The 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.
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Analysis of Plasmodium falciparum diversity in natural infections by deep sequencingThe malaria parasite cation ATPase PfATP4 and its role in the mechanism of action of a new arsenal of antimalarial drugsUDP-galactose and acetyl-CoA transporters as Plasmodium multidrug resistance genesThe molecular basis of folate salvage in Plasmodium falciparum: characterization of two folate transportersPfNT2, a permease of the equilibrative nucleoside transporter family in the endoplasmic reticulum of Plasmodium falciparumRoles for two aminopeptidases in vacuolar hemoglobin catabolism in Plasmodium falciparumThe plasma membrane permease PfNT1 is essential for purine salvage in the human malaria parasite Plasmodium falciparumTransport of nucleosides across the Plasmodium falciparum parasite plasma membrane has characteristics of PfENT1Characterization of two putative potassium channels in Plasmodium falciparumMalaria parasite type 4 equilibrative nucleoside transporters (ENT4) are purine transporters with distinct substrate specificityNa(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarialsAntimalarial exposure delays Plasmodium falciparum intra-erythrocytic cycle and drives drug transporter genes expressionNovel polymorphisms in Plasmodium falciparum ABC transporter genes are associated with major ACT antimalarial drug resistanceGenome wide adaptations of Plasmodium falciparum in response to lumefantrine selective drug pressureTargeting purine and pyrimidine metabolism in human apicomplexan parasitesLocalization of the ATP-binding cassette (ABC) transport proteins PfMRP1, PfMRP2, and PfMDR5 at the Plasmodium falciparum plasma membraneThe novel putative transporter NPT1 plays a critical role in early stages of Plasmodium berghei sexual developmentCationic amino acid transporters play key roles in the survival and transmission of apicomplexan parasitesIdentification and functional analysis of the primary pantothenate transporter, PfPAT, of the human malaria parasite Plasmodium falciparumA lactate and formate transporter in the intraerythrocytic malaria parasite, Plasmodium falciparumFunctional profiles of orphan membrane transporters in the life cycle of the malaria parasiteRecombinant vacuolar iron transporter family homologue PfVIT from human malaria-causing Plasmodium falciparum is a Fe(2+)/H(+)exchangerGenomic analysis of nucleoside transporters in Diptera and functional characterization of DmENT2, a Drosophila equilibrative nucleoside transporter.A computational model of gene expression reveals early transcriptional events at the subtelomeric regions of the malaria parasite, Plasmodium falciparum.Genome comparison of human and non-human malaria parasites reveals species subset-specific genes potentially linked to human disease.Genome-wide detection of serpentine receptor-like proteins in malaria parasitesComputational analysis of constraints on noncoding regions, coding regions and gene expression in relation to Plasmodium phenotypic diversity.Comparative transcriptional and genomic analysis of Plasmodium falciparum field isolates.Eating at the table of another: metabolomics of host-parasite interactions.Life cycle studies of the hexose transporter of Plasmodium species and genetic validation of their essentialityTransmembrane segment 11 appears to line the purine permeation pathway of the Plasmodium falciparum equilibrative nucleoside transporter 1 (PfENT1).Reconstruction and flux-balance analysis of the Plasmodium falciparum metabolic network.A class of tricyclic compounds blocking malaria parasite oocyst development and transmission.Plasmodial sugar transporters as anti-malarial drug targets and comparisons with other protozoa.Submicroscopic and asymptomatic Plasmodium falciparum and Plasmodium vivax infections are common in western Thailand - molecular and serological evidence.Purine import into malaria parasites as a target for antimalarial drug development.Yeast-based high-throughput screen identifies Plasmodium falciparum equilibrative nucleoside transporter 1 inhibitors that kill malaria parasitesPurine and pyrimidine pathways as targets in Plasmodium falciparum.Gene selective mRNA cleavage inhibits the development of Plasmodium falciparum.Proteomics of the human malaria parasite Plasmodium falciparum
P2860
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P2860
The 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
The 'permeome' of the malaria ...... teins of Plasmodium falciparum
@nl
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@ast
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@en
type
label
The 'permeome' of the malaria ...... teins of Plasmodium falciparum
@nl
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@ast
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@en
prefLabel
The 'permeome' of the malaria ...... teins of Plasmodium falciparum
@nl
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@ast
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@en
P2860
P50
P921
P3181
P356
P1433
P1476
The 'permeome' of the malaria ...... eins of Plasmodium falciparum.
@en
P2093
Janice L Abbey
John D Clements
P2860
P2888
P3181
P356
10.1186/GB-2005-6-3-R26
P407
P577
2005-03-02T00:00:00Z
P5875
P6179
1030027610