会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • USE OF GENES AS MOLECULAR MARKERS IN DIAGNOSIS OF SCHIZOPHRENIA AND DIAGNOSTIC KIT FOR THE SAME
    • 作为分子标记使用基因分子标记物及其诊断试剂盒
    • WO2005106026B1
    • 2006-01-19
    • PCT/HU2005000044
    • 2005-05-02
    • Y OF SCIENCES BIOLOG RES CT OFPUSKAS LASZLOZVARA AGNESSANTHA MIKLOSSZEKERES GYOERGYJANKA ZOLTAN
    • PUSKAS LASZLOZVARA AGNESSANTHA MIKLOSSZEKERES GYOERGYJANKA ZOLTAN
    • C12Q1/68
    • C12Q1/6883C12Q2600/136C12Q2600/158
    • Drug-naive and drug-free schizophrenic PBL were screened to identify additional markers that are differentially expressed compared to healthy individuals using microarray and quantitative real-time PCR (QRT-PCR) techniques. Genes for dopamine D 2 receptor (DRD2) and inwardly rectifying potassium channel (Kir2.3) were found to be overexpressed in microarray analysis. Increased mRNA levels were confirmed by QRT-PCR using SybrGreen method and dual labeled TaqMan probes. The invention relates to a method for diagnosing schizophrenia in a subject comprising assessing level or the expression level of at least one of the following genes or proteins: Kir2.3 or DRD2 or a gene encoding Kir2.3 or DRD2. The invention further relates to agents and uses thereof, said agents specifically binding to said proteins or nucleic acids encoding them, diagnostic kits and screening methods. Use of both molecular markers allow prediction of schizophrenia and help to follow the efficiency of drugs in therapy in order to provide a more tailored medication for schizophrenic patients.
    • 筛选无天真和无药物精神分裂症的PBL,以鉴定与使用微阵列和定量实时PCR(QRT-PCR)技术的健康个体差异表达的其他标志物。 发现多巴胺D 2受体(DRD2)和内向整流钾通道(Kir2.3)的基因在微阵列分析中过表达。 使用SybrGreen方法和双重标记的TaqMan探针通过QRT-PCR证实增加的mRNA水平。 本发明涉及一种诊断受试者精神分裂症的方法,包括评估至少一种以下基因或蛋白质的水平或表达水平:Kir2.3或DRD2或编码Kir2.3或DRD2的基因。 本发明还涉及其药剂及其用途,所述药剂特异性结合所述蛋白质或编码它们的核酸,诊断试剂盒和筛选方法。 使用两种分子标记物可以预测精神分裂症,并有助于遵循药物在治疗中的效率,以便为精神分裂症患者提供更加定制的药物。