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科学研究

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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
 

2011年发表论文

 

1.              Jiang, L., Liu, Y., Feng, Y., Hu, Z., Mei, L., Long, L., Chen, H., Xue, J., Xia, K., and He, C. (2011). Gene localization in a Chinese family with autosomal dominant non-syndromic deafness. Acta Otolaryngol, 131: 1061-8.

2.              Men, M., Jiang, L., Wang, H., Liu, Y., Hu, Z., He, C., and Feng, Y. (2011). Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation. Acta Otolaryngol, 131: 970-5.

3.              Zhan, X., and Desiderio, D.M. (2011). Nitroproteins Identified in Human Ex-smoker Bronchoalveolar Lavage Fluid. Aging Dis, 2: 100-15.

4.              Hannibal, M.C., Buckingham, K.J., Ng, S.B., Ming, J.E., Beck, A.E., McMillin, M.J., Gildersleeve, H.I., Bigham, A.W., Tabor, H.K., Mefford, H.C., Cook, J., Yoshiura, K., Matsumoto, T., Matsumoto, N., Miyake, N., Tonoki, H., Naritomi, K., Kaname, T., Nagai, T., Ohashi, H., Kurosawa, K., Hou, J.W., Ohta, T., Liang, D., Sudo, A., Morris, C.A., Banka, S., Black, G.C., Clayton-Smith, J., Nickerson, D.A., Zackai, E.H., Shaikh, T.H., Donnai, D., Niikawa, N., Shendure, J., and Bamshad, M.J. (2011). Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. Am J Med Genet A, 155A: 1511-6.

5.              Wu, L., Liao, X., Wang, H., Zhou, Z., Lv, W., and Liang, D. (2011). A patient with apparently reciprocal translocation and cryptic 10p deletion. Am J Med Genet A, 155A: 1753-5.

6.              Wu, L., Meng, D., Zhou, Z., Du, J., Long, Z., and Liang, D. (2011). A family with partial duplication/deletion 4p due to a balanced t (4; 15) (p16.2; p11.2) translocation. Am J Med Genet A, 155A: 656-9.

7.              Wu, L., Peng, J., Wei, C., Liu, G., Wang, G., Li, K., and Yin, F. (2011). Characterization, using comparative proteomics, of differentially expressed proteins in the hippocampus of the mesial temporal lobe of epileptic rats following treatment with valproate. Amino Acids, 40: 221-38.

8.              Li, J., Chen, X., Zhao, S., Hu, X., Chen, C., Ouyang, F., Liu, Q., Ding, R., Shi, Q., Su, J., Kuang, Y., Chang, J., Li, F., and Xie, H. (2011). Demographic and clinical characteristics and risk factors for infantile hemangioma: a Chinese case-control study. Arch Dermatol, 147: 1049-56.

9.              Choo, Y.S., Tang, C., and Zhang, Z. (2011). Critical role of PINK1 in regulating Parkin protein levels in vivo. Arch Neurol, 68: 684-5.

10.          Zhou, Y., Li, Y., Mao, L., and Peng, H. (2011). Periodontal healing by periodontal ligament cell sheets in a teeth replantation model. Arch Oral Biol, 57: 169-76.

11.          Qu, J., Ren, X., Hou, R.Y., Dai, X.P., Zhao, Y.C., Xu, X.J., Zhang, W., Zhou, G., Zhou, H.H., and Liu, Z.Q. (2011). The protective effect of magnesium lithospermate B against glucose-induced intracellular oxidative damage. Biochem Biophys Res Commun, 411: 32-9.

12.          Qin, B., Xiao, B., Liang, D., Xia, J., Li, Y., and Yang, H. (2011). MicroRNAs expression in ox-LDL treated HUVECs: MiR-365 modulates apoptosis and Bcl-2 expression. Biochem Biophys Res Commun, 410: 127-33.

13.          Jiang, L., Chen, H., Jiang, W., Hu, Z., Mei, L., Xue, J., He, C., Liu, Y., Xia, K., and Feng, Y. (2011). Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome. Biochem Biophys Res Commun, 408: 620-4.

14.          Wang, D., Liu, F., Wang, L., Huang, S., and Yu, J. (2011). Nonsynonymous substitution rate (Ka) is a relatively consistent parameter for defining fast-evolving and slow-evolving protein-coding genes. Biol Direct, 6: 13.

