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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
 

2012年发表论文

 

1.              Wang, L., Wu, M., Wen, Z., Xia, Q.P., Yan, H.F., and Luo, Z.Y. (2012). Isolation and characterization of microsatellite loci in the endangered tree Diplopanax stachyanthus (Araliaceae). Am J Bot, 99: e167-9.

2.              Luo, C., Yang, Y.F., Yin, B.L., Chen, J.L., Huang, C., Zhang, W.Z., Wang, J., Zhang, H., Yang, J.F., and Tan, Z.P. (2012). Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome. Am J Med Genet A, 158A: 1918-23.

3.              Chen, J.L., Yang, Y.F., Huang, C., Wang, J., Yang, J.F., and Tan, Z.P. (2012). Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies. Am J Med Genet A, 158A: 685-8.

4.              Wu, R.R., Jin, H., Gao, K., Twamley, E.W., Ou, J.J., Shao, P., Wang, J., Guo, X.F., Davis, J.M., Chan, P.K., and Zhao, J.P. (2012). Metformin for treatment of antipsychotic-induced amenorrhea and weight gain in women with first-episode schizophrenia: a double-blind, randomized, placebo-controlled study. Am J Psychiatry, 169: 813-21.

5.              Ma, C., Yeung, E.S., Qi, S., and Han, R. (2012). Highly sensitive detection of microRNA by chemiluminescence based on enzymatic polymerization. Anal Bioanal Chem, 402: 2217-20.

6.              Ma, C., Chen, H., Han, R., He, H., and Zeng, W. (2012). Fluorescence detection of adenosine triphosphate using smart probe. Anal Biochem, 429: 8-10.

7.              Liu, Q.P., Wu, L.S., Li, F.F., Liu, S., Su, J., Kuang, Y.H., Chen, C., Xie, X.Y., Jiang, M.H., Zhao, S., Chen, M.L., and Chen, X. (2012). The association between GJB2 gene polymorphism and psoriasis: a verification study. Arch Dermatol Res, 304: 769-72.

8.              Lu, J.H., Tan, J.Q., Durairajan, S.S., Liu, L.F., Zhang, Z.H., Ma, L., Shen, H.M., Chan, H.Y., and Li, M. (2012). Isorhynchophylline, a natural alkaloid, promotes the degradation of alpha-synuclein in neuronal cells via inducing autophagy. Autophagy, 8: 98-108.

9.              Zheng, X.R., Zhang, S.S., Yin, F., Tang, J.L., Yang, Y.J., Wang, X., and Zhong, L. (2012). Neuroprotection of VEGF-expression neural stem cells in neonatal cerebral palsy rats. Behav Brain Res, 230: 108-15.

10.          Kuang, Y.H., Patel, J.P., Sodani, K., Wu, C.P., Liao, L.Q., Patel, A., Tiwari, A.K., Dai, C.L., Chen, X., Fu, L.W., Ambudkar, S.V., Korlipara, V.L., and Chen, Z.S. (2012). OSI-930 analogues as novel reversal agents for ABCG2-mediated multidrug resistance. Biochem Pharmacol, 84: 766-74.

11.          Liang, D., Zhou, Z., Meng, D., Du, J., Wen, J., Niikawa, N., and Wu, L. (2012). Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p. Birth Defects Res A Clin Mol Teratol, 94: 549-52.

12.          Qin, B., Xiao, B., Liang, D., Li, Y., Jiang, T., and Yang, H. (2012). MicroRNA let-7c inhibits Bcl-xl expression and regulates ox-LDL-induced endothelial apoptosis. BMB Rep, 45: 464-9.

13.          Liu, J.P., Zhan, X.Q., Li, M.Y., Li, G.Q., Zhang, P.F., Xiao, Z.F., Shao, M.Y., Peng, F., Hu, R., and Chen, Z.C. (2012). Mitochondrial proteomics of nasopharyngeal carcinoma metastasis. BMC Medical Genomics, 5: 62.

14.          Gong, Z.C., Huang, Q., Dai, X.P., Lei, G.H., Lu, H.B., Yin, J.Y., Xu, X.J., Qu, J., Pei, Q., Dong, M., Zhou, B.T., Shen, J., Zhou, G., Zhou, H.H., and Liu, Z.Q. (2012). NeuroD1 A45T and PAX4 R121W polymorphisms are associated with plasma glucose level of repaglinide monotherapy in Chinese patients with type 2 diabetes. Br J Clin Pharmacol, 74: 501-9.

15.          Li, L., Dai, H.J., Ye, M., Wang, S.L., Xiao, X.J., Zheng, J., Chen, H.Y., Luo, Y.H., and Liu, J. (2012). Lycorine induces cell-cycle arrest in the G0/G1 phase in K562 cells via HDAC inhibition. Cancer Cell Int, 12: 49.

