Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 37

1.

Structure-Function Studies of the Bacillus subtilis Ric Proteins Identify the Fe-S Cluster-Ligating Residues and Their Roles in Development and RNA Processing.

Adusei-Danso F, Khaja FT, DeSantis M, Jeffrey PD, Dubnau E, Demeler B, Neiditch MB, Dubnau D.

mBio. 2019 Sep 17;10(5). pii: e01841-19. doi: 10.1128/mBio.01841-19.

2.

A protein complex supports the production of Spo0A-P and plays additional roles for biofilms and the K-state in Bacillus subtilis.

Dubnau EJ, Carabetta VJ, Tanner AW, Miras M, Diethmaier C, Dubnau D.

Mol Microbiol. 2016 Aug;101(4):606-24. doi: 10.1111/mmi.13411. Epub 2016 Jun 2.

3.

Cholesterol is not an essential source of nutrition for Mycobacterium tuberculosis during infection.

Yang X, Gao J, Smith I, Dubnau E, Sampson NS.

J Bacteriol. 2011 Mar;193(6):1473-6. doi: 10.1128/JB.01210-10. Epub 2011 Jan 21.

4.

A thiolase of Mycobacterium tuberculosis is required for virulence and production of androstenedione and androstadienedione from cholesterol.

Nesbitt NM, Yang X, Fontán P, Kolesnikova I, Smith I, Sampson NS, Dubnau E.

Infect Immun. 2010 Jan;78(1):275-82. doi: 10.1128/IAI.00893-09. Epub 2009 Oct 12.

5.

Cholesterol metabolism increases the metabolic pool of propionate in Mycobacterium tuberculosis.

Yang X, Nesbitt NM, Dubnau E, Smith I, Sampson NS.

Biochemistry. 2009 May 12;48(18):3819-21. doi: 10.1021/bi9005418.

6.

Rv1106c from Mycobacterium tuberculosis is a 3beta-hydroxysteroid dehydrogenase.

Yang X, Dubnau E, Smith I, Sampson NS.

Biochemistry. 2007 Aug 7;46(31):9058-67. Epub 2007 Jul 14.

7.

The Mycobacterium tuberculosis PhoPR two-component system regulates genes essential for virulence and complex lipid biosynthesis.

Walters SB, Dubnau E, Kolesnikova I, Laval F, Daffe M, Smith I.

Mol Microbiol. 2006 Apr;60(2):312-30.

8.

responses of mycobacterium tuberculosis to growth in the mouse lung.

Dubnau E, Chan J, Mohan VP, Smith I.

Infect Immun. 2005 Jun;73(6):3754-7.

9.

Mycobacterium tuberculosis gene expression in macrophages.

Dubnau E, Smith I.

Microbes Infect. 2003 Jun;5(7):629-37. Review.

PMID:
12787739
10.

Role of the extracytoplasmic-function sigma factor sigma(H) in Mycobacterium tuberculosis global gene expression.

Manganelli R, Voskuil MI, Schoolnik GK, Dubnau E, Gomez M, Smith I.

Mol Microbiol. 2002 Jul;45(2):365-74.

11.

Mycobacterium tuberculosis genes induced during infection of human macrophages.

Dubnau E, Fontán P, Manganelli R, Soares-Appel S, Smith I.

Infect Immun. 2002 Jun;70(6):2787-95.

12.

Oxygenated mycolic acids are necessary for virulence of Mycobacterium tuberculosis in mice.

Dubnau E, Chan J, Raynaud C, Mohan VP, Lanéelle MA, Yu K, Quémard A, Smith I, Daffé M.

Mol Microbiol. 2000 May;36(3):630-7.

13.

Differential expression of 10 sigma factor genes in Mycobacterium tuberculosis.

Manganelli R, Dubnau E, Tyagi S, Kramer FR, Smith I.

Mol Microbiol. 1999 Jan;31(2):715-24.

14.

Mutations in the cmaB gene are responsible for the absence of methoxymycolic acid in Mycobacterium bovis BCG Pasteur.

Dubnau E, Marrakchi H, Smith I, Daffé M, Quémard A.

Mol Microbiol. 1998 Sep;29(6):1526-8. No abstract available.

15.

Structure of a hydroxymycolic acid potentially involved in the synthesis of oxygenated mycolic acids of the Mycobacterium tuberculosis complex.

