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Mitochondrion
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August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases
Marco Crimi, Sara Galbiati, Monica Sciacco, et al.
Journal of the Neurological Sciences
|
September 11, 2002
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients
Roberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, et al.
Muscle & Nerve
|
August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoform
Sabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Human Mutation
|
October 29, 2002
A collection of 33 novel human mtDNA homoplasmic variants
Marco Crimi, Monica Sciacco, Sara Galbiati, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 25, 2005
Skeletal muscle gene expression profiling in mitochondrial disorders
Marco Crimi, Andreina Bordoni, Giorgia Menozzi, et al.
Biomolecules
|
June 26, 2026
IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives
Angela Messina, Angelo Palmigiano, Donata Agata Romeo, et al.
Journal of Neurology
|
June 11, 2003
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects
Roberto Del Bo, Giacomo Pietro Comi, Roberto Giorda, et al.
Clinical Immunology (Orlando, Fla.)
|
February 22, 2011
Dual role of anti-TNF therapy: enhancement of TCR-mediated T cell activation in peripheral blood and inhibition of inflammation in target tissues
Francesca Bosè, Lorenzo Raeli, Cecilia Garutti, et al.
Hepatology (Baltimore, Md.)
|
July 2, 2011
Genetic variation in the interleukin-28B gene is not associated with fibrosis progression in patients with chronic hepatitis C and known date of infection
Francesco Marabita, Alessio Aghemo, Stella De Nicola, et al.
Neurology
|
June 11, 2003
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome
Marco Crimi, Sara Galbiati, Isabella Moroni, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Mitochondrion
|
August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases
Marco Crimi, Sara Galbiati, Monica Sciacco, et al.
Journal of the Neurological Sciences
|
September 11, 2002
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients
Roberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, et al.
Muscle & Nerve
|
August 20, 2004
Developmental and tissue-specific regulation of a novel dysferlin isoform
Sabrina Salani, Sabrina Lucchiari, Francesco Fortunato, et al.
Human Mutation
|
October 29, 2002
A collection of 33 novel human mtDNA homoplasmic variants
Marco Crimi, Monica Sciacco, Sara Galbiati, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 25, 2005
Skeletal muscle gene expression profiling in mitochondrial disorders
Marco Crimi, Andreina Bordoni, Giorgia Menozzi, et al.
Biomolecules
|
June 26, 2026
IgG Glycosylation Analysis in Patients with Ring14 Syndrome Unveils Novel Pathomechanisms and New Therapy Perspectives
Angela Messina, Angelo Palmigiano, Donata Agata Romeo, et al.
Journal of Neurology
|
June 11, 2003
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects
Roberto Del Bo, Giacomo Pietro Comi, Roberto Giorda, et al.
Clinical Immunology (Orlando, Fla.)
|
February 22, 2011
Dual role of anti-TNF therapy: enhancement of TCR-mediated T cell activation in peripheral blood and inhibition of inflammation in target tissues
Francesca Bosè, Lorenzo Raeli, Cecilia Garutti, et al.
Hepatology (Baltimore, Md.)
|
July 2, 2011
Genetic variation in the interleukin-28B gene is not associated with fibrosis progression in patients with chronic hepatitis C and known date of infection
Francesco Marabita, Alessio Aghemo, Stella De Nicola, et al.
Neurology
|
June 11, 2003
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome
Marco Crimi, Sara Galbiati, Isabella Moroni, et al.
Page
of 4