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Frontiers in Physiology
|
November 8, 2021
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic Diseases
Maria Sofia Falzarano, Rachele Rossi, Andrea Grilli, et al.
Human Gene Therapy
|
August 18, 2016
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype
Maria Sofia Falzarano, Domenico D'Amario, Andrea Siracusano, et al.
Biorxiv : the Preprint Server for Biology
|
June 6, 2025
Mapping satellite glial cell heterogeneity reveals distinct spatial organization and signifies functional diversity in the dorsal root ganglion
Ole A Ahlgreen, Mads W Hansen, Jonas Baake, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 24, 2025
Mapping Satellite Glial Cell Heterogeneity Reveals Distinct Spatial Organization and Implies Functional Diversity in the Dorsal Root Ganglion
Ole Andreas Ahlgreen, Mads Würgler Hansen, Jonas Baake, et al.
Neurobiology of Disease
|
June 24, 2026
Morphine reprograms brain-derived extracellular vesicle cargo associated with synaptic remodeling in the prefrontal cortex
Pedro H Gobira, Savio Bastos, Rachele Rossi, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
November 4, 2024
A nanoencapsulated oral formulation of fenretinide promotes local and metastatic breast cancer dormancy in HER2/neu transgenic mice
Maria Laura De Angelis, Federica Francescangeli, Eleonora Aricò, et al.
International Journal of Molecular Sciences
|
November 27, 2024
Network Analysis of miRNA and Cytokine Landscape in Human Hematopoiesis
Alessandro Vici, Germana Castelli, Federica Francescangeli, et al.
Frontiers in Physiology
|
July 26, 2021
Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse Model and Patients
Rachele Rossi, Maria Sofia Falzarano, Hana Osman, et al.
Human Mutation
|
May 26, 2017
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
Alessia Nasca, Chiara Scotton, Irina Zaharieva, et al.
Frontiers in Genetics
|
February 12, 2019
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family
Stefania Bigoni, Marcella Neri, Chiara Scotton, et al.
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Search research articles
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Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Frontiers in Physiology
|
November 8, 2021
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential <i>in vitro</i> Model for Rare Genetic Diseases
Maria Sofia Falzarano, Rachele Rossi, Andrea Grilli, et al.
Human Gene Therapy
|
August 18, 2016
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype
Maria Sofia Falzarano, Domenico D'Amario, Andrea Siracusano, et al.
Biorxiv : the Preprint Server for Biology
|
June 6, 2025
Mapping satellite glial cell heterogeneity reveals distinct spatial organization and signifies functional diversity in the dorsal root ganglion
Ole A Ahlgreen, Mads W Hansen, Jonas Baake, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 24, 2025
Mapping Satellite Glial Cell Heterogeneity Reveals Distinct Spatial Organization and Implies Functional Diversity in the Dorsal Root Ganglion
Ole Andreas Ahlgreen, Mads Würgler Hansen, Jonas Baake, et al.
Neurobiology of Disease
|
June 24, 2026
Morphine reprograms brain-derived extracellular vesicle cargo associated with synaptic remodeling in the prefrontal cortex
Pedro H Gobira, Savio Bastos, Rachele Rossi, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
November 4, 2024
A nanoencapsulated oral formulation of fenretinide promotes local and metastatic breast cancer dormancy in HER2/neu transgenic mice
Maria Laura De Angelis, Federica Francescangeli, Eleonora Aricò, et al.
International Journal of Molecular Sciences
|
November 27, 2024
Network Analysis of miRNA and Cytokine Landscape in Human Hematopoiesis
Alessandro Vici, Germana Castelli, Federica Francescangeli, et al.
Frontiers in Physiology
|
July 26, 2021
Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse Model and Patients
Rachele Rossi, Maria Sofia Falzarano, Hana Osman, et al.
Human Mutation
|
May 26, 2017
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
Alessia Nasca, Chiara Scotton, Irina Zaharieva, et al.
Frontiers in Genetics
|
February 12, 2019
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family
Stefania Bigoni, Marcella Neri, Chiara Scotton, et al.
Page
of 5