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Cell Stem Cell|December 2, 2022
3D ECM-rich environment sustains the identity of naive human iPSCsElisa Cesare, Anna Urciuolo, Hannah T Stuart, et al.Acta Neuropathologica Communications|March 22, 2023
Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variantNastasia Cardone, Melissa Moula, Rianne J Baelde, et al.BMC Medical Genetics|August 17, 2012
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotypeSimona Brioschi, Francesca Gualandi, Chiara Scotton, et al.International Journal of Molecular Sciences|November 27, 2024
ICOSLG Is Associated with Anti-PD-1 and Concomitant Antihistamine Treatment Response in Advanced MelanomaDomenico Mallardo, Mario Fordellone, Margaret Ottaviano, et al.Frontiers in Genetics|February 12, 2019
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani FamilyStefania Bigoni, Marcella Neri, Chiara Scotton, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 26, 2009
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mousePaola Rimessi, Patrizia Sabatelli, Marina Fabris, et al.Journal of Experimental & Clinical Cancer Research : CR|February 14, 2025
Suppression of Spry1 reduces HIF1α-dependent glycolysis and impairs angiogenesis in BRAF-mutant cutaneous melanomaBarbara Montico, Giorgio Giurato, Roberto Guerrieri, et al.Nucleus (Austin, Tex.)|April 26, 2018
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processesPia Bernasconi, Nicola Carboni, Giulia Ricci, et al.Frontiers in Genetics|July 29, 2020
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular DystrophyChiara Passarelli, Rita Selvatici, Alberto Carrieri, et al.Journal of Cell Science|March 6, 2016
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathyChiara Scotton, Matteo Bovolenta, Elena Schwartz, et al.Pageof 9