Results 1 to 20 of 26
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Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?Dorfman, R; Nalpathamkalam, T; Taylor, C; Gonska, T; Keenan, K; Yuan, XW; Corey, M; Tsui, LC; Zielenski, J; Durie, P201081
Modifier gene study of meconium ileus in cystic fibrosis: Statistical considerations and gene mapping resultsDorfman, R; Li, W; Sun, L; Lin, F; Wang, Y; Sandford, A; Paré, PD; McKay, K; Kayserova, H; Piskackova, T; MacEk, M; Czerska, K; Sands, D; Tiddens, H; Margarit, S; Repetto, G; Sontag, MK; Accurso, FJ; Blackman, S; Cutting, GR; Tsui, LC; Corey, M; Durie, P; Zielenski, J; Strug, LJ2009136
Complex two-gene modulation of lung disease severity in children with cystic fibrosisDorfman, R; Sandford, A; Taylor, C; Huang, B; Frangolias, D; Wang, Y; Sang, R; Pereira, L; Sun, L; Berthiaume, Y; Tsui, LC; Paré, PD; Durie, P; Corey, M; Zielenski, J2008172
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, P20061,426
The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitisBishop, MD; Freedman, SD; Zielenski, J; Ahmed, N; Dupuis, A; Martin, S; Ellis, L; Shea, J; Hopper, I; Corey, M; Kortan, P; Haber, G; Ross, C; Tzountzouris, J; Steele, L; Ray, PN; Tsui, LC; Durie, PR2005879
The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrantsMeiZahav, M; Durie, P; Zielenski, J; Solomon, M; Tullis, E; Tsui, LC; Corey, M2005801
Glucose intolerance in children with cystic fibrosisSolomon, MP; Wilson, DC; Corey, M; Kalnins, D; Zielenski, J; Tsui, LC; Pencharz, P; Durie, P; Sweezey, NB2003442
Locus CFM1: a potential modifier of pancreatic disease in children with cystic fibrosisSontag, MK; Hokanson, JE; Marshall, JA; Corey, M; Zerbe, GO; Tsui, L-C; Zielenski, J; Accurso, FJ2003277
Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreasAhmed, N; Corey, M; Forstner, G; Zielenski, J; Tsui, LC; Ellis, L; Tullis, E; Durie, P2003357
Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout miceHaston, CK; McKerlie, C; Newbigging, S; Corey, M; Rozmahel, R; Tsui, LC2002216
Mapping of genetic factors influencing the weight of cystic fibrosis knockout miceHaston, CK; Corey, M; Tsui, LC2002211
Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitisDurno, C; Corey, M; Zielenski, J; Tullis, E; Tsui, LC; Durie, P2002187
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 [3]Zielenski, J; Corey, M; Rozmahel, R; Markiewicz, D; Aznarez, I; Casals, T; Larriba, S; Mercier, B; Cutting, GR; Krebsova, A; Macek M, Jr; Langfelder Schwind, E; Marshall, BC; DecelieGermana, J; Claustres, M; Palacio, A; Bal, J; Nowakowska, A; Ferec, C; Estivill, X; Durie, P; Tsui, LC1999153
CFTR gene mutations and the pancreatic phenotypeDurie, PR; Ahmed, N; Corey, M; Zielenski, J; Ellis, L; Tullis, E; Tsui, LC1999124
Genotype/phenotype in relation to lung diseaseDurie, PR; Tullis, E; Corey, M; Ellis, L; Martin, S; Jarvi, K; Zielenski, J; Gilljam, M; Tsui, LC199895
Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurementsWilson, DC; Ellis, L; Zielenski, J; Corey, M; Ip, WF; Tsui, LC; Tullis, E; Knowles, MR; Durie, PR1998294
Defining the modifiers of CF pathophysiologyRozmahel, R; Nguyen, V; Corey, M; Haston, CK; Kent, G; Bear, C; Durie, P; Tsui, LC1998127
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, PR1995246
Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Markiewicz, D; Chen, HS; Schappert, K; Seller, A; Durie, P; Corey, M; Tsui, LC1995285
CFTR gene variant for patients with congenital absence of vas deferens [3]Zielenski, J; Patrizio, P; Corey, M; Handelin, B; Markiewicz, D; Asch, R; Tsui, LC1995207
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