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M J Bennett

Showing results (231-240 of 351) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1984
Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardationM J Bennett, G P Hosking, M F Smith, et al.
Annals of Clinical Biochemistry|January 1, 1994
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spotsM J Bennett, M C Ragni, R J Ostfeld, et al.
Journal of Neurochemistry|June 1, 1976
A study of glycolytic and pentose phosphate shunt enzymes in relationship to the altered permeability in the blood-brain barrierM J Bennett, K M Ogilvy, G M Blake, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Combined malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiencies: an inborn error of beta-alanine, L-valine and L-alloisoleucine metabolism?K M Gibson, C F Lee, M J Bennett, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defectM J Bennett, R G Gray, D M Isherwood, et al.
Biochemistry|August 20, 1996
Structure of 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase complexed with NADP+M J Bennett, B P Schlegel, J M Jez, et al.
International Journal of Radiation Oncology, Biology, Physics|February 1, 1991
Marrow antioxidant enzyme activity in tumor-bearing and non-tumor-bearing mice following vincristine treatmentR M Johnke, D P Loven, R S Abernathy, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Archives of Pathology & Laboratory Medicine|July 1, 1997
Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyR H Amirkhan, C F Timmons, K O Brown, et al.
Pageof 36

Showing results (231-240 of 351) with videos related to

Sort By:
Pageof 36
Journal of Inherited Metabolic Disease|January 1, 1984
Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardationM J Bennett, G P Hosking, M F Smith, et al.
Annals of Clinical Biochemistry|January 1, 1994
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spotsM J Bennett, M C Ragni, R J Ostfeld, et al.
Journal of Neurochemistry|June 1, 1976
A study of glycolytic and pentose phosphate shunt enzymes in relationship to the altered permeability in the blood-brain barrierM J Bennett, K M Ogilvy, G M Blake, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Combined malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiencies: an inborn error of beta-alanine, L-valine and L-alloisoleucine metabolism?K M Gibson, C F Lee, M J Bennett, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defectM J Bennett, R G Gray, D M Isherwood, et al.
Biochemistry|August 20, 1996
Structure of 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase complexed with NADP+M J Bennett, B P Schlegel, J M Jez, et al.
International Journal of Radiation Oncology, Biology, Physics|February 1, 1991
Marrow antioxidant enzyme activity in tumor-bearing and non-tumor-bearing mice following vincristine treatmentR M Johnke, D P Loven, R S Abernathy, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Archives of Pathology & Laboratory Medicine|July 1, 1997
Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyR H Amirkhan, C F Timmons, K O Brown, et al.
Pageof 36