15.          Cheng, G., Gong, Q., Gai, N., Xiong, D.H., Yu, Y.J., Zeng, Q.R., and Hu, W.X. (2011). Karyopherin alpha 2 (KPNA2) is associated with the natural resistance to Schistosoma japanicum infection in Microtus fortis. Biomed Pharmacother, 65: 230-7.

16.          Wang, J.L., Cao, L., Li, X.H., Hu, Z.M., Li, J.D., Zhang, J.G., Liang, Y., San, A., Li, N., Chen, S.Q., Guo, J.F., Jiang, H., Shen, L., Zheng, L., Mao, X., Yan, W.Q., Zhou, Y., Shi, Y.T., Ai, S.X., Dai, M.Z., Zhang, P., Xia, K., Chen, S.D., and Tang, B.S. (2011). Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias. Brain, 134: 3493-501.

17.          Wang, C.Y., Xu, Q., Weng, L., Zhang, Q., Zhang, H.N., Guo, J.F., Tan, L.M., Tang, J.G., Yan, X.X., and Tang, B.S. (2011). Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease. Brain Res, 1385: 293-7.

18.          Liu, J., Sun, Q.Y., Tang, B.S., Hu, L., Yu, R.H., Wang, L., Shi, C.H., Yan, X.X., Pan, Q., Xia, K., and Guo, J.F. (2011). PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population. Brain Res, 1392: 116-20.

19.          Li, D., Guo, R., Chen, Q.Q., Hu, C.P., and Chen, X. (2011). Increased plasma level of asymmetric dimethylarginine in hypertensive rats facilitates platelet aggregation: role of plasma tissue factor. Can J Physiol Pharmacol, 89: 151-8.

20.          Yin, J.Y., Shen, J., Dong, Z.Z., Huang, Q., Zhong, M.Z., Feng, D.Y., Zhou, H.H., Zhang, J.T., and Liu, Z.Q. (2011). Effect of eIF3a on response of lung cancer patients to platinum-based chemotherapy by regulating DNA repair. Clin Cancer Res, 17: 4600-9.

21.          Sheng, F.F., Dai, X.P., Qu, J., Lei, G.H., Lu, H.B., Wu, J., Xu, X.J., Pei, Q., Dong, M., Liu, Y.Z., Zhou, H.H., and Liu, Z.Q. (2011). NAMPT -3186C/T polymorphism affects repaglinide response in Chinese patients with Type 2 diabetes mellitus. Clin Exp Pharmacol Physiol, 38: 550-4.

22.          Dong, M., Gong, Z.C., Dai, X.P., Lei, G.H., Lu, H.B., Fan, L., Qu, J., Zhou, H.H., and Liu, Z.Q. (2011). Serine racemase rs391300 G/A polymorphism influences the therapeutic efficacy of metformin in Chinese patients with diabetes mellitus type 2. Clin Exp Pharmacol Physiol, 38: 824-9.

23.          Tan, Z.P., Huang, C., Xu, Z.B., Yang, J.F., and Yang, Y.F. (2011). Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle. Clin Genet, 82: 466-71.

24.          Du, J., Hu, Y.C., Tang, B.S., Chen, C., Luo, Y.Y., Zhan, Z.X., Zhao, G.H., Jiang, H., Xia, K., and Shen, L. (2011). Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1. Clin Neurol Neurosurg, 113: 480-2.

25.          Yin, J.-Y., Han, L.-F., Huang, Q., Xu, X.-J., Zhou, H.-H., and Liu, Z.-Q. (2011). ABCC1 polymorphism Arg723Gln (2168G > A) is associated with lung cancer susceptibility in a Chinese population. Clin Exp Pharmacol Physiol, 38: 632-37.

26.          Liu, J., Mohandas, N., and An, X. (2011). Membrane assembly during erythropoiesis. Curr Opin Hematol, 18: 133-8.

27.          Matsuda, I., Hasegawa, S., Liang, D.S., and Harvey, D. (2011). Attitudes of Genetic Decision Making in Culturally Diverse Populations. EJAIB, 21: 159-64.

28.          Tian, L.M., Xie, H.F., Xiao, X., Yang, T., Hu, Y.H., Wang, W.Z., Liu, L.S., Chen, X., and Li, J. (2011). Study on the roles of beta-catenin in hydrogen peroxide-induced senescence in human skin fibroblasts. Exp Dermatol, 20: 836-8.

29.          Zhou, X., Hu, X., He, W., Tang, X., Shi, Q., Zhang, Z., and Yan, R. (2011). Interaction between amyloid precursor protein and Nogo receptors regulates amyloid deposition. FASEB J, 25: 3146-56.

