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    • 71. 发明申请
    • METHODS FOR QUANTIFYING MICRORNA PRECURSORS
    • 定量微生物前体的方法
    • US20090123917A1
    • 2009-05-14
    • US11816767
    • 2006-02-24
    • Thomas D. Schmittigen
    • Thomas D. Schmittigen
    • C12Q1/68
    • C12Q1/6876C12Q1/68C12Q2525/207
    • Provided herein is a sensitive, high throughput, real-time PCR assay to monitor the expression of miRNA precursors. Gene specific primers and reverse transcriptase were used to convert the primary precursors and pre-miRNAs to cDNA. The expression of 23 miRNA precursors in six human cancer cell lines was assayed using the PCR assay. The miRNA precursors accumulated to different levels when compared to each other or when a single precursor is compared in the various cell lines. The precursor expression profile of three miRNAs determined by the PCR assay was identical to the mature miRNA expression profile determined by Northern blotting. We propose that the PCR assay may be scaled up to include all of the 150+ known human miRNA genes and can easily be adaptable to other organisms such as plants, C. elegans and Drosophila.
    • 本文提供了一种灵敏,高通量的实时PCR测定法,用于监测miRNA前体的表达。 基因特异性引物和逆转录酶用于将初级前体和前体miRNAs转化为cDNA。 使用PCR测定法检测6种人类癌细胞系中23种miRNA前体的表达。 当彼此相比时,或者当在各种细胞系中比较单个前体时,miRNA前体累积到不同水平。 通过PCR测定确定的三种miRNA的前体表达谱与通过Northern印迹测定的成熟miRNA表达谱相同。 我们建议PCR测定可以扩大到包括所有150多种已知的人类miRNA基因,并且可以容易地适应于其它生物如植物,秀丽隐杆线虫和果蝇。
    • 76. 发明授权
    • Multi-criterial decision making system and method
    • 多标准决策制度和方法
    • US07437343B1
    • 2008-10-14
    • US11553126
    • 2006-10-26
    • John R. JosephsonBalakrishnan ChandrasekaranMark CarrollNaresh Sundaram Iyer
    • John R. JosephsonBalakrishnan ChandrasekaranMark CarrollNaresh Sundaram Iyer
    • G06F17/00G06N5/04
    • G06Q10/06Y10S707/99933
    • An architecture is disclosed for assistance with exploration of design and other decision spaces and for making decisions. These decision spaces may be very large. The architecture consists of three main components: A Seeker acquires candidates by generating or retrieving them, along with their scores according to one or more criteria. A Filter locates a relatively small number of promising candidates that are retained for further analysis. Various filters may be used to locate the promising candidates. A Viewer allows a user to examine trade-off diagrams, and other linked displays, that present the filtered candidates for evaluation, analysis, further exploration, and narrowing the choice set. The computational load of the Seeker may be distributed among a large number of clients in a client-server computing environment.
    • 披露了一种架构,用于协助探索设计和其他决策空间以及作出决策。 这些决策空间可能非常大。 该架构由三个主要组成部分组成:寻求者根据一个或多个标准通过生成或检索它们以及其分数来获取候选者。 过滤器定位了相对较少数量的有希望的候选人,用于进一步分析。 可以使用各种滤波器来定位有希望的候选者。 查看器允许用户检查权衡图和其他链接显示,呈现过滤的候选人进行评估,分析,进一步探索和缩小选择集。 Seeker的计算负载可以分布在客户端 - 服务器计算环境中的大量客户端之间。
    • 79. 发明申请
    • PDK-1/AKT SIGNALING INHIBITORS
    • PDK-1 / AKT信号抑制剂
    • US20080146815A1
    • 2008-06-19
    • US11864612
    • 2007-09-28
    • Ching-Shih Chen
    • Ching-Shih Chen
    • C07D257/04C07D231/10
    • C07D231/12
    • A new class of phosphoinositide-dependent kinase-1 (PDK-1) inhibitors of formula I: wherein X is selected from the group consisting of alkyl and haloalkyl; Ar is an aryl radical selected from the group consisting of phenyl, biphenyl, naphthyl, anthryl, phenanthryl, and fluorenyl; and wherein Ar is optionally substituted with one or more radicals selected from the group consisting of halo, C1-C4 alkyl, C1-C4 haloalkyl, azido, C1-C4 azidoalkyl, aryl, alkylaryl, haloaryl, haloalkylaryl, and combinations thereof, and R is selected from the group consisting of nitrile, acetonitrile, ethylnitrile, propylnitrile, carboxamide, amidine, tetrazole, oxime, hydrazone, acetamidine, aminoacetamide, guanidine, and urea. Also provided are methods of using the compounds for the treatment and prevention of cancer in humans.
    • 新型的式I的磷酸肌醇依赖性激酶-1(PDK-1)抑制剂:其中X选自烷基和卤代烷基; Ar是选自苯基,联苯基,萘基,蒽基,菲基和芴基的芳基; 并且其中Ar任选被一个或多个选自以下的基团取代:卤素,C 1 -C 4烷基,C 1〜 C 4卤代烷基,叠氮基,C 1 -C 4 - 叠氮基烷基,芳基,烷基芳基,卤代芳基,卤代烷基芳基及其组合,并且选择R 腈,乙腈,丙腈,甲酰胺,脒,四唑,肟,腙,乙脒,氨基乙酰胺,胍和尿素组成的组。 还提供了使用该化合物治疗和预防人类癌症的方法。