., Zhou, X., Song, G., Liu, Z., Zhou, H. and Zhang, W. (2017). Identification of novel variants associated with warfarin stable dosage by use of a two-stage extreme phenotype strategy. J Thromb Haemost 15(1): 28-37.

53.     Liu, H., Zhang, L., Sun, J., Chen, W., Li, S., Wang, Q., Yu, H., Xia, Z., Jin, X. and Wang, C. (2017). Endoplasmic Reticulum Protein SCAP Inhibits Dengue Virus NS2B3 Protease by Suppressing Its K27-Linked Polyubiquitylation. J Virol 91(9): doi: 10.1128/JVI.02234-02216.

54.     Wu, R., Chen, L., Liu, D., Huang, J., Zhang, J., Xiao, X., Lei, M., Chen, Y. and He, H. (2017). Preparation of Antioxidant Peptides from Salmon Byproducts with Bacterial Extracellular Proteases. Mar Drugs 15(1): doi: 10.3390/md15010004.

55.     Guo, W., Liu, F., Chen, J., Wu, R., Li, L., Zhang, Z., Chen, H. and Zhao, J. (2017). Hyperactivity of the default-mode network in first-episode, drug-naive schizophrenia at rest revealed by family-based case-control and traditional case-control designs. Medicine (Baltimore) 96(13): e6223.

56.     He, H., Li, H. and Liu, D. (2017). In Situ Demonstration and Characteristic Analysis of the Protease Using Substrate Immersing Zymography. Methods Mol Biol 1626: 205-212.

57.     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. (2017). Knockout of 4.1B triggers malignant transformation in SV40T-immortalized mouse embryo fibroblast cells. Mol Carcinog 56(2): 538-549.

58.     Wang, J., Liu, H., Ma, C., Wang, J., Zhong, L. and Wu, K. (2017). Label-free monitoring of DNA polymerase activity based on a thrombin-binding aptamer G-quadruplex. Mol Cell Probes 32: 13-17.

59.     Guo, T., Yang, K., Liu, L., Tan, Z. P. and Luo, H. (2017). Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy. Mol Med Rep 15(5): 2977-2982.

60.     Wu, P. F., Jin, J. Y., Li, J. J., He, J. Q., Fan, L. L., Jin, M., Huang, H., Xia, K., Tang, J. Y. and Xiang, R. (2017). A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome. Mol Med Rep 15(6): 3735-3738.

61.     Hu, Z., Zhong, B., Tan, J., Chen, C., Lei, Q. and Zeng, L. (2017). The Emerging Role of Epigenetics in Cerebral Ischemia. Mol Neurobiol 54(3): 1887-1905.

62.     Zhang, X., Wu, Y., Cai, F., Liu, S., Bromley-Brits, K., Xia, K. and Song, W. (2017). A Novel Alzheimer-Associated SNP in Tmp21 Increases Amyloidogenesis. Mol Neurobiol: doi:10.1007/s12035-12017-10459-12039.

63.     Stessman, H. A., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., Vives, L., Lin, J., Turner, T. N., Santen, G., Ruivenkamp, C., Kriek, M., van Haeringen, A., Aten, E., Friend, K., Liebelt, J., Barnett, C., Haan, E., Shaw, M., Gecz, J., Anderlid, B. M., Nordgren, A., Lindstrand, A., Schwartz, C., Kooy, R. F., Vandeweyer, G., Helsmoortel, C., Romano, C., Alberti, A., Vinci, M., Avola, E., Giusto, S., Courchesne, E., Pramparo, T., Pierce, K., Nalabolu, S., Amaral, D. G., Scheffer, I. E., Delatycki, M. B., Lockhart, P. J., Hormozdiari, F., Harich, B., Castells-Nobau, A., Xia, K., Peeters, H., Nordenskjold, M., Schenck, A., Bernier, R. A. and Eichler, E. E. (2017). Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. Nat Genet 49(4): 515-526.

