Results 1 to 6 of 6
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TypeTitleAuthor(s)YearViews
Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentialsWilschanski, M; Dupuis, A; Ellis, L; Jarvi, K; Zielenski, J; Tullis, E; Martin, S; Corey, M; Tsui, LC; Durie, P20061,427
 
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNARozmahel, R; Gyömörey, K; Plyte, S; Nguyen, V; Wilschanski, M; Durie, P; Bear, CE; Tsui, LC1997399
 
Erratum: Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor (Nature Genetics (1996) 12 (280-287))Rozmahel, R; Wilschanski, M; Matin, A; Plyte, S; Oliver, M; Auerbach, W; Moore, A; Forstner, J; Durie, P; Nadeau, J; Bear, C; Tsui, LC199663
 
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factorRozmahel, R; Wilschanski, M; Matin, A; Plyte, S; Oliver, M; Auerbach, W; Moore, A; Forstner, J; Durie, P; Nadeau, J; Bear, C; Tsui, LC1996301
 
Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutationsWilschanski, M; Zielenski, J; Markiewicz, D; Tsui, LC; Corey, M; Levison, H; Durie, PR1995248
 
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia [21]Jarvi, K; Zielenski, J; Wilschanski, M; Durie, P; Buckspan, M; Tullis, E; Markiewicz, D; Tsui, LC199595
 
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