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    • 3. 发明申请
    • DIAGNOSTIC PHENOTYPE ASSAY FOR ENGINEERED CELLS AND TISSUES
    • 用于工程细胞和组织的诊断性PHENOTYPE测定
    • WO2004000867A1
    • 2003-12-31
    • PCT/US2002/019705
    • 2002-07-31
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIANISHIMURA, IchiroIIDA, Keisuke
    • NISHIMURA, IchiroIIDA, Keisuke
    • C07H21/02
    • C12Q1/6883C12Q2600/158
    • The present invention provides an improved method for assessing, monitoring and/or determining the phenotype of cells and tissues. One aspect of the present invention is a method of fabricating phenotype specific gene (PSGs) and house keeping gene (HKGs) targets onto a microarray. Another aspect of the present invention provides a composition PSGs and HKGs as targets for high throughput assays including microarray analyses. Another aspect of the present invention is accessing, monitoring and/or determining the phenotype of tissue engineered cells derived from stem cells including embryonic stem cells, embryonic germ cells, fetal stem cells and adult stem cells by hybridizing cDNA probes to either PSG or HKG targets. These methods employ at least 25 PSG targets and no greater than 5000 HKG targets.
    • 本发明提供用于评估,监测和/或确定细胞和组织表型的改进方法。 本发明的一个方面是将表型特异性基因(PSG)和家族保持基因(HKG)靶标制造到微阵列上的方法。 本发明的另一方面提供组合物PSG和HKG作为包括微阵列分析的高通量测定的靶标。 本发明的另一方面是通过将cDNA探针与PSG或HKG靶物杂交来获取,监测和/或确定衍生自干细胞的组织工程细胞的表型,包括胚胎干细胞,胚胎生殖细胞,胎儿干细胞和成体干细胞 。 这些方法使用至少25个PSG目标和不超过5000个HKG目标。
    • 7. 发明申请
    • WIT 3.0, NOVEL GENE TO CONTROL SOFT TISSUE WOUND HEALING
    • WIT 3.0,新基因控制软组织治疗
    • WO2002100250A2
    • 2002-12-19
    • PCT/US2002/018828
    • 2002-06-12
    • THE REGENTS OF THE UNIVERSITY OF CALIFORNIANISHIMURA, IchiroSUKOTJO, Cortino
    • NISHIMURA, IchiroSUKOTJO, Cortino
    • A61B
    • C07K14/47A61K38/00
    • The present invention provides a method of treatment to improve wound healing and to minimize/prevent abnormal scarring caused by tissue contraction and fibrosis formation by providing a specific gene, Wit 3.0 alpha and beta sequences that is differentially expressed in wounded oral mucosa cells, relative to their decreased expression in non-wounded oral mucosa cells. One aspect of the invention is a method to treat soft tissue wound using anti-sense nucleic acid technologies. Another aspect of the present invention is a method to treat soft tissue wound using sense nucleic acid technologies. These methods can employ a complimentary nucleic acid sequence that is greater than 85% identity to Wit 3.0 alpha and/or beta sequences or greater than 90% identity to the deduced amino acids thereof.
    • 本发明提供了一种治疗方法,其通过提供在受伤的口腔粘膜细胞中差异表达的特异性基因Wit3.0α和β序列,来改善伤口愈合并且最小化/预防由组织收缩和纤维化形成引起的异常瘢痕形成 其在非伤口口腔粘膜细胞中的表达降低。 本发明的一个方面是使用反义核酸技术治疗软组织伤口的方法。 本发明的另一方面是使用有义核酸技术治疗软组织伤口的方法。 这些方法可以使用与Wit3.0α和/或β序列大于85%同一性或与其推导的氨基酸大于90%同一性的互补核酸序列。