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Search for publications relevant for "regulator cftr gene"
regulator cftr gene
Publication
Class
Person
Publication
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publication
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis
1996 |
Central Library of Charles University
publication
The origin of the major cystic fibrosis mutation (ΔF508) in European populations
1994 |
Second Faculty of Medicine
publication
Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%
1997 |
Second Faculty of Medicine
publication
Missense variations in the cystic fibrosis gene: Heteroduplex formation in the F508C mutation
1992 |
Central Library of Charles University
publication
Drug therapy for cystic fibrosis
2010 |
Second Faculty of Medicine
publication
A mutation in CFTR produces different phenotypes depending on chromosomal background
1993 |
Central Library of Charles University
publication
Mutations in the Amiloride-Sensitive Epithelial Sodium Channel in Patients With Cystic Fibrosis-Like Disease
2009 |
Second Faculty of Medicine
publication
Cystic fibrosis in adults
+3
2014 |
Second Faculty of Medicine
publication
Complete Ascertainment of Intragenic Copy Number Mutations (CNMs) in the CFTR Gene and its Implications for CNM Formation at Other Autosomal Loci
2010 |
Second Faculty of Medicine
publication
The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy
1991 |
Second Faculty of Medicine
publication
Antineutrophil cytoplasmic autoantibodies (ANCA) in children with cystic fibrosis
1998 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign
2004 |
Second Faculty of Medicine
publication
Cystic Fibrosis Revisited - a Review Study
2017 |
Publication without faculty affiliation
publication
Mutant CFTR Drives TWIST1 mediated epithelial-mesenchymal transition
2020 |
Second Faculty of Medicine
publication
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
2000 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival
1997 |
Second Faculty of Medicine