Results 1 to 17 of 17
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TypeTitleAuthor(s)YearViews
Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout miceHaston, CK; McKerlie, C; Newbigging, S; Corey, M; Rozmahel, R; Tsui, LC2002218
 
Alleles at the Nicastrin locus modify presenilin 1-deficiency phenotypeRozmahel, R; Mount, HTJ; Chen, F; Nguyen, V; Huang, J; Erdebil, S; Liauw, J; Yu, G; Hasegawa, H; Gu, Y; Song, YQ; Schmidt, SD; Nixon, RA; Mathews, PM; Bergeron, C; Fraser, P; Westaway, D; St GeorgeHyslop, P2002118
 
Carboxyl-terminal fragments of alzheimer β-amlyloid precursor protein accumulate in restricted and unpredicted intracellular compartments in presenilin 1-deficient cellsChen, F; Yang, DS; Petanceska, S; Yang, A; Tandon, A; Yu, G; Rozmahel, R; Ghiso, J; Nishimura, M; Zhang, DM; Kawarai, T; Levesque, G; Mills, J; Levesque, L; Song, YQ; Rogaeva, E; Westaway, D; Mount, H; Gandy, S; St GeorgeHyslop, P; Fraser, PE2000140
 
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, LC1999155
 
Defining the modifiers of CF pathophysiologyRozmahel, R; Nguyen, V; Corey, M; Haston, CK; Kent, G; Bear, C; Durie, P; Tsui, LC1998129
 
Amplification of CFTR exon 9 sequences to multiple locations in the human genomeRozmahel, R; Heng, HHQ; Duncan, AMV; Shi, XM; Rommens, JM; Tsui, LC1997271
 
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, LC1997400
 
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, LC199664
 
In vivo measurements of ion transport in long-living CF miceWilschanski, MA; Rozmahel, R; Beharry, S; Kent, G; Li, C; Tsui, LC; Durie, P; Bear, CE1996224
 
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, LC1996303
 
Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulatorYorifuji, T; Lemna, WK; Ballard, CF; Rosenbloom, CL; Rozmahel, R; Plavsic, N; Tsui, LC; Beaudet, AL1991213
 
Molecular genetics of cystic fibrosisTsui, LC; Rommens, J; Kerem, B; Rozmahel, R; Zielenski, J; Kennedy, D; Markiewicz, D; Plavsic, N; Chou, JL; Bozon, D; Dobbs, M1991151
 
Characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator geneChou, JL; Rozmahel, R; Tsui, LC1991260
 
Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) geneZielenski, J; Rozmahel, R; Bozon, D; Kerem, BS; Grzelczak, Z; Riordan, JR; Rommens, J; Tsui, LC1991343
 
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNARiordan, JR; Rommens, JM; Kerem, BS; Alon, N; Rozmahel, R; Grzelczak, Z; Zielinski, J; Lok, S; Plavsic, N; Chou, JL; Drumm, ML; Iannuzzi, MC; Collins, FS; Tsui, LC1989638
 
Identification of the cystic fibrosis gene: Chromosome walking and jumpingRommens, JM; Iannuzzi, MC; Kerem, BS; Drumm, ML; Melmer, G; Dean, M; Rozmahel, R; Cole, JL; Kennedy, D; Hidaka, N; Zsiga, M; Buchwald, M; Riordan, JR; Tsui, LC; Collins, FS1989465
 
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis geneRommens, JM; Zengerling, S; Burns, J; Melmer, G; Kerem, B; Plavsic, N; Zsiga, M; Kennedy, D; Markiewicz, D; Rozmahel, R; Riordan, JR; Buchwald, M; Tsui, L1988291
 
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