16.          Omran, A., Peng, J., Shrestha, B., Ashhab, M.U., and Yin, F. (2012). Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report. Case Rep Pediatr, 2012: 352751.

17.          Chen, Y., Bates, D.L., Dey, R., Chen, P.H., Machado, A.C., Laird-Offringa, I.A., Rohs, R., and Chen, L. (2012). DNA Binding by GATA Transcription Factor Suggests Mechanisms of DNA Looping and Long-Range Gene Regulation. Cell Rep, 2: 1197-206.

18.          Pan, Y., Hu, M., Liang, H., Wang, J.J., and Tang, L.J. (2012). The expression of the PIWI family members miwi and mili in mice testis is negatively affected by estrogen. Cell Tissue Res, 350: 177-81.

19.          Peng, J., Deng, X., He, F., Omran, A., Zhang, C., Yin, F., and Liu, J. (2012). Role of ventriculoperitoneal shunt surgery in grade IV tubercular meningitis with hydrocephalus. Childs Nerv Syst, 28: 209-15.

20.          Xiong, Z., Luo, S., Xu, X., Zhang, L., Peng, H., Li, W., Xue, J., Chen, X., Hu, Z., and Xia, K. (2012). Novel FLG mutations associated with ichthyosis vulgaris in the Chinese population. Clin Exp Dermatol, 37: 177-80.

21.          Liu, L., Xie, H., Chen, X., Shi, W., Xiao, X., Lei, D., and Li, J. (2012). Differential response of normal human epidermal keratinocytes and HaCaT cells to hydrogen peroxide-induced oxidative stress. Clin Exp Dermatol, 37: 772-80.

22.          Li, M., Li, C., Li, D., Xie, Y., Shi, J., Li, G., Guan, Y., Zhang, P., Peng, F., Xiao, Z., and Chen, Z. (2012). Periostin, a stroma-associated protein, correlates with tumor invasiveness and progression in nasopharyngeal carcinoma. Clin Exp Metastasis, 29: 865-77.

23.          Zhou, B.T., Zhou, Q.H., Yin, J.Y., Li, G.L., Xu, X.J., Qu, J., Liu, D., Zhou, H.H., and Liu, Z.Q. (2012). Comprehensive analysis of the association of SCN1A gene polymorphisms with the retention rate of carbamazepine following monotherapy for new-onset focal seizures in the Chinese Han population. Clin Exp Pharmacol Physiol, 39: 379-84.

24.          Dai, X.P., Huang, Q., Yin, J.Y., Guo, Y., Gong, Z.C., Lei, M.X., Jiang, T.J., Zhou, H.H., and Liu, Z.Q. (2012). KCNQ1 gene polymorphisms are associated with the therapeutic efficacy of repaglinide in Chinese type 2 diabetic patients. Clin Exp Pharmacol Physiol, 39: 462-8.

25.          Xu, X., Duan, L., Zhou, B., Ma, R., Zhou, H., and Liu, Z. (2012). Genetic polymorphism of copper transporter protein 1 is related to platinum resistance in Chinese non-small cell lung carcinoma patients. Clin Exp Pharmacol Physiol, 39: 786-92.

26.          Xu, X., Zhang, L., Tong, P., Xun, G., Su, W., Xiong, Z., Zhu, T., Zheng, Y., Luo, S., Pan, Y., Xia, K., and Hu, Z. (2012). Exome sequencing identifies UPF3B as the causative gene for a Chinese non-syndrome mental retardation pedigree. Clin Genet, doi:10.1111/cge.12014.

27.          Qiao, G., Yang, L., Li, Z., Ying, H., Hassen, Y., Yin, F., and Zhang, J. (2012). Program death-1 regulates peripheral T cell tolerance via an anergy-independent mechanism. Clin Immunol, 143: 128-33.

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

29.          Qu, J., Zhou, B.T., Yin, J.Y., Xu, X.J., Zhao, Y.C., Lei, G.H., Tang, Q., Zhou, H.H., and Liu, Z.Q. (2012). ABCC2 polymorphisms and haplotype are associated with drug resistance in Chinese epileptic patients. CNS Neurosci Ther, 18: 647-51.

30.          Zhou, B.T., Zhou, Q.H., Yin, J.Y., Li, G.L., Qu, J., Xu, X.J., Liu, D., Zhou, H.H., and Liu, Z.Q. (2012). Effects of SCN1A and GABA receptor genetic polymorphisms on carbamazepine tolerability and efficacy in Chinese patients with partial seizures: 2-year longitudinal clinical follow-up. CNS Neurosci Ther, 18: 566-72.