64.     Geisheker, M. R., Heymann, G., Wang, T., Coe, B. P., Turner, T. N., Stessman, H. A. F., Hoekzema, K., Kvarnung, M., Shaw, M., Friend, K., Liebelt, J., Barnett, C., Thompson, E. M., Haan, E., Guo, H., Anderlid, B. M., Nordgren, A., Lindstrand, A., Vandeweyer, G., Alberti, A., Avola, E., Vinci, M., Giusto, S., Pramparo, T., Pierce, K., Nalabolu, S., Michaelson, J. J., Sedlacek, Z., Santen, G. W. E., Peeters, H., Hakonarson, H., Courchesne, E., Romano, C., Kooy, R. F., Bernier, R. A., Nordenskjold, M., Gecz, J., Xia, K., Zweifel, L. S. and Eichler, E. E. (2017). Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nat Neurosci: doi:  10.1038/nn.4589.

65.     Wang, C., Peng, H., Li, J., Ding, D., Chen, Z., Long, Z., Peng, Y., Zhou, X., Ye, W., Li, K., Xu, Q., Ai, S., Song, C., Weng, L., Qiu, R., Xia, K., Tang, B. and Jiang, H. (2017). Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD. Neurobiol Aging 53: 192 e195-192 e110.

66.     Yan, W., Tang, B., Zhou, X., Lei, L., Li, K., Sun, Q., Xu, Q., Yan, X., Guo, J. and Liu, Z. (2017). TMEM230 mutation analysis in Parkinson's disease in a Chinese population. Neurobiol Aging 49: 219 e211-219 e213.

67.     Xiao, Z., Peng, J., Wu, L., Arafat, A. and Yin, F. (2017). The effect of IL-1beta on synaptophysin expression and electrophysiology of hippocampal neurons through the PI3K/Akt/mTOR signaling pathway in a rat model of mesial temporal lobe epilepsy. Neurol Res 39(7): 640-648.

68.     Liu, L., Li, X., Hu, Z., Mao, X., Zi, X., Xia, K., Tang, B. and Zhang, R. (2017). IGHMBP2-related clinical and genetic features in a cohort of Chinese Charcot-Marie-Tooth disease type 2 patients. Neuromuscul Disord 27(2): 193-199.

69.     Hu, M. L., Zong, X. F., Mann, J. J., Zheng, J. J., Liao, Y. H., Li, Z. C., He, Y., Chen, X. G. and Tang, J. S. (2017). A Review of the Functional and Anatomical Default Mode Network in Schizophrenia. Neurosci Bull 33(1): 73-84.

70.     Zhou, H., Zhang, L. L., Zou, X. B., Luo, X. R., Xia, K., Wu, L. J., Wang, Y. M., Xu, X., Ge, X. L., Jiang, Y. H., Fombonne, E., Yan, W. L. and Wang, Y. (2017). Chinese Norms for the Autism Spectrum Rating Scale. Neuroscience Bulletin 33(2): 161-167.

71.     Zhou, H., Zhang, L. L., Luo, X. R., Wu, L. J., Zou, X. B., Xia, K., Wang, Y. M., Xu, X., Ge, X. L., Jiang, Y. H., Fombonne, E., Yan, W. L. and Wang, Y. (2017). Modifying the Autism Spectrum Rating Scale (6-18 years) to a Chinese Context: An Exploratory Factor Analysis. Neuroscience Bulletin 33(2): 175-182.

72.     Yang, Y., Yuan, J., Yao, X., Zhang, R., Yang, H., Zhao, R., Guo, J., Jin, K., Mei, H., Luo, Y., Zhao, L., Tu, M. and Zhu, Y. (2017). BMPR1B mutation causes Pierre Robin sequence. Oncotarget 8(16): 25864-25871.

73.     Yang, J., Zhao, H., Ma, Y., Shi, G., Song, J., Tang, Y., Li, S., Li, T., Liu, N., Tang, F., Gu, J., Zhang, L., Zhang, Z., Zhang, X., Jin, Y. and Le, W. (2017). Early pathogenic event of Alzheimer's disease documented in iPSCs from patients with PSEN1 mutations. Oncotarget 8(5): 7900-7913.

