Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies

Antimalarial chemotherapy relies on combination therapies (ACTs) consisting of an artemisinin derivative and a partner drug. Here, the authors study the effects of globally prevalent mutations in a multidrug resistance transporter (PfMDR1) on the parasite’s susceptibility to ACT drugs.

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Autores principales: M. Isabel Veiga, Satish K. Dhingra, Philipp P. Henrich, Judith Straimer, Nina Gnädig, Anne-Catrin Uhlemann, Rowena E. Martin, Adele M. Lehane, David A. Fidock
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Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/dbb046e77b4e470caabc3ad9b066a983
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spelling oai:doaj.org-article:dbb046e77b4e470caabc3ad9b066a9832021-12-02T14:39:15ZGlobally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies10.1038/ncomms115532041-1723https://doaj.org/article/dbb046e77b4e470caabc3ad9b066a9832016-05-01T00:00:00Zhttps://doi.org/10.1038/ncomms11553https://doaj.org/toc/2041-1723Antimalarial chemotherapy relies on combination therapies (ACTs) consisting of an artemisinin derivative and a partner drug. Here, the authors study the effects of globally prevalent mutations in a multidrug resistance transporter (PfMDR1) on the parasite’s susceptibility to ACT drugs.M. Isabel VeigaSatish K. DhingraPhilipp P. HenrichJudith StraimerNina GnädigAnne-Catrin UhlemannRowena E. MartinAdele M. LehaneDavid A. FidockNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
M. Isabel Veiga
Satish K. Dhingra
Philipp P. Henrich
Judith Straimer
Nina Gnädig
Anne-Catrin Uhlemann
Rowena E. Martin
Adele M. Lehane
David A. Fidock
Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
description Antimalarial chemotherapy relies on combination therapies (ACTs) consisting of an artemisinin derivative and a partner drug. Here, the authors study the effects of globally prevalent mutations in a multidrug resistance transporter (PfMDR1) on the parasite’s susceptibility to ACT drugs.
format article
author M. Isabel Veiga
Satish K. Dhingra
Philipp P. Henrich
Judith Straimer
Nina Gnädig
Anne-Catrin Uhlemann
Rowena E. Martin
Adele M. Lehane
David A. Fidock
author_facet M. Isabel Veiga
Satish K. Dhingra
Philipp P. Henrich
Judith Straimer
Nina Gnädig
Anne-Catrin Uhlemann
Rowena E. Martin
Adele M. Lehane
David A. Fidock
author_sort M. Isabel Veiga
title Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
title_short Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
title_full Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
title_fullStr Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
title_full_unstemmed Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies
title_sort globally prevalent pfmdr1 mutations modulate plasmodium falciparum susceptibility to artemisinin-based combination therapies
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/dbb046e77b4e470caabc3ad9b066a983
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