30.          Zhao, J., and Li, Y.P. (2011). Middle cerebral artery thrombosis following IVF and ovarian hyperstimulation: a case report. Fertil Steril, 95: 2435.

31.          Fang, C.Y., Xue, J.J., Tan, L., Jiang, C.H., Gao, Q.P., Liang, D.S., and Wu, L.Q. (2011). A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia. Genet Mol Res, 10: 3539-44.

32.          Wu, L.Q., Hu, J.J., Xue, J.J., and Liang, D.S. (2011). Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome. Genet Mol Res, 10: 2517-22.

33.          Wu, L.S., Li, F.F., Sun, L.D., Li, D., Su, J., Kuang, Y.H., Chen, G., Chen, X.P., and Chen, X. (2011). A miRNA-492 binding-site polymorphism in BSG (basigin) confers risk to psoriasis in central south Chinese population. Hum Genet, 130: 749-57.

34.          Damaye, C.A., Wu, L., Peng, J., He, F., Zhang, C., Lan, Y., Walijee, S.M., and Yin, F. (2011). An experimental study on dynamic morphological changes and expression pattern of GFAP and synapsin i in the hippocampus of MTLE models for immature rats. Int J Neurosci, 121: 575-88.

35.          Hu, Z., Yu, C., Li, J., Wang, Y., Liu, D., Xiang, X., Su, W., Pan, Q., Xie, L., and Xia, K. (2011). A novel locus for congenital simple microphthalmia family mapping to 17p12-q12. Invest Ophthalmol Vis Sci, 52: 3425-9.

36.          Guo, W.B., Liu, F., Xue, Z.M., Yu, Y., Ma, C.Q., Tan, C.L., Sun, X.L., Chen, J.D., Liu, Z.N., Xiao, C.Q., Chen, H.F., and Zhao, J.P. (2011). Abnormal neural activities in first-episode, treatment-naive, short-illness-duration, and treatment-response patients with major depressive disorder: a resting-state fMRI study. J Affect Disord, 135: 326-31.

37.          Tan, J., Zhang, T., Jiang, L., Chi, J., Hu, D., Pan, Q., Wang, D., and Zhang, Z. (2011). Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein. J Biol Chem, 286: 29654-62.

38.          Sun, X., Wu, Y., Chen, B., Zhang, Z., Zhou, W., Tong, Y., Yuan, J., Xia, K., Gronemeyer, H., Flavell, R.A., and Song, W. (2011). Regulator of calcineurin 1 (RCAN1) facilitates neuronal apoptosis through caspase-3 activation. J Biol Chem, 286: 9049-62.

39.          Peng, Z., Tang, Y., Luo, H., Jiang, F., Yang, J., Sun, L., and Li, J.D. (2011). Disease-causing mutation in PKR2 receptor reveals a critical role of positive charges in the second intracellular loop for G-protein coupling and receptor trafficking. J Biol Chem, 286: 16615-22.

40.          Yi, M., Yang, J., Chen, X., Li, J., Li, X., Wang, L., Tan, Y., Xiong, W., Zhou, M., McCarthy, J.B., Li, G., Xiang, B., and Xie, H. (2011). RASSF1A suppresses melanoma development by modulating apoptosis and cell-cycle progression. J Cell Physiol, 226: 2360-9.

41.          Pei, Q., Yang, G.P., Li, Z.J., Peng, X.D., Fan, J.H., and Liu, Z.Q. (2011). Simultaneous analysis of amoxicillin and sulbactam in human plasma by HPLC-DAD for assessment of bioequivalence. J Chromatogr B Analyt Technol Biomed Life Sci, 879: 2000-4.

42.          Wang, L., Guo, J.F., Nie, L.L., Luo, L., Zuo, X., Shen, L., Jiang, H., Yan, X.X., Xia, K., Pan, Q., and Tang, B.S. (2011). Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population. J Clin Neurosci, 18: 541-4.

43.          Wang, L., Guo, J.F., Zhang, W.W., Xu, Q., Zuo, X., Shi, C.H., Luo, L.Z., Liu, J., Hu, L., Hu, Y.C., Yan, X.X., and Tang, B.S. (2011). Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson's disease. J Clin Neurosci, 18: 1699-701.

44.          Xie, H., Liu, L., Shi, W., Xiao, X., Tian, L., Jian, D., Chen, X., and Li, J. (2011). Down regulation of CD147 boosts the premature senescence in human skin fibroblasts by destroying the redox balance and inhibiting klotho. J Dermatol Sci, 64: 243-5.

