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M Zeviani

Showing results (71-80 of 184) with videos related to

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Human Molecular Genetics|April 1, 1997
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags databaseV Tiranti, A Savoia, F Forti, et al.
Neuromuscular Disorders : NMD|April 30, 1999
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonusV Tiranti, F Carrara, P Confalonieri, et al.
Minerva Pediatrica|March 1, 1991
[Metabolic myopathies]G Finocchiaro, M Zeviani, B Garavaglia, et al.
Journal of Medical Genetics|January 15, 2000
Leigh syndrome transmitted by uniparental disomy of chromosome 9V Tiranti, E Lamantea, G Uziel, et al.
Electrophoresis|September 23, 2000
Separation of intact pyruvate dehydrogenase complex using blue native agarose gel electrophoresisN S Henderson, L G Nijtmans, J G Lindsay, et al.
Journal of Neurology|August 1, 1995
Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathyG M Fabrizi, V Tiranti, C Mariotti, et al.
FEBS Letters|May 6, 1991
Evidence that nebulin is a protein-ruler in muscle thin filamentsS Labeit, T Gibson, A Lakey, et al.
Lancet (London, England)|July 20, 1991
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR)M Zeviani, C Gellera, C Antozzi, et al.
Neurology|September 1, 2006
POLG1 in idiopathic Parkinson diseaseW Tiangyou, G Hudson, D Ghezzi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) geneM Zeviani, F Muntoni, N Savarese, et al.
Pageof 19

Showing results (71-80 of 184) with videos related to

Sort By:
Pageof 19
Human Molecular Genetics|April 1, 1997
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags databaseV Tiranti, A Savoia, F Forti, et al.
Neuromuscular Disorders : NMD|April 30, 1999
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonusV Tiranti, F Carrara, P Confalonieri, et al.
Minerva Pediatrica|March 1, 1991
[Metabolic myopathies]G Finocchiaro, M Zeviani, B Garavaglia, et al.
Journal of Medical Genetics|January 15, 2000
Leigh syndrome transmitted by uniparental disomy of chromosome 9V Tiranti, E Lamantea, G Uziel, et al.
Electrophoresis|September 23, 2000
Separation of intact pyruvate dehydrogenase complex using blue native agarose gel electrophoresisN S Henderson, L G Nijtmans, J G Lindsay, et al.
Journal of Neurology|August 1, 1995
Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathyG M Fabrizi, V Tiranti, C Mariotti, et al.
FEBS Letters|May 6, 1991
Evidence that nebulin is a protein-ruler in muscle thin filamentsS Labeit, T Gibson, A Lakey, et al.
Lancet (London, England)|July 20, 1991
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR)M Zeviani, C Gellera, C Antozzi, et al.
Neurology|September 1, 2006
POLG1 in idiopathic Parkinson diseaseW Tiangyou, G Hudson, D Ghezzi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) geneM Zeviani, F Muntoni, N Savarese, et al.
Pageof 19