The Plasmodium falciparum translationally controlled tumor protein homolog and its reaction with the antimalarial drug artemisinin
about
Artemisinin-resistant malaria: research challenges, opportunities, and public health implicationsYeast model uncovers dual roles of mitochondria in action of artemisinin.Artemisinin and a Series of Novel Endoperoxide Antimalarials Exert Early Effects on Digestive Vacuole MorphologyPurified E255L Mutant SERCA1a and Purified PfATP6 Are Sensitive to SERCA-type Inhibitors but Insensitive to ArtemisininsArtemisinin, an Endoperoxide Antimalarial, Disrupts the Hemoglobin Catabolism and Heme Detoxification Systems in Malarial ParasiteHaem-activated promiscuous targeting of artemisinin in Plasmodium falciparumA molecular marker of artemisinin-resistant Plasmodium falciparum malariaCharacterization of fortilin, a novel antiapoptotic proteinThe mRNA of the translationally controlled tumor protein P23/TCTP is a highly structured RNA, which activates the dsRNA-dependent protein kinase PKRArtemisinin-based antimalarial research: application of biotechnology to the production of artemisinin, its mode of action, and the mechanism of resistance of Plasmodium parasitesMuddled mechanisms: recent progress towards antimalarial target identificationExpression of the gene and processed pseudogenes encoding the human and rabbit translationally controlled tumour protein (TCTP)The activities of current antimalarial drugs on the life cycle stages of Plasmodium: a comparative study with human and rodent parasitesReal-time imaging of the intracellular glutathione redox potential in the malaria parasite Plasmodium falciparumGene encoding a deubiquitinating enzyme is mutated in artesunate- and chloroquine-resistant rodent malaria parasitesLigand binding reveals a role for heme in translationally-controlled tumor protein dimerization.Translationally controlled tumor protein is a novel biological target for neurofibromatosis type 1-associated tumorsReaction of artemisinin with haemoglobin: implications for antimalarial activity.A controlled trial to assess the effect of quinine, chloroquine, amodiaquine, and artesunate on Loa loa microfilaremia.Role of pfmdr1 amplification and expression in induction of resistance to artemisinin derivatives in Plasmodium falciparum.Immune mimicry in malaria: Plasmodium falciparum secretes a functional histamine-releasing factor homolog in vitro and in vivo.Mechanisms of artemisinin resistance in the rodent malaria pathogen Plasmodium yoelii.Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription.Malaria parasites can develop stable resistance to artemisinin but lack mutations in candidate genes atp6 (encoding the sarcoplasmic and endoplasmic reticulum Ca2+ ATPase), tctp, mdr1, and cg10.Plasmodium drug targets outside the genetic control of the parasite.Antimalarial action of artesunate involves DNA damage mediated by reactive oxygen speciesDiscovery, mechanisms of action and combination therapy of artemisininEmerging targets for antimalarial drugs.Plasmodium falciparum isolates from southern Ghana exhibit polymorphisms in the SERCA-type PfATPase6 though sensitive to artesunate in vitro.Phenotypic and genotypic analysis of in vitro-selected artemisinin-resistant progeny of Plasmodium falciparumAntimalarial Effects of Iranian Flora Artemisia sieberi on Plasmodium berghei In Vivo in Mice and Phytochemistry Analysis of Its Herbal Extracts.Phospho-TCTP as a therapeutic target of Dihydroartemisinin for aggressive breast cancer cells.In Vivo Antimalarial Effects of Iranian Flora Artemisia khorassanica against Plasmodium berghei and Pharmacochemistry of its Natural ComponentsAn integrative analysis of small molecule transcriptional responses in the human malaria parasite Plasmodium falciparumLack of association of the S769N mutation in Plasmodium falciparum SERCA (PfATP6) with resistance to artemisinins.Mechanisms of in vitro resistance to dihydroartemisinin in Plasmodium falciparum.Artemisinin resistance in Plasmodium falciparum: A process linked to dormancy?Prospects for the treatment of drug-resistant malaria parasites.Accumulation of artemisinin trioxane derivatives within neutral lipids of Plasmodium falciparum malaria parasites is endoperoxide-dependent.Recent highlights in antimalarial drug resistance and chemotherapy research.
P2860
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P2860
The Plasmodium falciparum translationally controlled tumor protein homolog and its reaction with the antimalarial drug artemisinin
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
name
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@ast
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@en
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@nl
type
label
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@ast
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@en
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@nl
prefLabel
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@ast
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@en
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@nl
P2093
P2860
P921
P3181
P356
P1476
The Plasmodium falciparum tran ...... antimalarial drug artemisinin
@en
P2093
C A Yowell
D J Walker
J Bhisutthibhan
P A Hossler
S R Meshnick
P2860
P304
P3181
P356
10.1074/JBC.273.26.16192
P407
P577
1998-06-26T00:00:00Z