Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Dolors Balsa"'
Autor:
Elvira Bailón, Juan Román, Isabel Ramis, Pedro Michelena, Dolors Balsa, Manuel Merlos, Antonio Zarzuelo, Julio Gálvez, Mònica Comalada
Publikováno v:
Journal of Pharmacological Sciences, Vol 109, Iss 2, Pp 315-318 (2009)
The aim of the present study was to evaluate the inmunomodulatory effects of UR-1505, a new salicylate derivative, on the T helper (Th)2 / humoral response produced during dextran sodium sulfate (DSS)-induced rat colitis. In the in vitro studies, UR-
Externí odkaz:
https://doaj.org/article/3bd372bc9ae4413bb44c5924ef51f0b6
Autor:
David Calzada, Tamara Aranda, Marta Escutia, Dolors Balsa, Francisca Alvarez, Cristobalina Mayorga, María Salas, Maria Antonia Odena, Eliandre Oliveira, Mariona Pascal
Publikováno v:
Journal of Allergy and Clinical Immunology. 149:AB47
Autor:
Juan Román, Antonio Zarzuelo, Julio Gálvez, Jordi Xaus, Manuel Merlos, Margarita Cueto-Sola, B Arribas, Desirée Camuesco, Natividad Garrido-Mesa, Mònica Comalada, G Janer, Dolors Balsa, Elvira Bailón, María Elena Rodríguez-Cabezas
Publikováno v:
British Journal of Pharmacology. 165:729-740
BACKGROUND AND PURPOSE Dersalazine sodium (DS) is a new chemical entity formed by combining, through an azo bond, a potent platelet activating factor (PAF) antagonist (UR-12715) with 5-aminosalicylic acid (5-ASA). DS has been demonstrated to have ant
Publikováno v:
Plasmid; Vol 63
Plasmid
Plasmid
The emergence and spread of pathogenic bacteria that have become resistant to multiple antibiotics through lateral gene transfer have created the need of novel antimicrobials. Toxin-antitoxin (TA) modules, which have been implicated in plasmid mainte
Autor:
Dolors Balsa, M Ballarín, C. Salcedo, S Pérez-del-Pulgar, S Davalillo, J Cabellos, A.G. Fernández, Carmen Lagunas
Publikováno v:
British Journal of Pharmacology. 156:807-817
Background and purpose: Highly selective M3 muscarinic receptor antagonists may represent a better treatment for overactive bladder syndrome, diminishing side effects. Cardiac side effects of non-selective antimuscarinics have been associated with ac
Autor:
Julio Gálvez, Mònica Comalada, Manuel Merlos, Antonio Zarzuelo, Dolors Balsa, Pedro Michelena, Isabel Ramis, Juan Román, Elvira Bailón
Publikováno v:
Journal of Pharmacological Sciences, Vol 109, Iss 2, Pp 315-318 (2009)
The aim of the present study was to evaluate the inmunomodulatory effects of UR-1505, a new salicylate derivative, on the T helper (Th)2 / humoral response produced during dextran sodium sulfate (DSS)-induced rat colitis. In the in vitro studies, UR-
Publikováno v:
Journal of Neural Transmission. 114:707-712
It has been accepted that, as required mechanistically, the neutral form of the amine is the substrate for monoamine oxidase, despite the amine pK (a) of above 9.5. The pH dependence of the kinetic parameters for kynuramine oxidation by purified huma
Publikováno v:
FEMS Microbiology Reviews
Type II (proteic) toxin–antitoxin (TA) operons are widely spread in bacteria and archaea. They are organized as operons in which, usually, the antitoxin gene precedes the cognate toxin gene. The antitoxin generally acts as a transcriptional self-re
Autor:
Manuel Espinosa, Suzanne K. Christensen, Concha Nieto, Dolors Balsa, Teresa Pellicer, Kenn Gerdes
Publikováno v:
Molecular Microbiology. 59:1280-1296
Proteic toxin-antitoxin (TA) loci were first identified in bacterial plasmids, and they were regarded as involved in stable plasmid maintenance by a so-called 'addiction' mechanism. Later, chromosomally encoded TA loci were identified and their funct
Autor:
Juan C. Alonso, Dolors Balsa, Izhack Cherny, Susanne K. Christensen, Manuel Espinosa, Djordje Francuski, Ehud Gazit, Kenn Gerdes, Ed Hitchin, M. Teresa Martín, Concepción Nieto, Karin Overweg, Teresa Pellicer, Wolfram Saenger, Heinz Welfle, Karin Welfle, Jerry Wells
Publikováno v:
Enzyme-Mediated Resistance to Antibiotics
This chapter focuses on the proteic toxin-antitoxin (TA) systems. TA systems function as vitally important regulatory systems in bacteria and represent ideal targets for the development of novel antibiotic therapeutic agents. A broad mechanistic unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4f6e34bf6f6c0df56660973054375b7
https://doi.org/10.1128/9781555815615.ch19
https://doi.org/10.1128/9781555815615.ch19