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R J Pollitt

Showing results (31-40 of 133) with videos related to

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The Biochemical Journal|May 1, 1971
Proteins of normal hair and of cystine-deficient hair from mentally retarded siblingsR J Pollitt, P D Stonier
Biochemical Medicine|December 1, 1972
The estimation of glutarate in urine using gas chromatography mass spectrometry with an internal isotopic standardC R Lee, R J Pollitt
Journal of Inherited Metabolic Disease|July 3, 2007
Population quantile-quantile plots for monitoring assay performance in newborn screeningR J Pollitt, A J Matthews
Archives of Disease in Childhood|November 3, 1998
Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UKR J Pollitt, J V Leonard
The Biochemical Journal|October 15, 1985
Tracer studies of the interconversion of R- and S-methylmalonic semialdehydes in manN J Manning, R J Pollitt
Journal of Chromatography|June 18, 1975
Quantitative aspects of urinary indolo-3-acetic acid and 5-hydroxyindole-3-acetic acid excretionJ A Hoskins, R J Pollitt
Tetrahedron|July 1, 1970
The anhydrides of argininosuccinic acidC R Lee, R J Pollitt
The Biochemical Journal|July 1, 1974
The glycoasparagines in urine of a patient with aspartylglycosaminuriaR J Pollitt, K M Pretty
Biochemical and Biophysical Research Communications|March 16, 1992
Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondriaK Carpenter, R J Pollitt, B Middleton
Journal of Inherited Metabolic Disease|January 1, 1991
The long-chain 3-hydroxyacyl-CoA dehydrogenase of human liver mitochondriaK Carpenter, B Middleton, R J Pollitt
Pageof 14

Showing results (31-40 of 133) with videos related to

Sort By:
Pageof 14
The Biochemical Journal|May 1, 1971
Proteins of normal hair and of cystine-deficient hair from mentally retarded siblingsR J Pollitt, P D Stonier
Biochemical Medicine|December 1, 1972
The estimation of glutarate in urine using gas chromatography mass spectrometry with an internal isotopic standardC R Lee, R J Pollitt
Journal of Inherited Metabolic Disease|July 3, 2007
Population quantile-quantile plots for monitoring assay performance in newborn screeningR J Pollitt, A J Matthews
Archives of Disease in Childhood|November 3, 1998
Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UKR J Pollitt, J V Leonard
The Biochemical Journal|October 15, 1985
Tracer studies of the interconversion of R- and S-methylmalonic semialdehydes in manN J Manning, R J Pollitt
Journal of Chromatography|June 18, 1975
Quantitative aspects of urinary indolo-3-acetic acid and 5-hydroxyindole-3-acetic acid excretionJ A Hoskins, R J Pollitt
Tetrahedron|July 1, 1970
The anhydrides of argininosuccinic acidC R Lee, R J Pollitt
The Biochemical Journal|July 1, 1974
The glycoasparagines in urine of a patient with aspartylglycosaminuriaR J Pollitt, K M Pretty
Biochemical and Biophysical Research Communications|March 16, 1992
Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondriaK Carpenter, R J Pollitt, B Middleton
Journal of Inherited Metabolic Disease|January 1, 1991
The long-chain 3-hydroxyacyl-CoA dehydrogenase of human liver mitochondriaK Carpenter, B Middleton, R J Pollitt
Pageof 14