45.          Liao, X., Liang, D., Li, Y., Xi, H., Quan, Y., and Wu, L. (2011). Mutation analysis of the SRY, NR5A1, and DHH genes in six Chinese 46,XY women. J Matern Fetal Neonatal Med, 24: 863-6.

46.          Qiong, Z., Yanping, L., Deep, J.P., and Lin, Z. (2011). Treatment of cornual heterotopic pregnancy via selective reduction without feticide drug. J Minim Invasive Gynecol, 18: 766-8.

47.          Peng, J., He, F., Zhang, C., Deng, X., and Yin, F. (2011). Protein kinase C-alpha signals P115RhoGEF phosphorylation and RhoA activation in TNF-alpha-induced mouse brain microvascular endothelial cell barrier dysfunction. J Neuroinflammation, 8: 28.

48.          Kong, X., Ouyang, X., Tao, H., Liu, H., Li, L., Zhao, J., Xue, Z., Wang, F., Jiang, S., Shan, B., and Liu, Z. (2011). Complementary diffusion tensor imaging study of the corpus callosum in patients with first-episode and chronic schizophrenia. J Psychiatry Neurosci, 36: 120-5.

49.          Tao, H., Guo, S., Ge, T., Kendrick, K.M., Xue, Z., Liu, Z., and Feng, J. (2011). Depression uncouples brain hate circuit. Mol Psychiatry, doi10.1038/mp.

50.          Hu, Y.J., Xiao, D., Liu, X.H., Wu, L.Q., and Liang, D.S. (2011). Improvement of Gene Targeting at the Human rDNA Locus by Zinc Finger Nucleases. Mol Ther, 19: S267.

51.          Peng, J., Wu, L.Q., Liu, X.H., and Liang, D.S. (2011). Nonviral-Mediated Endostatin Delivery Results in Inhibition of Fibrosarcoma Growth. Mol Ther, 19: S267-68.

52.          Hu, J., Liang, D., Xue, J., Liu, J., and Wu, L. (2011). A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus. Mol Vis, 17: 715-22.

53.          Lei, L.F., Wang, J.L., Zhang, S., Jiang, H., Shen, L., Xu, Q., Yan, X.X., Yi, Y., Pan, Q., Xia, K., and Tang, B.S. (2011). Prenatal diagnosis of spinocerebellar ataxia type 3/Machado-Joseph disease in mainland China A case report. Neural Regeneration Res, 26: 2047-49.

54.          Fan, Y., Liu, Y., Wu, H., Hao, Y., Liu, H., Liu, Z., and Jiang, T. (2011). Discriminant analysis of functional connectivity patterns on Grassmann manifold. Neuroimage, 56: 2058-67.

55.          Wang, Y.Z., Liang, Q.H., Ramkalawan, H., Wang, Y.L., Yang, Y.F., Zhou, W.B., Tian, F.F., Li, J., and Yang, H. (2011). Expression of Toll-like receptors 2, 4 and 9 in patients with Guillain-Barre syndrome. Neuroimmunomodulation, 19: 60-8.

56.          Jiang, H., Shi, Y.T., Wang, J.L., Tang, B.S., Wang, J.Y., Peng, Z.F., and Xiao, D.S. (2011). A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literature. Neurol Sci, 32: 305-7.

57.          Guo, J.F., Wang, L., He, D., Yang, Q.H., Duan, Z.X., Zhang, X.W., Nie, L.L., Yan, X.X., and Tang, B.S. (2011). Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism. Neurol Sci, 32: 35-40.

58.          Tan, X.L., Yang, Q.D., Liu, X.J., Xiao, B., and Tang, B.S. (2011). Teaching NeuroImages: False-positive magnetic resonance sign in spontaneous spinal CSF leak. Neurology, 76: e15.

59.          Shi, C.H., Tang, B.S., Wang, L., Lv, Z.Y., Wang, J., Luo, L.Z., Shen, L., Jiang, H., Yan, X.X., Pan, Q., Xia, K., and Guo, J.F. (2011). PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort. Neurology, 77: 75-81.

60.          Yao, L.Y., Guo, J.F., Wang, L., Yu, R.H., Sun, Q.Y., Pan, Q., Xia, K., Tang, B.S., and Shen, L. (2011). LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's disease. Neurosci Lett, 495: 35-8.

