会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 7. 发明申请
    • METHOD OF NOCICEPTOR DIFFERENTIATION OF HUMAN EMBRYONIC STEM CELLS AND USES THEREOF
    • 人胚胎干细胞标记分化方法及其用途
    • US20130183674A1
    • 2013-07-18
    • US13697274
    • 2011-05-19
    • Lorenz StuderStuart M. Chambers
    • Lorenz StuderStuart M. Chambers
    • C12N5/0793
    • C12N5/062C12N5/0618C12N5/0626C12N2501/13C12N2501/15C12N2501/155C12N2501/16C12N2501/40C12N2501/415C12N2501/727C12N2506/02C12N2506/45G01N33/5023G01N33/5058
    • The present invention relates to the field of stem cell biology, in particular the linage specific differentiation of pluripotent or multipotent stem cells, which can include, but is not limited to, human embryonic stem cells (hESC), human induced pluripotent stem cells (hiPSC), somatic stem cells, cancer stem cells, or any other cell capable of lineage specific differentiation. Specifically described are methods to direct the lineage specific differentiation of hESC and/or hiPSC to nociceptors (i.e. nociceptor cells) using novel culture conditions. The nociceptors made using the methods of the present invention are further contemplated for various uses including, but limited to, use in in vitro drug discovery assays, pain research, and as a therapeutic to reverse disease of, or damage to, the peripheral nervous system (PNS). Further, compositions and methods are provided for producing melanocytes from human pluripotent stem cells for use in disease modeling.
    • 本发明涉及干细胞生物学领域,特别是多能干细胞或多能干细胞的细胞特异性分化,其可包括但不限于人胚胎干细胞(hESC),人诱导多能干细胞(hiPSC ),体细胞干细胞,癌症干细胞或能够谱系特异性分化的任何其他细胞。 具体描述的是使用新的培养条件将hESC和/或hiPSC的谱系特异性分化指向伤害感受器(即伤害感受器细胞)的方法。 使用本发明的方法制备的伤害感受器进一步考虑用于各种用途,包括但不限于用于体外药物发现测定,疼痛研究以及作为逆转外周神经系统疾病或损害的治疗剂 (PNS)。 此外,提供用于从人多能干细胞产生用于疾病建模的黑素细胞的组合物和方法。
    • 8. 发明授权
    • Cell expansion system for use in neural transplantation
    • 用于神经移植的细胞扩增系统
    • US06787356B1
    • 2004-09-07
    • US09744384
    • 2001-03-16
    • Lorenz StuderRon D. McKay
    • Lorenz StuderRon D. McKay
    • C12N502
    • C12N5/0619C12N2500/10C12N2500/38C12N2501/815
    • The invention provides a method of culturing cells which includes a proliferating step in which the number of precursor cells is expanded and a differentiating step in which the expanded precursor cells develop into neuronal cells. The proliferating step includes the step of incubating the precursor cells in proliferating medium which includes basic fibroblast growth factor (bFGF). The differentiating step includes incubating the precursor cells in differentiation media in a manner effective to form a cellular aggregate that is not adhered to any surface of the incubation vessel. In a preferred embodiment, the cells arc incubated in a roller tube. The differentiation media can also include at least one differentiating agent. The invention also provides a method for treating a neurological disorder, such as Parkinson's disease, a method of introducing a gene product into a brain of a patient, an assay for neurologically active substances, and a cell culture.
    • 本发明提供一种培养细胞的方法,其包括扩增前体细胞数量的增殖步骤和扩增的前体细胞发育成神经元细胞的分化步骤。 增殖步骤包括将前体细胞在包括碱性成纤维细胞生长因子(bFGF)的增殖培养基中孵育的步骤。 微分步骤包括以有效形成未附着于培养容器的任何表面的细胞聚集体的方式将分化培养基中的前体细胞孵育。 在优选的实施方案中,将细胞在辊管中保温。 分化培养基还可以包括至少一种分化剂。 本发明还提供了治疗诸如帕金森病的神经障碍的方法,将基因产物引入患者脑中的方法,神经活性物质的测定和细胞培养。