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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI AG 2020-10-01
Saila:International Journal of Molecular Sciences
Gaiak:
cystic fibrosis
CFTR
proteomics
DIGE-MALDI/TOF
biomarker
Sarrera elektronikoa:https://www.mdpi.com/1422-0067/21/19/7415
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