IN VIVO METHOD FOR THE EVALUATION OF A COMPOUND-TARGET INTERACTION
    64.
    发明申请
    IN VIVO METHOD FOR THE EVALUATION OF A COMPOUND-TARGET INTERACTION 审中-公开
    用于评估化合物 - 目标相互作用的体内方法

    公开(公告)号:WO2012010240A1

    公开(公告)日:2012-01-26

    申请号:PCT/EP2011/003055

    申请日:2011-06-20

    CPC classification number: G01N33/573 G01N33/5088 G01N2333/91215 G01N2500/00

    Abstract: The invention relates to a method for evaluation of a compound-target interaction in vivo, comprising the steps of administering the compound to an animal, taking a body fluid sample of the animal, determining the concentration of the compound in the body fluid sample, taking a cellular sample of the animal containing the target, preparing a protein preparation of said cellular sample, providing an immobilised ligand capable of binding to the target, contacting the protein preparation with the immobilised ligand under conditions allowing the formation of a complex between the immobilised ligand and the target, determining the amount of complexes formed in step, and correlating the amount of complexes with the concentration of the compound in the body fluid sample.

    Abstract translation: 本发明涉及一种用于评价体内化合物 - 靶相互作用的方法,包括以下步骤:向动物施用化合物,服用动物的体液样品,测定体液样品中化合物的浓度,取 制备含有该靶标的动物的细胞样品,制备所述细胞样品的蛋白质制剂,提供能够结合靶标的固定化配体,使蛋白质制剂与固定的配体在允许在固定化配体之间形成复合物的条件下接触 和靶标,确定步骤中形成的络合物的量,并且将复合物的量与体液样品中化合物的浓度相关联。

    METHODS OF QUANTITATIVE DETERMINATION OF NEUROGENESIS IN VIVO
    66.
    发明申请
    METHODS OF QUANTITATIVE DETERMINATION OF NEUROGENESIS IN VIVO 审中-公开
    定量测定血液中神经细胞的方法

    公开(公告)号:WO2011066987A1

    公开(公告)日:2011-06-09

    申请号:PCT/EP2010/007358

    申请日:2010-12-03

    CPC classification number: G01N33/5058

    Abstract: The present invention relates to methods for quantifying neurogenesis in vivo. These method combine the isolation of purified nuclei from the brain tissue, the specific labelling of the nuclei of newly generated neurons thereof, and the counting of these nuclei. Density sedimentation is suitable for the separation of the nuclei of the cells from the complex debris of the brain tissue. As a matter of course the markers which are used for that identification have to be presented on the surface of the nuclei or within the nuclei. FACS analysis is the preferred method for counting the differentially labelled nuclei of proliferating neurons and the ones of other neural cells.

    Abstract translation: 本发明涉及用于定量体内神经发生的方法。 这些方法结合了纯化的核从脑组织的分离,其新产生的神经元核的特异性标记,以及这些细胞核的计数。 密度沉降适用于从脑组织的复杂碎片分离细胞核。 当然,用于该鉴定的标记物必须呈现在细胞核的表面或核内。 FACS分析是计数增殖神经元和其他神经细胞的差异标记细胞核的首选方法。

    NOVEL TISSUE PROTECTIVE ERYTHROPOIETIN RECEPTOR (NEPOR) AND METHODS OF USE
    68.
    发明申请
    NOVEL TISSUE PROTECTIVE ERYTHROPOIETIN RECEPTOR (NEPOR) AND METHODS OF USE 审中-公开
    新型组织保护性ERYTHROPOIETIN受体(NEPOR)及其使用方法

    公开(公告)号:WO2010136192A1

    公开(公告)日:2010-12-02

    申请号:PCT/EP2010/003201

    申请日:2010-05-26

    Abstract: There is disclosed a molecular composition(s) of a novel tissue protective erythropoietin (EPO) binding receptor protein complex, termed NEPOR. Presence of NEPOR components on a tumour allows EPO to impinge on the survival of associated cells thereby enhancing tumour progression and negatively effecting patient survival. Presence of NEPOR represents a prognostic bio marker for poorer patient outcome. Thus, methods are provided for stratifying patients having a tumour as suitable (i.e. NEPOR not present) or non-suitable (i.e., NEPOR present) for EPO treatment, comprising: (a) isolating a tissue sample from an individual who is receiving or is a candidate for receiving erythropoietin, (b) determining the level of expression of the NEPOR gene(s) (mRNA) and/or the presence of the NEPOR gene product (protein) from the isolated tissue, and (c) correlating the presence of an NEPOR gene expression product or the presence of NEPOR protein to a physiological response to the treatment with erythropoietin. Furthermore, by disclosing the molecular compositions of NEPOR species, there are disclosed methods for rationally identifying/designing NEPOR modulating therapeutics. Methods also are provided for treating neurological insults such as stroke (via enhancement of NEPOR activity) and cancer (via down-regulation of cyto- protective signaling from NEPOR).

    Abstract translation: 公开了一种称为NEPOR的新型组织保护促红细胞生成素(EPO)结合受体蛋白复合物的分子组成。 在肿瘤上存在NEPOR成分允许EPO影响相关细胞的存活,从而增强肿瘤进展并对患者的存活产生负面影响。 NEPOR的存在代表较差的患者结局的预后生物标志物。 因此,提供了用于对具有适合的肿瘤(即NEPOR不存在)或不适合(即,存在的NEPOR)的患者进行EPO治疗的分层方法,其包括:(a)从接受或正在接受的个体分离组织样品 接受促红细胞生成素的候选物,(b)从分离的组织中确定NEPOR基因(mRNA)的表达水平和/或NEPOR基因产物(蛋白质)的存在,以及(c) NEPOR基因表达产物或NEPOR蛋白的存在对促红细胞生成素治疗的生理反应。 此外,通过公开NEPOR种类的分子组成,公开了合理鉴定/设计NEPOR调节治疗剂的方法。 还提供用于治疗诸如中风(通过增强NEPOR活性)和癌症(通过下调NEPOR的细胞保护性信号传导)的神经学损伤的方法。

    USE OF THIABENDAZOLE AND DERIVATIVES THEREOF FOR THE THERAPHY OF NEUROLOGICAL CONDITIONS
    69.
    发明申请
    USE OF THIABENDAZOLE AND DERIVATIVES THEREOF FOR THE THERAPHY OF NEUROLOGICAL CONDITIONS 审中-公开
    用于神经病学条件的噻吗咔唑及其衍生物的用途

    公开(公告)号:WO2010127878A2

    公开(公告)日:2010-11-11

    申请号:PCT/EP2010/002861

    申请日:2010-05-10

    CPC classification number: A61K31/4184

    Abstract: The present invention relates to the use of thiabendazole and derivatives thereof for the preparation of a pharmaceutical composition for treating and/or preventing a neuronal condition where there is a need of neuroprotection and/or neurcregeneration. Tiie invention furthermore relates to the use of thiabendazole and derivatives thereof for the in vitro differentiation of neuronal stem cells and the use of such pre-treated cells for stem cell therapy of neurological conditions.

    Abstract translation: 本发明涉及噻苯达唑及其衍生物在制备用于治疗和/或预防需要神经保护和/或神经再生的神经元状况的药物组合物中的应用。 蒂恩发明还涉及噻苯达唑及其衍生物用于神经元干细胞体外分化的用途,以及这些预处理细胞用于神经系统疾病干细胞治疗的用途。

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