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Results: 1 to 20 of 118

1.

Integrin αvβ3 acting as membrane receptor for thyroid hormones mediates angiogenesis in malignant T cells.

Cayrol F, Díaz Flaqué MC, Fernando T, Yang SN, Sterle HA, Bolontrade M, Amorós M, Isse B, Farías RN, Ahn H, Tian YF, Tabbò F, Singh A, Inghirami G, Cerchietti L, Cremaschi GA.

Blood. 2015 Jan 29;125(5):841-51. doi: 10.1182/blood-2014-07-587337. Epub 2014 Dec 8.

PMID:
25488971
2.

Thyroid hormones-membrane interaction: reversible association of hormones with organized phospholipids with changes in fluidity and dipole potential.

Issé BA, Yunes Quartino P, Fidelio GD, Farías RN.

Chem Phys Lipids. 2013 Oct-Nov;175-176:131-7. doi: 10.1016/j.chemphyslip.2013.08.007. Epub 2013 Sep 30.

PMID:
24091073
3.

Macrophage environment turns otherwise MccJ25-resistant Salmonella into sensitive.

Pomares MF, Corbalán NS, Adler C, de Cristóbal R, Farías RN, Delgado MA, Vincent PA.

BMC Microbiol. 2013 May 1;13:95. doi: 10.1186/1471-2180-13-95.

4.

Cu(II)-reduction by Escherichia coli cells is dependent on respiratory chain components.

Volentini SI, Farías RN, Rodríguez-Montelongo L, Rapisarda VA.

Biometals. 2011 Oct;24(5):827-35. doi: 10.1007/s10534-011-9436-3. Epub 2011 Mar 10.

PMID:
21390523
5.

Cooperative nongenomic and genomic actions on thyroid hormone mediated-modulation of T cell proliferation involve up-regulation of thyroid hormone receptor and inducible nitric oxide synthase expression.

Barreiro Arcos ML, Sterle HA, Paulazo MA, Valli E, Klecha AJ, Isse B, Pellizas CG, Farias RN, Cremaschi GA.

J Cell Physiol. 2011 Dec;226(12):3208-18. doi: 10.1002/jcp.22681.

PMID:
21344381
6.

Redox-active tyrosine residue in the microcin J25 molecule.

Chalón MC, Wilke N, Pedersen J, Rufini S, Morero RD, Cortez L, Chehín RN, Farias RN, Vincent PA.

Biochem Biophys Res Commun. 2011 Mar 18;406(3):366-70. doi: 10.1016/j.bbrc.2011.02.047. Epub 2011 Feb 15.

PMID:
21329661
7.

Sensitization of microcin J25-resistant strains by a membrane-permeabilizing peptide.

Pomares MF, Delgado MA, Corbalán NS, Farías RN, Vincent PA.

Appl Environ Microbiol. 2010 Oct;76(20):6837-42. doi: 10.1128/AEM.00307-10. Epub 2010 Aug 27.

8.

Glyceraldehyde-3-phosphate dehydrogenase tetramer dissociation and amyloid fibril formation induced by negatively charged membranes.

Cortez LM, Avila CL, Bugeau CM, Farías RN, Morero RD, Chehín RN.

FEBS Lett. 2010 Feb 5;584(3):625-30. doi: 10.1016/j.febslet.2009.12.012. Epub 2009 Dec 13.

9.

Tyrosine 9 is the key amino acid in microcin J25 superoxide overproduction.

Chalon MC, Bellomio A, Solbiati JO, Morero RD, Farias RN, Vincent PA.

FEMS Microbiol Lett. 2009 Nov;300(1):90-6. doi: 10.1111/j.1574-6968.2009.01770.x. Epub 2009 Aug 28.

10.

Protective effect of 3,5,3'-triiodothyroacetic and 3,5,3',5'-tetraiodothyroacetic acids on serum albumin fibrillation.

Cortez LM, Farías RN, Chehín RN.

Eur Biophys J. 2009 Sep;38(7):857-63. doi: 10.1007/s00249-009-0448-7. Epub 2009 Apr 18.

PMID:
19381627
11.

Phosphate-enhanced stationary-phase fitness of Escherichia coli is related to inorganic polyphosphate level.

Schurig-Briccio LA, Farías RN, Rintoul MR, Rapisarda VA.

J Bacteriol. 2009 Jul;191(13):4478-81. doi: 10.1128/JB.00082-09. Epub 2009 Apr 17.

12.

Protection against oxidative stress in Escherichia coli stationary phase by a phosphate concentration-dependent genes expression.

Schurig-Briccio LA, Farías RN, Rodríguez-Montelongo L, Rintoul MR, Rapisarda VA.

Arch Biochem Biophys. 2009 Mar 1;483(1):106-10. doi: 10.1016/j.abb.2008.12.009. Epub 2008 Dec 27.

PMID:
19138658
13.

A critical phosphate concentration in the stationary phase maintains ndh gene expression and aerobic respiratory chain activity in Escherichia coli.

Schurig-Briccio LA, Rintoul MR, Volentini SI, Farías RN, Baldomà L, Badía J, Rodríguez-Montelongo L, Rapisarda VA.

FEMS Microbiol Lett. 2008 Jul;284(1):76-83. doi: 10.1111/j.1574-6968.2008.01188.x. Epub 2008 May 17.

14.

Protective action of ppGpp in microcin J25-sensitive strains.

Pomares MF, Vincent PA, Farías RN, Salomón RA.

J Bacteriol. 2008 Jun;190(12):4328-34. doi: 10.1128/JB.00183-08. Epub 2008 Apr 11.

15.

Microcin J25 has dual and independent mechanisms of action in Escherichia coli: RNA polymerase inhibition and increased superoxide production.

Bellomio A, Vincent PA, de Arcuri BF, Farías RN, Morero RD.

J Bacteriol. 2007 Jun;189(11):4180-6. Epub 2007 Mar 30.

16.

Linear array of conserved sequence motifs to discriminate protein subfamilies: study on pyridine nucleotide-disulfide reductases.

Avila CL, Rapisarda VA, Farías RN, De Las Rivas J, Chehín R.

BMC Bioinformatics. 2007 Mar 16;8:96.

17.

Efficacy of microcin J25 in biomatrices and in a mouse model of Salmonella infection.

Lopez FE, Vincent PA, Zenoff AM, Salomón RA, Farías RN.

J Antimicrob Chemother. 2007 Apr;59(4):676-80. Epub 2007 Mar 12.

18.

Molecular view by fourier transform infrared spectroscopy of the relationship between lactocin 705 and membranes: speculations on antimicrobial mechanism.

Castellano P, Vignolo G, Farías RN, Arrondo JL, Chehín R.

Appl Environ Microbiol. 2007 Jan;73(2):415-20. Epub 2006 Oct 27.

19.

The Cu(II)-reductase NADH dehydrogenase-2 of Escherichia coli improves the bacterial growth in extreme copper concentrations and increases the resistance to the damage caused by copper and hydroperoxide.

Rodríguez-Montelongo L, Volentini SI, Farías RN, Massa EM, Rapisarda VA.

Arch Biochem Biophys. 2006 Jul 1;451(1):1-7. Epub 2006 May 17.

PMID:
16759635
20.

Microcin J25 uptake: His5 of the MccJ25 lariat ring is involved in interaction with the inner membrane MccJ25 transporter protein SbmA.

de Cristóbal RE, Solbiati JO, Zenoff AM, Vincent PA, Salomón RA, Yuzenkova J, Severinov K, Farías RN.

J Bacteriol. 2006 May;188(9):3324-8.

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