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Response of M. tuberculosis to 8 hour exposure to vitamin C
PubMed Similar studies Analyze with GEO2R
Temporal response of Mycobacterium tuberculosis H37Rv to vitamin C exposure.
PubMed Full text in PMC Similar studies Analyze with GEO2R
In vitro dormancy achieved by multiple stresses in Mycobacterium tuberculosis
Hypoxia is NOT THE MAIN stress When M. tuberculosis is in a dormancy-LIKE FATTY ACID environment
PubMed Full text in PMC Similar studies SRA Run Selector
In-vivo Gene Signatures of Mycobacterium tuberculosis In C3HeB/FeJ Mice
Role of M. tuberculosis dosS and dosT in CO sensing
Dose response of carbon monoxide treatment of M. tuberculosis
Role of M. tuberculosis in CO sensing
Mycobacterium tuberculosis H37Rv (WT) versus Mut1 and Comp1
PubMed Full text in PMC Similar studies
Effect of small M. tuberculosis RNA MTS1338 on the transcriptome under various stress conditions
Differentially regulated genes induced in Mycobacterium by in vitro acid-nitrosative multi-stress
Differentially regulated genes induced in Mycobacterium tuberculosis by in vitro acid-nitrosative multi-stress
Differentially regulated genes induced in Mycobacterium smegmatis by in vitro acid-nitrosative multi-stress
Transcriptional Profile of Mycobacterium tuberculosis Replicating in Human Type II Alveolar Epithelial A549 cell line
Gene expression profiling of THP-1 cells on treatment with vitamin C
The Mycobacterium tuberculosis Rv2745c Plays an Important Role in Responding to Redox Stress
A Lysosomal In Vitro Exposure (LivE) Model to Identify Pathways Critical for Mycobacterium tuberculosis Intracellular Persistence
Intricate genetic program underlying hypoxia-induced dormancy in Mycobacterium tuberculosis revealed by high-resolution transcriptional time-course
Reaeration timecourse from a defined hypoxia model
Mycobacterium tuberculosis gene expression during adaptation to stationary phase and low-oxygen dormancy
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