Abnormal n-6 fatty acid metabolism in cystic fibrosis contributes to pulmonary symptoms-Reference-Cited by-同舟云学术

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Abnormal n-6 fatty acid metabolism in cystic fibrosis contributes to pulmonary symptoms

Published:2020-09 Issue: Volume:160 Page:102156
ISSN:0952-3278
Container-title:Prostaglandins, Leukotrienes and Essential Fatty Acids
language:en
Short-container-title:Prostaglandins, Leukotrienes and Essential Fatty Acids

Author:

Wheelock Craig E.,Strandvik Birgitta

Funder

Royal Academy of Sciences and Art

Swedish Research Council

Swedish Heart Lung Foundation

Publisher

Elsevier BV

Subject

Cell Biology,Clinical Biochemistry

Reference165 articles.

1. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989

2. Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice;Castellani;J. Cyst. Fibr.,2008

3. Molecular genetics of cystic fibrosis transmembrane conductance regulator: genotype and phenotype;Sosnay;Pediatr. Clin. N Am.,2016

4. CFTR mutation combinations producing frequent complex alleles with different clinical and functional outcomes;El-Seedy;Hum. Mut.,2012

5. Gel-forming mucin interactome drives mucus viscoelasticity;Demouveaux;Adv. Colloid. Interface Sci.,2018

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