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D Johnsen

Showing results (81-90 of 91) with videos related to

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Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
The British Journal of Nutrition|October 29, 2009
Differential effects of dietary fatty acids on the cerebral distribution of plasma-derived apo B lipoproteins with amyloid-betaRyusuke Takechi, Susan Galloway, Menuka M S Pallebage-Gamarallage, et al.
Heliyon|March 4, 2024
New avenues for residual stress analysis in ultrathin atomic layer deposited free-standing membranes through release of micro-cantileversS Burgmann, M J Lid, H J D Johnsen, et al.
The Medical Journal of Australia|January 7, 1991
The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratoryN G Laing, M E Mears, D C Chandler, et al.
Scientific Reports|April 29, 2014
Time-resolved double-slit interference pattern measurement with entangled photonsPiotr Kolenderski, Carmelo Scarcella, Kelsey D Johnsen, et al.
The Journal of Pediatrics|July 1, 1972
Pathogenesis of Leigh's encephalomyelopathyT T Tang, T A Good, P R Dyken, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 21, 2007
Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouseSue Fletcher, Kaite Honeyman, Abbie M Fall, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.
American Journal of Human Genetics|August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 geneCharalampos L Karadimas, Tuan H Vu, Stephen A Holve, et al.
Brain : a Journal of Neurology|February 15, 2015
Expanding the phenotype of GMPPB mutationsMacarena Cabrera-Serrano, Roula Ghaoui, Gianina Ravenscroft, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
The British Journal of Nutrition|October 29, 2009
Differential effects of dietary fatty acids on the cerebral distribution of plasma-derived apo B lipoproteins with amyloid-betaRyusuke Takechi, Susan Galloway, Menuka M S Pallebage-Gamarallage, et al.
Heliyon|March 4, 2024
New avenues for residual stress analysis in ultrathin atomic layer deposited free-standing membranes through release of micro-cantileversS Burgmann, M J Lid, H J D Johnsen, et al.
The Medical Journal of Australia|January 7, 1991
The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratoryN G Laing, M E Mears, D C Chandler, et al.
Scientific Reports|April 29, 2014
Time-resolved double-slit interference pattern measurement with entangled photonsPiotr Kolenderski, Carmelo Scarcella, Kelsey D Johnsen, et al.
The Journal of Pediatrics|July 1, 1972
Pathogenesis of Leigh's encephalomyelopathyT T Tang, T A Good, P R Dyken, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 21, 2007
Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouseSue Fletcher, Kaite Honeyman, Abbie M Fall, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletionK J Nowak, P Walsh, R L Jacob, et al.
American Journal of Human Genetics|August 16, 2006
Navajo neurohepatopathy is caused by a mutation in the MPV17 geneCharalampos L Karadimas, Tuan H Vu, Stephen A Holve, et al.
Brain : a Journal of Neurology|February 15, 2015
Expanding the phenotype of GMPPB mutationsMacarena Cabrera-Serrano, Roula Ghaoui, Gianina Ravenscroft, et al.
Pageof 10