61.          Guo, X., Zhai, J., Wei, Q., Twamley, E.W., Jin, H., Fang, M., Hu, M., and Zhao, J. (2011). Neurocognitive effects of first- and second-generation antipsychotic drugs in early-stage schizophrenia: a naturalistic 12-month follow-up study. Neurosci Lett, 503: 141-6.

62.          Hu, M., Chen, J., Li, L., Zheng, Y., Wang, J., Guo, X., Wu, R., and Zhao, J. (2011). Semantic fluency and executive functions as candidate endophenotypes for the early diagnosis of schizophrenia in Han Chinese. Neurosci Lett, 502: 173-7.

63.          He, F., Peng, J., Deng, X.L., Yang, L.F., Wu, L.W., Zhang, C.L., and Yin, F. (2011). RhoA and NF-kappaB are involved in lipopolysaccharide-induced brain microvascular cell line hyperpermeability. Neurosci, 188: 35-47.

64.          He, J., Ye, J., Cai, Y., Riquelme, C., Liu, J.O., Liu, X., Han, A., and Chen, L. (2011). Structure of p300 bound to MEF2 on DNA reveals a mechanism of enhanceosome assembly. Nucleic Acids Res, 39: 4464-74.

65.          Shu, X.S., Geng, H., Li, L., Ying, J., Ma, C., Wang, Y., Poon, F.F., Wang, X., Ying, Y., Yeo, W., Srivastava, G., Tsao, S.W., Yu, J., Sung, J.J., Huang, S., Chan, A.T., and Tao, Q. (2011). The epigenetic modifier PRDM5 functions as a tumor suppressor through modulating WNT/beta-catenin signaling and is frequently silenced in multiple tumors. PLoS One, 6: e27346.

66.          Wei, Q., Kang, Z., Diao, F., Shan, B., Li, L., Zheng, L., Guo, X., Liu, C., Zhang, J., and Zhao, J. (2011). Association of the ZNF804A gene polymorphism rs1344706 with white matter density changes in Chinese schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry, 36: 122-7.

67.          Guo, W.B., Sun, X.L., Liu, L., Xu, Q., Wu, R.R., Liu, Z.N., Tan, C.L., Chen, H.F., and Zhao, J.P. (2011). Disrupted regional homogeneity in treatment-resistant depression: a resting-state fMRI study. Prog Neuropsychopharmacol Biol Psychiatry, 35: 1297-302.

68.          He, Y., Xun, G., Xia, K., Hu, Z., Lv, L., Deng, Z., and Zhao, J. (2011). No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population. Psychiatry Res, 187: 462-4.

69.          Guo, X., Fang, M., Zhai, J., Wang, B., Wang, C., Hu, B., Sun, X., Lv, L., Lu, Z., Ma, C., Guo, T., Xie, S., Twamley, E.W., Jin, H., and Zhao, J. (2011). Effectiveness of maintenance treatments with atypical and typical antipsychotics in stable schizophrenia with early stage: 1-year naturalistic study. Psychopharmacology (Berl), 216: 475-84.

70.          Ou, J.J., Xun, G.L., Wu, R.R., Li, L.H., Fang, M.S., Zhang, H.G., Xie, S.P., Shi, J.G., Du, B., Yuan, X.Q., and Zhao, J.P. (2011). Efficacy and safety of escitalopram versus citalopram in major depressive disorder: a 6-week, multicenter, randomized, double-blind, flexible-dose study. Psychopharmacology (Berl), 213: 639-46.

71.          Ma, L., Tan, Z., Teng, Y., Hoersch, S., and Horvitz, H.R. (2011). In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans. RNA, 17: 2201-11.

72.          Aggarwal, N.K., Tao, H., Xu, K., Stefanovics, E., Zhening, L., and Rosenheck, R.A. (2011). Comparing the PANSS in Chinese and American inpatients: cross-cultural psychiatric analyses of instrument translation and implementation. Schizophr Res, 132: 146-52.

73.          Li, G., Xiao, Z., Liu, J., Li, C., Li, F., and Chen, Z. (2011). Cancer: a proteomic disease. Sci China Life Sci, 54: 403-8.

74.          Jian, D., Jiang, D., Su, J., Chen, W., Hu, X., Kuang, Y., Xie, H., Li, J., and Chen, X. (2011). Diethylstilbestrol enhances melanogenesis via cAMP-PKA-mediating up-regulation of tyrosinase and MITF in mouse B16 melanoma cells. Steroids, 76: 1297-304.

