网站标志
会员登录信息
您好,欢迎光临!   [请登录]   [免费注册]
商品搜索
点评详情
发布于:2020-9-3 03:17:51  访问:69 次 回复:0 篇
版主管理 | 推荐 | 删除 | 删除并扣分
Ive splicing and expressed in distinct subsets of neurons. Neuron fourteen(three):497?07. nine. Treutlein
(2010) Trans-synaptic interaction of GluRdelta2 and neurexin through Cbln1 mediates synapse Fisetin Biological Activity pubmed ID:https://www.ncbi.nlm.nih.gov/pubmed/26262685 development in the cerebellum. Sj lom B, Elleby B, Wallgren K, Jonsson BH, Lindskog S (1996) Two stage mutations convert a catalytically inactive Mibampator In Vivo Carbonic anhydrase-related protein (CARP) to an active enzyme. FEBS Lett 398(two?):322?25. sixteen. Nishimori I, et al. (2013) TRi-1 Autophagy Restoring catalytic exercise towards the human carbonic anhydrase (CA) similar proteins VIII, X and XI affords isoforms with higher catalytic performance and susceptibility to anion inhibition. Bioorg Med Chem Lett 23(1):256?sixty. 17. Aspatwar A, Tolvanen ME, Parkkila S (2010) Phylogeny and expression of carbonic anhydrase-related proteins. BMC Mol Biol 11:25. 18. Barnea G, et al. (1993) Identification of a carbonic anhydrase-like area within the extracellular location of RPTP gamma defines a completely new subfamily of receptor tyrosine phosphatases. Mol Mobile Biol 13(3):1497?506. 19. Peles E, et al. (1995) The carbonic anhydrase domain of receptor tyrosine phosphatase beta is often a purposeful ligand with the axonal cell recognition molecule contactin. Cell eighty two(two):251?60. twenty. Bouyain S, Watkins DJ (2010) The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct users with the contactin loved ones of neural recognition molecules. Proc Natl Acad Sci United states 107(six):2443?448.21. Jiao Y, et al. (2005) Carbonic anhydrase-related protein VIII deficiency is linked by using a unique lifelong gait disorder in waddles mice. Genetics 171(3):1239?246. 22. T kmen S, et al. (2009) CA8 mutations induce a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait. PLoS Genet five(five):e1000487. 23. Kaya N, et al. (2011) Phenotypical spectrum of cerebellar ataxia connected which has a novel mutation within the CA8 gene, encoding carbonic anhydrase (CA) VIII. Am J Med Genet B Neuropsychiatr Genet 156B(7):826?34. 24. Anderson GR, et al. (2015) -Neurexins regulate neural circuits by regulating synaptic endocannabinoid signaling. Cell 162(3):593?06. twenty five. Gokce PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/25580973 O, S hof TC (2013) Membrane-tethered monomeric neurexin LNS-domain triggers synapse formation. J Neurosci 33(36):14617?4628. 26. Aspatwar A, et al.Ive splicing and expressed in distinct subsets of neurons. Neuron fourteen(3):497?07. nine. Treutlein B, Gokce O, Quake SR, S hof TC (2014) Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing. Proc Natl Acad Sci Usa 111(13):E1291 1299. 10. Schreiner D, et al. (2014) Specific combinatorial alternate splicing generates brain region-specific repertoires of neurexins. Neuron 84(2):386?ninety eight. eleven. Ichtchenko K, et al. (1995) Neuroligin 1: A splice site-specific ligand for beta-neurexins. Cell eighty one(3):435?43. twelve. Ko J, Fuccillo MV, Malenka RC, S hof TC (2009) LRRTM2 features to be a neurexin ligand in endorsing excitatory synapse development. Neuron sixty four(six):791?ninety eight. thirteen. Uemura T, et al. (2010) Trans-synaptic conversation of GluRdelta2 and neurexin via Cbln1 mediates synapse PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/26262685 development from the cerebellum.
共0篇回复 每页10篇 页次:1/1
共0篇回复 每页10篇 页次:1/1
我要回复
回复内容
验 证 码
看不清?更换一张
匿名发表 
当前位置
脚注信息
Copyright ? 2009-2010 All Rights Reserved. 家电商城网站管理系统 版权所有   沪ICP备01234567号
服务时间:周一至周日 08:30 — 20:00  全国订购及服务热线:021-98765432 
联系地址:上海市某某路某大厦20楼B座2008室   邮政编码:210000   智能建站 提供