REACTIVATION OF X CHROMOSOME GENES
    4.
    发明申请
    REACTIVATION OF X CHROMOSOME GENES 审中-公开
    X染色体基因的反应

    公开(公告)号:US20160313304A1

    公开(公告)日:2016-10-27

    申请号:US15138208

    申请日:2016-04-25

    CPC classification number: G01N33/5023

    Abstract: Methods of prohibiting Xist-dependent silencing of X chromosome genes include targeting the required Xist silencing complex components including SHARP, SMRT, HDAC3, SAF-A, LBR, and the respective binding sites of SHARP, LBR, and SAF-A on Xist, thereby prohibiting Xist repression, allowing for reactivation of the silenced X chromosome genes.

    Abstract translation: 禁止X染色体基因Xist依赖性沉默的方法包括靶向所需的Xist沉默复合物成分,包括SHARP,SMRT,HDAC3,SAF-A,LBR,以及Xist上SHARP,LBR和SAF-A的相应结合位点,从而 禁止Xist镇压,允许重新激活沉默的X染色体基因。

    HDAC inhibitor compositions for reactivation of the X chromosome

    公开(公告)号:US11197881B2

    公开(公告)日:2021-12-14

    申请号:US16345666

    申请日:2017-10-27

    Abstract: A reactivation composition for activating or re-activating expression of a silenced X chromosome gene in a cell includes a non-cytotoxic histone deacetylase (HDAC) inhibitor. The reactivation composition includes the non-cytotoxic HDAC inhibitor and may further include a DNA methylation inhibitor. A method of activating or re-activating expression of a silenced X chromosome gene in a cell includes administering a reactivation composition including a non-cytotoxic HDAC inhibitor. The method of activating or re-activating expression of a silenced X chromosome gene may further includes administering a reactivation composition that includes a non-cytotoxic HDAC inhibitor and an inhibitor of DNA methylation.

    METHODS FOR IDENTIFYING MACROMOLECULE INTERACTIONS

    公开(公告)号:US20190187156A1

    公开(公告)日:2019-06-20

    申请号:US15466861

    申请日:2017-03-22

    CPC classification number: G01N33/6875 C12N15/1065

    Abstract: A method for identifying interactions of DNA, RNA, and/or protein molecules in a cell includes distributing a cell lysate or fraction thereof into a plurality of lysate suspensions, adding a unique nucleotide tag to each lysate suspension to tag each DNA, RNA, and/or protein, pooling the tagged suspensions, and repeating the tagging, pooling, and sorting (distributing) as desired to decrease the probability that non-interacting molecules will receive all of the same nucleotide tags.

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