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R Rozen

Showing results (61-70 of 154) with videos related to

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Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.
Genomics|February 10, 1995
Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10K C Arden, C S Viars, K Fu, et al.
Diabete & Metabolisme|May 1, 1988
Oleate metabolism and endogenous triacylglycerol hydrolysis in isolated hepatocytes from rats fed a high-fat dietM I Malewiak, R Rozen, X Le Liepvre, et al.
Annales De La Nutrition Et De L'Alimentation|January 1, 1976
[Short term effects of diets with high levels of dithiocarbamates on carbohydrate and lipid metabolism of rat liver]F Faudemay, G Griffaton, F Dupuy, et al.
The Journal of Nutrition, Health & Aging|April 1, 2008
Dietary and genetic compromise in folate availability reduces acetylcholine, cognitive performance and increases aggression: critical role of S-adenosyl methionineA Chan, F Tchantchou, V Graves, et al.
American Journal of Human Genetics|March 1, 1991
Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral diseaseD M Slipetz, J R Aprille, P R Goodyer, et al.
The Journal of Biological Chemistry|November 5, 1988
Primary structure of a human trifunctional enzyme. Isolation of a cDNA encoding methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetaseD W Hum, A W Bell, R Rozen, et al.
American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.
European Journal of Clinical Nutrition|November 1, 1989
Energy expenditure economy induced by decrease in lean body mass in anorexia nervosaJ C Melchior, D Rigaud, R Rozen, et al.
Kidney International|May 1, 1996
Molecular genetics of cystinuria in French Canadians: identification of four novel mutations in type I patientsJ Horsford, I Saadi, J Raelson, et al.
Pageof 16

Showing results (61-70 of 154) with videos related to

Sort By:
Pageof 16
Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.
Genomics|February 10, 1995
Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10K C Arden, C S Viars, K Fu, et al.
Diabete & Metabolisme|May 1, 1988
Oleate metabolism and endogenous triacylglycerol hydrolysis in isolated hepatocytes from rats fed a high-fat dietM I Malewiak, R Rozen, X Le Liepvre, et al.
Annales De La Nutrition Et De L'Alimentation|January 1, 1976
[Short term effects of diets with high levels of dithiocarbamates on carbohydrate and lipid metabolism of rat liver]F Faudemay, G Griffaton, F Dupuy, et al.
The Journal of Nutrition, Health & Aging|April 1, 2008
Dietary and genetic compromise in folate availability reduces acetylcholine, cognitive performance and increases aggression: critical role of S-adenosyl methionineA Chan, F Tchantchou, V Graves, et al.
American Journal of Human Genetics|March 1, 1991
Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral diseaseD M Slipetz, J R Aprille, P R Goodyer, et al.
The Journal of Biological Chemistry|November 5, 1988
Primary structure of a human trifunctional enzyme. Isolation of a cDNA encoding methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetaseD W Hum, A W Bell, R Rozen, et al.
American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.
European Journal of Clinical Nutrition|November 1, 1989
Energy expenditure economy induced by decrease in lean body mass in anorexia nervosaJ C Melchior, D Rigaud, R Rozen, et al.
Kidney International|May 1, 1996
Molecular genetics of cystinuria in French Canadians: identification of four novel mutations in type I patientsJ Horsford, I Saadi, J Raelson, et al.
Pageof 16