(Q48269045)

10 February 2018

title

Reappraising the effects of artemisinin on the ATPase activity of PfATP6 and SERCA1a E255L expressed in Xenopus laevis oocytes. (English)

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10 February 2018

Erratum: Reappraising the effects of artemisinin on the ATPase activity of PfATP6 and SERCA1a E255L expressed in Xenopus laevis oocytes.

main subject

artemisinin

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African clawed frog

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Xenopus laevis oocyte

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based on heuristic

inferred from title

corrigendum / erratum

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author

Poul Nissen

5

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10 February 2018

Michael V Clausen

object named as

Michael Voldsgaard Clausen

2

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author name string

Stéphanie David-Bosne

1

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10 February 2018

Hanne Poulsen

3

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10 February 2018

Jesper Vuust Møller

4

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10 February 2018

Marc le Maire

6

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10 February 2018

publication date

1 January 2016

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10 February 2018

Nature Structural & Molecular Biology

published in

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10 February 2018

volume

23

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10 February 2018

issue

1

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10 February 2018

page(s)

1-2

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10 February 2018

https://scigraph.springernature.com/pub.10.1038/nsmb.3156

exact match

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cites work

Artemisinins target the SERCA of Plasmodium falciparum

1 reference

A single amino acid residue can determine the sensitivity of SERCAs to artemisinins

31 March 2020

1 reference

Purified E255L Mutant SERCA1a and Purified PfATP6 Are Sensitive to SERCA-type Inhibitors but Insensitive to Artemisinins

31 March 2020

1 reference

A molecular marker of artemisinin-resistant Plasmodium falciparum malaria

31 March 2020

1 reference

Molecular analysis of pfatp6 and pfmdr1 polymorphisms and their association with in vitro sensitivity in Plasmodium falciparum isolates from the Thai-Myanmar border.

31 March 2020

1 reference

Geographic structuring of the Plasmodium falciparum sarco(endo)plasmic reticulum Ca2+ ATPase (PfSERCA) gene diversity

31 March 2020

1 reference

Investigations into the role of the Plasmodium falciparum SERCA (PfATP6) L263E mutation in artemisinin action and resistance

31 March 2020

1 reference

Artemisinins and the biological basis for the PfATP6/SERCA hypothesis

31 March 2020

1 reference

A single amino acid residue can determine the sensitivity of SERCAs to artemisinins

31 March 2020

1 reference

Pumped up: reflections on PfATP6 as the target for artemisinins

31 March 2020

1 reference

The Plasmodium falciparum Ca 2+ -ATPase PfATP6: insensitive to artemisinin, but a potential drug target

31 March 2020

1 reference

Antimalarial screening via large-scale purification of Plasmodium falciparum Ca2+-ATPase 6 and in vitro studies

31 March 2020

1 reference

Expression and functional characterization of a Plasmodium falciparum Ca2+-ATPase (PfATP4) belonging to a subclass unique to apicomplexan organisms

31 March 2020

1 reference

Na(+) regulation in the malaria parasite Plasmodium falciparum involves the cation ATPase PfATP4 and is a target of the spiroindolone antimalarials

31 March 2020

1 reference

Spiroindolones, a potent compound class for the treatment of malaria

31 March 2020

1 reference

Genome editing in the human malaria parasite Plasmodium falciparum using the CRISPR-Cas9 system.

31 March 2020

1 reference

Drug resistance. K13-propeller mutations confer artemisinin resistance in Plasmodium falciparum clinical isolates

31 March 2020

1 reference

Drug resistance. Population transcriptomics of human malaria parasites reveals the mechanism of artemisinin resistance

31 March 2020

1 reference

Genetic architecture of artemisinin-resistant Plasmodium falciparum

31 March 2020

1 reference

Spread of artemisinin-resistant Plasmodium falciparum in Myanmar: a cross-sectional survey of the K13 molecular marker

31 March 2020

1 reference

A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria

31 March 2020

1 reference

Targeting the cell stress response of Plasmodium falciparum to overcome artemisinin resistance

31 March 2020

1 reference

Occurrence of pfatpase6 Single Nucleotide Polymorphisms Associated with Artemisinin Resistance among Field Isolates of Plasmodium falciparum in North-Eastern Tanzania

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26733217

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NSMB.3156

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10 February 2018

Dimensions Publication ID

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10 February 2018