Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis

10.1128/mBio.00679-16

Saved in:

Bibliographic Details
Main Authors:	Gengenbacher, M, Nieuwenhuizen, N, Vogelzang, A, Liu, H, Kaiser, P, Schuerer, S, Lazar, D, Wagner, I, Mollenkopf, H.-J, Kaufmann, S.H.E
Other Authors:	MEDICINE
Format:	Article
Published:	2020
Subjects:	BCG vaccine cell protein guanosine triphosphatase immunoglobulin G inflammasome interleukin 18 LC3 protein transcriptome ubiquilin protein unclassified drug bacterial protein reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone) animal cell animal experiment animal model animal tissue apoptosis Article B lymphocyte bacterial gene bacterial load BCG vaccination CD4+ T lymphocyte cell activation cell differentiation controlled study drug efficacy drug safety Gbps gene gene gene deletion gene expression regulation genetic analysis helper cell Ifi204 gene IL 18 gene IL 1beta gene immune response immunocompetent cell in vitro study inflammation lung tuberculosis mouse nonhuman nuoG gene priority journal protein localization transcriptome analysis tuberculosis upregulation animal gene expression profiling genetics immunology lung lymph node microbiology Mycobacterium bovis pathology Tuberculosis, Pulmonary vaccination Animals Bacterial Load Bacterial Proteins BCG Vaccine Electron Transport Complex I Gene Deletion Gene Expression Profiling Inflammasomes Lung Lymph Nodes Mice Vaccination
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/183721
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

id	sg-nus-scholar.10635-183721
record_format	dspace
spelling	sg-nus-scholar.10635-1837212024-11-08T17:48:51Z Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis Gengenbacher, M Nieuwenhuizen, N Vogelzang, A Liu, H Kaiser, P Schuerer, S Lazar, D Wagner, I Mollenkopf, H.-J Kaufmann, S.H.E MEDICINE BCG vaccine cell protein guanosine triphosphatase immunoglobulin G inflammasome interleukin 18 LC3 protein transcriptome ubiquilin protein unclassified drug bacterial protein BCG vaccine inflammasome reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone) animal cell animal experiment animal model animal tissue apoptosis Article B lymphocyte bacterial gene bacterial load BCG vaccination CD4+ T lymphocyte cell activation cell differentiation controlled study drug efficacy drug safety Gbps gene gene gene deletion gene expression regulation genetic analysis helper cell Ifi204 gene IL 18 gene IL 1beta gene immune response immunocompetent cell in vitro study inflammation lung tuberculosis mouse nonhuman nuoG gene priority journal protein localization transcriptome analysis tuberculosis upregulation animal gene expression profiling genetics immunology lung lymph node microbiology Mycobacterium bovis pathology Tuberculosis, Pulmonary vaccination Animals Bacterial Load Bacterial Proteins BCG Vaccine Electron Transport Complex I Gene Deletion Gene Expression Profiling Inflammasomes Lung Lymph Nodes Mice Mycobacterium bovis Tuberculosis, Pulmonary Vaccination 10.1128/mBio.00679-16 mBio 7 3 e00679-16 2020-11-19T09:38:46Z 2020-11-19T09:38:46Z 2016 Article Gengenbacher, M, Nieuwenhuizen, N, Vogelzang, A, Liu, H, Kaiser, P, Schuerer, S, Lazar, D, Wagner, I, Mollenkopf, H.-J, Kaufmann, S.H.E (2016). Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis. mBio 7 (3) : e00679-16. ScholarBank@NUS Repository. https://doi.org/10.1128/mBio.00679-16 21612129 https://scholarbank.nus.edu.sg/handle/10635/183721 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	BCG vaccine cell protein guanosine triphosphatase immunoglobulin G inflammasome interleukin 18 LC3 protein transcriptome ubiquilin protein unclassified drug bacterial protein BCG vaccine inflammasome reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone) animal cell animal experiment animal model animal tissue apoptosis Article B lymphocyte bacterial gene bacterial load BCG vaccination CD4+ T lymphocyte cell activation cell differentiation controlled study drug efficacy drug safety Gbps gene gene gene deletion gene expression regulation genetic analysis helper cell Ifi204 gene IL 18 gene IL 1beta gene immune response immunocompetent cell in vitro study inflammation lung tuberculosis mouse nonhuman nuoG gene priority journal protein localization transcriptome analysis tuberculosis upregulation animal gene expression profiling genetics immunology lung lymph node microbiology Mycobacterium bovis pathology Tuberculosis, Pulmonary vaccination Animals Bacterial Load Bacterial Proteins BCG Vaccine Electron Transport Complex I Gene Deletion Gene Expression Profiling Inflammasomes Lung Lymph Nodes Mice Mycobacterium bovis Tuberculosis, Pulmonary Vaccination
spellingShingle	BCG vaccine cell protein guanosine triphosphatase immunoglobulin G inflammasome interleukin 18 LC3 protein transcriptome ubiquilin protein unclassified drug bacterial protein BCG vaccine inflammasome reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone) animal cell animal experiment animal model animal tissue apoptosis Article B lymphocyte bacterial gene bacterial load BCG vaccination CD4+ T lymphocyte cell activation cell differentiation controlled study drug efficacy drug safety Gbps gene gene gene deletion gene expression regulation genetic analysis helper cell Ifi204 gene IL 18 gene IL 1beta gene immune response immunocompetent cell in vitro study inflammation lung tuberculosis mouse nonhuman nuoG gene priority journal protein localization transcriptome analysis tuberculosis upregulation animal gene expression profiling genetics immunology lung lymph node microbiology Mycobacterium bovis pathology Tuberculosis, Pulmonary vaccination Animals Bacterial Load Bacterial Proteins BCG Vaccine Electron Transport Complex I Gene Deletion Gene Expression Profiling Inflammasomes Lung Lymph Nodes Mice Mycobacterium bovis Tuberculosis, Pulmonary Vaccination Gengenbacher, M Nieuwenhuizen, N Vogelzang, A Liu, H Kaiser, P Schuerer, S Lazar, D Wagner, I Mollenkopf, H.-J Kaufmann, S.H.E Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
description	10.1128/mBio.00679-16
author2	MEDICINE
author_facet	MEDICINE Gengenbacher, M Nieuwenhuizen, N Vogelzang, A Liu, H Kaiser, P Schuerer, S Lazar, D Wagner, I Mollenkopf, H.-J Kaufmann, S.H.E
format	Article
author	Gengenbacher, M Nieuwenhuizen, N Vogelzang, A Liu, H Kaiser, P Schuerer, S Lazar, D Wagner, I Mollenkopf, H.-J Kaufmann, S.H.E
author_sort	Gengenbacher, M
title	Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
title_short	Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
title_full	Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
title_fullStr	Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
title_full_unstemmed	Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis
title_sort	deletion of nuog from the vaccine candidate mycobacterium bovis bcg δurec:: hly improves protection against tuberculosis
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/183721
_version_	1821208499678347264

Deletion of nuoG from the vaccine candidate Mycobacterium bovis BCG ΔureC:: Hly improves protection against tuberculosis

Similar Items