31.          He, F., Peng, J., Deng, X.L., Yang, L.F., Camara, A.D., Omran, A., Wang, G.L., Wu, L.W., Zhang, C.L., and Yin, F. (2012). Mechanisms of tumor necrosis factor-alpha-induced leaks in intestine epithelial barrier. Cytokine, 59: 264-72.

32.          Omran, A., Peng, J., Zhang, C., Xiang, Q.L., Xue, J., Gan, N., Kong, H., and Yin, F. (2012). Interleukin-1beta and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy. Epilepsia, 53: 1215-24.

33.          Luo, H., Xie, L., Wang, S.Z., Chen, J.L., Huang, C., Wang, J., Yang, J.F., Zhang, W.Z., Yang, Y.F., and Tan, Z.P. (2012). Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly. Eur J Med Genet, 55: 646-9.

34.          Ge, S., Mao, Y., Yi, Y., Xie, D., Chen, Z., and Xiao, Z. (2012). Comparative proteomic analysis of secreted proteins from nasopharyngeal carcinoma-associated stromal fibroblasts and normal fibroblasts. Exp Ther Med, 3: 857-60.

35.          Zhang, H., Luo, H., Chen, H., Mei, L., He, C., Jiang, L., Li, J.D., and Feng, Y. (2012). Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2. FEBS Lett, 586: 4126-31.

36.          Peng, J., Deng, X., Wang, G., Duan, Y., and Yin, F. (2012). A retrospective analysis of pathological and clinical diagnoses: report of 240 pediatric autopsies. Fetal Pediatr Pathol, 31: 63-73.

37.          Deng, G., Jiang, C., and Li, Y.X. (2012). Clinical utility of the mood and anxiety symptom questionnaire in a chinese sample of patients with pancreatic cancer. Gastroenterol Nurs, 35: 193-8.

38.          Peng, H., Zhang, Y., Long, Z., Zhao, D., Guo, Z., Xue, J., Xie, Z., Xiong, Z., Xu, X., Su, W., Wang, B., Xia, K., and Hu, Z. (2012). A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family. Gene, 502: 168-71.

39.          Huang, C., Yang, Y.F., Yin, N., Chen, J.L., Wang, J., Zhang, H., and Tan, Z.P. (2012). Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion. Gene, 498: 308-10.

40.          Guo, H., Xun, G., Peng, Y., Xiang, X., Xiong, Z., Zhang, L., He, Y., Xu, X., Liu, Y., Lu, L., Long, Z., Pan, Q., Hu, Z., Zhao, J., and Xia, K. (2012). Disruption of Contactin 4 in two subjects with autism in Chinese population. Gene, 505: 201-5.

41.          Huang, C., Yang, Y.F., Zhang, H., Xie, L., Chen, J.L., Wang, J., Tan, Z.P., and Luo, H. (2012). Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China. Genet Mol Res, 11: 2321-7.

42.          Zhong, Q., Liang, D., Liu, J., Xue, J., and Wu, L. (2012). Mutation analysis in Chinese patients with Cornelia de Lange syndrome. Genet Test Mol Biomarkers, 16: 1130-4.

43.          Hu, Z., Xiong, Z., Xu, X., Li, F., Lu, L., Li, W., Su, J., Liu, Y., Liu, D., Xie, Z., Peng, Y., Kuang, Y., Wu, L., Zhang, J., Pan, Q., Tang, B., Chen, X., and Xia, K. (2012). Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population. Hum Genet, 131: 1269-74.

44.          Zhang, H., Chen, H., Luo, H., An, J., Sun, L., Mei, L., He, C., Jiang, L., Jiang, W., Xia, K., Li, J.D., and Feng, Y. (2012). Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II. Hum Genet, 131: 491-503.

45.          Choo, Y.S., Vogler, G., Wang, D., Kalvakuri, S., Iliuk, A., Tao, W.A., Bodmer, R., and Zhang, Z. (2012). Regulation of parkin and PINK1 by neddylation. Hum Mol Genet, 21: 2514-23.

46.          Qurashi, A., Liu, H., Ray, L., Nelson, D.L., Duan, R., and Jin, P. (2012). Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila. Hum Mol Genet, 21: 2068-75.

47.          Wang, T., Pan, Q., Lin, L., Szulwach, K.E., Song, C.X., He, C., Wu, H., Warren, S.T., Jin, P., Duan, R., and Li, X. (2012). Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum. Hum Mol Genet, 21: 5500-10.

48.          Zhu, L., Li, Y., and Xu, A. (2012). Influence of controlled ovarian hyperstimulation on uterine peristalsis in infertile women. Hum Reprod, 27: 2684-9.

49.          Ramkalawan, H., Wang, Y.Z., Hurbungs, A., Yang, Y.F., Tian, F.F., Zhou, W.B., Li, J., Yang, H., Xiao, B., and Zhang, W. (2012). Pioglitazone, PPARgamma agonist, attenuates experimental autoimmune neuritis. Inflammation, 35: 1338-47.

