Role of CFTR in Epithelial to Mesenchymal Transition (EMT) by functional genomics

Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein cause Cystic Fibrosis (CF), the most common life-shortening monogenic condition in Caucasians. Recent evidence indicates that in addition to being an anion channel CFTR plays a role in other cellular processes, inclu...

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Detalhes bibliográficos
Autor principal: Quaresma, Margarida C (author)
Formato: doctoralThesis
Idioma:eng
Publicado em: 2022
Assuntos:
CFTR
Fibrose Quística
Transição Epitélio-Mesenquima (EMT)
Cancro
Biologia de Sistemas
Cystic Fibrosis
Epithelial-Mesenchymal Transition (EMT)
Cancer
Systems Biology
Domínio/Área Científica::Ciências Naturais::Ciências Biológicas
Texto completo:http://hdl.handle.net/10451/53669
País:Portugal
Oai:oai:repositorio.ul.pt:10451/53669

Texto Completo

http://hdl.handle.net/10451/53669

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