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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
 

2010年发表论文

 

1.       Guo X, Zhai J, Liu Z, Fang M, Wang B, Wang C, Hu B, Sun X, Lv L, Lu Z, Ma C, He X, Guo T, Xie S, Wu R, Xue Z, Chen J, Twamley EW, Jin H, Zhao J. (2010) Effect of antipsychotic medication alone vs combined with psychosocial intervention on outcomes of early-stage schizophrenia: A randomized 1-year study.Arch Gen Psychiat.67: 895-904.

2.       Wang JL, Yang X, Xia K, Hu ZM, Weng L, Jin X, Jiang H, Zhang P, Shen L, Guo JF, Li N, Li YR, Lei LF, Zhou J, Du J, Zhou YF, Pan Q, Wang J, Wang J, Li RQ, Tang BS. (2010) Identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.Brain.133: 3510-3518.

3.       Yuan XL, Guo JF, Shi ZH, Xiao ZQ, Yan XX, Zhao BL, Tang BS. (2010) R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial disfunction and oxidative stress.Brain res.1351: 229-237.

4.       Chen H, Jiang L, Xie Z, Mei L, He C, Hu Z, Xia K, Feng Y. (2010) Novel mutations of PAX3 MITF and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.Biochem Biophys Res Commun.397: 70-74.

5.       Huang S. (2010) The overlap feature of the genetic equidistance result a fundamental biological phenomenon overlooked for nearly half of a century.Biological Theory.5: 40-52.

6.       Guo H, Peng D, Xu M, Xue J, Lu L, Xu X, Liu Y, Xiong Z, Pan Q, Hu Z, Xia K. (2010) Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population.Clin Dysmorphol.19: 206-208.

7.       Shen JD, Liang DS, Zhou ZM, XiaY, Long ZG, Wu LQ. (2010) Pallister-Killian Syndrome: meiosis II non-disjunction may be the first step in the formation of isochromosome 12p.Chinese Med J-peking (Engl).123: 3482-3485.

8.       Xu Q, Li QH, Wang JL, Jiang H, Shen L, Li XH, Tang BS.(2010) A spinocerebellar Ataxia Family with Expanded Alleles in the Tata-Binding Protein Gene and Ataxin-3 Gene.Int J Neurosci. 120: 159-161.

9.       Li N, Li H, Jiang H, Shen L, Yan X, Guo J, Song Y, Yang Q, Wang Y, Li X, Xiang R, Zi X, Long X, Hu Z, Pan Q, Xia K, Tang B. (2010) Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.Int J Neurosci.120: 217-221.

10.     Wang X, Wang H, Xia Y, Jiang H, Shen L, Wang S, Shen R, Huang L, Wang J, Xu Q, Li X, Luo X, Tang BS. (2010) A neuropathological study at autopsy of early onset spinocerebellar ataxia 6.J Clin Neurosci.30: 1-4.

11.        Guo JF,Zhang XW,Nie LL,Zhang HN,Liao B,Li J,Wang L,Yan XX,Tang BS. (2010) Mutation analysis of Parkin PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism.J Neurol.257: 1170-1175.

12.     Lu H, Kuang YH, Su J, Chang J, Wu LS, Kanekura T, Li D, Chen ML, Chen X. (2010) CD147 is highly expressed on peripheral blood neutrophils from patients with psoriasis and induces neutrophil chemotaxis.J Dermatol.37: 1053-1056.

13.     Xia K, Xiong H, Shin Y, Wang D, Deerinck T, Takahashi H, Ellisman MH, Lipton SA, Tong G, Descalzi G, Zhang D, Zhuo M, Zhang Z. (2010) Roles of KChIP1 in the regulation of GABA-mediated transmission and behavioral anxiety.Mol Brain.3: 23.

14.     Zhou WB, Li JD, Wang XC, Hu RM.(2010) Stable knockdown of TPPP3 by RNA interference in Lewis lung carcinoma cell inhibits tumor growth and metastasis.Mol Cell Biochem. 343: 231-238.

