High conservation of sequences involved in cystic fibrosis mutations in five mammalian species
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference13 articles.
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2. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients;Dean;Cell,1990
3. The search for South European cystic fibrosis mutations: Identification of two new mutations, four variants, and intronic sequences;Gasparini;Genomics,1991
4. A deletion of two nucleotides in exon 10 of the CFTR gene in a soviet family with cystic fibrosis causing early infant death;Ivaschenko;Genomics,1991
5. Identification of the cystic fibrosis gene: Genetic analysis;Kerem;Science,1989
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1. Bioelectric Properties of Chloride Channels in Human, Pig, Ferret, and Mouse Airway Epithelia;American Journal of Respiratory Cell and Molecular Biology;2007-03
2. A domain mimic increases ΔF508 CFTR trafficking and restores cAMP-stimulated anion secretion in cystic fibrosis epithelia;American Journal of Physiology-Cell Physiology;2004-07
3. Phylogenetic analysis of cystic fibrosis transmembrane conductance regulator gene in mammalian species argues for the development of a rabbit model for cystic fibrosis;Molecular Biology and Evolution;1997-04-01
4. L'analyse phylogénétique du gène CFTR plaide pour l'utilisation du lapin comme modèle animal dans la mucoviscidose;médecine/sciences;1997
5. Animal studies of cystic fibrosis;Molecular Medicine Today;1995-10
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