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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Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: MDPI AG 2020-10-01
Serija:International Journal of Molecular Sciences
Teme:
cystic fibrosis
CFTR
proteomics
DIGE-MALDI/TOF
biomarker
Online pristup:https://www.mdpi.com/1422-0067/21/19/7415
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