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Showing results (31-40 of 51) with videos related to

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Pediatric Research|August 14, 1999
Surface hydrophobicity is increased in the ileum and proximal colon of cystic fibrosis miceC Chung, L van Hoof, Z Policova, et al.
Gut|July 17, 2003
Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreasN Ahmed, M Corey, G Forstner, et al.
American Journal of Respiratory and Critical Care Medicine|October 14, 1998
Relation between alpha, beta, and gamma human amiloride- sensitive epithelial Na+ channel mRNA levels and nasal epithelial potential difference in healthy menG Otulakowski, S Flueckiger-Staub, L Ellis, et al.
British Journal of Haematology|September 13, 2001
Immune function in patients with Shwachman-Diamond syndromeY Dror, H Ginzberg, I Dalal, et al.
Human Mutation|January 1, 1995
Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ Zielenski, D Markiewicz, H S Chen, et al.
The New England Journal of Medicine|November 29, 1990
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508)E Kerem, M Corey, B S Kerem, et al.
Human Molecular Genetics|July 1, 1997
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNAR Rozmahel, K Gyömörey, S Plyte, et al.
JAMA|June 22, 1999
Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermiaV Mak, J Zielenski, L C Tsui, et al.
Human Reproduction (Oxford, England)|February 3, 2000
Cystic fibrosis gene mutations and infertile men with primary testicular failureV Mak, J Zielenski, L C Tsui, et al.
Biochemical and Biophysical Research Communications|February 27, 1996
In vivo measurements of ion transport in long-living CF miceM A Wilschanski, R Rozmahel, S Beharry, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Pediatric Research|August 14, 1999
Surface hydrophobicity is increased in the ileum and proximal colon of cystic fibrosis miceC Chung, L van Hoof, Z Policova, et al.
Gut|July 17, 2003
Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreasN Ahmed, M Corey, G Forstner, et al.
American Journal of Respiratory and Critical Care Medicine|October 14, 1998
Relation between alpha, beta, and gamma human amiloride- sensitive epithelial Na+ channel mRNA levels and nasal epithelial potential difference in healthy menG Otulakowski, S Flueckiger-Staub, L Ellis, et al.
British Journal of Haematology|September 13, 2001
Immune function in patients with Shwachman-Diamond syndromeY Dror, H Ginzberg, I Dalal, et al.
Human Mutation|January 1, 1995
Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) geneJ Zielenski, D Markiewicz, H S Chen, et al.
The New England Journal of Medicine|November 29, 1990
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508)E Kerem, M Corey, B S Kerem, et al.
Human Molecular Genetics|July 1, 1997
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNAR Rozmahel, K Gyömörey, S Plyte, et al.
JAMA|June 22, 1999
Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermiaV Mak, J Zielenski, L C Tsui, et al.
Human Reproduction (Oxford, England)|February 3, 2000
Cystic fibrosis gene mutations and infertile men with primary testicular failureV Mak, J Zielenski, L C Tsui, et al.
Biochemical and Biophysical Research Communications|February 27, 1996
In vivo measurements of ion transport in long-living CF miceM A Wilschanski, R Rozmahel, S Beharry, et al.
Pageof 6