journal1 ›› 2014, Vol. 22 ›› Issue (9): 949-951.DOI: 10.11852/zgetbjzz2014-22-09-16
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Received:2014-01-14
Online:2014-09-10
Published:2014-09-10
张颖1, 衣明纪1, 刘世国2
通讯作者:
衣明纪,E-mail:yimji@126.com
作者简介:张颖(1988-), 女, 山东人, 在读硕士研究生, 主要研究方向为发育行为儿科。
基金资助:CLC Number:
张颖, 衣明纪, 刘世国. Tourette综合征易感基因研究进展[J]. 中国儿童保健杂志, 2014, 22(9): 949-951.
| [1] Liu SG,Zhang XH,Yin YY,et al.An association analysis between 5-HTTLPR polymorphism and obsessive-compulsive disorder,Tourette syndrome in a Chinese Han population[J].CNS Neurosci Ther,2011,17(6):793-795. [2] Robertson MM.The Gilles de la Tourette syndrome:the current status[J].Arch Dis Child Educ Pract Ed,2012,97(5):166-175. [3] Chou IC,Tsai CH,Lee CC,et al.Association analysis between Tourette's syndrome and dopamine D1 receptor gene in Taiwanese children[J].Psychiatr Genet,2004,14(4):219-221. [4] Herzberg I,Valencia-Duarte AV,Kay VA,et al.Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate[J].Psychiatr Genet,2010,20(4):179-183. [5] 吴华,吴志英,王柠,等.福建省Tourette综合征DRD4基因第3外显子48bp VNTR多态性[J].中国神经精神疾病杂志,2010,36(8):468-471. [6] 季卫东,周家秀,杨闯,等.抽动秽语综合征汉族患者的执行功能及与多巴胺D4受体第3外显子48bp可重复序列多态性[J].中国心理卫生杂志,2010,24(8):568-573. [7] 卢瑶,麻宏伟,郗春艳,等.多巴胺D4受体基因启动子区多态性与慢性抽动障碍的关联研究[J].中国当代儿科杂志,2006,8(5):357-360. [8] 郑兰兰,韩振靓,张心华,等.中国汉族Tourette综合征与多巴胺转运体可变串联重复序列多态性的关联分析[J].中华医学遗传学杂志,2013,30(5):594-597. [9] Jijun L,Zaiwang L,Anyuan L,et al.Abnormal expression of dopamine and serotonin transporters associated with the pathophysiologic mechanism of Tourette syndrome[J].Neurol India,2010,58(4):523-529. [10] Ozbay F,Wigg KG,Turanli ET,et al.Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome[J].Am J Med Genet B Neuropsychiatr Genet,2006,141B(6):673-677. [11] 刘红,王晓芳,张本恕,等.多巴胺β羟化酶基因TaqⅠ酶切多态性与抽动秽语综合征:病例对照研究[J].中国现代神经疾病杂志,2009,9(1):60-64. [12] Guo Y,Deng X,Jankovic J,et al.Mutation screening of the HTR2B gene in patients with Tourette syndrome[J].Neurosci Lett,2012,526(2):150-153. [13] Dehning S,Muller N,Matz J,et al.A genetic variant of HTR2C may play a role in the manifestation of Tourette syndrome[J].Psychiatr Genet,2010,20(1):35-38. [14] Guo Y,Su L,Zhang J,et al.Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome[J].Psychiatr Genet,2012,22(6):300-303. [15] 郑兰兰,周瑞玲,岳涛,等.中国汉族Tourette综合征患者HTR-2A102T/C多态性的家系关联分析[J].中华行为医学与脑科学杂志,2012,21(11):1003-1005. [16] Hu XZ,Lipsky RH,Zhu G,et al.Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder[J].Am J Hum Genet,2006,78(5):815-826. [17] Moya PR,Wendland JR,Rubenstein LM,et al.Common and rare alleles of the serotonin transporter gene,SLC6A4,associated with Tourette's disorder[J].Mov Disord,2013,28(9):1263-1270. [18] 徐通,周翊.儿童抽动障碍病因及发病机制[J].中国实用儿科杂志,2012,27(7):502-505. [19] Cheng YH,Zheng Y,He F,et al.Detection of autoantibodies and increased concentrations of interleukins in plasma from patients with Tourette's syndrome[J].J Mol Neurosci,2012,48(1):219-224. [20] 王美建,王修海,王培林,等.抽动秽语综合征4个炎症因子基因SNP位点家系传递不平衡分析[J].齐鲁医学杂志,2012,27(5):432-433,436. [21] Liu S,Yi M,Qi F,et al.No significant association between Catechol-O-methyl transferase (COMT) -287A/G gene polymorphism and Tourette's syndrome in family-based association study in Chinese Han population[J].Eur Child Adolesc Psychiatry,2011,20(11-12):593-596. [22] 孙锦华,郭兰婷,袁爱花,等.抽动秽语综合征与儿茶酚氧位甲基转移酶基因多态性的关联研究[J].中华行为医学与脑科学杂志,2012,21(5):403-406. [23] Lei J,Deng X,Zhang J,et al.Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome[J].Am J Med Genet B Neuropsychiatr Genet,2012,159B(1):72-76. [24] Karagiannidis I,Dehning S,Sandor P,et al.Support of the histaminergic hypothesis in Tourette syndrome:association of the histamine decarboxylase gene in a large sample of families[J].J Med Genet,2013,50(11):760-764. [25] Paschou P,Stylianopoulou E,Karagiannidis I,et al.Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome[J].Genes Brain Behav,2012,11(4):444-451. [26] Lin WY,Lee CC,Liu HP,et al.Association of genetic variations in X-ray repair cross-complementing group 1 and Tourette syndrome[J].J Clin Lab Anal,2012,26(5):321-324. [27] Wu BT,Lin WY,Chou IC,et al.Association of poly(ADP-ribose) polymerase-1 polymorphism with Tourette syndrome[J].Neurol Sci,2013,34(11):1911-1916. |
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