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Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis
(Soc Brasileira Pneumologia TisiologiaBrasilia DfBrasil, 2013)
Mutações do gene cystic fibrosis transmembrane conductance regulator e deleções dos genes glutationa S-transferase em pacientes com fibrose cística no BrasilCystic fibrosis transmembrane conductance regulator gene mutations and glutathione S-transferase null genotypes in cystic fibrosis patients in Brazil
(Sociedade Brasileira de Pneumologia e Tisiologia, 2012)
Correlación genotipo-fenotipo de un grupo de pacientes con fibrosis quística
(Soc. Médica Santiago, 2002)
Background: Cystic fibrosis (CF) is the most common lethal autosomic disease in Caucasians, with a global incidence of 1:3000 newborns. More than 900 mutations have been described, involving the Cystic Fibrosis Transmembrane ...
Correlación genotipo-fenotipo de un grupo de pacientes con fibrosis quística
(Sociedad Médica de Santiago, 2002)
Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis
(Soc Brasileira Pneumologia TisiologiaBrasilia DfBrasil, 2013)
Type IV B pili are required for invasion but not for adhesion of Salmonella enterica serovar Typhi into BHK epithelial cells in a cystic fibrosis transmembrane conductance regulator-independent manner
(2011)
The cystic fibrosis transmembrane conductance regulator (CFTR) has been proposed as an epithelial cell receptor for the entry of Salmonella Typhi but not Salmonella Typhimurium. The bacterial ligand recognized by CFTR is ...