The binding modes and binding affinities of artemisinin derivatives with Plasmodium falciparum Ca2+-ATPase (PfATP6).
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A plausible mechanism for the antimalarial activity of artemisinin: A computational approachHistone deacetylases 1 and 3 but not 2 mediate cytokine-induced beta cell apoptosis in INS-1 cells and dispersed primary islets from rats and are differentially regulated in the islets of type 1 diabetic childrenLysine deacetylase inhibition prevents diabetes by chromatin-independent immunoregulation and β-cell protectionHistone deacetylase 3 supports endochondral bone formation by controlling cytokine signaling and matrix remodeling.Specific inhibition of histone deacetylase 8 reduces gene expression and production of proinflammatory cytokines in vitro and in vivoMolecular insights of protein contour recognition with ligand pharmacophoric sites through combinatorial library design and MD simulation in validating HTLV-1 PR inhibitors.Lack of association of the S769N mutation in Plasmodium falciparum SERCA (PfATP6) with resistance to artemisinins.Characterization of the Plasmodium falciparum sarcoplasmic/endoplasmic reticulum Ca2+-ATPase gene in samples from Equatorial Guinea before implementation of artemisinin-based combination therapy.Mechanism of artemisinin resistance for malaria PfATP6 L263 mutations and discovering potential antimalarials: An integrated computational approach.Class I lysine deacetylases facilitate glucocorticoid-induced transcription.The therapeutic potential of epigenetics in autoimmune diseases.Suppression of T cell functions by hydroxamic acid-based histone deacetylase inhibitors.Structure-based drug design studies of the interactions of ent-kaurane diterpenes derived from Wedelia paludosa with the Plasmodium falciparum sarco/endoplasmic reticulum Ca²⁺-ATPase PfATP6.Investigations into the role of the Plasmodium falciparum SERCA (PfATP6) L263E mutation in artemisinin action and resistance.Docking and in silico ADMET studies of noraristeromycin, curcumin and its derivatives with Plasmodium falciparum SAH hydrolase: a molecular drug target against malaria.Improper protein trafficking contributes to artemisinin sensitivity in cells lacking the KDAC Rpd3p.An HDAC6 Inhibitor Confers Protection and Selectively Inhibits B-Cell Infiltration in DSS-Induced Colitis in Mice.Targeting Channels and Transporters in Protozoan Parasite Infections.Differential Anti-inflammatory Activity of HDAC Inhibitors in Human Macrophages and Rat ArthritisInhibiting histone deacetylase 1 suppresses both inflammation and bone loss in arthritisArtemisinin biosynthesis in Artemisia annua and metabolic engineering: questions, challenges, and perspectives
P2860
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P2860
The binding modes and binding affinities of artemisinin derivatives with Plasmodium falciparum Ca2+-ATPase (PfATP6).
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@ast
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@en
The binding modes and binding ...... smodium falciparum Ca2+-ATPase
@nl
type
label
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@ast
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@en
The binding modes and binding ...... smodium falciparum Ca2+-ATPase
@nl
prefLabel
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@ast
The binding modes and binding ...... lciparum Ca2+-ATPase (PfATP6).
@en
The binding modes and binding ...... smodium falciparum Ca2+-ATPase
@nl
P2093
P2860
P921
P1476
The binding modes and binding ...... alciparum Ca2+-ATPase (PfATP6)
@en
P2093
Abhishek Dubey
Harvinder Singh
Mani Srivastava
Piyush Ranjan
Pradeep Kumar Naik
Prasad Bajaj
Rishay Kumar
P2860
P2888
P304
P356
10.1007/S00894-010-0726-4
P50
P577
2010-05-12T00:00:00Z