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FEBS Letters|June 8, 2001
Shy1p occurs in a high molecular weight complex and is required for efficient assembly of cytochrome c oxidase in yeastL G Nijtmans, M Artal Sanz, M Bucko, et al.Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.Acta Neuropathologica|January 1, 1994
Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber levelA Prelle, G Fagiolari, N Checcarelli, et al.Plant Disease|August 11, 2025
Bacillus Species Interfere with Infective Structures of Colletotrichum spp. and Reduce Symptoms of Apple Bitter Rot in Post-HarvestDébora Petermann, Nicolly C Xavier, Rafaele Regina Moreira, et al.Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.Neurology|July 1, 1991
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studiesS Servidei, M Zeviani, G Manfredi, et al.Genomics|April 1, 1988
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32M Zeviani, B T Darras, R Rizzuto, et al.Human Mutation|April 24, 2001
Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiencyM O Péquignot, R Dey, M Zeviani, et al.Archives of Neurology|November 1, 1986
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiencyM Zeviani, D H Van Dyke, S Servidei, et al.Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.Pageof 18