scholarly article | Q13442814 |
P50 | author | Sébastien Gagneux | Q47007290 |
Mireia Coscolla | Q56523288 | ||
P2093 | author name string | Mireilla Coscolla | |
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Variation among genome sequences of H37Rv strains of Mycobacterium tuberculosis from multiple laboratories | Q33962971 | ||
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Virulence of Mycobacterium tuberculosis CDC1551 and H37Rv in rabbits evaluated by Lurie's pulmonary tubercle count method. | Q34001917 | ||
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Lipids of putative relevance to virulence in Mycobacterium tuberculosis: correlation of virulence with elaboration of sulfatides and strongly acidic lipids | Q34102661 | ||
Massive gene duplication event among clinical isolates of the Mycobacterium tuberculosis W/Beijing family | Q34119298 | ||
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Genomic deletions suggest a phylogeny for the Mycobacterium tuberculosis complex | Q42679362 | ||
Association of Mycobacterium tuberculosis complex isolates of BOVIS and Central Asian (CAS) genotypic lineages with extrapulmonary disease | Q44131747 | ||
Clinical strains of Mycobacterium tuberculosis display a wide range of virulence in guinea pigs | Q44306950 | ||
Mycobacterium tuberculosis infection causes different levels of apoptosis and necrosis in human macrophages and alveolar epithelial cells. | Q44553442 | ||
Strain-related virulence of the dominant Mycobacterium tuberculosis strain in the Canadian province of Manitoba | Q44557232 | ||
Differential pattern of cytokine expression by macrophages infected in vitro with different Mycobacterium tuberculosis genotypes | Q44738814 | ||
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Guinea-pig alveolar macrophages kill Mycobacterium tuberculosis in vitro, but killing is independent of susceptibility to hydrogen peroxide or triggering of the respiratory burst | Q46231108 | ||
VIRULENCE IN THE GUINEA-PIG AND SUSCEPTIBLITY TO HYDROGEN PEROXIDE OF ISONIAZID-SENSITIVE TUBERCLE BACILLI FROM SOUTH INDIAN PATIENTS. | Q46299477 | ||
Diversity of in vitro cytokine responses by human macrophages to infection by mycobacterium tuberculosis strains | Q46361152 | ||
Absence of an association between Mycobacterium tuberculosis genotype and clinical features in children with tuberculous meningitis | Q46461006 | ||
VIRULENCE IN THE GUINEA-PIG, SUSCEPTIBILITY TO HYDROGEN PEROXIDE, AND CATALASE ACTIVITY OF ISONIAZID-SENSITIVE TUBERCLE BACILLI FROM SOUTH INDIAN AND BRITISH PATIENTS. | Q46799337 | ||
Hypervirulent M. tuberculosis W/Beijing strains upregulate type I IFNs and increase expression of negative regulators of the Jak-Stat pathway | Q46828227 | ||
Enhanced capacity of a widespread strain of Mycobacterium tuberculosis to grow in human macrophages | Q47328803 | ||
Association between the infectivity of Mycobacterium tuberculosis strains and their efficiency for extrarespiratory infection | Q47690978 | ||
Virulence of selected Mycobacterium tuberculosis clinical isolates in the rabbit model of meningitis is dependent on phenolic glycolipid produced by the bacilli | Q48864122 | ||
A mechanism of virulence: virulent Mycobacterium tuberculosis strain H37Rv, but not attenuated H37Ra, causes significant mitochondrial inner membrane disruption in macrophages leading to necrosis. | Q52569105 | ||
Virulent clinical isolates of Mycobacterium tuberculosis grow rapidly and induce cellular necrosis but minimal apoptosis in murine macrophages. | Q53610312 | ||
Mycobacterium tuberculosis, Beijing genotype strains not associated with radiological presentation of pulmonary tuberculosis. | Q53892460 | ||
Virulence, immunopathology and transmissibility of selected strains of Mycobacterium tuberculosis in a murine model. | Q54495954 | ||
Variable human minisatellite-like regions in the Mycobacterium tuberculosis genome | Q56834474 | ||
Molecular epidemiology of tuberculosis | Q57095977 | ||
Myths and misconceptions: the origin and evolution of Mycobacterium tuberculosis | Q57984677 | ||
Transmission of Tuberculosis in New York City -- An Analysis by DNA Fingerprinting and Conventional Epidemiologic Methods | Q58265072 | ||
Infection withMycobacterium tuberculosisBeijing Genotype Strains Is Associated with Polymorphisms inSLC11A1/NRAMP1in Indonesian Patients with Tuberculosis | Q58379339 | ||
Mycobacterium tuberculosis lipids regulate cytokines, TLR-2/4 and MHC class II expression in human macrophages | Q58608724 | ||
A glycolipid of hypervirulent tuberculosis strains that inhibits the innate immune response | Q59057817 | ||
