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    • 6. 发明申请
    • ALGORITHMS FOR OUTCOME PREDICTION IN PATIENTS WITH NODE-POSITIVE CHEMOTHERAPY-TREATED BREAST CANCER
    • 患有结直肠癌治疗乳腺癌的患者的预后预测方法
    • US20110166838A1
    • 2011-07-07
    • US12999522
    • 2009-06-16
    • Mathias GehrmannRalf KronenwettUdo StroppChristian Von TörneKarsten Weber
    • Mathias GehrmannRalf KronenwettUdo StroppChristian Von TörneKarsten Weber
    • G06F7/60
    • C12Q1/6886C12Q2600/106C12Q2600/112C12Q2600/118C12Q2600/136C12Q2600/158G16B20/00G16B25/00G16B40/00
    • The invention relates to methods for predicting an outcome of cancer in a patient suffering from cancer, said patient having been previously diagnosed as node positive and treated with cytotoxic chemotherapy, said method comprising determining in a biological sample from said patient an expression level of a plurality of genes selected from the group consisting of ACTG1, CAl2, CALM2, CCND1, CHPT1, CLEC2B, CTSB, CXCL13, DCN, DHRS2, EIF4B, ERBB2, ESR1, FBXO28, GABRP, GAPDH, H2AFZ, IGFBP3, IGHG1, IGKC, KCTD3, KIAA0101, KRT17, MLPH, MMP1, NAT1, NEK2, NR2F2, OAZ1, PCNA, PDLIM5, PGR, PPIA, PRC1, RACGAP1, RPL37A, SOX4, TOP2A, UBE2C and VEGF; ABCB1, ABCG2, ADAM15, AKR1C1, AKR1C3, AKT1, BANF1, BCL2, BIRC5, BRMS1, CASP10, CCNE2, CENPJ, CHPT1, EGFR, CTTN, ERBB3, ERBB4, FBLN1, FIP1L1, FLT1, FLT4, FNTA, GATA3, GSTP1, Herstatin, IGF1R, IGHM, KDR, KIT, CKRT5, SLC39A6, MAPK3, MAPT, MKI67, MMP7, MTA1, FRAP1, MUC1, MYC, NCOA3, NFIB, OLFM1, TP53, PCNA, PI3K, PPERLD1, RAB31, RAD54B, RAF1, SCUBE2, STAU, TINF2, TMSL8, VGLL1, TRA@, TUBA1, TUBB, TUBB2A.
    • 本发明涉及用于预测患有癌症的患者的癌症结果的方法,所述患者先前被诊断为淋巴结阳性并用细胞毒性化疗治疗,所述方法包括在来自所述患者的生物样品中确定多个表达水平 选自ACTG1,CA2,CALM2,CCND1,CHPT1,CLEC2B,CTSB,CXCL13,DCN,DHRS2,EIF4B,ERBB2,ESR1,FBXO28,GABRP,GAPDH,H2AFZ,IGFBP3,IGHG1,IGKC,KCTD3, KIAA0101,KRT17,MLPH,MMP1,NAT1,NEK2,NR2F2,OAZ1,PCNA,PDLIM5,PGR,PPIA,PRC1,RACGAP1,RPL37A,SOX4,TOP2A,UBE2C和VEGF; ABCB1,ABCG2,ADAM15,AKR1C1,AKR1C3,AKT1,BANF1,BCL2,BIRC5,BRMS1,CASP10,CCNE2,CENPJ,CHPT1,EGFR,CTTN,ERBB3,ERBB4,FBLN1,FIP1L1,FLT1,FLT4,FNTA,GATA3,GSTP1, Herbatin,IGF1R,IGHM,KDR,KIT,CKRT5,SLC39A6,MAPK3,MAPT,MKI67,MMP7,MTA1,FRAP1,MUC1,MYC,NCOA3,NFIB,OLFM1,TP53,PCNA,PI3K,PPERLD1,RAB31,RAD54B,RAF1, SCUBE2,STAU,TINF2,TMSL8,VGLL1,TRA @,TUBA1,TUBB,TUBB2A。
    • 10. 发明申请
    • Single nucleotide polymorphisms sensitively predicting adverse drug reactions (adr) and drug efficacy
    • 单核苷酸多态性敏感地预测不良药物反应(adr)和药物功效
    • US20070128597A1
    • 2007-06-07
    • US10525278
    • 2003-08-18
    • Stephan SchwersHarald KallabisUdo Stropp
    • Stephan SchwersHarald KallabisUdo Stropp
    • C12Q1/68C07H21/04C12P21/06C07K14/705
    • C12Q1/6883C12Q2600/106C12Q2600/156G01N33/6893G01N2800/32G01N2800/52
    • Single Nucleotide Polymorphisms sensitively predicting Advserse Drug Reactions (ADR) and Drug Efficacy Abs tract. The invention provides diagnostic methods and kits including oligo and/or polynucleotides or derivatives, including as well antibodies determining whether a human subject is at risk of getting adverse drug reaction after statin therapy or whether the human subject is a high or low responder or a good a or bad metabolizer of statins. The invention provides further diagnostic methods and kits including antibodies determining whether a human subject is at risk for a cardiovascular disease. Still further the invention provides polymorphic sequences and other genes. The present invention further relates to isolated polynucleotides encoding a phenotype associated (PA) gene polypeptide useful in methods to identify therapeutic agents and useful for preparation of a medicament to treat cardiovascular disease or influence drug response, the polynucleotide is selected from the group comprising: SEQ ID 1-168 with allelic variation as indicated in the sequences section contained in a functional surrounding like full length cDNA for PA gene polypeptide and with or without the PA gene promoter sequence.
    • 单核苷酸多态性灵敏预测Advancese药物反应(ADR)和药物功效性Abs。 本发明提供了包括寡核苷酸和/或多核苷酸或衍生物的诊断方法和试剂盒,包括确定人类受试者在他汀类药物治疗后是否有获得不良药物反应风险的抗体,还是人类受试者是高反应者还是低反应者 他汀类药物或代谢物。 本发明提供了进一步的诊断方法和试剂盒,包括确定人受试者是否处于心血管疾病风险的抗体。 本发明还提供了多态序列和其他基因。 本发明还涉及编码可用于鉴定治疗剂并用于制备治疗心血管疾病或影响药物应答的药物的方法中的表型相关(PA)基因多肽的分离的多核苷酸,所述多核苷酸选自SEQ ID NO: ID 1-168,其具有如包含在功能性周围的序列部分中所示的等位基因变异,如PA基因多肽的全长cDNA并具有或不具有PA基因启动子序列。