Pages that link to "Q28487335"
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The following pages link to Molecular basis of intrinsic macrolide resistance in the Mycobacterium tuberculosis complex (Q28487335):
Displaying 50 items.
- Structural and Functional Characterization of Rv2966c Protein Reveals an RsmD-like Methyltransferase from Mycobacterium tuberculosis and the Role of Its N-terminal Domain in Target Recognition (Q27667462) (← links)
- Structural basis for S-adenosylmethionine binding and methyltransferase activity by mitochondrial transcription factor B1 (Q27678821) (← links)
- The structure of Rv2372c identifies an RsmE-like methyltransferase from Mycobacterium tuberculosis (Q27689443) (← links)
- Ancestral antibiotic resistance in Mycobacterium tuberculosis (Q28486382) (← links)
- Characterization of peptidyl-tRNA hydrolase encoded by open reading frame Rv1014c of Mycobacterium tuberculosis H37Rv (Q28486643) (← links)
- TLR13 recognizes bacterial 23S rRNA devoid of erythromycin resistance-forming modification (Q28586721) (← links)
- The mycobacterial antibiotic resistance determinant WhiB7 acts as a transcriptional activator by binding the primary sigma factor SigA (RpoV). (Q30353252) (← links)
- Identification of novel leads applying in silico studies for Mycobacterium multidrug resistant (MMR) protein (Q31141792) (← links)
- Genes required for intrinsic multidrug resistance in Mycobacterium avium (Q33206220) (← links)
- Molecular basis of intrinsic macrolide resistance in clinical isolates of Mycobacterium fortuitum (Q33209766) (← links)
- Mycobacterium smegmatis Erm(38) is a reluctant dimethyltransferase (Q33222431) (← links)
- Methyltransferase Erm(37) slips on rRNA to confer atypical resistance in Mycobacterium tuberculosis (Q33223661) (← links)
- Mycobacterium tuberculosis interactome analysis unravels potential pathways to drug resistance (Q33395486) (← links)
- New Insights in to the Intrinsic and Acquired Drug Resistance Mechanisms in Mycobacteria (Q33600161) (← links)
- Mycobacterium neoaurum and Mycobacterium bacteremicum sp. nov. as Causes of Mycobacteremia (Q33706133) (← links)
- In vitro and in vivo activities of macrolide derivatives against Mycobacterium tuberculosis (Q33722005) (← links)
- Rapid assessment of antibacterial activity against Mycobacterium ulcerans by using recombinant luminescent strains (Q33962755) (← links)
- The mycobacterial transcriptional regulator whiB7 gene links redox homeostasis and intrinsic antibiotic resistance (Q34070418) (← links)
- Assessment of clarithromycin susceptibility in strains belonging to the Mycobacterium abscessus group by erm(41) and rrl sequencing (Q34528945) (← links)
- Intrinsic macrolide resistance of the Mycobacterium tuberculosis complex is inducible (Q34721591) (← links)
- First linezolid-resistant clinical isolates of Mycobacterium tuberculosis (Q35758951) (← links)
- Pharmacogenomic strategies against resistance development in microbial infections (Q35785222) (← links)
- Epigenetic Segregation of Microbial Genomes from Complex Samples Using Restriction Endonucleases HpaII and McrB. (Q35884126) (← links)
- Application of molecular genetic methods in macrolide, lincosamide and streptogramin resistance diagnostics and in detection of drug-resistant Mycobacterium tuberculosis (Q36003067) (← links)
- Subinhibitory Doses of Aminoglycoside Antibiotics Induce Changes in the Phenotype of Mycobacterium abscessus. (Q36075849) (← links)
- Importance of the genetic diversity within the Mycobacterium tuberculosis complex for the development of novel antibiotics and diagnostic tests of drug resistance (Q36396241) (← links)
- Bacterial genome sequencing and its use in infectious diseases (Q36982025) (← links)
- A novel gene, erm(41), confers inducible macrolide resistance to clinical isolates of Mycobacterium abscessus but is absent from Mycobacterium chelonae (Q37144788) (← links)
- N-methylation of a bactericidal compound as a resistance mechanism in Mycobacterium tuberculosis. (Q37161540) (← links)
- Structure-activity relationships of macrolides against Mycobacterium tuberculosis (Q37257892) (← links)
- WhiB7, an Fe-S-dependent transcription factor that activates species-specific repertoires of drug resistance determinants in actinobacteria (Q37348910) (← links)
- Prospects for the Future Using Genomics and Proteomics in Clinical Microbiology (Q37884605) (← links)
- WhiB7, a transcriptional activator that coordinates physiology with intrinsic drug resistance in Mycobacterium tuberculosis. (Q38056150) (← links)
- Molecular biology of drug resistance in Mycobacterium tuberculosis (Q38062402) (← links)
- Speculative strategies for new antibacterials: all roads should not lead to Rome (Q38101243) (← links)
- Clinical detection and characterization of bacterial pathogens in the genomics era. (Q38320332) (← links)
- Antibiotic resistance mechanisms in M. tuberculosis: an update (Q38830420) (← links)
- Resistance to Macrolide Antibiotics in Public Health Pathogens (Q38928353) (← links)
- Antimicrobial resistance in Mycobacterium tuberculosis: mechanistic and evolutionary perspectives. (Q39038482) (← links)
- Antagonism between Front-Line Antibiotics Clarithromycin and Amikacin in the Treatment of Mycobacterium abscessus Infections Is Mediated by the whiB7 Gene (Q40065950) (← links)
- In Silico Prediction of Antibiotic Resistance in Mycobacterium ulcerans Agy99 through Whole Genome Sequence Analysis (Q40117191) (← links)
- Acyldepsipeptide antibiotics kill mycobacteria by preventing the physiological functions of the ClpP1P2 protease (Q40776051) (← links)
- Aminoglycoside-modifying enzymes determine the innate susceptibility to aminoglycoside antibiotics in rapidly growing mycobacteria. (Q41532035) (← links)
- Susceptibility of Mycobacterium bovis BCG vaccine strains to antituberculous antibiotics (Q42111827) (← links)
- Recent progress towards understanding genetic variation in the Mycobacterium abscessus complex (Q42234240) (← links)
- Diversity and evolution of drug resistance mechanisms in Mycobacterium tuberculosis (Q42673180) (← links)
- Virtual screening and experimental verification to identify potential inhibitors of the ErmC methyltransferase responsible for bacterial resistance against macrolide antibiotics (Q46882307) (← links)
- Discovery of the first macrolide antibiotic binding protein in Mycobacterium tuberculosis: a new antibiotic resistance drug target (Q49924164) (← links)
- Whole genome sequence analysis of Mycobacterium bovis bacillus Calmette-Guérin (BCG) Tokyo 172: a comparative study of BCG vaccine substrains (Q51834838) (← links)
- Identification of N6,N6-Dimethyladenosine in Transfer RNA from Mycobacterium bovis Bacille Calmette-Guérin (Q57058346) (← links)