In Vivo Phenotypic Dominance in Mouse Mixed Infections withMycobacterium tuberculosisClinical Isolates | Q60914355 | ||
Protein expression by a Beijing strain differs from that of another clinical isolate and Mycobacterium tuberculosis H37Rv | Q62084119 | ||
Colonisation by Streptococcus pneumoniae and Staphylococcus aureus in healthy children | Q63916849 | ||
An outbreak involving extensive transmission of a virulent strain of Mycobacterium tuberculosis | Q64133339 | ||
Virulence of tubercle bacilli isolated from patients with tuberculosis in Bangalore, India | Q70361424 | ||
Differences in mannose receptor-mediated uptake of lipoarabinomannan from virulent and attenuated strains of Mycobacterium tuberculosis by human macrophages | Q71755919 | ||
Prevention of pneumococcal disease by vaccination: does serotype replacement matter? | Q73176006 | ||
Temporal trends in the population structure of Bordetella pertussis during 1949-1996 in a highly vaccinated population | Q74587898 | ||
Pathogenic Mycobacterium tuberculosis evades apoptosis of host macrophages by release of TNF-R2, resulting in inactivation of TNF-alpha | Q77186410 | ||
Mycobacterium tuberculosis CDC1551 induces a more vigorous host response in vivo and in vitro, but is not more virulent than other clinical isolates | Q77823582 | ||
A comparison of the virulence in Guinea-pigs of south indian and British tubercle bacilli | Q78838887 | ||
Evolution, population structure, and phylogeography of genetically monomorphic bacterial pathogens | Q37266513 | ||
Clinical relevance of Mycobacterium tuberculosis plcD gene mutations | Q37282843 | ||
Role of the type III secretion system in a hypervirulent lineage of Bordetella bronchiseptica. | Q37333410 | ||
Drivers of tuberculosis epidemics: the role of risk factors and social determinants | Q37459996 | ||
Differential monocyte activation underlies strain-specific Mycobacterium tuberculosis pathogenesis | Q37521603 | ||
Group B streptococci escape host immunity by deletion of tandem repeat elements of the alpha C protein | Q37630658 | ||
Infectiousness, reproductive fitness and evolution of drug-resistant Mycobacterium tuberculosis. | Q37634147 | ||
Recent and rapid emergence of W-Beijing strains of Mycobacterium tuberculosis in Cape Town, South Africa | Q38424744 | ||
An assay to compare the infectivity of Mycobacterium tuberculosis isolates based on aerosol infection of guinea pigs and assessment of bacteriology | Q38447337 | ||
Comparison of strains of mycobacterium tuberculosis from british, ugandan and asian immigrant patients: A study in bacteriophage typing, susceptibility to hydrogen peroxide and sensitivity to thiophen-2-carbonic acid hydrazide | Q38893176 | ||
ALOX5 variants associated with susceptibility to human pulmonary tuberculosis | Q39064559 | ||
Virulence and Resistance to Superoxide, Low pH and Hydrogen Peroxide among Strains of Mycobacterium tuberculosis | Q39182715 | ||
The epidemiology of tuberculosis in San Francisco. A population-based study using conventional and molecular methods | Q39388568 | ||
The Correlation of Bacteriophage Types of Mycobacterium tuberculosis with Guinea-pig Virulence and In vitro-indicators of Virulence | Q39506456 | ||
Growth rate of mycobacteria in mice as an unreliable indicator of mycobacterial virulence. | Q39512426 | ||
Transmission of tuberculosis in a jail | Q39519951 | ||
Mycobacterium tuberculosis CDC1551 is resistant to reactive nitrogen and oxygen intermediates in vitro | Q39655566 | ||
Drug-resistant strains of Mycobacterium tuberculosis exhibit a range of virulence for mice | Q39821342 | ||
Mycobacterial growth and sensitivity to H2O2 killing in human monocytes in vitro | Q39831579 | ||
Reduced TNF-alpha and IFN-gamma responses to Central Asian strain 1 and Beijing isolates of Mycobacterium tuberculosis in comparison with H37Rv strain | Q39859674 | ||
Induction of cell death in human macrophages by a highly virulent Korean Isolate of Mycobacterium tuberculosis and the virulent strain H37Rv | Q39895901 | ||
Changing Mycobacterium tuberculosis population highlights clade-specific pathogenic characteristics. | Q40021876 | ||
The competitive cost of antibiotic resistance in Mycobacterium tuberculosis | Q40311130 | ||
Global phylogeny of Mycobacterium tuberculosis based on single nucleotide polymorphism (SNP) analysis: insights into tuberculosis evolution, phylogenetic accuracy of other DNA fingerprinting systems, and recommendations for a minimal standard SNP se | Q34303290 | ||
Stable association between strains of Mycobacterium tuberculosis and their human host populations | Q34308443 | ||
Mycobacterium tuberculosis Beijing genotype and risk for treatment failure and relapse, Vietnam | Q34555065 | ||
