Search research articles
Contact Us
Filters
Showing results (41-50 of 346) with videos related to
Page
of 35
Sort By:
FEBS Letters
|
June 14, 2002
The dystrophin gene is alternatively spliced throughout its coding sequence
M Sironi, R Cagliani, U Pozzoli, et al.
Plos Genetics
|
February 23, 2010
Genome-wide identification of susceptibility alleles for viral infections through a population genetics approach
Matteo Fumagalli, Uberto Pozzoli, Rachele Cagliani, et al.
Journal of Cellular and Molecular Medicine
|
December 6, 2019
Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights
Matteo Saladini, Monica Nizzardo, Alessandra Govoni, et al.
European Journal of Biochemistry
|
April 1, 1979
beta-Like globin RNA sequences in hemoglobin Lepore disease
B Giglioni, P Comi, R Taramelli, et al.
Molecular Neurobiology
|
May 24, 2020
The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer's Disease and Parkinson's Disease
Giacomo Monzio Compagnoni, Alessio Di Fonzo, Stefania Corti, et al.
Genome Biology
|
December 22, 2006
Gene function and expression level influence the insertion/fixation dynamics of distinct transposon families in mammalian introns
Manuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Human Molecular Genetics
|
June 9, 2016
iPSC-derived LewisX+CXCR4+β1-integrin+ neural stem cells improve the amyotrophic lateral sclerosis phenotype by preserving motor neurons and muscle innervation in human and rodent models
Monica Nizzardo, Monica Bucchia, Agnese Ramirez, et al.
Cell Transplantation
|
October 10, 2012
Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectives
Monica Nizzardo, Chiara Simone, Marianna Falcone, et al.
Progress in Neurobiology
|
August 6, 2011
ALS genetic modifiers that increase survival of SOD1 mice and are suitable for therapeutic development
Giulietta Riboldi, Monica Nizzardo, Chiara Simone, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 28, 2025
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature
Sabrina Lucchiari, Francesca Magri, Martina Rimoldi, et al.
Page
of 35
Search research articles
Search
Showing results (41-50 of 346) with videos related to
Sort By:
Page
of 35
FEBS Letters
|
June 14, 2002
The dystrophin gene is alternatively spliced throughout its coding sequence
M Sironi, R Cagliani, U Pozzoli, et al.
Plos Genetics
|
February 23, 2010
Genome-wide identification of susceptibility alleles for viral infections through a population genetics approach
Matteo Fumagalli, Uberto Pozzoli, Rachele Cagliani, et al.
Journal of Cellular and Molecular Medicine
|
December 6, 2019
Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights
Matteo Saladini, Monica Nizzardo, Alessandra Govoni, et al.
European Journal of Biochemistry
|
April 1, 1979
beta-Like globin RNA sequences in hemoglobin Lepore disease
B Giglioni, P Comi, R Taramelli, et al.
Molecular Neurobiology
|
May 24, 2020
The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer's Disease and Parkinson's Disease
Giacomo Monzio Compagnoni, Alessio Di Fonzo, Stefania Corti, et al.
Genome Biology
|
December 22, 2006
Gene function and expression level influence the insertion/fixation dynamics of distinct transposon families in mammalian introns
Manuela Sironi, Giorgia Menozzi, Giacomo P Comi, et al.
Human Molecular Genetics
|
June 9, 2016
iPSC-derived LewisX+CXCR4+β1-integrin+ neural stem cells improve the amyotrophic lateral sclerosis phenotype by preserving motor neurons and muscle innervation in human and rodent models
Monica Nizzardo, Monica Bucchia, Agnese Ramirez, et al.
Cell Transplantation
|
October 10, 2012
Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectives
Monica Nizzardo, Chiara Simone, Marianna Falcone, et al.
Progress in Neurobiology
|
August 6, 2011
ALS genetic modifiers that increase survival of SOD1 mice and are suitable for therapeutic development
Giulietta Riboldi, Monica Nizzardo, Chiara Simone, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 28, 2025
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature
Sabrina Lucchiari, Francesca Magri, Martina Rimoldi, et al.
Page
of 35