50.          Fang, M., Chen, H., Li, L.H., Wu, R., Li, Y., Liu, L., Ye, M., Huang, J., Zhu, S., Wang, G., Zhang, Q., Zheng, H., Zhang, L., Wang, B., Zhou, J., and Zhao, J.P. (2012). Comparison of risperidone oral solution and intramuscular haloperidol with the latter shifting to oral therapy for the treatment of acute agitation in patients with schizophrenia. Int Clin Psychopharmacol, 27: 107-13.

51.          Ai, S., Shen, L., Guo, J., Feng, X., and Tang, B. (2012). DNA methylation as a biomarker for neuropsychiatric diseases. Int J Neurosci, 122: 165-76.

52.          Jia, D., Tang, B., Chen, Z., Shi, Y., Sun, Z., Zhang, L., Wang, J., Xia, K., and Jiang, H. (2012). Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds. Int J Neurosci, 122: 560-2.

53.          Song, C.Y., Guo, J.F., Liu, Y., and Tang, B.S. (2012). Autophagy and Its Comprehensive Impact on ALS. Int J Neurosci, 122: 695-703.

54.          Chen, J.D., Liu, F., Xun, G.L., Chen, H.F., Hu, M.R., Guo, X.F., Xiao, C.Q., Wooderson, S.C., Guo, W.B., and Zhao, J.P. (2012). Early and late onset, first-episode, treatment-naive depression: same clinical symptoms, different regional neural activities. J Affect Disord, 143: 56-63.

55.          Xu, Y., Cao, L.Q., Jin, L.Y., Chen, Z.C., Zeng, G.Q., Tang, C.E., Li, G.Q., Duan, C.J., Peng, F., Xiao, Z.Q., and Li, C. (2012). Quantitative proteomic study of human lung squamous carcinoma and normal bronchial epithelial acquired by laser capture microdissection. J Biomed Biotechnol, 2012: 510418.

56.          Ma, C., Han, R., Qi, S., and Yeung, E.S. (2012). Selective transport of single protein molecules inside gold nanotubes. J Chromatogr A, 1238: 11-4.

57.          Zhao, J., and Li, Y. (2012). Adenosine triphosphate content in human unfertilized oocytes, undivided zygotes and embryos unsuitable for transfer or cryopreservation. J Int Med Res, 40: 734-9.

58.          Chen, S., Zuo, X., Yang, M., Lu, H., Wang, N., Wang, K., Tu, Z., Chen, G., Liu, M., Liu, K., and Xiao, X. (2012). Severe multiple organ injury in HSF1 knockout mice induced by lipopolysaccharide is associated with an increase in neutrophil infiltration and surface expression of adhesion molecules. J Leukoc Biol, 92: 851-7.

59.          Omran, A., Sahmoud, S., Peng, J., Ashhab, U., and Yin, F. (2012). Thrombocytopenia and absent radii (TAR) syndrome associated with bilateral congenital cataract: a case report. J Med Case Rep, 6: 168.

60.          Xu, Q., Guo, H., Zhang, X., Tang, B., Cai, F., Zhou, W., and Song, W. (2012). Hypoxia regulation of ATP13A2 (PARK9) gene transcription. J Neurochem, [Epub ahead of print].

61.          Hu, Y., Tang, B., Guo, J., Wu, X., Sun, Q., Shi, C., Hu, L., Wang, C., Wang, L., Tan, L., Shen, L., Yan, X., and Zhang, H. (2012). Variant in the 3' region of SNCA associated with Parkinson's disease and serum alpha-synuclein levels. J Neurol, 259: 497-504.

62.          Zhang, B.R., Tian, J., Yan, Y.P., Yin, X.Z., Zhao, G.H., Wu, Z.Y., Gu, W.H., Xia, K., and Tang, B.S. (2012). CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese families. J Neurol Sci, 312: 92-6.

63.          Zhan, X.Q., Liu, J., and Chen, Z.C. (2012). Identification of mitochondrial proteins related to nasopharyneal carcinoma metastasis. J Protomics Bioinformatics, 5: 6-32.

64.          Liu, Y., Hu, Z., Xun, G., Peng, Y., Lu, L., Xu, X., Xiong, Z., Xia, L., Liu, D., Li, W., Zhao, J., and Xia, K. (2012). Mutation analysis of the NRXN1 gene in a Chinese autism cohort. J Psychiatr Res, 46: 630-4.

65.          Guo, W.B., Liu, F., Chen, J.D., Gao, K., Xue, Z.M., Xu, X.J., Wu, R.R., Tan, C.L., Sun, X.L., Liu, Z.N., Chen, H.F., and Zhao, J.P. (2012). Abnormal neural activity of brain regions in treatment-resistant and treatment-sensitive major depressive disorder: a resting-state fMRI study. J Psychiatr Res, 46: 1366-73.

