Objective To develop a new method for analysis of protein phosphorylation modification in cultured neuron.
目的建立一种对神经细胞中的磷酸化蛋白质进行分离分析的方法。
Observation the space-time change of cortex nerve stem cell in newborn rat orientation differentiation to cholinergic neuron by cell cultured and immunocyte chemistry methods.
方法采用细胞培养技术、免疫细胞化学方法观察新生大鼠皮层神经干细胞向胆碱能神经元定向分化的时空变化。
Results the rat embryo neuron axon could be elongated and cultured on the PLGA membrane.
结果鼠胚的神经元和神经轴突束可以在PLGA生物膜上延长和继续培养。
Objective To study the effect of different concentration of taurine on cultured cortex neuron growth and exist.
目的研究不同浓度牛磺酸对原代培养的皮层神经元生长及存活的影响。
Results Proper concentration taurine promoted cultured cortex neuron to exist, and to format networks among neurons.
结果适当浓度的牛磺酸能够促进培养的皮层神经元存活，突起生长，促进神经元间网络的形成。
Conclusions: CGRP can activate spinal neuron cultured in vitro.
结论：CGRP能激活脊髓神经元。
The primary processes of neuron like cells in Co cultured groups were obviously longer than that in control groups.
这些神经元样细胞的初级突起比对照组的明显增长。
Conclusion The results suggested that 2,5-HD can decrease the endogenous NGF levels in both cultured DRG sensory neurons and VSC4.1 motor neuron cells of rats.
结论2 ，5 己二酮可降低大鼠DRG感觉神经元和脊髓前角运动神经元（VSC4 。 1细胞）、内源性NGF的表达水平，并进一步抑制了两类细胞的生长与存活。
Methods Cortical neuron in embrayonal rats was cultured in non serum ;
方法无血清培养胚鼠皮层神经元；
Methods Cortical neuron in embrayonal rats was cultured in non serum ;
方法无血清培养胚鼠皮层神经元；
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