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Mostrando ítems 41-50 de 179
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)
Fibrosis quística. Aspectos diagnósticos.
(2013-07-10)
La fibrosis quística (FQ) es una de las enfermedades genéticas mortales más frecuentes en la raza caucásica. Se caracteriza por
una disfunción de las glándulas exocrinas, con insuficiencia pancreática y bronconeumopatía ...
CFTR chloride channel activity modulates the mitochondrial morphology in cultured epithelial cells
(Pergamon-Elsevier Science Ltd, 2021-06)
The impairment of the CFTR channel activity, a cAMP-activated chloride (Cl−) channel responsible for cystic fibrosis (CF), has been associated with a variety of mitochondrial alterations such as modified gene expression, ...
c- Src and its role in cystic fibrosis
(Elsevier Gmbh, 2016-10)
Cystic fibrosis (CF) is a lethal inherited disease produced by mutations in the gene encoding the CFTR chloride channel. Loss of function in the CFTR gene is associated with a not much noticed increased expression and ...
Extracellular pH and lung infections in cystic fibrosis
(Elsevier, 2018)
Abstract: Cystic fibrosis (CF) is an autosomal recessive disease caused by CFTR mutations. It is characterized by high NaCl concentration in sweat and the production of a thick and sticky mucus, occluding secretory ducts, ...
N-acetyl cysteine reverts the proinflammatory state induced by cigarette smoke extract in lung Calu-3 cells
(Elsevier, 2018-06)
Chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF) are lethal pulmonary diseases. Cigarette consumption is the main cause for development of COPD, while CF is produced by mutations in the CFTR gene. ...
A Genética na Fibrose Cística
(HCPA/FAMED/UFRGS, 2011)
Estudio de la expresión del gen CISD1 mediada por la actividad del CFTRStudy of gene expression mediated CISD1 CFTR activity
(Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires, 2010)