66.          Wang, Y.W., Ren, J.H., Xia, K., Wang, S.H., Yin, T.F., Xie, D.H., and Li, L.H. (2012). Effect of mitomycin on normal dermal fibroblast and HaCat cell: an in vitro study. J Zhejiang Univ Sci B, 13: 997-1005.

67.          Han, R., Wang, G., Qi, S., Ma, C., and Yeung, E.S. (2012). Electrophoretic Migration and Axial Diffusion of Individual Nanoparticles in Cylindrical Nanopores. J Phys Chem C, 116: 18460-68.

68.          Xu, X., Ren, H., Zhou, B., Zhao, Y., Yuan, R., Ma, R., Zhou, H., and Liu, Z. (2012). Prediction of copper transport protein 1 (CTR1) genotype on severe cisplatin induced toxicity in non-small cell lung cancer (NSCLC) patients. Lung Cancer, 77: 438-42.

69.          Omran, A., Elimam, D., He, F., Peng, J., and Yin, F. (2012). Potential role of blood microRNAs as non-invasive biomarkers for early detection of asymptomatic coronary atherosclerosis in obese children with metabolic syndrome. Med Hypotheses, 79: 889-93.

70.          Guan, R., Wen, X.Y., Wu, J., Duan, R., Cao, H., Lam, S., Hou, D., Wang, Y., Hu, J., and Chen, Z. (2012). Knockdown of ZNF403 inhibits cell proliferation and induces G2/M arrest by modulating cell-cycle mediators. Mol Cell Biochem, 365: 211-22.

71.          Ma, C. (2012). Highly sensitive detection of alkaline phosphatase using molecular beacon probes based on enzymatic polymerization. Mol Cell Probes, 26: 113-5.

72.          Ma, C., Xia, K., Chen, H., Zeng, W., Han, R., and Tang, J. (2012). Label-free highly sensitive detection of telomerase activity in cancer cell by chemiluminescence imaging. Mol Cell Probes, 26: 212-4.

73.          Liu, W., Li, L., Khan, M.A., and Zhu, F. (2012). Popular molecular markers in bacteria. Mol Gen Mikrobiol Virusol: 14-7.

74.          Xue, J., Peng, J., Zhou, M., Zhong, L., Yin, F., Liang, D., and Wu, L. (2012). Novel compound heterozygous mutation of MLYCD in a Chinese patient with malonic aciduria. Mol Genet Metab, 105: 79-83.

75.          Zhang, S.Q., Jiang, T., Li, M., Zhang, X., Ren, Y.Q., Wei, S.C., Sun, L.D., Cheng, H., Li, Y., Yin, X.Y., Hu, Z.M., Wang, Z.Y., Liu, Y., Guo, B.R., Tang, H.Y., Tang, X.F., Ding, Y.T., Wang, J.B., Li, P., Wu, B.Y., Wang, W., Yuan, X.F., Hou, J.S., Ha, W.W., Wang, W.J., Zhai, Y.J., Wang, J., Qian, F.F., Zhou, F.S., Chen, G., Zuo, X.B., Zheng, X.D., Sheng, Y.J., Gao, J.P., Liang, B., Zhu, J., Xiao, F.L., Wang, P.G., Cui, Y., Li, H., Liu, S.X., Gao, M., Fan, X., Shen, S.K., Zeng, M., Sun, G.Q., Xu, Y., Hu, J.C., He, T.T., Li, Y.R., Yang, H.M., Yu, Z.Y., Zhang, H.F., Hu, X., Yang, K., Zhao, S.X., Zhou, Y.W., Liu, J.J., Du, W.D., Zhang, L., Xia, K., Yang, S., Wang, J., and Zhang, X.J. (2012). Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis. Nat Genet, 44: 1156-60.

76.          Zhong, L., Yan, K., Liu, C., Xue, J., Wu, L., and Yin, F. (2012). Clinical reasoning: a young man with reversible paralysis, cerebral white matter lesions, and peripheral neuropathy. Neurology, 79: e70-2.

77.          Qiu, F., Qiu, C.Y., Liu, Y.Q., Wu, D., Li, J.D., and Hu, W.P. (2012). Potentiation of acid-sensing ion channel activity by the activation of 5-HT(2) receptors in rat dorsal root ganglion neurons. Neuropharmacology, 63: 494-500.

78.          Tian, J.Y., Tang, B.S., Shi, C.H., Lv, Z.Y., Li, K., Yu, R.L., Shen, L., Yan, X.X., and Guo, J.F. (2012). Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population. Neurosci Lett, 514: 156-8.

