Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Isabel Carvalho-Oliveira"'
Autor:
Mark K. Titulaer, Ruvalic M. Buijs-Offerman, Martina Wilke, Jamil Aarbiou, Bob J. Scholte, Thomas Schettgen, Thomas Kraus, Theo M. Luider, Nuno Charro, Deborah Penque, Peter Burgers, Isabel Carvalho-Oliveira
Publikováno v:
Journal of Proteome Research, 8(7), 3606-3616. American Chemical Society
Combined results from laser capture microdissection of mouse airway epithelial cells followed by high power (MALDI-FTICR) MS, and fluorescent two-dimensional gel elctrophoresis (2D-DIGE) of the whole lung, allowed us to identify proteins differential
Autor:
Rita Cordeiro, Deborah Penque, Baltazar Nunes, Philippe Lehours, Lurdes Monteiro, Ana I. Mendes, Armelle Ménard, Isabel Carvalho-Oliveira, Mónica Oleastro, Jonathan Ferrand, Francis Mégraud
Publikováno v:
The Journal of infectious diseases. 198(9)
BACKGROUND homB codes for a putative Helicobacter pylori outer membrane protein and has previously been associated with peptic ulcer disease (PUD) in children. METHODS A total of 190 H. pylori strains isolated from children and adults were studied to
Publikováno v:
Expert Review of Molecular Diagnosis, 7(4), 407-417. Taylor & Francis Ltd
Genetically modified mouse strains are important research tools for the study of numerous human diseases. These models provide us with differentiated tissues, which are not often available from human sources. Furthermore, they allow for testing the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2eeaefb401168783825426d8320ee26
https://pure.eur.nl/en/publications/94d4532d-4d98-4ea7-82b9-95bdddfdc224
https://pure.eur.nl/en/publications/94d4532d-4d98-4ea7-82b9-95bdddfdc224
Autor:
Zsuzsanna Bebok, Eric J. Sorscher, Ceinwen Menai Harris, Margaret A. McPherson, Iolo Doull, Deborah Penque, Valerie Eubanks, Robert L. Dormer, John P. Clancy, Filipa Mendes, Godfried M. Roomans, Anca Dragomir, Margarida D. Amaral, Isabel Carvalho-Oliveira
Publikováno v:
Journal of Cystic Fibrosis. :43-48
Reliable methods for determining the localisation of mutant CFTR protein in native cells from CF individuals are necessary to allow the degree of mislocalisation of any genotype to be defined and to assess the effect of therapeutic agents on CFTR tra
Autor:
Deborah Penque, Isabel Carvalho-Oliveira, Alexandra Efthymiadou, Rui Malhó, Maria Tzetis, Margarida D. Amaral, Emmanuel Kanavakis, Paulo Nogueira
Publikováno v:
CIÊNCIAVITAE
Scopus-Elsevier
Scopus-Elsevier
The intracellular localization of cystic fibrosis transmembrane conductance regulator (CFTR) in native tissues is a major issue in the study of mutation, processing, and trafficking effects in CFTR and in the evaluation of therapeutic strategies in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b96e8d705ebe8d9e4d69f370bc0faf3
http://www.scopus.com/inward/record.url?eid=2-s2.0-0742322867&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0742322867&partnerID=MN8TOARS