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Molecular analysis of 23 exons of the cftr gene in brazilian patients leads to the finding of rare cystic fibrosis mutations
(Wayne State University Press, 2012)
Mitochondrial alterations and oxidative stress in cystic fibrosis
(Springer Nature, 2022)
Molecular analysis of 23 exons of the cftr gene in brazilian patients leads to the finding of rare cystic fibrosis mutations
(Wayne State University Press, 2005)
The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function
(Dominik Hartl, University of Tübingen, Germany, 2012)
Abstract: Cystic fibrosis (CF) is a frequent and lethal autosomal recessive disease. It results from different possible mutations in the CFTR gene, which encodes the CFTR chloride channel. We have previously studied the ...
Propuesta de atención de manejo paliativo del paciente adulto portador de enfermedad de fibrosis quística
(2022)
La fibrosis quística es una enfermedad que se considera que afecta al menos a 100 000 personas en todo el mundo, a nivel nacional tenemos actualmente 22 pacientes con fibrosis quística en edad adulta. Las mutaciones en el ...
CFTR Polymorphisms in Patients with Alcoholic Chronic Pancreatitis
(KARGER, 2009)
Introduction: Pancreas susceptibility to alcohol is variable and only 5-10% of chronic alcohol abusers develop chronic pancreatitis; the role of genetic factors in this process is unknown. The CFTR gene encodes a protein ...