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FEBS Letters
|
July 29, 2000
ATP-dependent regulation of nuclear Ca(2+) levels in plant cells
T 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 groups
A B Moser, M Rasmussen, S Naidu, et al.
Human Mutation
|
January 1, 1995
Mutational analysis of patients with X-linked adrenoleukodystrophy
F 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 deficiency
M 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 diseases
P 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 plants
T 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 adrenoleukodystrophy
P A Watkins, S J Gould, M A Smith, et al.
Neurochemical Research
|
May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes
K 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 entity
S 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 system
J Moss, P Bruni, J A Hsia, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
FEBS Letters
|
July 29, 2000
ATP-dependent regulation of nuclear Ca(2+) levels in plant cells
T 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 groups
A B Moser, M Rasmussen, S Naidu, et al.
Human Mutation
|
January 1, 1995
Mutational analysis of patients with X-linked adrenoleukodystrophy
F 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 deficiency
M 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 diseases
P 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 plants
T 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 adrenoleukodystrophy
P A Watkins, S J Gould, M A Smith, et al.
Neurochemical Research
|
May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes
K 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 entity
S 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 system
J Moss, P Bruni, J A Hsia, et al.
Page
of 11