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M Zeviani

Showing results (121-130 of 184) with videos related to

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Cell|January 13, 1995
Identification and characterization of a spinal muscular atrophy-determining geneS Lefebvre, L Bürglen, S Reboullet, et al.
American Journal of Human Genetics|March 7, 1998
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosidesX Estivill, N Govea, E Barceló, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
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
<i>Bacillus</i> Species Interfere with Infective Structures of <i>Colletotrichum</i> 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.
Pageof 19

Showing results (121-130 of 184) with videos related to

Sort By:
Pageof 19
Cell|January 13, 1995
Identification and characterization of a spinal muscular atrophy-determining geneS Lefebvre, L Bürglen, S Reboullet, et al.
American Journal of Human Genetics|March 7, 1998
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosidesX Estivill, N Govea, E Barceló, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
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
<i>Bacillus</i> Species Interfere with Infective Structures of <i>Colletotrichum</i> 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.
Pageof 19