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pro vyhledávání: '"Fibrose cística/tratamento farmacológico"'
Autor:
Athanazio, Rodrigo Abensur, Tanni, Suzana Erico, Ferreira, Juliana, Dalcin, Paulo de Tarso Roth, Fuccio, Marcelo B de, Esposito, Concetta, Canan, Mariane Gonçalves Martynychen, Coelho, Liana Sousa, Firmida, Mônica de Cássia, Almeida, Marina Buarque de, Marostica, Paulo José Cauduro, Monte, Luciana de Freitas Velloso, Souza, Edna Lúcia, Pinto, Leonardo Araujo, Rached, Samia Zahi, Oliveira, Verônica Stasiak Bednarczuk de, Riedi, Carlos Antonio, Silva Filho, Luiz Vicente Ribeiro Ferreira da
Publikováno v:
Jornal Brasileiro de Pneumologia, Volume: 49, Issue: 2, Article number: e20230040, Published: 15 MAY 2023
Cystic fibrosis (CF) is a genetic disease that results in dysfunction of the CF transmembrane conductance regulator (CFTR) protein, which is a chloride and bicarbonate channel expressed in the apical portion of epithelial cells of various organs. Dys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::95a8034dce24a319cfbd844d3432cb56
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132023000200400&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132023000200400&lng=en&tlng=en
