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Items: 1 to 20 of 90

1.

Mce3R, a TetR-type transcriptional repressor, controls the expression of a regulon involved in lipid metabolism in Mycobacterium tuberculosis.

de la Paz Santangelo M, Klepp L, Nuñez-García J, Blanco FC, Soria M, García-Pelayo MC, Bianco MV, Cataldi AA, Golby P, Jackson M, Gordon SV, Bigi F.

Microbiology. 2009 Jul;155(Pt 7):2245-55. doi: 10.1099/mic.0.027086-0. Epub 2009 Apr 23.

PMID:
19389781
2.

Study of the role of Mce3R on the transcription of mce genes of Mycobacterium tuberculosis.

Santangelo MP, Blanco FC, Bianco MV, Klepp LI, Zabal O, Cataldi AA, Bigi F.

BMC Microbiol. 2008 Feb 27;8:38. doi: 10.1186/1471-2180-8-38.

3.

Regulation of the Escherichia coli allantoin regulon: coordinated function of the repressor AllR and the activator AllS.

Rintoul MR, Cusa E, Baldomà L, Badia J, Reitzer L, Aguilar J.

J Mol Biol. 2002 Dec 6;324(4):599-610.

PMID:
12460564
5.
6.

Negative transcriptional regulation of the mce3 operon in Mycobacterium tuberculosis.

Santangelo MP, Goldstein J, Alito A, Gioffré A, Caimi K, Zabal O, Zumárraga M, Romano MI, Cataldi AA, Bigi F.

Microbiology. 2002 Oct;148(Pt 10):2997-3006.

PMID:
12368433
7.

Comparison of mammalian cell entry operons of mycobacteria: in silico analysis and expression profiling.

Kumar A, Chandolia A, Chaudhry U, Brahmachari V, Bose M.

FEMS Immunol Med Microbiol. 2005 Feb 1;43(2):185-95.

8.

A highly conserved transcriptional repressor controls a large regulon involved in lipid degradation in Mycobacterium smegmatis and Mycobacterium tuberculosis.

Kendall SL, Withers M, Soffair CN, Moreland NJ, Gurcha S, Sidders B, Frita R, Ten Bokum A, Besra GS, Lott JS, Stoker NG.

Mol Microbiol. 2007 Aug;65(3):684-99.

9.

Mycobacterium tuberculosis mammalian cell entry operon (mce) homologs in Mycobacterium other than tuberculosis (MOTT).

Haile Y, Caugant DA, Bjune G, Wiker HG.

FEMS Immunol Med Microbiol. 2002 Jun 3;33(2):125-32.

10.
11.

Mammalian cell-entry proteins encoded by the mce3 operon of Mycobacterium tuberculosis are expressed during natural infection in humans.

Ahmad S, El-Shazly S, Mustafa AS, Al-Attiyah R.

Scand J Immunol. 2004 Oct;60(4):382-91. Erratum in: Scand J Immunol. 2005 Mar;61(3):297.

12.

Identification and characterization of two divergently transcribed iron regulated genes in Mycobacterium tuberculosis.

Rodriguez GM, Gold B, Gomez M, Dussurget O, Smith I.

Tuber Lung Dis. 1999;79(5):287-98. Erratum in: Tuber Lung Dis 1999;79(6):382.

PMID:
10707257
15.

Mce2R from Mycobacterium tuberculosis represses the expression of the mce2 operon.

Santangelo Mde L, Blanco F, Campos E, Soria M, Bianco MV, Klepp L, Alito A, Zabal O, Cataldi A, Bigi F.

Tuberculosis (Edinb). 2009 Jan;89(1):22-8. doi: 10.1016/j.tube.2008.09.002. Epub 2008 Nov 22.

PMID:
19027363
16.

Transcriptional regulation of stress response and motility functions in Helicobacter pylori is mediated by HspR and HrcA.

Roncarati D, Danielli A, Spohn G, Delany I, Scarlato V.

J Bacteriol. 2007 Oct;189(20):7234-43. Epub 2007 Aug 10.

17.
18.

Arginine regulon of Escherichia coli K-12. A study of repressor-operator interactions and of in vitro binding affinities versus in vivo repression.

Charlier D, Roovers M, Van Vliet F, Boyen A, Cunin R, Nakamura Y, Glansdorff N, Piérard A.

J Mol Biol. 1992 Jul 20;226(2):367-86.

PMID:
1640456
19.

The DtxR regulon of Corynebacterium glutamicum.

Wennerhold J, Bott M.

J Bacteriol. 2006 Apr;188(8):2907-18.

20.

Bacillus subtilis LmrA is a repressor of the lmrAB and yxaGH operons: identification of its binding site and functional analysis of lmrB and yxaGH.

Yoshida K, Ohki YH, Murata M, Kinehara M, Matsuoka H, Satomura T, Ohki R, Kumano M, Yamane K, Fujita Y.

J Bacteriol. 2004 Sep;186(17):5640-8.

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