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    • 3. 发明申请
    • CLASSIFICATION METHOD AND TREATMENT FOR ENDOMETRIAL CANCERS
    • 子宫内膜癌的分类方法和治疗
    • WO2017008165A1
    • 2017-01-19
    • PCT/CA2016/050829
    • 2016-07-13
    • BRITISH COLUMBIA CANCER AGENCY BRANCH
    • MCALPINE, JessicaTALHOUK, AlineHUNTSMAN, David
    • G01N33/574A61B10/00A61B5/00A61K45/00
    • G01N33/57442A61B10/0291A61K45/00C12Q1/6886C12Q2600/112C12Q2600/118C12Q2600/156G01N33/6875G01N2800/52G01N2800/56
    • Classification of endometrial cancers by morphologic features is inconsistent, and yields limited prognostic and predictive information. A method of classifying endometrial cancers and treating based on classification comprises obtaining a sample from a subject having endometrial cancer; evaluating the sample for: (a) a hypermutated mismatch repair protein comprising high microsatellite instability phenotype to classify the cancer as: (i) mismatch repair abnormal if present or mismatched repair microsatellite stable if absent; (b) subsequently evaluating the mismatch repair microsatellite stable sample from (a) for a POLE exonuclease domain mutation to classify the cancer as (ii) POLE mutated if present or POLE wild type if absent; and (c) subsequently evaluating the POLE wildtype sample from (b) for a p53 copy number abnormality comprising a high copy number or a low copy number to classify the cancer as (iii) p53 wild type, absent abnormality, and as (iv) p53 abnormal if present.
    • 通过形态学特征对子宫内膜癌的分类不一致,产生有限的预后和预测信息。 分类子宫内膜癌的方法和基于分类的治疗包括从具有子宫内膜癌的受试者获得样品; 评估样品:(a)包含高微卫星不稳定性表型的高度遗传性错配修复蛋白,以将癌症分类为:(i)如果存在错配修复异常或不匹配的修复微卫星如果不存在则稳定; (b)随后评估来自(a)的错配修复微卫星稳定样品,用于POLE核酸外切酶突变以将癌症分类为(ii)如果存在POLE突变或如果不存在则为POLE野生型; 和(c)随后评估来自(b)的包含高拷贝数或低拷贝数的p53拷贝数异常的POLE野生型样品,以将癌症分类为(iii)p53野生型,无异常,以及(iv) 如果存在p53异常
    • 5. 发明申请
    • T-CELL EPITOPE IDENTIFICATION
    • T细胞抗体鉴定
    • WO2015143558A1
    • 2015-10-01
    • PCT/CA2015/050230
    • 2015-03-25
    • BRITISH COLUMBIA CANCER AGENCY BRANCH
    • HOLT, RobertSHARMA, Govinda
    • C12Q1/68C12N5/10C12Q1/02C40B30/06C40B40/02G01N33/567C07K14/74
    • G01N33/6878C12N15/1037C12N15/1086C12Q1/6886C12Q2600/158G01N33/5091G01N33/56972G01N33/6845
    • The present invention is a method for determining the identity of the epitopes recognized by T-cells. The method consists of expressing an encoded library of candidate epitope sequences in a recipient reporter cell capable of providing a detectable signal upon cytotoxic attack from a single cognate T-cell followed by contacting the reporter cells with T-cells of interest. The reporter cells with a single indicating cytotoxic attack from a T-cell are isolated and then analyzed by next-generation sequencing in order to identify the epitope sequences. Specifically disclosed is a method in which a library of candidate epitope-encoding nucleic acids are expressed in cells which feature a membrane-bound major histocompatibility complex (MHC) protein, said library produced by transfection of plasmids featuring both a nucleotide encoding the candidate epitope and a nucleotide encoding a FRET-based fluorescent protein cleaved by granzyme.
    • 本发明是确定由T细胞识别的表位的身份的方法。 该方法包括在受体报道细胞中表达候选表位序列的编码文库,其能够在来自单个同源T细胞的细胞毒性攻击后提供可检测信号,随后将报道细胞与感兴趣的T细胞接触。 分离具有来自T细胞的单一指示细胞毒性攻击的报道细胞,然后通过下一代测序进行分析,以鉴定表位序列。 具体公开了一种方法,其中候选表位编码核酸的文库在具有膜结合主要组织相容性复合物(MHC)蛋白的细胞中表达,所述文库通过转染具有编码候选表位的核苷酸的质粒和 编码由颗粒酶切割的基于FRET的荧光蛋白的核苷酸。