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L Knight

Showing results (741-750 of 1,163) with videos related to

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Allergy|November 21, 2018
Bacillus subtilis exopolysaccharide prevents allergic eosinophiliaJulie A Swartzendruber, Ryan W Incrocci, Samantha A Wolf, et al.
Journal of Economic Entomology|July 21, 2000
Particle films for suppression of the codling moth (Lepidoptera: Tortricidae) in apple and pear orchardsT R Unruh, A L Knight, J Upton, et al.
Journal of Cardiothoracic and Vascular Anesthesia|March 20, 2001
A comparison of neuropsychologic deficits after extracardiac and intracaradiac surgeryM J Andrew, R A Baker, J Bennetts, et al.
The Biochemical Journal|May 25, 2002
Peroxisome-proliferator-activated receptor-alpha (PPARalpha) deficiency leads to dysregulation of hepatic lipid and carbohydrate metabolism by fatty acids and insulinMary C Sugden, Karen Bulmer, Geoffrey F Gibbons, et al.
Journal of Molecular Biology|March 26, 1998
Differential cleavage of LexA and UmuD mediated by recA Pro67 mutants: implications for common LexA and UmuD binding sites on RecAJ T Konola, A Guzzo, J B Gow, et al.
Annals of Internal Medicine|March 18, 2003
The impact of protein intake on renal function decline in women with normal renal function or mild renal insufficiencyEric L Knight, Meir J Stampfer, Susan E Hankinson, et al.
Atherosclerosis|April 1, 1991
Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjectsB L Knight, Y F Perombelon, A K Soutar, et al.
Archives of Internal Medicine|July 28, 2004
Lifetime nonnarcotic analgesic use and decline in renal function in womenGary C Curhan, Eric L Knight, Bernard Rosner, et al.
Tissue Engineering. Part C, Methods|November 4, 2011
Development of methods for studying the differentiation of human mesenchymal stem cells under cyclic compressive strainEfstathios Michalopoulos, Richard L Knight, Sotirios Korossis, et al.
Human Molecular Genetics|November 1, 1995
A mutation (T-45C) in the promoter region of the low-density-lipoprotein (LDL)-receptor gene is associated with a mild clinical phenotype in a patient with heterozygous familial hypercholesterolaemia (FH)X M Sun, C Neuwirth, D P Wade, et al.
Pageof 117

Showing results (741-750 of 1,163) with videos related to

Sort By:
Pageof 117
Allergy|November 21, 2018
Bacillus subtilis exopolysaccharide prevents allergic eosinophiliaJulie A Swartzendruber, Ryan W Incrocci, Samantha A Wolf, et al.
Journal of Economic Entomology|July 21, 2000
Particle films for suppression of the codling moth (Lepidoptera: Tortricidae) in apple and pear orchardsT R Unruh, A L Knight, J Upton, et al.
Journal of Cardiothoracic and Vascular Anesthesia|March 20, 2001
A comparison of neuropsychologic deficits after extracardiac and intracaradiac surgeryM J Andrew, R A Baker, J Bennetts, et al.
The Biochemical Journal|May 25, 2002
Peroxisome-proliferator-activated receptor-alpha (PPARalpha) deficiency leads to dysregulation of hepatic lipid and carbohydrate metabolism by fatty acids and insulinMary C Sugden, Karen Bulmer, Geoffrey F Gibbons, et al.
Journal of Molecular Biology|March 26, 1998
Differential cleavage of LexA and UmuD mediated by recA Pro67 mutants: implications for common LexA and UmuD binding sites on RecAJ T Konola, A Guzzo, J B Gow, et al.
Annals of Internal Medicine|March 18, 2003
The impact of protein intake on renal function decline in women with normal renal function or mild renal insufficiencyEric L Knight, Meir J Stampfer, Susan E Hankinson, et al.
Atherosclerosis|April 1, 1991
Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjectsB L Knight, Y F Perombelon, A K Soutar, et al.
Archives of Internal Medicine|July 28, 2004
Lifetime nonnarcotic analgesic use and decline in renal function in womenGary C Curhan, Eric L Knight, Bernard Rosner, et al.
Tissue Engineering. Part C, Methods|November 4, 2011
Development of methods for studying the differentiation of human mesenchymal stem cells under cyclic compressive strainEfstathios Michalopoulos, Richard L Knight, Sotirios Korossis, et al.
Human Molecular Genetics|November 1, 1995
A mutation (T-45C) in the promoter region of the low-density-lipoprotein (LDL)-receptor gene is associated with a mild clinical phenotype in a patient with heterozygous familial hypercholesterolaemia (FH)X M Sun, C Neuwirth, D P Wade, et al.
Pageof 117