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G Forstner

Showing results (101-110 of 130) with videos related to

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The Biochemical Journal|November 1, 1978
Enhancement of the viscosity of mucin by serum albuminS J List, B P Findlay, G G Forstner, et al.
The Biochemical Journal|May 1, 1987
Characterization and localization of the putative 'link' component in rat small-intestinal mucinR E Fahim, R D Specian, G G Forstner, et al.
Digestive Diseases and Sciences|October 1, 1985
Altered PABA pharmacokinetics in cystic fibrosis. Implications for bentiromide testG Koren, Z Weizman, G Forstner, et al.
Gut|September 1, 1980
Effect of cimetidine and sodium bicarbonate on pancreatic replacement therapy in cystic fibrosisP R Durie, L Bell, W Linton, et al.
Gastroenterology|January 1, 1984
Colipase and lipase secretion in childhood-onset pancreatic insufficiency. Delineation of patients with steatorrhea secondary to relative colipase deficiencyK J Gaskin, P R Durie, L Lee, et al.
The Journal of Pediatrics|December 1, 1978
Iatrogenic hyperuricemia in children with cystic fibrosisG P Davidson, F M Hassel, D Crozier, et al.
The Journal of Clinical Investigation|February 1, 1992
Binding of nonmucoid Pseudomonas aeruginosa to normal human intestinal mucin and respiratory mucin from patients with cystic fibrosisU Sajjan, J Reisman, P Doig, et al.
The Biochemical Journal|September 1, 1979
The role of disulphide bonds in human intestinal mucinJ F Forstner, I Jabbal, R Qureshi, et al.
Pediatric Research|July 1, 1982
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosisK J Gaskin, P R Durie, M Corey, et al.
The Journal of Pediatrics|September 1, 1995
Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosisR T Couper, M Corey, P R Durie, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
The Biochemical Journal|November 1, 1978
Enhancement of the viscosity of mucin by serum albuminS J List, B P Findlay, G G Forstner, et al.
The Biochemical Journal|May 1, 1987
Characterization and localization of the putative 'link' component in rat small-intestinal mucinR E Fahim, R D Specian, G G Forstner, et al.
Digestive Diseases and Sciences|October 1, 1985
Altered PABA pharmacokinetics in cystic fibrosis. Implications for bentiromide testG Koren, Z Weizman, G Forstner, et al.
Gut|September 1, 1980
Effect of cimetidine and sodium bicarbonate on pancreatic replacement therapy in cystic fibrosisP R Durie, L Bell, W Linton, et al.
Gastroenterology|January 1, 1984
Colipase and lipase secretion in childhood-onset pancreatic insufficiency. Delineation of patients with steatorrhea secondary to relative colipase deficiencyK J Gaskin, P R Durie, L Lee, et al.
The Journal of Pediatrics|December 1, 1978
Iatrogenic hyperuricemia in children with cystic fibrosisG P Davidson, F M Hassel, D Crozier, et al.
The Journal of Clinical Investigation|February 1, 1992
Binding of nonmucoid Pseudomonas aeruginosa to normal human intestinal mucin and respiratory mucin from patients with cystic fibrosisU Sajjan, J Reisman, P Doig, et al.
The Biochemical Journal|September 1, 1979
The role of disulphide bonds in human intestinal mucinJ F Forstner, I Jabbal, R Qureshi, et al.
Pediatric Research|July 1, 1982
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosisK J Gaskin, P R Durie, M Corey, et al.
The Journal of Pediatrics|September 1, 1995
Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosisR T Couper, M Corey, P R Durie, et al.
Pageof 13