Proteomic analysis of nasal cells from cystic fibrosis patients and non-cystic fibrosis control individuals: Search for novel biomarkers of cystic fibrosis lung disease

Author:

Roxo-Rosa Mónica,da Costa Gonçalo,Luider Theo M.,Scholte Bob J.,Coelho Ana V.,Amaral Margarida D.,Penque Deborah

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Reference48 articles.

1. Cystic fibrosis: molecular biology and therapeutic implications

2. Degradation of CFTR by the ubiquitin-proteasome pathway

3. Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP.

4. , , , The Metabolic and Molecular Basis of Inherited Disease, McGraw-Hill, NY, 1995, pp.  3799–3876.

5. , , , The Metabolic and Molecular Basis of Inherited Disease, McGraw-Hill, NY, 2001, pp.  5121–5188.

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