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2篇 您的检索式:作者名="K.Y.Cheng"
    题名 作者 年代 出处 被引量
1Microstructural Stability of a Single Crystal Superalloy DD8 during Thermal Exposure显示文摘五分钱底单身者水晶合金 DD8 的微结构稳定性被调查了。标准热对待在在当演员组下面的 950 ° C .While 的显示出的好微结构稳定性调节的标本,一种像杆的阶段猛抛在内部当演员组标本的树枝状的区域在热暴露期间。阶段,让电子消息传输方式组织,与也预言的 Cr.Thermo 计算被充实在 Cr 富有的电子消息传输方式分阶段执行的约 950 ° C .The 的一个电子消息传输方式阶段的降水被看作 alpha-Cr 并且在当演员组条件下面由于 Cr 的分离形成了。K.Y.Cheng D.H.Kim Y.S.Yoo C.Y.Jo T.Jin Z.Q.Hu 2008Journal of Materials Science & Technology2008,24,1:2
2APPL2 Negatively Regulates Olfactory Functions by Switching Fate Commitments of Neural Stem Cells in Adult Olfactory Bulb via Interaction with Notch1 Signaling显示文摘Adult olfactory neurogenesis plays critical roles in maintaining olfactory functions.Newly-generated neurons in the subventricular zone migrate to the olfactory bulb(OB) and determine olfactory discrimination,but the mechanisms underlying the regulation of olfactory neurogenesis remain unclear.Our previous study indicated the potential of APPL2(adaptor protein,phosphotyrosine interacting with PH domain and leucine zipper 2) as a modulating factor for neurogenesis in the adult olfactory system.In the present study,we report how APPL2 affects neurogenesis in the OB and thereby mediates olfactory discrimination by using both in vitro neural stem cells(NSCs) and an in vivo animal model-APPL2 transgenic(Tg) mice.In the in vitro study,we found that APPL2 overexpression resulted in NSCs switching from neuronal differentiation to gliogenesis while APPL2 knockdown promoted neurogenesis.In the in vivo study,APPL2 Tg mice had a higher population of glial cells and dampened neuronal production in the olfactory system,including the corpus callosum,OB,and rostral migratory stream.Adult APPL2 Tg mice displayed impaired performance in olfactory discrimination tests compared with wild-type mice.Furthermore,we found that an interaction of APPL2 with Notch1 contributed to the roles of APPL2 in modulating the neurogenic lineage-switching and olfactory behaviors.In conclusion,APPL2 controls olfactory discrimination by switching the fate choice of NSCs via interaction with Notch1 signaling.Chong Gao Tingting Yan Xingmiao Chen Kenneth K.Y.Cheng Aimin Xu Jiangang Shen 2020Neuroscience Bulletin2020,36,9:0
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