79.          Zhang, H.N., Guo, J.F., He, D., Lei, L.F., Wang, Y.Q., Wang, C.Y., Tan, L.M., Yan, X.X., Shen, L., and Tang, B.S. (2012). Lower serum UA levels in Parkinson's disease patients in the Chinese population. Neurosci Lett, 514: 152-5.

80.          Guo, W.B., Liu, F., Xue, Z.M., Gao, K., Wu, R.R., Ma, C.Q., Liu, Z.N., Xiao, C.Q., Chen, H.F., and Zhao, J.P. (2012). Altered white matter integrity in young adults with first-episode, treatment-naive, and treatment-responsive depression. Neurosci Lett, 522: 139-44.

81.          Chen, Z., Li, X., Tang, B., Wang, J., Shi, Y., Sun, Z., Zhang, L., Pan, Q., Xia, K., and Jiang, H. (2012). Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population. Neurosci Lett, 520: 16-9.

82.          Tian, J.Y., Guo, J.F., Wang, L., Sun, Q.Y., Yao, L.Y., Luo, L.Z., Shi, C.H., Hu, Y.C., Yan, X.X., and Tang, B.S. (2012). Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neurosci Lett, 516: 207-11.

83.          Li, K., Tang, B.S., Yu, R.L., Lv, Z.Y., Sun, Q.Y., Li, Q., Xia, K., Yan, X.X., and Guo, J.F. (2012). Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population. Neurosci Lett, 517: 56-9.

84.          Wei, Q., Diao, F., Kang, Z., Gan, Z., Han, Z., Zheng, L., Li, L., Guo, X., Shan, B., Liu, C., Zhao, J., and Zhang, J. (2012). The effect of DISC1 on regional gray matter density of schizophrenia in Han Chinese population. Neurosci Lett, 517: 21-4.

85.          Liu, Y.T., Tang, B.S., Wang, J.L., Guan, W.J., Shen, L., Shi, Y.T., Zhou, Y., Yan, X.X., Xia, K., and Jiang, H. (2012). Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population. Neurosci Lett, 528: 51-4.

86.          Jayathilaka, N., Han, A., Gaffney, K.J., Dey, R., Jarusiewicz, J.A., Noridomi, K., Philips, M.A., Lei, X., He, J., Ye, J., Gao, T., Petasis, N.A., and Chen, L. (2012). Inhibition of the function of class IIa HDACs by blocking their interaction with MEF2. Nucleic Acids Res, 40: 5378-88.

87.          Long, D., Zeng, J., Wu, L.Q., Tang, L.S., Wang, H.L., and Wang, H. (2012). Vitreous amyloidosis in two large mainland Chinese kindreds resulting from transthyretin variant Lys35Thr and Leu55Arg. Ophthalmic Genet, 33: 28-33.

88.          Lv, Z., Guo, J., Sun, Q., Li, K., Yu, R., Tian, J., Yan, X., and Tang, B. (2012). Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population. Parkinsonism Relat Disord, 18: 641-4.

89.          Guo, J.F., Sun, Q.Y., Lv, Z.Y., Yu, R.L., Li, K., Zhang, Y.H., Tian, J.Y., Xia, K., Yan, X.X., and Tang, B.S. (2012). VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population. Parkinsonism Relat Disord, 18: 983-5.

90.          Li, Y.M., Zhao, J.P., Ou, J.J., and Wu, R.R. (2012). Efficacy and tolerability of ziprasidone vs. olanzapine in naive first-episode schizophrenia: a 6-week, randomized, open-label, flexible-dose study. Pharmacopsychiatry, 45: 177-81.

91.          Ma, L., Gao, X., Luo, J., Huang, L., Teng, Y., and Horvitz, H.R. (2012). The Caenorhabditis elegans gene mfap-1 encodes a nuclear protein that affects alternative splicing. PLoS Genet, 8: e1002827.

92.          Chi, J., Li, L., Liu, M., Tan, J., Tang, C., Pan, Q., Wang, D., and Zhang, Z. (2012). Pathogenic connexin-31 forms constitutively active hemichannels to promote necrotic cell death. PLoS One, 7: e32531.

93.          Li, B., Zhang, G., Li, C., He, D., Li, X., Zhang, C., Tang, F., Deng, X., Lu, J., Tang, Y., Li, R., Chen, Z., and Duan, C. (2012). Identification of JAK2 as a mediator of FIP1L1-PDGFRA-induced eosinophil growth and function in CEL. PLoS One, 7: e34912.

94.          Liu, F., Guo, W., Yu, D., Gao, Q., Gao, K., Xue, Z., Du, H., Zhang, J., Tan, C., Liu, Z., Zhao, J., and Chen, H. (2012). Classification of different therapeutic responses of major depressive disorder with multivariate pattern analysis method based on structural MR scans. PLoS One, 7: e40968.