Snapshot of moving and expanding clones of Mycobacterium tuberculosis and their global distribution assessed by spoligotyping in an international study | Q34991344 | ||
Comparing genomes within the species Mycobacterium tuberculosis | Q35033207 | ||
Molecular epidemiology of tuberculosis: current insights | Q35070843 | ||
A deletion defining a common Asian lineage of Mycobacterium tuberculosis associates with immune subversion | Q35108344 | ||
Beijing genotype of Mycobacterium tuberculosis is significantly associated with human immunodeficiency virus infection and multidrug resistance in cases of tuberculous meningitis | Q35220932 | ||
Population-based study of deletions in five different genomic regions of Mycobacterium tuberculosis and possible clinical relevance of the deletions | Q35220950 | ||
Virulence ranking of some Mycobacterium tuberculosis and Mycobacterium bovis strains according to their ability to multiply in the lungs, induce lung pathology, and cause mortality in mice | Q35435985 | ||
Association between Mycobacterium tuberculosis Beijing/W lineage strain infection and extrathoracic tuberculosis: Insights from epidemiologic and clinical characterization of the three principal genetic groups of M. tuberculosis clinical isolates | Q35690557 | ||
The W-Beijing lineage of Mycobacterium tuberculosis overproduces triglycerides and has the DosR dormancy regulon constitutively upregulated | Q35759546 | ||
A recently evolved sublineage of the Mycobacterium tuberculosis Beijing strain family is associated with an increased ability to spread and cause disease | Q35784560 | ||
Silent nucleotide polymorphisms and a phylogeny for Mycobacterium tuberculosis | Q35872892 | ||
Virulence of a Mycobacterium tuberculosis clinical isolate in mice is determined by failure to induce Th1 type immunity and is associated with induction of IFN-alpha /beta | Q35894501 | ||
Beijing/W genotype Mycobacterium tuberculosis and drug resistance | Q36029451 | ||
Different Strains ofMycobacterium tuberculosisCause Various Spectrums of Disease in the Rabbit Model of Tuberculosis | Q36046773 | ||
Effects of genetic variability of Mycobacterium tuberculosis strains on the presentation of disease | Q36070678 | ||
Large sequence polymorphisms classify Mycobacterium tuberculosis strains with ancestral spoligotyping patterns. | Q36098732 | ||
Genetic susceptibility to mycobacterial disease in humans | Q36414900 | ||
Relationship between Mycobacterium tuberculosis genotype and the clinical phenotype of pulmonary and meningeal tuberculosis | Q36539881 | ||
The emergence of Beijing family genotypes of Mycobacterium tuberculosis and low-level protection by bacille Calmette-Guérin (BCG) vaccines: is there a link? | Q36565187 | ||
Mycobacterium bovis BCG vaccine strains lack narK2 and narX induction and exhibit altered phenotypes during dormancy | Q36710576 | ||
The phenolic glycolipid of Mycobacterium tuberculosis differentially modulates the early host cytokine response but does not in itself confer hypervirulence | Q36747037 | ||
Global phylogeography of Mycobacterium tuberculosis and implications for tuberculosis product development. | Q36797710 | ||
Disseminated disease severity as a measure of virulence of Mycobacterium tuberculosis in the guinea pig model | Q36948262 | ||
Growth characteristics of recent sputum isolates of Mycobacterium tuberculosis in guinea pigs infected by the respiratory route | Q36970963 | ||
Progression to active tuberculosis, but not transmission, varies by Mycobacterium tuberculosis lineage in The Gambia | Q37001570 | ||
Mycobacterium tuberculosis Beijing genotype emerging in Vietnam | Q37093922 | ||
Vaccine-induced immunity circumvented by typical Mycobacterium tuberculosis Beijing strains. | Q37133287 | ||
Major Mycobacterium tuberculosis lineages associate with patient country of origin | Q37156812 | ||
Use of spoligotyping and large sequence polymorphisms to study the population structure of the Mycobacterium tuberculosis complex in a cohort study of consecutive smear-positive tuberculosis cases in The Gambia | Q37156954 | ||
The clinical consequences of strain diversity in Mycobacterium tuberculosis | Q37177756 | ||
Systems biology of persistent infection: tuberculosis as a case study | Q37184399 | ||
P433 | issue | 1 | |
P921 | main subject | Mycobacterium tuberculosis | Q130971 |
tuberculosis | Q12204 | ||
biodiversity | Q47041 | ||
P304 | page(s) | e43-e59 | |
P577 | publication date | 2010-01-01 | |
P1433 | published in | Drug discovery today. Disease mechanisms | Q27721894 |
P1476 | title | Does M. tuberculosis genomic diversity explain disease diversity? | |
P478 | volume | 7 |
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