METHOD AND APPARATUS FOR BRAIDING MICRO STRANDS
    6.
    发明申请
    METHOD AND APPARATUS FOR BRAIDING MICRO STRANDS 审中-公开
    消除微观结构的方法和装置

    公开(公告)号:WO2010059832A1

    公开(公告)日:2010-05-27

    申请号:PCT/US2009/065156

    申请日:2009-11-19

    IPC分类号: D04C3/00

    CPC分类号: D04C3/42

    摘要: A method and apparatus for fabricating microbraided structures is provided. A microbraiding device includes first and second carrier members that are movable with respect to each other. Each carrier includes a plurality of shelters. Spool-less strands of microfiber are retained in shuttles that are movable between the first and second shelters under magnetic forces. The microbraid structure is fabricated as the shuttles move between the first shelters, and as the first carrier member moves relative to the second carrier member.

    摘要翻译: 提供了一种用于制造微阵列结构的方法和装置。 微型装置包括可相对于彼此移动的第一和第二承载构件。 每个载体包括多个收容所。 无纺布的超细纤维束被保留在可在磁力下在第一和第二收容所之间移动的梭子中。 随着梭子在第一遮蔽物之间移动,并且当第一承载构件相对于第二承载构件移动时,制作微框架结构。

    PHOTOLABILE DINITROINDOLINYL BASED COMPOUNDS
    7.
    发明申请
    PHOTOLABILE DINITROINDOLINYL BASED COMPOUNDS 审中-公开
    可溶性丁基酚基酚化合物

    公开(公告)号:WO2008094922A1

    公开(公告)日:2008-08-07

    申请号:PCT/US2008/052331

    申请日:2008-01-29

    CPC分类号: C07F9/5728 C07D209/08

    摘要: The present invention relates to photolabile or photoreleasable compounds including a caging moiety linked to an effector moiety, wherein the compounds are capable of releasing the effector moiety on irradiation, typically by flash irradiation with UV light. These compounds are particularly suitable for focal 2-photon uncaging The photoreleasable compounds can be used to deliver effector moieties such as carboxylic acids, preferably, neuroactive amino acids to sites where their activity is required. In preferred embodiments of the invention, the caging moiety is based on 4-carboxymethoxy-5,7-dinitroinlinyl and derivatives thereof.

    摘要翻译: 本发明涉及光不稳定或光可释放化合物,其包括与效应子部分连接的笼状部分,其中所述化合物通常通过紫外线的闪光照射在照射时释放效应部分。 这些化合物特别适用于焦点2光子褪色。可光致发光的化合物可用于将效应部分如羧酸,优选神经活性氨基酸递送至需要其活性的位点。 在本发明的优选实施方案中,笼状部分基于4-羧基甲氧基-5,7-二硝基苯乙烯基及其衍生物。

    MIR-155 ENHANCEMENT OF CD8+ T CELL IMMUNITY
    8.
    发明申请
    MIR-155 ENHANCEMENT OF CD8+ T CELL IMMUNITY 审中-公开
    MIR-155增强CD8 + T细胞免疫

    公开(公告)号:WO2014059248A1

    公开(公告)日:2014-04-17

    申请号:PCT/US2013/064503

    申请日:2013-10-11

    IPC分类号: C12N5/071 C12N15/00 A61K48/00

    摘要: The present invention provides novel methods of enhancing CD8+ T cell mediated immunity (also referred to as "CD8+ T cell immunity") in a patient having a diseased state. In particular, the present invention provides for the enhanced expression of miR-155 in a population of patient specific T cells through the introduction of a nucleic acid molecule encoding a miR-155 transcript or a nucleic acid molecule encoding a chimeric antigen receptor and a miR-155 transcript into those cells, followed by the reintroduction of the T cells into the patient. The present invention also provides methods of enhancing the expansion of these T cells relative to control cells. Increased expansion of CD8+ T cells following enhanced miR-155 expression is directly related to enhanced CD8+ T cell immunity. The present invention further provides methods of enhancing anti-cancer immunity in a patient through the increased expression of miR-155 in patient specific T cells.

    摘要翻译: 本发明提供了具有疾病状态的患者中增强CD8 + T细胞介导的免疫(也称为“CD8 + T细胞免疫”)的新方法。 特别地,本发明通过引入编码miR-155转录物的核酸分子或编码嵌合抗原受体和miR的核酸分子来提供miR-155在患者特异性T细胞群体中的增强表达 -155转录到这些细胞中,随后将T细胞重新引入患者体内。 本发明还提供了相对于对照细胞增强这些T细胞的扩增的方法。 增强的miR-155表达后CD8 + T细胞的增加与增强的CD8 + T细胞免疫直接相关。 本发明还提供了通过增加miR-155在患者特异性T细胞中的表达来增强患者抗癌免疫的方法。

    NOVEL SIGMA RECEPTOR LIGANDS AND METHODS OF MODULATING CELLULAR PROTEIN HOMEOSTASIS USING SAME
    9.
    发明申请
    NOVEL SIGMA RECEPTOR LIGANDS AND METHODS OF MODULATING CELLULAR PROTEIN HOMEOSTASIS USING SAME 审中-公开
    新型SIGMA受体配体和使用相同方法调节细胞蛋白家族成员的方法

    公开(公告)号:WO2014015157A2

    公开(公告)日:2014-01-23

    申请号:PCT/US2013/051110

    申请日:2013-07-18

    IPC分类号: A61K31/155

    摘要: The present invention includes compounds useful in preventing, treating or ameliorating Sigma-related disorders or diseases. The compounds of the invention may modulate cellular protein homeostasis, which includes: translation initiation, folding, processing, transport, and degradation (including ubiquitin selective autophagy) of proteins. The present invention also includes methods of preventing, treating or ameliorating a Sigma-related disorder or disease in a subject in need thereof, the method comprising administering to the subject an effective amount of a Sigma-modulating compound. The present invention also includes methods of preventing, treating or ameliorating a Sigma-related disorder or disease in a subject in need thereof, the method comprising administering to the subject an effective amount of a Sigma-modulating compound, further comprising administering an effective amount of a compound that inhibits the ubiquitin proteasome system (UPS) and/or autophagic survival pathways.

    摘要翻译: 本发明包括可用于预防,治疗或改善Sigma相关疾病或疾病的化合物。 本发明的化合物可以调节细胞蛋白质体内平衡,其包括蛋白质的翻译起始,折叠,加工,转运和降解(包括遍在蛋白选择性自噬)。 本发明还包括在有需要的受试者中预防,治疗或改善与Sigma相关的病症或疾病的方法,所述方法包括向受试者施用有效量的Sigma-调节化合物。 本发明还包括在有需要的受试者中预防,治疗或改善与Sigma相关的病症或疾病的方法,所述方法包括向所述受试者施用有效量的Sigma-调节化合物,所述方法还包括给予有效量的 一种抑制泛素蛋白酶体系统(UPS)和/或自噬存活途径的化合物。