95.          Liu, X., Wu, Y., Li, Z., Yang, J., Xue, J., Hu, Y., Feng, M., Niu, W., Yang, Q., Lei, M., Xia, J., Wu, L., and Liang, D. (2012). Targeting of the human coagulation factor IX gene at rDNA locus of human embryonic stem cells. PLoS One, 7: e37071.

96.          Yin, J.Y., Huang, Q., Zhao, Y.C., Zhou, H.H., and Liu, Z.Q. (2012). Meta-analysis on pharmacogenetics of platinum-based chemotherapy in non small cell lung cancer (NSCLC) patients. PLoS One, 7: e38150.

97.          Li, J.D., Hu, W.P., and Zhou, Q.Y. (2012). The circadian output signals from the suprachiasmatic nuclei. Prog Brain Res, 199: 119-27.

98.          Guo, W.B., Liu, F., Xue, Z.M., Xu, X.J., Wu, R.R., Ma, C.Q., Wooderson, S.C., Tan, C.L., Sun, X.L., Chen, J.D., Liu, Z.N., Xiao, C.Q., Chen, H.F., and Zhao, J.P. (2012). Alterations of the amplitude of low-frequency fluctuations in treatment-resistant and treatment-response depression: a resting-state fMRI study. Prog Neuropsychopharmacol Biol Psychiatry, 37: 153-60.

99.          Guo, W.B., Liu, F., Chen, J.D., Xu, X.J., Wu, R.R., Ma, C.Q., Gao, K., Tan, C.L., Sun, X.L., Xiao, C.Q., Chen, H.F., and Zhao, J.P. (2012). Altered white matter integrity of forebrain in treatment-resistant depression: a diffusion tensor imaging study with tract-based spatial statistics. Prog Neuropsychopharmacol Biol Psychiatry, 38: 201-6.

100.       Guo, W.B., Liu, F., Xun, G.L., Hu, M.R., Guo, X.F., Xiao, C.Q., Chen, H.F., Wooderson, S.C., Chen, J.D., and Zhao, J.P. (2012). Reversal alterations of amplitude of low-frequency fluctuations in early and late onset, first-episode, drug-naive depression. Prog Neuropsychopharmacol Biol Psychiatry, 40C: 153-59.

101.       Zhou, W., Li, J.D., Hu, W.P., Cheng, M.Y., and Zhou, Q.Y. (2012). Prokineticin 2 is involved in the thermoregulation and energy expenditure. Regul Pept, 179: 84-90.

102.       Zhao, J., Zhang, Q., and Li, Y. (2012). The effect of endometrial thickness and pattern measured by ultrasonography on pregnancy outcomes during IVF-ET cycles. Reprod Biol Endocrinol, 10: 100.

103.       Xu, B., and Li, Y.P. (2012). Flexible ovarian stimulation in a poor responder: A case report and review of the literature. Reprod Biomed Online, 25: 441-2.

104.       Liu, H., Kaneko, Y., Ouyang, X., Li, L., Hao, Y., Chen, E.Y., Jiang, T., Zhou, Y., and Liu, Z. (2012). Schizophrenic patients and their unaffected siblings share increased resting-state connectivity in the task-negative network but not its anticorrelated task-positive network. Schizophr Bull, 38: 285-94.

105.       Pu, W., Li, L., Zhang, H., Ouyang, X., Liu, H., Zhao, J., Xue, Z., Xu, K., Tang, H., Shan, B., Liu, Z., and Wang, F. (2012). Morphological and functional abnormalities of salience network in the early-stage of paranoid schizophrenia. Schizophr Res, 141: 15-21.

106.       Huang, S. (2012). Primate phylogeny: molecular evidence for a pongid clade excluding humans and a prosimian clade containing tarsiers. Sci China Life Sci, 55: 709-25.

107.       Zeng, G.Q., Zhang, P.F., Li, C., Peng, F., Li, M.Y., Xu, Y., Yu, F.L., Chen, M.J., Yi, H., Li, G.Q., Chen, Z.C., and Xiao, Z.Q. (2012). Comparative Proteome Analysis of Human Lung Squamous Carcinoma using Two Different Methods: Two-Dimensional Gel Electrophoresis and iTRAQ Analysis. Technol Cancer Res Treat, 11: 395-408.

108.       王淑玲, 刘静 (2012). 泛素-蛋白酶体通路与白血病. 生命的化学: 871-75.

109.       王鸿涵, 冯永, 王行炜, 梅凌云, 陈红胜, 蒋璐, 门美超, 张华, 李海波, 刘亚兰, 卢焰梅, 贺楚峰 (2012). 一个迟发性非综合征型常染色体显性遗传性聋家系表型特征及致病基因初步探讨. 听力学及言语疾病杂志: 309-13.

