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    • 45. 发明公开
    • Dopaminergic neuron-like cell cluster and method for preparing the same
    • 多巴胺神经元ähnlicherZellhaufen und Verfahren zur Herstellung davon
    • EP2845899A1
    • 2015-03-11
    • EP14179316.6
    • 2014-07-31
    • Daegu Gyeongbuk Institute of Science and Technology
    • Jeon, Won BaeLee, Kyeong MinJung, Gwon Soo
    • C12N5/0793
    • C12N5/0619C12N2501/01C12N2501/113C12N2501/727C12N2501/999C12N2533/50
    • Disclosed are a dopaminergic neuron-like cell cluster exhibiting a far higher level of a dopaminergic neuron marker, compared to conventional 2D or 3D cultured cells, and a method for preparing the same. The cell cluster can be more effectively differentiated into dopaminergic neurons in the presence of a differentiation-inducing factor, so that it is suitable for use in studying neurodegenerative diseases such as Parkinson's disease. In addition, the cell cluster can express factors reinforcing intercellular interaction at an improved level, and is free of cellular toxicity and safe to the body, easy to culture with high productivity, superior in biocompatibility, and highly unlikely to undergo mutations. Also provided is a dish for culturing a 3D dopaminergic neuron-like cell cluster on a mass scale; which guarantees the 3D dopaminergic neuron-like cell cluster superior biocompatibility, freedom of cellular toxicity, minimal mutagenicity, and improvement in the expression of factors reinforcing intercellular interaction.
    • 与传统的2D或3D培养细胞相比,公开了表现出更高水平的多巴胺能神经元标记物的多巴胺能神经元样细胞簇及其制备方法。 在分化诱导因子的存在下,细胞簇可以更有效地分化为多巴胺能神经元,使其适用于研究神经变性疾病如帕金森病。 此外,细胞簇可以表达增强细胞间相互作用的因子,并且没有细胞毒性并且对身体安全,容易以高生产率培养,生物相容性优异,并且极不可能经历突变。 还提供了用于大规模培养3D多巴胺能神经元样细胞簇的皿; 其保证3D多巴胺能神经元样细胞簇优异的生物相容性,细胞毒性自由,最小致突变性,以及增强细胞间相互作用因子表达的改善。
    • 46. 发明授权
    • MYELINATION OF CONGENITALLY DYSMYELINATED FOREBRAINS USING OLIGODENDROCYTE PROGENITOR CELLS
    • 维吾尔族维吾尔族维吾尔族维吾尔族
    • EP1480521B1
    • 2015-02-25
    • EP03742750.7
    • 2003-02-14
    • CORNELL RESEARCH FOUNDATION, INC.
    • GOLDMAN, Steven A.ROY, NeetaWINDREM, Martha
    • A01N63/00A01N65/00C12N5/00C12N5/02
    • C12N5/0623A61K35/12A61K35/30C12N5/0618C12N5/0619C12N5/0622C12N2510/00G01N33/5005G01N33/56966Y02A50/467
    • One form of the present invention is directed to a method ofremyelinating demyelinated axons by treating the demyelinated axons with oligodendrocyte progenitor cells under conditions which permit remyelination of the axons. Another aspect of the present invention relates to a method of treating a subject having a condition mediated by a loss of myelin or a loss of oligodendrocytes by administering to the subject oligodendrocyte progenitor cells under conditions effective to treat the condition mediated by a loss of myelin or a loss of oligodendrocytes. A further aspect of the present invention relates to an in vitro method of identifying and separating oligodendrocyte progenitor cells from a mixed population containing other mammalian brain or spinal cord cell types. This further aspect of the present invention involves removing neurons and neuronal progenitor cells from the mixed population to produce a treated mixed population. Oligodendrocyte progenitor cells are then separated from the treated mixed population to form an enriched population of oligodendrocyte progenitor cells.
    • 本发明的一种形式涉及通过在允许轴突再髓鞘化的条件下用少突胶质祖细胞处理脱髓鞘化的轴突来再髓鞘化的轴突的方法。 本发明的另一方面涉及通过在有效治疗由髓磷脂损失介导的病症的条件下给予少突胶质祖细胞的方法来治疗具有由髓磷脂损失或少突胶质细胞损失介导的病症的受试者的方法,或 少突胶质细胞的丧失。 本发明的另一方面涉及从含有其它哺乳动物脑或脊髓细胞类型的混合群体中鉴定和分离少突胶质祖细胞祖细胞的体外方法。 本发明的另一方面涉及从混合群体中去除神经元和神经元祖细胞以产生经处理的混合群体。 然后从处理的混合群体中分离少突胶质细胞祖细胞以形成少突胶质细胞祖细胞的富集群体。