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P A Watkins

Showing results (71-80 of 104) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|June 6, 1998
Characterization of phytanoyl-Coenzyme A hydroxylase in human liver and activity measurements in patients with peroxisomal disordersG A Jansen, S J Mihalik, P A Watkins, et al.
Nature Genetics|November 5, 1997
Identification of PAHX, a Refsum disease geneS J Mihalik, J C Morrell, D Kim, et al.
American Journal of Medical Genetics|May 17, 1996
Urinary bile acids and peroxisomal bifunctional enzyme deficiencyM R Natowicz, J E Evans, R I Kelley, et al.
The Journal of Biological Chemistry|July 11, 1998
Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrationsP A Watkins, J F Lu, S J Steinberg, et al.
American Journal of Medical Genetics|June 5, 1995
Diagnoses of neuronal ceroid-lipofuscinosis by immunochemical methodsS Hosain, W E Kaufmann, G Negrin, et al.
The Journal of Cell Biology|May 1, 1977
Lipogenesis and the synthesis and secretion of very low density lipoprotein by avian liver cells in nonproliferating monolayer culture. Hormonal effectsD M Tarlow, P A Watkins, R E Reed, et al.
Biochemical and Biophysical Research Communications|December 4, 1996
Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humansG A Jansen, S J Mihalik, P A Watkins, et al.
Endocrinology|December 1, 1990
Luteinizing hormone causes rapid and transient changes in rat Leydig cell peroxisome volume and intraperoxisomal sterol carrier protein-2 contentS M Mendis-Handagama, P A Watkins, S J Gelber, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: recommendations for future researchR Katz, J A Hamilton, A A Spector, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctataG A Jansen, S J Mihalik, P A Watkins, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 6, 1998
Characterization of phytanoyl-Coenzyme A hydroxylase in human liver and activity measurements in patients with peroxisomal disordersG A Jansen, S J Mihalik, P A Watkins, et al.
Nature Genetics|November 5, 1997
Identification of PAHX, a Refsum disease geneS J Mihalik, J C Morrell, D Kim, et al.
American Journal of Medical Genetics|May 17, 1996
Urinary bile acids and peroxisomal bifunctional enzyme deficiencyM R Natowicz, J E Evans, R I Kelley, et al.
The Journal of Biological Chemistry|July 11, 1998
Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrationsP A Watkins, J F Lu, S J Steinberg, et al.
American Journal of Medical Genetics|June 5, 1995
Diagnoses of neuronal ceroid-lipofuscinosis by immunochemical methodsS Hosain, W E Kaufmann, G Negrin, et al.
The Journal of Cell Biology|May 1, 1977
Lipogenesis and the synthesis and secretion of very low density lipoprotein by avian liver cells in nonproliferating monolayer culture. Hormonal effectsD M Tarlow, P A Watkins, R E Reed, et al.
Biochemical and Biophysical Research Communications|December 4, 1996
Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humansG A Jansen, S J Mihalik, P A Watkins, et al.
Endocrinology|December 1, 1990
Luteinizing hormone causes rapid and transient changes in rat Leydig cell peroxisome volume and intraperoxisomal sterol carrier protein-2 contentS M Mendis-Handagama, P A Watkins, S J Gelber, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: recommendations for future researchR Katz, J A Hamilton, A A Spector, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctataG A Jansen, S J Mihalik, P A Watkins, et al.
Pageof 11