Serum-Based Proteomics Profiling in Adult Patients with Cystic Fibrosis

Cystic fibrosis (CF), the most common lethal autosomal recessive disorder among Caucasians, is caused by mutations in the CF transmembrane conductance regulator (CFTR) chloride channel gene. Despite significant advances in the management of CF patients, novel disease-related biomarkers and therapies...

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Detalhes bibliográficos
Main Authors: Hicham Benabdelkamel, Hanadi Alamri, Meshail Okla, Afshan Masood, Mai Abdel Jabar, Ibrahim O. Alanazi, Assim A. Alfadda, Imran Nizami, Majed Dasouki, Anas M. Abdel Rahman
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI AG 2020-10-01
Colecção:International Journal of Molecular Sciences
Assuntos:
cystic fibrosis
CFTR
proteomics
DIGE-MALDI/TOF
biomarker
Acesso em linha:https://www.mdpi.com/1422-0067/21/19/7415
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