74.     Liu, B., Chen, F., Wu, Y., Wang, X., Feng, M., Li, Z., Zhou, M., Wang, Y., Wu, L., Liu, X. and Liang, D. (2017). Enhanced tumor growth inhibition by mesenchymal stem cells derived from iPSCs with targeted integration of interleukin24 into rDNA loci. Oncotarget 8(25): 40791-40803.

75.     Heng, J., Zhang, F., Guo, X., Tang, L., Peng, L., Luo, X., Xu, X., Wang, S., Dai, L. and Wang, J. (2017). Integrated analysis of promoter methylation and expression of telomere related genes in breast cancer. Oncotarget 8(15): 25442-25454.

76.     Qin, L. X., Tan, J. Q., Zhang, H. N., Rizwana, K., Lu, J. H., Tang, J. G., Jiang, B., Shen, X. M., Guo, J. F., Tang, B. S., Tan, L. M. and Wang, C. Y. (2017). BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage. Oxid Med Cell Longev 2017: 5094934. doi: 5094910.5091155/5092017/5094934.

77.     Yin, J., Lu, Q., Yin, F., Wang, Y., He, F., Wu, L., Yang, L., Deng, X., Chen, C. and Peng, J. (2017). Effectiveness and Safety of Different Once-Daily Doses of Adrenocorticotropic Hormone for Infantile Spasms. Paediatr Drugs: 1-9. DOI: 10.1007/s40272-40017-40225-40275.

78.     Heng, J., Guo, X., Wu, W., Wang, Y., Li, G., Chen, M., Peng, L., Wang, S., Dai, L., Tang, L. and Wang, J. (2017). Integrated analysis of promoter mutation, methylation and expression of AKT1 gene in Chinese breast cancer patients. PLoS One 12(3): e0174022.

79.     Niu, Z., Feng, Y., Mei, L., Sun, J., Wang, X., Wang, J., Hu, Z., Dong, Y., Chen, H., He, C., Liu, Y., Cai, X., Liu, X. and Jiang, L. (2017). A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. PLoS One 12(5): e0178384.

80.     Qiu, J., Chen, X., Netrusov, A. I., Zhou, Q., Guo, D., Liu, X., He, H., Xin, X., Wang, Y. and Chen, L. (2017). Screening and Identifying Antioxidative Components in Ginkgo biloba Pollen by DPPH-HPLC-PAD Coupled with HPLC-ESI-MS2. PLoS One 12(1): e0170141.

81.     Guo, W., Liu, F., Chen, J., Wu, R., Li, L., Zhang, Z., Chen, H. and Zhao, J. (2017). Using short-range and long-range functional connectivity to identify schizophrenia with a family-based case-control design. Psychiatry research 264: 60-67.

82.     Zhu, Y. C., Yin, B. A., Wu, T. H., Ye, L. J., Chen, C. M., Zeng, Y. and Zhang, Y. O. (2017). Comparative study in infertile couples with and without Chlamydia trachomatis genital infection. Reproductive Health 14: 9.

83.     Li, R., Zhao, J. and Wu, R. (2017). Predictors of menstruation restoration during metformin administration for treatment of antipsychotic drug-induced amenorrhea: A post hoc analysis. Schizophr Res: doi: 10.1016/j.schres.2017.1003.1019.

84.     Meyers, J., Smith, R., Wu, R., Liu, Y., Wang, J., Jin, H., Davis, J. and Zhao, J. (2017). COGNITIVE FUNCTION DEFICITS IN HIGH-RISK, FIRST-EPISODE, AND CHRONIC SCHIZOPHRENIA. Schizophrenia Bulletin. 43: S175-S176.

85.     Ma, R., Deng, L., Xia, Y., Wei, X., Cao, Y., Guo, R., Zhang, R., Guo, J., Liang, D. and Wu, L. (2017). A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies. Sci Rep 7: 44446.

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106.   牛志杰#, 冯永, 梅凌云, 孙捷, 陈红胜, 贺楚峰, 刘亚兰, 王雪萍, 文杰, 蒋璐* (2017). 非综合征型X连锁隐性遗传耳聋家系临床表型及遗传学特征分析. 中华耳科学杂志 15(02): 195-200.

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