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Andreina Bordoni

Showing results (11-20 of 54) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 25, 2005
Skeletal muscle gene expression profiling in mitochondrial disordersMarco Crimi, Andreina Bordoni, Giorgia Menozzi, et al.
Journal of the Neurological Sciences|March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological studyRoberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 5, 2018
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III miceSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of the Neurological Sciences|February 19, 2010
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairmentDario Ronchi, Roberta Virgilio, Andreina Bordoni, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Annals of Neurology|September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaEleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Nucleic Acids Research|September 18, 2008
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybridsPeter Seibel, Chiara Di Nunno, Christian Kukat, et al.
Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.
Neurology|June 11, 2003
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndromeMarco Crimi, Sara Galbiati, Isabella Moroni, et al.
Neurobiology of Aging|August 21, 2003
High mutational burden in the mtDNA control region from aged muscles: a single-fiber studyRoberto Del Bo, Marco Crimi, Monica Sciacco, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 25, 2005
Skeletal muscle gene expression profiling in mitochondrial disordersMarco Crimi, Andreina Bordoni, Giorgia Menozzi, et al.
Journal of the Neurological Sciences|March 13, 2009
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological studyRoberta Virgilio, Dario Ronchi, Andreina Bordoni, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 5, 2018
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III miceSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Journal of the Neurological Sciences|February 19, 2010
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairmentDario Ronchi, Roberta Virgilio, Andreina Bordoni, et al.
Biochimica Et Biophysica Acta|August 6, 2014
Glycogen storage disease type III: A novel Agl knockout mouse modelSerena Pagliarani, Sabrina Lucchiari, Gianna Ulzi, et al.
Annals of Neurology|September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaEleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Nucleic Acids Research|September 18, 2008
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybridsPeter Seibel, Chiara Di Nunno, Christian Kukat, et al.
Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.
Neurology|June 11, 2003
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndromeMarco Crimi, Sara Galbiati, Isabella Moroni, et al.
Neurobiology of Aging|August 21, 2003
High mutational burden in the mtDNA control region from aged muscles: a single-fiber studyRoberto Del Bo, Marco Crimi, Monica Sciacco, et al.
Pageof 6