Are the PE‐PGRS proteins of Mycobacterium tuberculosis variable surface antigens?
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Sayera Banu | M. Prevost | S. Cole | N. Honoré | D. Philpott | S. Banu | Marie‐Christine Prévost | Dana Philpott | Stewart T. Cole | Nadine Honoré | Brigitte Saint‐Joanis | B. Saint‐Joanis
[1] J. Ulmer,et al. Immunization with DNA. , 1994, Journal of immunological methods.
[2] B. Barrell,et al. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.
[3] S T Cole,et al. Learning from the genome sequence of Mycobacterium tuberculosis H37Rv , 1999, FEBS letters.
[4] M. Chaussee,et al. Characterization of the recD gene of Neisseria gonorrhoeae MS11 and the effect of recD inactivation on pilin variation and DNA transformation. , 1999, Microbiology.
[5] Michael Gribskov,et al. Combining evidence using p-values: application to sequence homology searches , 1998, Bioinform..
[6] M B Hinman,et al. Synthetic spider silk: a modular fiber. , 2000, Trends in biotechnology.
[7] N. Federspiel,et al. Granuloma-specific expression of Mycobacterium virulence proteins from the glycine-rich PE-PGRS family. , 2000, Science.
[8] P. Andersen,et al. Mapping and identification of Mycobacterium tuberculosis proteins by two‐dimensional gel electrophoresis, microsequencing and immunodetection , 2000, Electrophoresis.
[9] H. Seifert,et al. Comparisons between Colony Phase Variation ofNeisseria gonorrhoeae FA1090 and Pilus, Pilin, and S-Pilin Expression , 1998, Infection and Immunity.
[10] T. Whittam,et al. Restricted structural gene polymorphism in the Mycobacterium tuberculosis complex indicates evolutionarily recent global dissemination. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[11] B. Robertson,et al. Genetic variation in pathogenic bacteria. , 1992, Trends in genetics : TIG.
[12] S. Cole,et al. Use of site-directed mutagenesis to probe the structure, function and isoniazid activation of the catalase/peroxidase, KatG, from Mycobacterium tuberculosis. , 1999, The Biochemical journal.
[13] C. Wills,et al. DNA microsatellites: agents of evolution? , 1999, Scientific American.
[14] K. Papavinasasundaram,et al. Expression of a Gene for a Porin-Like Protein of the OmpA Family from Mycobacterium tuberculosisH37Rv , 1998, Journal of bacteriology.
[15] B. Barrell,et al. Use of a Mycobacterium tuberculosisH37Rv Bacterial Artificial Chromosome Library for Genome Mapping, Sequencing, and Comparative Genomics , 1998, Infection and Immunity.
[16] T. Meyer,et al. Variation and control of protein expression in Neisseria. , 1990, Annual Review of Microbiology.
[17] J. Betts,et al. Comparison of the proteome of Mycobacterium tuberculosis strain H37Rv with clinical isolate CDC 1551. , 2000, Microbiology.
[18] J. Laclette,et al. The PE-PGRS glycine-rich proteins of Mycobacterium tuberculosis: a new family of fibronectin-binding proteins? , 1999, Microbiology.
[19] S. H. Kaufmann,et al. Comparative proteome analysis of Mycobacterium tuberculosis and Mycobacterium bovis BCG strains: towards functional genomics of microbial pathogens , 1999, Molecular microbiology.
[20] B. Ross,et al. Molecular cloning of a highly repeated DNA element from Mycobacterium tuberculosis and its use as an epidemiological tool , 1992, Journal of clinical microbiology.
[21] S. Cole,et al. Characterization of the highly abundant polymorphic GC-rich-repetitive sequence (PGRS) present in Mycobacterium tuberculosis , 1995, Archives of Microbiology.
[22] F. Plummer,et al. Bacterial antigenic variation, host immune response, and pathogen-host coevolution , 1993, Infection and immunity.