Quémard A, Lanéelle MA, Marrakchi H, Promé D, Dubnau E, Daffé M.

Eur J Biochem. 1997 Dec 15;250(3):758-63.

16.

Mycobacterium bovis BCG genes involved in the biosynthesis of cyclopropyl keto- and hydroxy-mycolic acids.

Dubnau E, Lanéelle MA, Soares S, Bénichou A, Vaz T, Promé D, Promé JC, Daffé M, Quémard A.

Mol Microbiol. 1997 Jan;23(2):313-22.

18.

inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis.

Banerjee A, Dubnau E, Quemard A, Balasubramanian V, Um KS, Wilson T, Collins D, de Lisle G, Jacobs WR Jr.

Science. 1994 Jan 14;263(5144):227-30.

PMID:
8284673
19.

Early spo gene expression in Bacillus subtilis: the role of interrelated signal transduction systems.

Smith I, Dubnau E, Predich M, Bai U, Rudner R.

Biochimie. 1992 Jul-Aug;74(7-8):669-78.

PMID:
1391046
20.

Regulation of spo0H, a gene coding for the Bacillus subtilis sigma H factor.

Weir J, Predich M, Dubnau E, Nair G, Smith I.

J Bacteriol. 1991 Jan;173(2):521-9.

21.

Temporal regulation of the Bacillus subtilis early sporulation gene spo0F.

Bai U, Lewandoski M, Dubnau E, Smith I.

J Bacteriol. 1990 Sep;172(9):5432-9.

23.

Bacillus sporulation gene spo0H codes for sigma 30 (sigma H).

Dubnau E, Weir J, Nair G, Carter L 3rd, Moran C Jr, Smith I.

J Bacteriol. 1988 Mar;170(3):1054-62.

24.

Regulation of spo0H, an early sporulation gene in bacilli.

Dubnau EJ, Cabane K, Smith I.

J Bacteriol. 1987 Mar;169(3):1182-91.

25.
26.

Transcriptional regulation of the spo0F gene of Bacillus subtilis.

Lewandoski M, Dubnau E, Smith I.

J Bacteriol. 1986 Nov;168(2):870-7.

27.

The complete DNA sequence and regulatory regions of the Bacillus licheniformis spoOH gene.

Ramakrishna N, Dubnau E, Smith I.

Nucleic Acids Res. 1984 Feb 24;12(4):1779-90.

28.

Bacillus subtilis spo0H gene.

Weir J, Dubnau E, Ramakrishna N, Smith I.

J Bacteriol. 1984 Feb;157(2):405-12.

29.

Cloning of an early sporulation gene in Bacillus subtilis.

Dubnau E, Ramakrishna N, Cabane K, Smith I.

J Bacteriol. 1981 Aug;147(2):622-32.

30.

Genetics and physiology of the rel system of Bacillus subtilis.

Smith I, Paress P, Cabane K, Dubnau E.

Mol Gen Genet. 1980;178(2):271-9.

PMID:
6248722
31.

Conditional mutations in the translational apparatus of Bacillus subtils.

Dubnau E, Pifko S, Sloma A, Cabane K, Smith I.

Mol Gen Genet. 1976 Aug 10;147(1):1-12.

PMID:
822278
32.

Nonsense mutations of the supX locus: further characterization of the supX mutant phenotype.

Dubnau E, Lenny AB, Margolin P.

Mol Gen Genet. 1973 Nov 12;126(3):191-200. No abstract available.

PMID:
4593755
33.

Suppression of promoter mutations by the pleiotropic supx mutations.

Dubnau E, Margolin P.

Mol Gen Genet. 1972;117(2):91-112. No abstract available.

PMID:
4561426
34.

Inactivation of a newly transferred gene in recombination-deficient recipients of Escherichia coli.

Dubnau E, Maas WK.

Mol Gen Genet. 1969;103(4):305-12. No abstract available.

PMID:
4896140
35.
36.

Behavior of three colicine factors and an R (drug resistance) factor in Hfr crosses in Salmonella typhimurium.

Dubnau E, Stocker BA.

Genet Res. 1967 Jun;9(3):283-97. No abstract available.

PMID:
4863199
37.

GENETICS OF PLASMIDS IN SALMONELLA TYPHIMURIUM.

DUBNAU E, STOCKER BA.

Nature. 1964 Dec 12;204:1112-3. No abstract available.

PMID:
14243403

Supplemental Content

Loading ...
Support Center