110.       宋延民, 龙莉莉, 杨茜, 李海燕, 唐北沙 (2012). 定位于1p36.121p35.1的良性家族性婴儿惊厥家系8个候选基因的排除克隆. 现代生物医学进展: 1233-35.

111.       田磊, 万文萃, 郭辉, 王天云, 卢杰, 夏昆, 金学民, 胡正茂 (2012). 高度近视家系ZNF644基因突变筛查. 眼科新进展: 447-49.

112.       张译升, 康亚男, 刘冬娥, 李玉梅, 李艳萍, 刘能辉, 陈仙花, 姚仲元, 周世敏, 张叶青 (2012). 部分卵子卵胞浆内单精子注射在辅助生殖技术中的应用价值. 医学临床研究, 29: 4.

113.       向秋莲, 张慈柳, 彭镜, 何芳, 吴丽文, 欧曼, 尹飞 (2012). TLR4MRP8在内侧颞叶癫痫幼大鼠海马中表达的动态变化. 中风与神经疾病杂志: 580-84.

114.       李娟, 龙志高, 戴和平 (2012). 世界首报染色体异常核型一例. 中国保健营养(中旬刊).

115.       廖鑫鑫, 沈璐 (2012). 帕金森病BOLD-fMRI研究进展. 中国临床医学影像杂志, 23.

116.       唐北沙 (2012). 神经系统遗传性疾病分子遗传学和分子诊断历史回顾与展望. 中国现代神经疾病杂志: 231-32.

117.       唐北沙, 江泓 (2012). 遗传性共济失调诊断与治疗专家策略. 中国现代神经疾病杂志: 266-74.

118.       王春荣, 江泓 (2012). 多聚谷氨酰胺病CAG重复序列动态突变机制研究进展. 中国现代神经疾病杂志, 12: 363-66.

119.       李娟, 龙志高, 文娟, 唐桂芝, 朱艳萍 (2012). 9Yqs携带者的临床遗传学分析. 中国优生与遗传杂志: 69-70.

120.       黑明燕, 陈佳, 邬玲仟, 余波, 谭彦娟, 赵玲玲 (2012). Cornelia de Lange综合征病例报告并17例文献复习. 中华儿科杂志, 50.

121.       向小爽, 孙占芳, 邝岚琼, 唐北沙, 江泓 (2012). 多系统萎缩影像学研究进展. 中华临床医师杂志(电子版), 6: 1806-08.

122.       刘新建, 唐北沙 (2012). 散发性共济失调的分类及诊断. 中华神经科杂志, 45.

123.       关文娟, 王俊岭, 唐北沙 (2012). 常染色体隐性小脑性遗传共济失调的遗传学特征及研究进展. 中华医学遗传学杂志, 29: 4.

124.       罗丽霞, 潘乾, 夏昆, 唐北沙, 江泓 (2012). 一例貌似强直性肌营养不良的脊肌萎缩症的临床、病理及基因诊断. 中华医学遗传学杂志, 29.

125.       王华, 席惠, 贾政军, 黄定梅, 周玉春, 邬玲仟 (2012). 应用单核苷酸多态芯片技术产前诊断四例胎儿新发染色体变异. 中华医学遗传学杂志, 29: 4.

126.       严伟倩, 王俊岭, 唐北沙 (2012). 热休克同源蛋白70羧基端作用蛋白的功能及其与神经退行性疾病的关系. 中华医学遗传学杂志, 29.

127.       詹自雄, 胡兆婷, 沈璐 (2012). 全外显子组测序在常染色体隐性遗传病致病基因克隆中的应用策略. 中华医学遗传学杂志, 29: 4.

128.       张如旭, 唐北沙 (2012). 腓骨肌萎缩症的分型与分子诊断流程. 中华医学遗传学杂志, 29: 5.

129.       占雅静, 资晓宏, 李琳, 李小波, 黄顺祥, 厉兰, 李锡癸, 胡正茂, 潘乾, 夏昆, 唐北沙, 张如旭 (2012). 中国汉族腓骨肌萎缩症家系的CX32基因突变和临床特点分析. 中华医学杂志, 92.

130.       张付峰, 卢晓琴, 周亚芳, 沈璐, 江泓, 严新翔, 唐北沙 (2012). K141N突变型小分子热休克蛋白22轴突转运障碍及其在CMT2L发病机制中的作用. 中华医学杂志, 92.

131.       张学伟, 郭纪锋, 艾三喜, 胡雅岑, 孙启英, 徐倩, 吕占云, 李凯, 董晓丽, 沈璐, 江泓, 潘乾, 夏昆, 严新翔, 唐北沙 (2012). 中国汉族帕金森病人microRNA-7变异分析. 中南大学学报(医学版), 37: 4.


     
     
     
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