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    • 32. 发明授权
    • Compositions and methods for early pregnancy diagnosis
    • 早孕诊断的组成和方法
    • US08182999B2
    • 2012-05-22
    • US12825223
    • 2010-06-28
    • Robert Michael RobertsJonathan Andrew GreenSancai Xie
    • Robert Michael RobertsJonathan Andrew GreenSancai Xie
    • G01N33/53
    • G01N33/689C07K14/47G01N2333/471G01N2800/368Y10S435/973
    • Pregnancy-associated glycoproteins (PAGs) are structurally related to the pepsins, thought to be restricted to the hoofed (ungulate) mammals and characterized by being expressed specifically in the outer epithelial cell layer (chorion/trophectoderm) of the placenta. By cloning expressed genes from ovine and bovine placental cDNA libraries, the inventors estimate that cattle, sheep, and most probably all ruminant Artiodactyla, possess possibly 100 or more PAG genes, many of which are placentally expressed. The PAGs are highly diverse in sequence, with regions of hypervariability confined largely to surface-exposed loops. Selected PAG that are products of the invasive binucleate cells, expressed highly in early pregnancy at the time of trophoblast invasion and expressed weakly, if at all, in late gestation are useful in the early diagnosis of pregnancy. In a preferred embodiment, the invention relates to immunoassays for detecting these PAGs.
    • 妊娠相关糖蛋白(PAG)在结构上与胃蛋白酶相关,被认为限于蹄(有蹄类)的哺乳动物,其特征在于在胎盘的外上皮细胞层(绒毛膜/滋养外胚层)中特异性表达。 通过克隆来自绵羊和牛胎盘cDNA文库的表达基因,本发明人估计,牛,绵羊和大多数所有反刍动物偶蹄类动物都具有100个或更多个PAG基因,其中许多是胎盘表达的。 PAG的序列高度多样化,高变区域主要局限于表面暴露的环路。 选择的PAG是侵入性双核细胞的产物,在滋养层侵袭时早期表达高度表达,如果在妊娠晚期,在妊娠早期诊断中很有用。 在优选的实施方案中,本发明涉及用于检测这些PAG的免疫测定。
    • 34. 发明申请
    • Methods and Apparatus for Screening for Chromosomal Abnormalities
    • 筛选染色体异常的方法和装置
    • US20110246077A1
    • 2011-10-06
    • US12986534
    • 2011-01-07
    • David Edmund Wright
    • David Edmund Wright
    • G06F19/00
    • G01N33/743G01N33/76G01N2333/471G01N2333/575G01N2800/387Y10S436/811Y10S436/814
    • This invention generally relates to methods, apparatus, and computer program code for antenatal screening for chromosomal abnormalities, in particular Down's Syndrome. A method of determining a likelihood of a fetus carried by a pregnant mother having a chromosomal abnormality, a first biological, parameter being suitable for screening said fetus for said chromosomal abnormality, the method comprising: receiving first data from a first stage of pregnancy of said mother, said first data comprising data representing a first value of said first biological parameter; receiving second data from a second, later stage of said pregnancy, said second data comprising data representing a second value of said first biological parameter; and determining likelihood data from said first and second data, said likelihood data representing the likelihood of said fetus having a chromosomal abnormality.
    • 本发明一般涉及用于染色体异常的产前筛查的方法,装置和计算机程序代码,特别是唐氏综合征。 一种确定由具有染色体异常的怀孕母亲携带的胎儿的可能性的方法,第一生物学参数适合于筛选所述胎儿用于所述染色体异常,所述方法包括:从所述第一阶段怀孕所述第一数据 所述第一数据包括表示所述第一生物参数的第一值的数据; 从所述怀孕的第二后期接收第二数据,所述第二数据包括表示所述第一生物参数的第二值的数据; 以及从所述第一和第二数据确定似然数据,所述似然数据表示所述胎儿具有染色体异常的可能性。
    • 36. 发明申请
    • Multimarker panel for diabetes type 1 and 2
    • 糖尿病1型和2型多标记面板
    • US20070015208A1
    • 2007-01-18
    • US11371871
    • 2006-03-09
    • Georg HessAndera HorschWerner Poppe
    • Georg HessAndera HorschWerner Poppe
    • G01N33/53
    • G01N33/6893G01N2333/471G01N2333/58G01N2333/70578G01N2800/32
    • The present invention relates to a method and means for diagnosing or risk stratification of co-morbidities, particularly cardiovascular complications in diabetes patients. The invention particularly relates to a method for diagnosing whether a diabetes patient is suffering from a cardiovascular complication or is at risk of suffering from a cardiovascular complication, said method comprising the steps of (a) measuring, preferably iii vitro, the level(s) of at least one cardiac hormone or a variant thereof in a sample from the patient, and (b) diagnosing the cardiovascular complication or the risk of suffering from cardiovascular complication by comparing the measured level(s) to known level(s) associated with the cardiovascular complication or risk. The present invention also relates to combining the measurement of markers comprising cardiac hormones, natriuretic peptides, inflammation-associated markers, angiogenesis markers, and markers for platelet activation. Preferred markers are brain natriuretic peptides (particularly NT-proBNP), PIGF, and sCD40L.
    • 本发明涉及用于诊断或风险分层的方法和手段,尤其是糖尿病患者的心血管并发症。 本发明特别涉及用于诊断糖尿病患者是否患有心血管并发症或患有心血管并发症的风险的方法,所述方法包括以下步骤:(a)优选地在体外测量水平, 的至少一种心脏激素或其变体,以及(b)通过将所测量的水平与已知水平相关联来诊断心血管并发症或患有心血管并发症的风险 心血管并发症或风险。 本发明还涉及将包含心脏激素,利尿钠肽,炎症相关标志物,血管生成标记物和用于血小板活化的标记物的标记物的测量结合在一起。 优选的标记物是脑利钠肽(特别是NT-proBNP),PIGF和sCD40L。