Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway
10.1371/journal.ppat.1007298
Saved in:
Main Authors: | , , , , , , , , , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Published: |
2019
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/161879 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
id |
sg-nus-scholar.10635-161879 |
---|---|
record_format |
dspace |
spelling |
sg-nus-scholar.10635-1618792024-05-08T09:52:07Z Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway Ye W. Chew M. Hou J. Lai F. Leopold S.J. Loo H.L. Ghose A. Dutta A.K. Chen Q. Ooi E.E. White N.J. Dondorp A.M. Preiser P. Chen J. MEDICINE MICROBIOLOGY AND IMMUNOLOGY DUKE-NUS MEDICAL SCHOOL BIOLOGICAL SCIENCES bilirubin CD69 antigen creatinine gamma interferon granulysin interferon induced helicase C domain containing protein 1 interleukin 2 receptor alpha lectin receptor lysosome associated membrane protein 1 natural killer cell receptor NKG2A natural killer cell receptor NKG2D IFIH1 protein, human interferon induced helicase C domain containing protein 1 adult Article cell heterogeneity confocal microscopy controlled study cytotoxicity discriminant analysis erythrocyte female flow cytometry gel electrophoresis gene expression hematocrit human human cell hypoglycemia immune response immunoassay malaria male membrane microparticle microarray analysis natural killer T cell parasitemia peripheral blood mononuclear cell Plasmodium falciparum protein expression respiratory failure reverse transcription RNA isolation signal transduction systolic blood pressure Western blotting antagonists and inhibitors cell culture CRISPR Cas system cytoplasm erythrocyte genetics immunology isolation and purification lymphocyte activation malaria falciparum membrane microparticle metabolism natural killer cell parasitology Cell-Derived Microparticles Cells, Cultured CRISPR-Cas Systems Cytoplasm Erythrocytes Humans Interferon-Induced Helicase, IFIH1 Killer Cells, Natural Lymphocyte Activation Malaria, Falciparum Plasmodium falciparum 10.1371/journal.ppat.1007298 PLoS Pathogens 14 10 e1007298 2019-11-08T06:41:37Z 2019-11-08T06:41:37Z 2018 Article Ye W., Chew M., Hou J., Lai F., Leopold S.J., Loo H.L., Ghose A., Dutta A.K., Chen Q., Ooi E.E., White N.J., Dondorp A.M., Preiser P., Chen J. (2018). Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway. PLoS Pathogens 14 (10) : e1007298. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.ppat.1007298 15537366 https://scholarbank.nus.edu.sg/handle/10635/161879 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101 |
institution |
National University of Singapore |
building |
NUS Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NUS Library |
collection |
ScholarBank@NUS |
topic |
bilirubin CD69 antigen creatinine gamma interferon granulysin interferon induced helicase C domain containing protein 1 interleukin 2 receptor alpha lectin receptor lysosome associated membrane protein 1 natural killer cell receptor NKG2A natural killer cell receptor NKG2D IFIH1 protein, human interferon induced helicase C domain containing protein 1 adult Article cell heterogeneity confocal microscopy controlled study cytotoxicity discriminant analysis erythrocyte female flow cytometry gel electrophoresis gene expression hematocrit human human cell hypoglycemia immune response immunoassay malaria male membrane microparticle microarray analysis natural killer T cell parasitemia peripheral blood mononuclear cell Plasmodium falciparum protein expression respiratory failure reverse transcription RNA isolation signal transduction systolic blood pressure Western blotting antagonists and inhibitors cell culture CRISPR Cas system cytoplasm erythrocyte genetics immunology isolation and purification lymphocyte activation malaria falciparum membrane microparticle metabolism natural killer cell parasitology Cell-Derived Microparticles Cells, Cultured CRISPR-Cas Systems Cytoplasm Erythrocytes Humans Interferon-Induced Helicase, IFIH1 Killer Cells, Natural Lymphocyte Activation Malaria, Falciparum Plasmodium falciparum |
spellingShingle |
bilirubin CD69 antigen creatinine gamma interferon granulysin interferon induced helicase C domain containing protein 1 interleukin 2 receptor alpha lectin receptor lysosome associated membrane protein 1 natural killer cell receptor NKG2A natural killer cell receptor NKG2D IFIH1 protein, human interferon induced helicase C domain containing protein 1 adult Article cell heterogeneity confocal microscopy controlled study cytotoxicity discriminant analysis erythrocyte female flow cytometry gel electrophoresis gene expression hematocrit human human cell hypoglycemia immune response immunoassay malaria male membrane microparticle microarray analysis natural killer T cell parasitemia peripheral blood mononuclear cell Plasmodium falciparum protein expression respiratory failure reverse transcription RNA isolation signal transduction systolic blood pressure Western blotting antagonists and inhibitors cell culture CRISPR Cas system cytoplasm erythrocyte genetics immunology isolation and purification lymphocyte activation malaria falciparum membrane microparticle metabolism natural killer cell parasitology Cell-Derived Microparticles Cells, Cultured CRISPR-Cas Systems Cytoplasm Erythrocytes Humans Interferon-Induced Helicase, IFIH1 Killer Cells, Natural Lymphocyte Activation Malaria, Falciparum Plasmodium falciparum Ye W. Chew M. Hou J. Lai F. Leopold S.J. Loo H.L. Ghose A. Dutta A.K. Chen Q. Ooi E.E. White N.J. Dondorp A.M. Preiser P. Chen J. Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
description |
10.1371/journal.ppat.1007298 |
author2 |
MEDICINE |
author_facet |
MEDICINE Ye W. Chew M. Hou J. Lai F. Leopold S.J. Loo H.L. Ghose A. Dutta A.K. Chen Q. Ooi E.E. White N.J. Dondorp A.M. Preiser P. Chen J. |
format |
Article |
author |
Ye W. Chew M. Hou J. Lai F. Leopold S.J. Loo H.L. Ghose A. Dutta A.K. Chen Q. Ooi E.E. White N.J. Dondorp A.M. Preiser P. Chen J. |
author_sort |
Ye W. |
title |
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
title_short |
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
title_full |
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
title_fullStr |
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
title_full_unstemmed |
Microvesicles from malaria-infected red blood cells activate natural killer cells via MDA5 pathway |
title_sort |
microvesicles from malaria-infected red blood cells activate natural killer cells via mda5 pathway |
publishDate |
2019 |
url |
https://scholarbank.nus.edu.sg/handle/10635/161879 |
_version_ |
1800913823640584192 |