15.     Sun QY, Guo JF, Wang L, Yu RH, Zuo X, Yao LY, Pan Q, Xia K, Tang BS. (2010) Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population.Movement Disord.25: 1005-1011.

16.     Liu D, Hu Z, Peng Y, Yu C, Liu Y, Mo X, Li X, Lu L, Xu X, Su W, Pan Q, Xia K. (2010) A novel nonsense mutation in the NDP gene in a Chinese family with Norrie disease.Mol Vis.16: 2653-2658

17.     Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B. (2010) Spinocerebellar ataxia type 11 in the Chinese Han population.Neurol Sci.31: 107-109.

18.        Guo JF,Wang L,He D,Yang QH,Duan ZX,Zhang XW,Nie LL,Yan XX,Tang BS. (2010) Clinical features and [(11)C]-CFT PET analysis of PARK2 PARK6 PARK7-linked autosomal recessive early onset Parkinsonism.Neurol Sci.

19.     JiangH,Shi YT, Wang JL,TangBS,WangJY, Peng ZF, XiaoDS. (2010) A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literature.Neurol Sci.

20.     Li N, Zhang J, Guo JF, Yan XX, Xia K, Tang BS. (2010) Novel mutation of SCN1A in familial generalized epilepsy with febrile seizures plus.Neurosci Lett.480: 211-214.

21.     Wang L, Guo JF, Zhang WW, Xu Q, Zuo X, Shi CH, Luo LZ, Liu J, Hu L, Hu YC, She L, Jiang H, Yan XX, Xia K , Pan Q, Tang BS. (2010) Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population.Neurosci Lett.473: 131-135.

22.     Luo LZ, Xu Q, Guo JF, Wang L, Shi CH, Wei JH, Long ZG, Pan Q, Tang BS, Xia K, Yan XX. (2010) FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patients.Neurosci Lett.482: 86-89.

23.     Zuo X, Jiang H, Guo JF, Yu RH, Sun QY, Hu L, Wang L, Yao LY, Shen L, Pan Q, Yan XX, Xia K, Tang BS. (2010) Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population.Neurosci Lett.481: 69-72.

24.        Guo J,Wei J,Liao S,Wang L,Jiang H,Tang BS. (2010) A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease.Neurosci Lett.468: 34-37.

25.        Wang L,Guo JF,Nie LL,Xu Q,Zuo X,Sun QY,Yan XX,Tang BS. (2010) A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.Neurosci Lett.468: 198-201.

26.     Wang X, Wang H, Xia Y, Jiang H, Shen L, Wang S, Shen R, Xu Q, Luo X, Tang BS. (2010) Spinocerebellar ataxia type 6: Systematic patho-anatomical study reveals different phylogenetically defined regions of the cerebellum and neural pathways undergo different evolutions of the degenerative process.Neuropathology.30: 501-514.

27.     He Y, Xun G, Xia K, Hu Z, Lv L, Deng Z, Zhao J. (2010)No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population.Psychiatry Res.

28.     Li X, Hu Z, He Y, Xiong Z, Long Z, Peng Y, Bu F, Ling J, Xun G, Mo X, Pan Q, Zhao J, Xia K. (2010) Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.Psychiatr Genet.20: 113-117.

29.     Mo X, Liu D, Li W, Hu Z, Hu Y, Li J, Guo J, Tang B, Zhang Z, Bai Y, Xia K. (2010) Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese population.Parkinsonism Relat D.16: 222-224.

30.     Xu Q, Jia D, Wang J, Guo J, Jiang H, Lei L, Shen L, Pan Q, Xia K, Yan X, Tang B. (2010) Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson's disease in mainland China.Parkinsonism Relat D.16: 700-702.

31.     Wang F, Huang S, Ma L. (2010) Caenorhabditis elegans operons contain a higher proportion of genes with multiple transcripts and use 3' splice sites differentially.PloS one.5: e12456.

32.    Lyu QF,Deng L,Xue SG,Cao SF,Liu XY,Jin W,Wu LQ,Kuang YP. (2010) New technique for mouse oocyte injection via a modified holding pipette.Reproductive BioMedicine. 21: 663-666.

     
     
     
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