首页> 外文OA文献 >Human Secreted Ly-6/uPAR Related Protein-1 (SLURP-1) Is a Selective Allosteric Antagonist of α7 Nicotinic Acetylcholine Receptor.

【2h】

Human Secreted Ly-6/uPAR Related Protein-1 (SLURP-1) Is a Selective Allosteric Antagonist of α7 Nicotinic Acetylcholine Receptor.

机译：人体分泌的Ly-6 / upaR相关蛋白-1（sLURp-1）是α7烟碱乙酰胆碱受体的选择性变构拮抗剂。

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Ekaterina N Lyukmanova; Mikhail A Shulepko; Denis Kudryavtsev; Maxim L Bychkov; Dmitrii S Kulbatskii; Igor E Kasheverov; Maria V Astapova; Alexey V Feofanov; Morten S Thomsen; Jens D Mikkelsen; Zakhar O Shenkarev; Victor I Tsetlin; Dmitry A Dolgikh; Mikhail P Kirpichnikov;
展开▼
作者单位

展开▼
年度 2016
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Human secreted Ly-6/uPAR related proteins: insights into specificity of interaction with acetylcholine receptors. Part 1: SLURP-1 exclusively binds to human alpha 7 nicotinic acetylcholine receptors on the outside of the orthosteric binding site [J] . Kulbatskii Dmitrii, Shulepko Mikhail, Shenkarev Zakhar, Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry . 2017,第S2期

机译：人分泌的LY-6 / UPAR相关蛋白质：识别与乙酰胆碱受体相互作用的特异性。第1部分：Slurp-1专门与人α7烟碱乙酰胆碱受体完全结合在矫形位置的外部
2. Down-regulation of secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related peptide-1 (SLURP-1), an endogenous allosteric alpha7 nicotinic acetylcholine receptor modulator, in murine and human asthmatic conditions. [J] . Narumoto O, Horiguchi K, Horiguchi S, Biochemical and Biophysical Research Communications . 2010,第4期

机译：在鼠类和人类哮喘病中，分泌的淋巴细胞抗原6 /尿激酶型纤溶酶原激活物受体相关肽1（SLURP-1）的下调，一种内源性变构α7烟碱乙酰胆碱受体调节剂。
3. 3D-QSAR and 3D-QSSR models of negative allosteric modulators facilitate the design of a novel selective antagonist of human α4β2 neuronal nicotinic acetylcholine receptors [J] . HendersonB.J., OracC.M., MacIagiewiczI., Bioorganic and Medicinal Chemistry Letters . 2012,第4期

机译：负变构调节剂的3D-QSAR和3D-QSSR模型有助于设计人α4β2神经元烟碱型乙酰胆碱受体的新型选择性拮抗剂
4. Allosteric Modulation of the Nicotinic Acetylcholine Receptor by Physostigmine [C] . LUCIE SVOBODOVá, JAN KRU?EK, TOMá? HENDRYCH, International Biophysics Symposium . 2005

机译：抗碱性乙酰胆碱受体的体溶氨基酮受体
5. Agonist and antagonist interactions with the nicotinic acetylcholine receptor. [D] . Hong, Filbert Hui-pek. 2004

机译：激动剂和拮抗剂与烟碱乙酰胆碱受体的相互作用。
6. Human Secreted Ly-6/uPAR Related Protein-1 (SLURP-1) Is a Selective Allosteric Antagonist of α7 Nicotinic Acetylcholine Receptor [O] . Ekaterina N. Lyukmanova, Mikhail A. Shulepko, Denis Kudryavtsev, -1

机译：人类分泌的Ly-6 / uPAR相关蛋白1（SLURP-1）是α7烟碱乙酰胆碱受体的选择性变构拮抗剂。
7. 3D-QSAR and 3D-QSSR models of negative allosteric modulators facilitate the design of a novel selective antagonist of human α4β2 neuronal nicotinic acetylcholine receptors [O] . Brandon J. Henderson, Crina M. Orac, Iwona Maciagiewicz, 2012

机译：3D-QSAR和3D-QSSR型号的负变构调制器促进了一种新颖的人α4β2神经元氰基乙酰胆碱受体的选择性拮抗剂的设计
8. Structural Characterization of the Putative Cholinergic Binding Region alpha(179-201) of the Nicotinic Acetylcholine Receptor. Part I. Review and Experimental Design. [R] . Height, J., Vincent, J. 1993

机译：烟碱乙酰胆碱受体的推定胆碱能结合区α（179-201）的结构表征。第一部分。审查和实验设计。

Human Secreted Ly-6/uPAR Related Protein-1 (SLURP-1) Is a Selective Allosteric Antagonist of α7 Nicotinic Acetylcholine Receptor.

著录项

引文网络

相似文献

相关主题

期刊订阅