Patient personalized translational tools in cystic fibrosis to transform data from bench to bed-side and back

Cystic fibrosis is a deadly multiorgan disorder caused by loss of function mutations in the gene that encodes for the cystic fibrosis transmembrane conductance regulator (CFTR) chloride/bicarbonate ion channel. More than 1,700 CFTR genetic variants exist that can cause CF, and majority of these are...

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Detalhes bibliográficos
Publicado no:Am J Physiol Gastrointest Liver Physiol
Main Authors: Arora, Kavisha, Yang, Fanmuyi, Brewington, John, McPhail, Gary, Cortez, Alexander R., Sundaram, Nambirajan, Ramananda, Yashaswini, Ogden, Herbert, Helmrath, Michael, Clancy, John P., Naren, Anjaparavanda P.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2021
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8285588/
https://ncbi.nlm.nih.gov/pubmed/33949881
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpgi.00095.2021
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