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P A Watkins

Showing results (91-100 of 104) with videos related to

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FEBS Letters|July 29, 2000
ATP-dependent regulation of nuclear Ca(2+) levels in plant cellsT D Bunney, P J Shaw, P A Watkins, et al.
The Journal of Pediatrics|July 1, 1995
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groupsA B Moser, M Rasmussen, S Naidu, et al.
Human Mutation|January 1, 1995
Mutational analysis of patients with X-linked adrenoleukodystrophyF Kok, S Neumann, C O Sarde, et al.
American Journal of Human Genetics|June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiencyM He, S L Rutledge, D R Kelly, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: applications to peroxisomal biogenesis diseasesP A Watkins, J A Hamilton, A Leaf, et al.
The Plant Cell|September 28, 2000
Association of phosphatidylinositol 3-kinase with nuclear transcription sites in higher plantsT D Bunney, P A Watkins, A F Beven, et al.
American Journal of Human Genetics|August 1, 1995
Altered expression of ALDP in X-linked adrenoleukodystrophyP A Watkins, S J Gould, M A Smith, et al.
Neurochemical Research|May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypesK D Smith, S Kemp, L T Braiterman, et al.
Neurology|July 1, 1988
Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entityS Naidu, G Hoefler, P A Watkins, et al.
Journal of Receptor Research|January 1, 1984
Pertussis toxin-catalyzed ADP-ribosylation: effects on the coupling of inhibitory receptors to the adenylate cyclase systemJ Moss, P Bruni, J A Hsia, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
FEBS Letters|July 29, 2000
ATP-dependent regulation of nuclear Ca(2+) levels in plant cellsT D Bunney, P J Shaw, P A Watkins, et al.
The Journal of Pediatrics|July 1, 1995
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groupsA B Moser, M Rasmussen, S Naidu, et al.
Human Mutation|January 1, 1995
Mutational analysis of patients with X-linked adrenoleukodystrophyF Kok, S Neumann, C O Sarde, et al.
American Journal of Human Genetics|June 15, 2007
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiencyM He, S L Rutledge, D R Kelly, et al.
Journal of Molecular Neuroscience : MN|August 2, 2001
Brain uptake and utilization of fatty acids: applications to peroxisomal biogenesis diseasesP A Watkins, J A Hamilton, A Leaf, et al.
The Plant Cell|September 28, 2000
Association of phosphatidylinositol 3-kinase with nuclear transcription sites in higher plantsT D Bunney, P A Watkins, A F Beven, et al.
American Journal of Human Genetics|August 1, 1995
Altered expression of ALDP in X-linked adrenoleukodystrophyP A Watkins, S J Gould, M A Smith, et al.
Neurochemical Research|May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypesK D Smith, S Kemp, L T Braiterman, et al.
Neurology|July 1, 1988
Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entityS Naidu, G Hoefler, P A Watkins, et al.
Journal of Receptor Research|January 1, 1984
Pertussis toxin-catalyzed ADP-ribosylation: effects on the coupling of inhibitory receptors to the adenylate cyclase systemJ Moss, P Bruni, J A Hsia, et al.
Pageof 11