Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R J Pollitt

Showing results (41-50 of 133) with videos related to

Pageof 14
Sort By:
Biochemical Society Transactions|February 1, 1993
A unique, membrane-bound, multifunctional enzyme from human liver mitochondria catalysing three steps of fatty acid beta-oxidationK Carpenter, R J Pollitt, B Middleton
Journal of Inherited Metabolic Disease|January 1, 1985
Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydesR J Pollitt, A Green, R Smith
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1978
The labelling of urinary acids after oral doses of deuterated L-phenylalanine and L-tyrosine in normal subjects. Quantitative studies with implications for the deuterated phenylalanine load test in phenylketonuriaV Fell, J A Hoskins, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1987
The incidence and presentation of dicarboxylic aciduriaM J Bennett, E Worthy, R J Pollitt
Biochemical Medicine|May 1, 1975
The occurrence of (S)-3,4-dihydroxybutyrate in human blood and urineV Fell, C R Lee, R J Pollitt
Biochemical Medicine and Metabolic Biology|August 1, 1987
Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblastsR G Gray, R J Pollitt, J Webley
Lancet (London, England)|December 20, 1986
Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant deathM J Bennett, S Variend, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1980
Alpha-aminoadipic aciduria: chemical and enzymatic studiesR G Gray, E M O'Neill, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 5, 1982
Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuriaR G Gray, S E Hill, R J Pollitt
Archives of Disease in Childhood|October 1, 1980
Detection of carbamyl phosphate synthetase 1 deficiency using duodenal biopsy samplesJ P Farriaux, J L Dhondt, R J Pollitt
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
Biochemical Society Transactions|February 1, 1993
A unique, membrane-bound, multifunctional enzyme from human liver mitochondria catalysing three steps of fatty acid beta-oxidationK Carpenter, R J Pollitt, B Middleton
Journal of Inherited Metabolic Disease|January 1, 1985
Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydesR J Pollitt, A Green, R Smith
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1978
The labelling of urinary acids after oral doses of deuterated L-phenylalanine and L-tyrosine in normal subjects. Quantitative studies with implications for the deuterated phenylalanine load test in phenylketonuriaV Fell, J A Hoskins, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1987
The incidence and presentation of dicarboxylic aciduriaM J Bennett, E Worthy, R J Pollitt
Biochemical Medicine|May 1, 1975
The occurrence of (S)-3,4-dihydroxybutyrate in human blood and urineV Fell, C R Lee, R J Pollitt
Biochemical Medicine and Metabolic Biology|August 1, 1987
Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblastsR G Gray, R J Pollitt, J Webley
Lancet (London, England)|December 20, 1986
Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant deathM J Bennett, S Variend, R J Pollitt
Journal of Inherited Metabolic Disease|January 1, 1980
Alpha-aminoadipic aciduria: chemical and enzymatic studiesR G Gray, E M O'Neill, R J Pollitt
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 5, 1982
Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuriaR G Gray, S E Hill, R J Pollitt
Archives of Disease in Childhood|October 1, 1980
Detection of carbamyl phosphate synthetase 1 deficiency using duodenal biopsy samplesJ P Farriaux, J L Dhondt, R J Pollitt
Pageof 14