该生物学家拥有包括将分子导入活体细胞的纳米注射器、人工骨科材料、结核病靶标治疗和细胞芯片平台等专利。
The biologist holds patents including a cell nanoinjector that introduces molecules into living cells, artificial bone materials, targets for tuberculosis therapy and cell microarray platforms.
他说，这些药物对于实验室内的人体细胞很有效果，但是在正式成为治疗手段之前还需进行药物毒理和临床实验，而这个过程大概需要五年或更长时间。
He said that the drugs have been effective on human cells in the laboratory but that toxicology and clinical trials would be needed before it could be adopted as a treatment.
该药物能够准确的将正确的染色体数目导入每一新细胞，产生非整倍体细胞，能够用于治疗由于肿瘤抑制基因突变导致的肿瘤。
Drugs that inhibit accurate delivery of the right number of chromosomes to each new cell, resulting in aneuploidy, would be used to destroy tumors caused by mutations in the tumor suppressors.
结果从28例实体瘤组织和肿瘤引流淋巴结中获取的TIL前体细胞，26例培养成功，其中23例TIL数量达到治疗数量级；
Results TIL were successfully cultured in 26 out of 28 samples obtained from tumor tissues or tumor draining lymph nodes(TDLN), of which 23 samples reached the number of therapy grade.
科学家们发现了可分化为人心脏所有类型主要细胞的出心脏干细胞，该发现打开了自体细胞用于治疗受损心脏之门。
Scientists have identified a cardiac stem cell that gives rise to all of the major cell types in the human heart. The find opens the way to using patients' own cells to heal their damaged hearts.
由于人体细胞的无义突变也可能敏感于反义试剂的抑制作用，这就为治疗由于无义突变导致的多种疾病提供了一个新途径。
Nonsense termination in human cells may also be susceptible to suppression by antisense agents, providing a new approach to address numerous diseases caused by nonsense mutations.
ES细胞和MAPC作为CSC的前体细胞，在心肌梗塞的干细胞移植治疗方面需经过向心肌谱系的提交过程。
As precursor of CSC, ES and MAPC may commit into myocardial lineage in transplanting stem cells to treat myocardial ischaemia.
治疗性克隆和体细胞重编程是制备患者特异性自体干细胞的两种不同策略，近期已取得了重大的研究进展。
The researches of therapeutic cloning and somatic cell reprogramming, two strategies used to generate patient-specific autologous stem cells, have recently made great progress.
结论胚胎干细胞来源的神经前体细胞移植PD大鼠纹状体后能分化为TH阳性的神经细胞，对PD有治疗作用。
ConclusionThe NPCs derived from ESc differentiated into TH-positive neurons after being grafted into the striatum of PD rats, which produced therapeutic effect on PD.
“治疗性克隆”是人类最关注的课题之一，而人体细胞核移植是治疗性克隆的基础和前提。
Therapeutic cloning is one of our major research objectives, and therapeutic cloning is based on human somatic cell nuclear transfer.
目的观察自体细胞因子诱导杀伤细胞(CIK细胞)治疗HBVDNA阳性肝硬化患者的近期疗效。
Objective to observe the therapeutic effect of autologous cytokine-induced killer cells (CIK) on HBV DNA positive patients with liver cirrhosis.
使用神经前体细胞或神经干细胞治疗将克服以上的困难。
The use of stem or CNS precursor cells would overcome many of these problems.
本文主要论述了内皮前体细胞的分离、培养、鉴定以及在血管生成治疗中的作用。
This review demonstrates the isolation, culture and identification of EPCs and the function in the therapeutic angiogenesis.
观察各组大鼠治疗后在Y-迷宫中的学习记忆成绩和梗死对侧海马锥体细胞树突和突触结构变化。
The ability of learning and memory was measured with Y-maze and the morphology and ultrastructure of contralateral hippocampal CA3 pyramidal neurons were detected after 4 weeks.
观察各组大鼠治疗后在Y-迷宫中的学习记忆成绩和梗死对侧海马锥体细胞树突和突触结构变化。
The ability of learning and memory was measured with Y-maze and the morphology and ultrastructure of contralateral hippocampal CA3 pyramidal neurons were detected after 4 weeks.
应用推荐