75.          Pei, J.H., Luo, S.Q., Zhong, Y., Chen, J.H., Xiao, H.W., and Hu, W.X. (2011). The association between non-Hodgkin lymphoma and methylation of p73. Tumour Biol, 32: 1133-8.

76.          李丽, 刘哲宁 (2011). 男女性别差异的脑形态学研究. 国际精神病学杂志: 231-34.

77.          欧建君, 赵靖平, 夏昆 (2011). 孤独症谱系障碍早期症状研究进展. 国际精神病学杂志: 250-54.

78.          朱芙蓉, 郑英君, 赵靖平 (2011). 精神分裂症的环境因素致病假说. 国际精神病学杂志: 146-50.

79.          朱晓岩, 侯荣耀, 许宏伟, 王玉春, 肖波, 杨期东, 唐北沙 (2011). 卵磷脂胆固醇酰基转移酶基因608C/T511C/T多态性与湖南地区汉族人卒中的关系. 国际脑血管病杂志, 19.

80.          伍新田, 朱榆红, 唐北沙 (2011). 脑海绵状血管瘤分子遗传学研究进展. 国际神经病学神经外科学杂志: 77-81.

81.          郭鹏, 张保刚, 王相斌, 宋福聪, 冯文霞, 唐北沙, 夏昆 (2011). 腓骨肌萎缩症1型和2型的临床与基因突变特点. 河北医药: 3530-32.

82.          侯德富, 关勇军, 万恂恂, 谭宇婷, 欧阳咏梅, 余艳辉, 陈主初 (2011). 一个新的NPCEDRG基因mRNA剪接变异体的克隆及鉴定. 湖南师范大学学报(医学版): 3-8.

83.          雷立芳, 叶湘漓, 唐北沙 (2011). 进行性核上性麻痹的个案分析. 湖南师范大学学报(医学版): 73-75.

84.          宋延民, 龙莉莉, 李海燕, 唐北沙, 邓景贵 (2011). 新的良性家族性婴儿惊厥位点候选基因的突变分析. 解放军医药杂志: 21-23+111.

85.          王娟, 胡茂荣, 赵靖平 (2011). 精神分裂症影像遗传学研究进展. 精神医学杂志: 388-91.

86.          李海燕, 李楠, 唐北沙, 齐尚书, 杨清成 (2011). Kennedy病的临床、病理及AR基因分析一例. 脑与神经疾病杂志: 342-44.

87.          彭镜, 吴蕾, 张慈柳, 尹飞 (2011). Dynamin-的功能结构域及其在突触囊泡内吞过程中的作用. 生理科学进展: 121-24.

88.          谭小宁, 周知, 谢小雷, 罗志勇 (2011). 雌激素受体信号通路在乳腺癌发生和治疗中的作用. 生命科学: 969-74.

89.          王克夷, 李家大 (2011). 细胞核质中的糖生物学. 生命科学: 526-32.

90.          侯德富, 关勇军, 关瑞, 欧阳咏梅, 余艳辉, 陈主初 (2011). NPCEDRG基因启动子的克隆及CCAAT/NFY结合位点初步分析. 生物化学与生物物理进展: 713-23.

91.          李丽, 贺修胜, 罗桥, 张志伟, 姚旭炯, 陈苏琼, 李春成, 王莉莉, 段蓉, 陈主初 (2011). STGC3基因缺失突变对CNE2细胞生长增殖能力的影响. 生物化学与生物物理进展: 248-53.

92.          曾爱源, 朱惊雷, 洪亢亢, 张灼华, 段然慧, 孙莉, 刘承伟, 魏小莉, 韦荔莉, 陈梅玲, 林小慧, 陈薇, 李清华 (2011). 沉默信息调节因子2SCA3/MJD转基因果蝇的神经保护作用及其与自噬的相关性研究. 生物化学与生物物理进展: 250-56.

93.          张春芳, 谭潭, 李建国, 马虹英, 陈主初, 段朝军 (2011). 冷藏对新鲜冰冻血浆诱导内皮细胞迁移的影响及其分子机制研究. 生物化学与生物物理进展: 528-35.

94.          邓利, 曾明, 匡延平, 邬玲仟, 吕祁峰 (2011). 小鼠卵子胞膜在显微穿刺中存活的膜特性因素研究. 生殖与避孕: 791-96.

95.          王春喻, 曹立, 唐北沙, 张海南, 郭纪锋, 廖书圣, 汤建光, 严新翔, 谭利明 (2011). OGCP代谢途径及Parkin对其代谢的影响. 四川大学学报(医学版), 42: 157-60.