[23] R. Lathigra,et al. Genetic and immunological analysis of Mycobacterium tuberculosis fibronectin-binding proteins , 1991, Infection and immunity.
[24] T. Meyer,et al. Common mechanism controlling phase and antigenic variation in pathogenic Neisseriae , 1987, Molecular microbiology.
[25] M. Brennan,et al. Comparative Immune Response to PE and PE_PGRS Antigens of Mycobacterium tuberculosis , 2001, Infection and Immunity.
[26] J. Ulmer,et al. Heterologous protection against influenza by injection of DNA encoding a viral protein. , 1993, Science.
[27] Stefan Imreh,et al. Inhibition of antigen processing by the internal repeat region of the EpsteinBarr virus nuclear antigen-1 , 1995, Nature.
[28] Donna L. Montgomery,et al. Immunogenicity and protective efficacy of a tuberculosis DNA vaccine , 1996, Nature Medicine.
[29] S T Cole,et al. Analysis of the proteome of Mycobacterium tuberculosis in silico. , 1999, Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.
[30] P. E. M. Fine,et al. Variation in protection by BCG: implications of and for heterologous immunity , 1995, The Lancet.
[31] S T Cole,et al. Analysis of the genome of Mycobacterium tuberculosis H37Rv. , 1998, Novartis Foundation symposium.
[32] S. Laal,et al. Antigens of Mycobacterium tuberculosis Expressed during Preclinical Tuberculosis: Serological Immunodominance of Proteins with Repetitive Amino Acid Sequences , 2001, Infection and Immunity.
[33] S. Norris,et al. Genetic Variation of the Borrelia burgdorferi Gene vlsE Involves Cassette-Specific, Segmental Gene Conversion , 1998, Infection and Immunity.
[34] B. Heym,et al. Implications of multidrug resistance for the future of short-course chemotherapy of tuberculosis: a molecular study , 1994, The Lancet.
[35] D van Soolingen,et al. Comparison of various repetitive DNA elements as genetic markers for strain differentiation and epidemiology of Mycobacterium tuberculosis , 1993, Journal of clinical microbiology.
[36] J. Gilsdorf. Antigenic Diversity and Gene Polymorphisms inHaemophilus influenzae , 1998, Infection and Immunity.
[37] H. Towbin,et al. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[38] W. Jacobs,et al. An integrated map of the genome of the tubercle bacillus, Mycobacterium tuberculosis H37Rv, and comparison with Mycobacterium leprae. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[39] J. Shiver,et al. Heterologous and homologous protection against influenza A by DNA vaccination: optimization of DNA vectors. , 1993, DNA and cell biology.
[40] P. Brennan,et al. Peptidoglycan-associated polypeptides of Mycobacterium tuberculosis , 1990, Journal of bacteriology.
[41] Charles Elkan,et al. Fitting a Mixture Model By Expectation Maximization To Discover Motifs In Biopolymer , 1994, ISMB.
[42] V. Fischetti,et al. Size variation in group A streptococcal M protein is generated by homologous recombination between intragenic repeats , 1987, Molecular and General Genetics MGG.
[43] P. Brennan,et al. Characterization of the major membrane protein of virulent Mycobacterium tuberculosis , 1992, Infection and immunity.
[44] H. Davis,et al. DNA-based immunization induces continuous secretion of hepatitis B surface antigen and high levels of circulating antibody. , 1993, Human molecular genetics.
[45] J. Gilsdorf,et al. Immunologic and Structural Relationships of the Minor Pilus Subunits among Haemophilus influenzaeIsolates , 1998, Infection and Immunity.
[46] S T Cole,et al. Use of an ordered cosmid library to deduce the genomic organization of Mycobacterium leprae , 1993, Molecular microbiology.
[47] A Ciechanover,et al. Inhibition of ubiquitin/proteasome-dependent protein degradation by the Gly-Ala repeat domain of the Epstein-Barr virus nuclear antigen 1. , 1997, Proceedings of the National Academy of Sciences of the United States of America.