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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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A B Moser

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American Journal of Medical Genetics|December 8, 1998

Developmental delay and growth failure caused by a peroxisomal disorder, dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiencyE R Elias, M Mobassaleh, A K Hajra, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1988

Increased levels of ceramide in the retina of a patient with Farber's diseaseM A Zarbin, W R Green, A B Moser, et al.

Journal of the Neurological Sciences|July 1, 1992

Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelinationC Theda, A B Moser, J M Powers, et al.

Annals of Neurology|December 1, 1990

Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesisM MacCollin, D C De Vivo, A B Moser, et al.

Neurochemical Pathology|August 1, 1986

Effects of subperineurial injections of very-long-chain and medium-chain fatty acids into rat sciatic nerveN C Sacktor, J Griffin, A B Moser, et al.

Acta Neuropathologica|August 12, 1999

Cerebellar atrophy in chronic rhizomelic chondrodysplasia punctata: a potential role for phytanic acid and calcium in the death of its Purkinje cellsJ M Powers, T P Kenjarski, A B Moser, et al.

The Journal of Biological Chemistry|August 14, 2001

Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesisH M Su, A B Moser, H W Moser, et al.

Biochemical and Biophysical Research Communications|October 15, 1990

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acidsM C McGuinness, A B Moser, H W Moser, et al.

Molecular Genetics and Metabolism|March 9, 1999

Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expressionL T Braiterman, P A Watkins, A B Moser, et al.

The Journal of Clinical Investigation|December 1, 1991

Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damageG Hoefler, E Paschke, S Hoefler, et al.

Pageof 9

Search research articles

Showing results (11-20 of 86) with videos related to

Sort By:

Pageof 9

American Journal of Medical Genetics|December 8, 1998

Developmental delay and growth failure caused by a peroxisomal disorder, dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiencyE R Elias, M Mobassaleh, A K Hajra, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1988

Increased levels of ceramide in the retina of a patient with Farber's diseaseM A Zarbin, W R Green, A B Moser, et al.

Journal of the Neurological Sciences|July 1, 1992

Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelinationC Theda, A B Moser, J M Powers, et al.

Annals of Neurology|December 1, 1990

Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesisM MacCollin, D C De Vivo, A B Moser, et al.

Neurochemical Pathology|August 1, 1986

Effects of subperineurial injections of very-long-chain and medium-chain fatty acids into rat sciatic nerveN C Sacktor, J Griffin, A B Moser, et al.

Acta Neuropathologica|August 12, 1999

Cerebellar atrophy in chronic rhizomelic chondrodysplasia punctata: a potential role for phytanic acid and calcium in the death of its Purkinje cellsJ M Powers, T P Kenjarski, A B Moser, et al.

The Journal of Biological Chemistry|August 14, 2001

Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesisH M Su, A B Moser, H W Moser, et al.

Biochemical and Biophysical Research Communications|October 15, 1990

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acidsM C McGuinness, A B Moser, H W Moser, et al.

Molecular Genetics and Metabolism|March 9, 1999

Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expressionL T Braiterman, P A Watkins, A B Moser, et al.

The Journal of Clinical Investigation|December 1, 1991

Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damageG Hoefler, E Paschke, S Hoefler, et al.

Pageof 9