A genomic library-based amplification approach (GL-PCR) for the mapping of multiple IS6110 insertion sites and strain differentiation of Mycobacterium tuberculosis-Reference-Cited by-同舟云学术

A genomic library-based amplification approach (GL-PCR) for the mapping of multiple IS6110 insertion sites and strain differentiation of Mycobacterium tuberculosis

Published:2006-11 Issue:2 Volume:67 Page:202-211
ISSN:0167-7012
Container-title:Journal of Microbiological Methods
language:en
Short-container-title:Journal of Microbiological Methods

Author:

Namouchi Amine,Mardassi Helmi

Publisher

Elsevier BV

Subject

Microbiology (medical),Molecular Biology,Microbiology

Reference36 articles.

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4. Evidence that mycobacterial PE_PGRS proteins are cell surface constituents that influence interactions with other cells;Brennan;Infect. Immun.,2001

5. Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain;Brosch;Infect. Immun.,1999

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1. Functional genetic variation in pe/ppe genes contributes to diversity in Mycobacterium tuberculosis lineages and potential interactions with the human host;Frontiers in Microbiology;2023-10-09

2. Transposition mechanism, molecular characterization and evolution of IS6110, the specific evolutionary marker of Mycobacterium tuberculosis complex;Molecular Biology Reports;2016-10-20

3. IS6110-5′3′FP: an automated typing approach for Mycobacterium tuberculosis complex strains simultaneously targeting and resolving IS6110 5′ and 3′ polymorphisms;International Journal of Infectious Diseases;2014-12

4. IS-seq: a novel high throughput survey of in vivo IS6110 transposition in multiple Mycobacterium tuberculosis genomes;BMC Genomics;2012-06-15

5. Comparative Analysis of Mycobacterium tuberculosis pe and ppe Genes Reveals High Sequence Variation and an Apparent Absence of Selective Constraints;PLoS ONE;2012-04-04