Serveur d'exploration SRAS - Curation (Ncbi)

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Peptide Fragments (isolation & purification) < Peptide Fragments (metabolism) < Peptide Fragments (pharmacology)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000650 (2004) Baomei Wang [République populaire de Chine] ; Huabiao Chen ; Xiaodong Jiang ; Minghui Zhang ; Tao Wan ; Nan Li ; Xiangyang Zhou ; Yanfeng Wu ; Feng Yang ; Yizhi Yu ; Xiaoning Wang ; Ruifu Yang ; Xuetao CaoIdentification of an HLA-A*0201-restricted CD8+ T-cell epitope SSp-1 of SARS-CoV spike protein.
000D15 (2005) Jin-Cun Zhao [République populaire de Chine] ; Zhen-Dong Zhao ; Wei Wang ; Xiao-Ming GaoProkaryotic expression, refolding, and purification of fragment 450-650 of the spike protein of SARS-coronavirus.
000F06 (2005) Ao Cheng [République populaire de Chine] ; Wei Zhang ; Youhua Xie ; Weihong Jiang ; Eddy Arnold ; Stefan G. Sarafianos ; Jianping DingExpression, purification, and characterization of SARS coronavirus RNA polymerase.
000F24 (2005) Haibin Luo [République populaire de Chine] ; Qing Chen ; Jing Chen ; Kaixian Chen ; Xu Shen ; Hualiang JiangThe nucleocapsid protein of SARS coronavirus has a high binding affinity to the human cellular heterogeneous nuclear ribonucleoprotein A1.
001338 (2005) Hai-Yan Wei [République populaire de Chine] ; Jian-Wei Wang ; Yang-Jing Ou ; Yan-Bin Wang ; Jian-Guo Qu ; Wei-Ming Zhao ; Tao Hong[Receptor-binding ability of fragments 260-600 and 397-796 of SARS-associated coronavirus spike protein].
001576 (2006) John S. Mills [États-Unis]Peptides derived from HIV-1, HIV-2, Ebola virus, SARS coronavirus and coronavirus 229E exhibit high affinity binding to the formyl peptide receptor.
001605 (2006) Minghai Zhou ; Dongping Xu ; Xiaojuan Li ; Hongtao Li ; Ming Shan ; Jiaren Tang ; Min Wang ; Fu-Sheng Wang ; Xiaodong Zhu ; Hua Tao ; Wei He ; Po Tien ; George F. GaoScreening and identification of severe acute respiratory syndrome-associated coronavirus-specific CTL epitopes.
001827 (2007) Marcius S. Almeida [États-Unis] ; Margaret A. Johnson ; Torsten Herrmann ; Michael Geralt ; Kurt WüthrichNovel beta-barrel fold in the nuclear magnetic resonance structure of the replicase nonstructural protein 1 from the severe acute respiratory syndrome coronavirus.
001D68 (2008) John Mark [Canada] ; Xuguang Li [Canada] ; Terry Cyr [Canada] ; Sylvie Fournier [Canada] ; Bozena Jaentschke [Canada] ; Mary Alice Hefford [Canada]SARS coronavirus: unusual lability of the nucleocapsid protein.
002040 (2009) Yanbo Lv ; Zhihua Ruan ; Li Wang ; Bing Ni ; Yuzhang WuIdentification of a novel conserved HLA-A*0201-restricted epitope from the spike protein of SARS-CoV
002560 (2012) Jun Huang [République populaire de Chine] ; Yingnan Cao [République populaire de Chine] ; Xianzhang Bu [République populaire de Chine] ; Changyou Wu [République populaire de Chine]Residue analysis of a CTL epitope of SARS-CoV spike protein by IFN-gamma production and bioinformatics prediction
002A26 (2015) Ying Liao ; Si Min Zhang ; Tuan Ling Neo ; James P. TamTryptophan-dependent membrane interaction and heteromerization with the internal fusion peptide by the membrane proximal external region of SARS-CoV spike protein.
002A52 (2015) Anirban Ghosh [Inde] ; Amit S. Pithadia [États-Unis] ; Jyotsna Bhat [Inde] ; Supriyo Bera [Inde] ; Anupam Midya [Inde] ; Carol A. Fierke [États-Unis] ; Ayyalusamy Ramamoorthy [États-Unis] ; Anirban Bhunia [Inde]Self-assembly of a nine-residue amyloid-forming peptide fragment of SARS corona virus E-protein: mechanism of self aggregation and amyloid-inhibition of hIAPP.
002B50 (2015) Natalia T. Freund [Israël, États-Unis] ; Anna Roitburd-Berman [Israël] ; Jianhua Sui [États-Unis, République populaire de Chine] ; Wayne A. Marasco [États-Unis] ; Jonathan M. Gershoni [Israël]Reconstitution of the receptor-binding motif of the SARS coronavirus
002E59 (2017) Alex L. Lai [États-Unis] ; Jean K. Millet [États-Unis] ; Susan Daniel [États-Unis] ; Jack H. Freed [États-Unis] ; Gary R. Whittaker [États-Unis]The SARS-CoV Fusion Peptide Forms an Extended Bipartite Fusion Platform that Perturbs Membrane Order in a Calcium-Dependent Manner.

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