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Pulmonary Ionocytes Challenge the Paradigm in Cystic Fibrosis.
Hawkins, Finn J; Kotton, Darrell N.
Afiliação
  • Hawkins FJ; Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, MA, USA; The Pulmonary Center, Boston University School of Medicine, Boston, MA, USA. Electronic address: hawk@bu.edu.
  • Kotton DN; Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, MA, USA; The Pulmonary Center, Boston University School of Medicine, Boston, MA, USA.
Trends Pharmacol Sci ; 39(10): 852-854, 2018 10.
Article em En | MEDLINE | ID: mdl-30213439
ABSTRACT
Two recent studies have identified novel airway cells termed pulmonary ionocytes that express higher levels of CFTR than other airway cells express. These findings raise new questions in the evolving debate about the physiological role of CFTR in lung epithelia and its importance in the pathogenesis of cystic fibrosis (CF).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Trends Pharmacol Sci Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Trends Pharmacol Sci Ano de publicação: 2018 Tipo de documento: Article