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European Journal of Human Genetics : EJHG|October 18, 2012
Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585Julia Schreml, Markus Riessland, Mario Paterno, et al.Human Molecular Genetics|August 14, 2010
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophyThomas M Wishart, Jack P-W Huang, Lyndsay M Murray, et al.Human Molecular Genetics|August 16, 2011
Reversible molecular pathology of skeletal muscle in spinal muscular atrophyChantal A Mutsaers, Thomas M Wishart, Douglas J Lamont, et al.Human Molecular Genetics|April 12, 2011
ApoE isoform-specific regulation of regeneration in the peripheral nervous systemLaura H Comley, Heidi R Fuller, Thomas M Wishart, et al.Journal of Anatomy|October 11, 2021
Neutralisation of SARS-CoV-2 by anatomical embalming solutionsFabio Quondamatteo, Dora E Corzo-Leon, Cecilia Brassett, et al.JCI Insight|October 5, 2016
Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophyRachael A Powis, Evangelia Karyka, Penelope Boyd, et al.Cellular and Molecular Gastroenterology and Hepatology|February 5, 2021
SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver DiseaseMarc-Olivier Deguise, Chantal Pileggi, Yves De Repentigny, et al.The Journal of Clinical Investigation|September 13, 2022
Microvasculopathy in spinal muscular atrophy is driven by a reversible autonomous endothelial cell defectHaiyan Zhou, Ying Hong, Mariacristina Scoto, et al.The Journal of Clinical Investigation|May 9, 2024
Hepatocyte-intrinsic SMN deficiency drives metabolic dysfunction and liver steatosis in spinal muscular atrophyDamien Meng-Kiat Leow, Yang Kai Ng, Loo Chien Wang, et al.Annals of Clinical and Translational Neurology|August 13, 2019
Abnormal fatty acid metabolism is a core component of spinal muscular atrophyMarc-Olivier Deguise, Giovanni Baranello, Chiara Mastella, et al.Pageof 5