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W Moser

Showing results (381-390 of 466) with videos related to

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Magnetic Resonance in Medicine|June 22, 2005
Magnetization transfer weighted imaging in the upper cervical spinal cord using cerebrospinal fluid as intersubject normalization reference (MTCSF imaging)Seth A Smith, Xavier Golay, Ali Fatemi, 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.
Journal of Animal Science|March 20, 2013
The heritabilities, phenotypic correlations, and genetic correlations of lean color and palatability measures from longissimus muscle in beef cattleP J Pratt, D W Moser, L D Thompson, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 13, 2012
Parents' information needs in tumor necrosis factor-α inhibitor treatment decisionsEllen A Lipstein, Daniel J Lovell, Lee A Denson, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 1997
A fibroblast cell line defective in alkyl-dihydroxyacetone phosphate synthase: a novel defect in plasmalogen biosynthesisN Nagan, A K Hajra, A K Das, et al.
Sports Health|October 26, 2024
Making Sense of Topical Pain Relief Options: Comparing Topical Analgesics in Efficacy and SafetyAndrew Clark Smith, M Seth Smith, Ryan P Roach, et al.
American Journal of Human Genetics|July 10, 2003
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationNaomi Matsumoto, Shigehiko Tamura, Satomi Furuki, 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.
Pageof 47

Showing results (381-390 of 466) with videos related to

Sort By:
Pageof 47
Magnetic Resonance in Medicine|June 22, 2005
Magnetization transfer weighted imaging in the upper cervical spinal cord using cerebrospinal fluid as intersubject normalization reference (MTCSF imaging)Seth A Smith, Xavier Golay, Ali Fatemi, 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.
Journal of Animal Science|March 20, 2013
The heritabilities, phenotypic correlations, and genetic correlations of lean color and palatability measures from longissimus muscle in beef cattleP J Pratt, D W Moser, L D Thompson, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 13, 2012
Parents' information needs in tumor necrosis factor-α inhibitor treatment decisionsEllen A Lipstein, Daniel J Lovell, Lee A Denson, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 1997
A fibroblast cell line defective in alkyl-dihydroxyacetone phosphate synthase: a novel defect in plasmalogen biosynthesisN Nagan, A K Hajra, A K Das, et al.
Sports Health|October 26, 2024
Making Sense of Topical Pain Relief Options: Comparing Topical Analgesics in Efficacy and SafetyAndrew Clark Smith, M Seth Smith, Ryan P Roach, et al.
American Journal of Human Genetics|July 10, 2003
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationNaomi Matsumoto, Shigehiko Tamura, Satomi Furuki, 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.
Pageof 47