96.          陈仙花, 李欣凝, 刘冬娥, 张叶青, 姚仲元, 周世敏, 郝好英, 李艳萍, 刘能辉, 邬玲仟 (2011). 不同质量玻璃化冻融胚胎移植对其妊娠结局的影响. 医学临床研究, 28: 1662-65.

97.          李琳, 张如旭, 孙贺东, 雷立芳, 袁毅, 潘乾, 夏昆, 胡正茂, 江泓, 唐北沙, 资晓宏 (2011). 原发性红斑肢痛症一家系排除与2q24.1-32区间连锁分析. 医学临床研究, 28.

98.          宋延民, 刘佳, 邓景贵, 唐北沙 (2011). 遗传性脊髓小脑共济失调7型一家系报告. 疑难病杂志: 208.

99.          郭鹏, 宋福聪, 王相斌, 冯文霞, 胡志强, 唐北沙, 夏昆 (2011). 常染色体显性遗传腓骨肌萎缩症的临床与基因突变特点. 中风与神经疾病杂志: 705-07.

100.       邓小鹿, 彭镜, 何芳, 杨丽芬, 吴丽文, 尹飞 (2011). TNF-α对小鼠脑微血管内皮细胞RhoA活性的影响. 中国病理生理杂志, 27: 1210-12+17.

101.       何芳, 彭镜, 邓小鹿, 杨丽芬, 吴丽文, 张慈柳, 尹飞 (2011). NF-κB参与脂多糖致永生化小鼠脑血管内皮细胞通透性增高的调控. 中国病理生理杂志: 1041-47.

102.       严雅萍, 彭丹涛, 田均, 迟静薇, 谭洁琼, 殷鑫浈, 浦佳丽, 夏昆, 张宝荣 (2011). 亨廷顿舞蹈病致病蛋白氨基端出核序列的研究及其对聚集体的影响. 中国科学:生命科学: 134-42.

103.       胡茂荣, 王娟, 李乐华, 陈晋东, 吴仁容, 赵靖平 (2011). 首发精神分裂症及其健康同胞神经心理功能的比较. 中国临床心理学杂志: 483-85+88.

104.       郝以辉, 高金松, 张会然, 欧阳萱, 刘海洪, 李幼辉, 宋学勤, 刘哲宁 (2011). 纤维追踪技术探索精神分裂症患者及其同胞的脑白质完整性. 中国神经精神疾病杂志: 725-29.

105.       魏钦令, 吴小立, 王继辉, 康庄, 张晋碚, 国效峰, 韩自力, 赵靖平 (2011). 有无冲动攻击行为首发精神分裂症脑灰质体积的比较. 中国神经精神疾病杂志: 625-28.

106.       侯德富, 关勇军, 关瑞, 万恂恂, 李国庆, 欧阳咏梅, 余艳辉, 陈主初 (2011). 鼻咽癌细胞系CNE2NPCEDRG基因mRNA剪接变异体分析. 中国生物化学与分子生物学报: 841-50.

107.       李海燕, 李楠, 唐北沙, 宋延民 (2011). 全面性癫伴热性惊厥附加症一家系的临床特点及SCN2A基因分析. 中国实用神经疾病杂志: 1-3.

108.       门美超, 薛晋杰, 潘乾, 田湘娥, 冯永 (2011). 引物延伸变性高效液相色谱法诊断遗传性非综合征性耳聋. 中国现代医学杂志: 1143-46.

109.       刘新建, 王俊岭, 唐北沙 (2011). 谷蛋白共济失调的研究进展. 中华神经科杂志, 44.

110.       侯荣耀, 朱晓岩, 郭瑞友, 许宏伟, 肖波, 杨期东, 唐北沙 (2011). 卵磷脂胆固醇酰基转移酶基因511C/T多态性与脑出血的关联研究. 中华神经医学杂志, 10.

111.       韩威威, 张琳, 江泓, 唐北沙 (2011). 脆性X相关震颤和()共济失调综合征. 中华医学遗传学杂志, 28.

112.       李书剑, 唐北沙, 赵国华, 张如旭, 夏昆, 潘乾 (2011). 腓骨肌萎缩症2L热休克蛋白B8过表达对细胞相对活力的影响. 中华医学遗传学杂志, 28.

113.       张如旭, 杨茜, 资晓宏, 李小波, 刘婷, 刘三妹, 李琳, 占雅静, 厉兰, 夏昆, 潘乾, 唐北沙 (2011). HSPB1R127W突变蛋白细胞内表达与神经丝轻链的共定位研究. 中华医学遗传学杂志, 28.

