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A B Moser

Showing results (61-70 of 86) with videos related to

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Journal of Neuropathology and Experimental Neurology|May 31, 2001
The dorsal root ganglia in adrenomyeloneuropathy: neuronal atrophy and abnormal mitochondriaJ M Powers, D P DeCiero, C Cox, et al.
Biochemical and Biophysical Research Communications|May 15, 1978
High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patientsN Kawamura, A B Moser, H W Moser, et al.
The New England Journal of Medicine|February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndromeA K Hajra, N S Datta, L G Jackson, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Orthotopic liver transplantation from a living-related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease typeL Van Maldergem, A B Moser, M-F Vincent, et al.
Journal of Neurochemistry|August 1, 1983
Myelin membrane from adrenoleukodystrophy brain white matter--biochemical propertiesF R Brown, W W Chen, D A Kirschner, et al.
Annals of Neurology|September 1, 1995
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficienciesP A Watkins, M C McGuinness, G V Raymond, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
A mouse model for X-linked adrenoleukodystrophyJ F Lu, A M Lawler, P A Watkins, et al.
Journal of the Neurological Sciences|February 1, 1987
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblastsR J Wanders, R B Schutgens, G Schrakamp, et al.
Pediatric Research|March 1, 1982
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal glandH W Moser, A B Moser, J M Powers, et al.
Human Molecular Genetics|March 21, 1998
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsL T Braiterman, S Zheng, P A Watkins, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Journal of Neuropathology and Experimental Neurology|May 31, 2001
The dorsal root ganglia in adrenomyeloneuropathy: neuronal atrophy and abnormal mitochondriaJ M Powers, D P DeCiero, C Cox, et al.
Biochemical and Biophysical Research Communications|May 15, 1978
High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patientsN Kawamura, A B Moser, H W Moser, et al.
The New England Journal of Medicine|February 14, 1985
Prenatal diagnosis of Zellweger cerebrohepatorenal syndromeA K Hajra, N S Datta, L G Jackson, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Orthotopic liver transplantation from a living-related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease typeL Van Maldergem, A B Moser, M-F Vincent, et al.
Journal of Neurochemistry|August 1, 1983
Myelin membrane from adrenoleukodystrophy brain white matter--biochemical propertiesF R Brown, W W Chen, D A Kirschner, et al.
Annals of Neurology|September 1, 1995
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficienciesP A Watkins, M C McGuinness, G V Raymond, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
A mouse model for X-linked adrenoleukodystrophyJ F Lu, A M Lawler, P A Watkins, et al.
Journal of the Neurological Sciences|February 1, 1987
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblastsR J Wanders, R B Schutgens, G Schrakamp, et al.
Pediatric Research|March 1, 1982
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal glandH W Moser, A B Moser, J M Powers, et al.
Human Molecular Genetics|March 21, 1998
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsL T Braiterman, S Zheng, P A Watkins, et al.
Pageof 9