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C T Moraes

Showing results (51-60 of 88) with videos related to

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Nature Genetics|July 1, 1993
A mitochondrial tRNA anticodon swap associated with a muscle diseaseC T Moraes, F Ciacci, E Bonilla, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
The American Journal of Pathology|September 1, 1988
Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patientsA F Miranda, E Bonilla, G Martucci, et al.
Pediatric Research|October 6, 1997
A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathyA Verma, D A Piccoli, E Bonilla, et al.
Annals of Neurology|June 1, 1991
Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromesM L Zupanc, C T Moraes, S Shanske, et al.
Journal of the Neurological Sciences|February 7, 1998
Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegiaB H Kiyomoto, C H Tengan, C T Moraes, et al.
Human Molecular Genetics|March 1, 1994
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243V Petruzzella, C T Moraes, M C Sano, et al.
American Journal of Medical Genetics|December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.
Nature Genetics|August 1, 1992
Molecular analysis of the muscle pathology associated with mitochondrial DNA deletionsC T Moraes, E Ricci, V Petruzzella, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Nature Genetics|July 1, 1993
A mitochondrial tRNA anticodon swap associated with a muscle diseaseC T Moraes, F Ciacci, E Bonilla, et al.
Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.
The American Journal of Pathology|September 1, 1988
Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patientsA F Miranda, E Bonilla, G Martucci, et al.
Pediatric Research|October 6, 1997
A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathyA Verma, D A Piccoli, E Bonilla, et al.
Annals of Neurology|June 1, 1991
Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromesM L Zupanc, C T Moraes, S Shanske, et al.
Journal of the Neurological Sciences|February 7, 1998
Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegiaB H Kiyomoto, C H Tengan, C T Moraes, et al.
Human Molecular Genetics|March 1, 1994
Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243V Petruzzella, C T Moraes, M C Sano, et al.
American Journal of Medical Genetics|December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.
Nature Genetics|August 1, 1992
Molecular analysis of the muscle pathology associated with mitochondrial DNA deletionsC T Moraes, E Ricci, V Petruzzella, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 9