Search research articles
Contact Us
Filters
Showing results (91-100 of 114) with videos related to
Page
of 12
Sort By:
Science Signaling
|
December 1, 2011
Gαi2 signaling promotes skeletal muscle hypertrophy, myoblast differentiation, and muscle regeneration
Giulia C Minetti, Jerome N Feige, Antonia Rosenstiel, et al.
Molecular and Cellular Biology
|
December 4, 2013
An antibody blocking activin type II receptors induces strong skeletal muscle hypertrophy and protects from atrophy
Estelle Lach-Trifilieff, Giulia C Minetti, KellyAnn Sheppard, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2000
Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype
F Galbiati, D Volonte, J B Chu, et al.
European Journal of Neurology
|
March 23, 2016
Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2
C Fiorillo, F Moro, G Brisca, et al.
Neurology
|
January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
C Bruno, E Bertini, A Federico, et al.
Clinical Genetics
|
September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I
S Assereto, A Robbiano, M Di Rocco, et al.
Neuromuscular Disorders : NMD
|
November 28, 2012
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases
M Mancuso, C Angelini, E Bertini, et al.
Biochemical and Biophysical Research Communications
|
September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract disease
M Traverso, S Assereto, E Gazzerro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 20, 2008
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease
M Traverso, C Bruno, A Broccolini, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 114) with videos related to
Sort By:
Page
of 12
Science Signaling
|
December 1, 2011
Gαi2 signaling promotes skeletal muscle hypertrophy, myoblast differentiation, and muscle regeneration
Giulia C Minetti, Jerome N Feige, Antonia Rosenstiel, et al.
Molecular and Cellular Biology
|
December 4, 2013
An antibody blocking activin type II receptors induces strong skeletal muscle hypertrophy and protects from atrophy
Estelle Lach-Trifilieff, Giulia C Minetti, KellyAnn Sheppard, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2000
Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype
F Galbiati, D Volonte, J B Chu, et al.
European Journal of Neurology
|
March 23, 2016
Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2
C Fiorillo, F Moro, G Brisca, et al.
Neurology
|
January 14, 2004
Clinical and molecular findings in patients with giant axonal neuropathy (GAN)
C Bruno, E Bertini, A Federico, et al.
Clinical Genetics
|
September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I
S Assereto, A Robbiano, M Di Rocco, et al.
Neuromuscular Disorders : NMD
|
November 28, 2012
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases
M Mancuso, C Angelini, E Bertini, et al.
Biochemical and Biophysical Research Communications
|
September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract disease
M Traverso, S Assereto, E Gazzerro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 20, 2008
Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease
M Traverso, C Bruno, A Broccolini, et al.
Page
of 12