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您的检索式：作者名="Pingfei Luo"
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| 1 | Selective Reduction of Nitroarenes with Molybdenum Disulfide显示文摘商业 MoS2 被发现是为到有在温和条件下面的肼的相应苯胺的硝基苯的减小的高度选择的催化剂。MoS2 比为到相应苯胺的功能的硝基苯的减小的高贵金属催化剂便宜得多不仅,而且更选择。有卤化物的硝基苯(F, Cl, Br 并且我) 有选择地被减少,并且相应苯胺在优秀收益被获得,并且没有 dehalogenation 被检测。功能的组象 NH2 那样,哦,链烯组在 nitro 混合物的减小期间被容忍。p-chloronitrobenzene 的减小与肼分别地在 MoS2 和 Pd/C 上被学习。p-chloroaniline 的收益与在完整的变换的 Pd/C 比那与 MoS2 是高得多的。 | Lei Huang Pingfei Luo Man Xiong Rizhi Chen Yong Wang Weihong Xing Jun Huang | 2013 | Chinese Journal of Chemistry2013，31，8： | 1 |
| 2 | ATP6V0d2 mediates leucine-induced mTORCI activation and polarization of macrophages显示文摘Dear Editor, mTORCI, as a center regulatory hub of metabolism, senses the cellular energy status, nutrition and extracellular stimuli and regulates cell growth, differentiation and functions of immune cells (Powell et al., 2012). Lysosomal localization of key signal comp orients is critical for mTORCI activati on: mTORCI activation requires co-localization of activated Rheb and mTORCI to the lysosome membrane (Buerger et al., 2006). Signals in eluding growth factors, cellular stresses and energy levels act on the disruption the formation of tuberous sclerosis complex (TSC) complex, comprised of TSC1, TSC2 and TBC1D7, which leads to the translocation and activation of Rheb on the lysosome membrane (Dibble et al., 2012). In response to nutrient levels, specifically the availability of amino acids and glucose (Efeyan et al., 2013), mTORCI is recruited to the lysosomal surface by Rag GTPases that are heterodimers of RagA or RagC bound to RagB or RagD. Multiple protein complexes have been implicated in regulation of mTORCI upon nutrient sensing including Ragulator, GATOR1, GATOR2, KICSTOR and vacuolar ATPases (Wolfson et al., 2017). Vacuolar ATPases are large multiple-protein complexes that acidify the lysosome and may mediate additional functions independent of their proton pump activity (Nishi and Forgac, 2002). | Pingfei Li Xiaofei Deng Jing Luo Yufei Chen Guoyu Bi Feili Gong Zhengping Wei Na Liu Huabin Li Arian Laurence Xiang-Ping Yang | 2019 | Protein & Cell2019，10，8： | 1 |
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