114.       何芳, 邬玲仟, 彭镜, 尹飞 (2011). 染色体荧光原位杂交检测确诊Angelman综合征一例. 中华医学杂志, 12: 863-64.

115.       郭辉, 胡正茂, 赵靖平, 夏昆 (2011). 孤独症遗传学(英文). 中南大学学报(医学版): 703-11.

116.       国效峰, 张展筹, 朱薇薇, 连楠, 吕海龙, 赵靖平 (2011). 伴与不伴糖尿病的精神分裂症认知功能的比较(英文). 中南大学学报(医学版): 724-27.

117.       李吉, 谢红付, 易梅, 彭乐芳, 雷丹, 陈翔, 简丹 (2011). 亲环素ACD147在皮肤衰老过程中表达的研究(英文). 中南大学学报(医学版): 203-11.

118.       刘能辉, 张振辉, 李艳萍, 刘冬娥, 陈仙花, 姚仲元 (2011). 不明原因不孕患者精子的精-卵相互作用实验及体外受精临床结局的研究. 中南大学学报(医学版): 439-47.

119.       刘勇, 唐亚梅, 蒲唯丹, 张向晖, 赵靖平 (2011). MK-801诱导的精神分裂症发育模型大鼠脑组织DA,DOPAC,GluGABA浓度的变化(英文). 中南大学学报(医学版): 712-19.

120.       门美超, 薛晋杰, 蒋璐, 王鸿涵, 潘乾, 冯永 (2011). 一种新的高效快速检测遗传性耳聋的方法(英文). 中南大学学报(医学版): 1079-84.

121.       谭巧, 刘能辉, 李艳萍, 刘冬娥, 陈仙花 (2011). 不同精子来源及参数对卵胞浆内单精子注射术结局的影响. 中南大学学报(医学版): 149-53.

122.       王俊岭, 沈璐, 雷立芳, 徐倩, 周洁, 刘玉涛, 关文娟, 潘乾, 夏昆, 唐北沙, 江泓 (2011). 中国大陆脊髓小脑性共济失调家系和散发病例的最新基因突变分析(英文). 中南大学学报(医学版): 482-89+56.

123.       吴仁容, 赵靖平, 邵平, 欧建君, 常麦会 (2011). 抗精神病药物所致体质量增加的遗传易感基因(英文). 中南大学学报(医学版): 720-23.

124.       张学伟, 张海南, 廖冰, 郭纪锋, 夏昆, 唐北沙 (2011). 早发性帕金森综合征的PINK1基因变异分析(英文). 中南大学学报(医学版): 490-97.

125.       雷立芳, 廖云杰, 廖伟华, 周洁, 袁毅, 王俊岭, 江泓, 沈璐, 唐北沙 (2011). 脊髓小脑性共济失调3/Machado-Joseph病患者小脑的磁共振波谱分析. 中南大学学报(医学版), 36511-9.

126.       周洁, 雷立芳, 廖鑫鑫, 王俊岭, 江泓, 唐北沙, 沈璐 (2011). 脊髓小脑性共济失调3/Machado-Joseph ICARSSARA评分相关因素分析. 中南大学学报(医学版), 36.

127.       周洁, 雷立芳, 师玉婷, 王俊岭, 江泓, 沈璐, 唐北沙 (2011). 脊髓小脑性共济失调3/ Machado-Joseph病血清NSES100B浓度的测定. 中南大学学报(医学版), 36.

128.       向新颖, 唐红梅, 胡正茂, 夏昆, 唐建华 (2011). 鼻咽癌患者糖基化磷脂酰肌醇特异性磷脂酶D活性及其表达水平的初步研究. 肿瘤药学: 450-56.

129.       董晓立, 郭纪锋, 严新翔 (2011). DJ-1与帕金森病. 卒中与神经疾病, 18: 58-61.

130.       刘小民, 朱梅佳, 李爱银, 王爱华, 关新华, 唐北沙 (2011). 带状疱疹性脊髓炎临床分析. 卒中与神经疾病: 286-88.

131.       詹自雄, 江泓, 沈璐, 张文娟, 唐北沙 (2011). 发作性睡病并OSAHS(1例报道及文献复习). 卒中与神经疾病: 231-33.

132.       左星, 孙启英, 唐北沙 (2011). LINGO1基因多态性与多系统萎缩相关性研究. 卒中与神经疾病: 3-5+16.


     
     
     
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