Showing results (21-30 of 180) with videos related to
Sort By:
Pageof 18
Gene|April 30, 1993
Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB)V Tiranti, M Rocchi, S DiDonato, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2000
Ultrastructural analysis of extraocular muscle in chronic progressive external ophthalmoplegiaA Carta, T D'Adda, F Carrara, et al.Italian Journal of Neurological Sciences|August 11, 2000
Nuclear gene defects in mitochondrial disordersM Zeviani, P Corona, L Nijtmans, et al.Human Molecular Genetics|November 5, 1999
Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybridsM Toompuu, V Tiranti, M Zeviani, et al.The Biochemical Journal|November 15, 1984
Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibresG Salviati, R Betto, D Danieli Betto, et al.Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.Human Molecular Genetics|September 25, 1997
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous systemG Battaglia, A Princivalle, F Forti, et al.International Journal of Clinical Pharmacology Research|December 4, 2004
Accelerated cardiomyopathy in maternally inherited diabetes and deafnessR A Mangiafico, M Zeviani, G Bartoloni, et al.Journal of Medical Genetics|May 3, 2005
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiencyM Bugiani, V Tiranti, L Farina, et al.Pageof 18