In situ cloning from pathological tissue specimens
    2.
    发明申请
    In situ cloning from pathological tissue specimens 有权
    病理组织标本的原位克隆

    公开(公告)号:US20090023593A1

    公开(公告)日:2009-01-22

    申请号:US11784677

    申请日:2007-04-09

    摘要: The present invention pertains to methods related to cloning nucleic acids from biological samples, particularly pathological tissue samples. This method includes hybridizing a population of oligonucleotide sequence probes comprising degenerate sequence tags to a fixed tissue, isolating the hybridized oligonucleotide sequence probes and amplifying the sequence tags in the hybridized oligonucleotide sequence probes. This method can be utilized to identify genes associated with disease and to quantitate the expression of disease-related transcripts. The method can also be used to identify truncated mRNAs.

    摘要翻译: 本发明涉及从生物样品,特别是病理组织样品中克隆核酸的方法。 该方法包括将包含简并序列标签的寡核苷酸序列探针的群体与固定组织杂交,分离杂交的寡核苷酸序列探针并扩增杂交的寡核苷酸序列探针中的序列标签。 该方法可用于鉴定与疾病相关的基因并定量疾病相关转录物的表达。 该方法也可用于鉴定截短的mRNA。

    Transcription factors in neuronal dendrites-dendritic protein synthesis and cell death
    5.
    发明授权
    Transcription factors in neuronal dendrites-dendritic protein synthesis and cell death 有权
    转录因子在神经元树突 - 树突状蛋白合成和细胞死亡

    公开(公告)号:US09114159B2

    公开(公告)日:2015-08-25

    申请号:US11990376

    申请日:2006-08-17

    CPC分类号: A61K48/005 A61K38/1709

    摘要: The present invention relates to methods of altering the competence of a dendrite and/or the viability of a neuron by modulating the level of Elk-1 in a dendrite. The present invention also provides methods of altering the ATP levels in a neuron, methods of isolating at least one protein of a mitochondrial permeability transition pore complex, methods of introducing an RNA into a neuron, methods of translating an RNA in a dendrite, methods of monitoring risk of neurodegeneration of a neuron, and methods of treatment for neurodegenerative diseases.

    摘要翻译: 本发明涉及通过调节枝晶中的Elk-1的水平来改变树突的能力和/或神经元的活力的方法。 本发明还提供了改变神经元中ATP水平的方法,分离至少一种线粒体通透性转换孔复合物的蛋白质的方法,将RNA引入神经元的方法,将树突状RNA翻译的方法, 监测神经元神经变性的风险,以及治疗神经退行性疾病的方法。

    Processes for genetic manipulations using promoters
    10.
    发明授权
    Processes for genetic manipulations using promoters 失效
    使用启动子的遗传操作过程

    公开(公告)号:US5891636A

    公开(公告)日:1999-04-06

    申请号:US922965

    申请日:1997-09-03

    CPC分类号: C12N15/1096 C12Q1/6865

    摘要: This invention relates to the use of promoters for ribonucleic acid amplification and other genetic manipulations. Processes are provided wherein complementary deoxyribonucleic acid (cDNA) is synthesized from a ribonucleic acid (RNA) sequence using a complementary primer linked to an RNA polymerase promoter region complement and then anti-sense RNA (aRNA) is transcribed from the cDNA by introducing an RNA polymerase capable of binding to the promoter region. Additional processes using the resulting aRNA are also described.

    摘要翻译: 本发明涉及用于核糖核酸扩增和其他遗传操作的启动子的用途。 提供了使用与RNA聚合酶启动子区域补体连接的互补引物从核糖核酸(RNA)序列合成互补脱氧核糖核酸(cDNA)的方法,然后通过引入RNA从cDNA转录反义RNA(aRNA) 能够结合启动子区域的聚合酶。 还描述了使用所得的aRNA的另外的方法。