about
Protein kinases of the human malaria parasite Plasmodium falciparum: the kinome of a divergent eukaryoteScreening marine resources to find novel chemical inhibitors of disease-relevant protein kinasesThe Entamoeba histolytica serum-inducible transmembrane kinase EhTMKB1-9 is involved in intestinal amebiasisData-mining approaches reveal hidden families of proteases in the genome of malaria parasiteEvidence from bioinformatics, expression and inhibition studies of phosphoinositide-3 kinase signalling in Giardia intestinalis.2,N6-disubstituted adenosine analogs with antitrypanosomal and antimalarial activities.Core genome components and lineage specific expansions in malaria parasites plasmodiumOptimization of luminescent assay for screening of cyclin-dependent kinase 2 inhibitorsInhibitory activities of epidermal growth factor receptor tyrosine kinase-targeted dihydroxyisoflavone and trihydroxydeoxybenzoin derivatives on Sarcocystis neurona, Neospora caninum, and Cryptosporidium parvum development.Deep Insight into the Phosphatomes of Parasitic Protozoa and a Web Resource ProtozPhosDB.In vitro screening for drug repositioning.Three-dimensional structures in the design of therapeutics targeting parasitic protozoa: reflections on the past, present and future.Kinetoplastid PPEF phosphatases: dual acylated proteins expressed in the endomembrane system of LeishmaniaDual action of the inhibitors of cyclin-dependent kinases: targeting of the cell-cycle progression and activation of wild-type p53 protein.Proteomics of the human malaria parasite Plasmodium falciparumAntimalarial drug discovery: targeting protein kinases.Reduced Activity of Mutant Calcium-Dependent Protein Kinase 1 Is Compensated in Plasmodium falciparum through the Action of Protein Kinase G.Plasmodium kinases as targets for new-generation antimalarials.Visceral leishmaniasis treatment: What do we have, what do we need and how to deliver it?The role of two novel regulatory sites in the activation of the cGMP-dependent protein kinase from Plasmodium falciparumHigh-throughput screening with the Eimeria tenella CDC2-related kinase2/cyclin complex EtCRK2/EtCYC3a.A novel protein phosphatase 2A (PP2A) is involved in the transformation of human protozoan parasite Trypanosoma cruzi.Target-similarity search using Plasmodium falciparum proteome identifies approved drugs with anti-malarial activity and their possible targets.Plasmodial Kinase Inhibitors: License to Cure?
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Protein kinases as drug targets in parasitic protozoa.
@ast
Protein kinases as drug targets in parasitic protozoa.
@de
Protein kinases as drug targets in parasitic protozoa.
@en
Protein kinases as drug targets in parasitic protozoa.
@fr
type
label
Protein kinases as drug targets in parasitic protozoa.
@ast
Protein kinases as drug targets in parasitic protozoa.
@de
Protein kinases as drug targets in parasitic protozoa.
@en
Protein kinases as drug targets in parasitic protozoa.
@fr
prefLabel
Protein kinases as drug targets in parasitic protozoa.
@ast
Protein kinases as drug targets in parasitic protozoa.
@de
Protein kinases as drug targets in parasitic protozoa.
@en
Protein kinases as drug targets in parasitic protozoa.
@fr
P1476
Protein kinases as drug targets in parasitic protozoa.
@en
P2093
Laurent Meijer
P304
P356
10.1016/S1471-4922(02)02321-8
P407
P577
2002-08-01T00:00:00Z