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Experimental Biology and Medicine (Maywood, N.J.)|January 26, 2026
Beginning of a new era of synthetic messenger RNA therapeutics: Comprehensive insights on mRNA drug design, development and applicationsSaumya Nishanga Heendeniya, Suxiang Chen, Saadia Bhatti, et al.Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.Oncogenesis|November 10, 2015
A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinomaA Stirnweiss, K McCarthy, J Oommen, et al.Plos One|January 9, 2016
Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping StrategiesZhi Yon Charles Toh, May Thandar Aung-Htut, Gavin Pinniger, et al.International Journal of Molecular Sciences|October 17, 2019
Systematic Approach to Developing Splice Modulating Antisense OligonucleotidesMay T Aung-Htut, Craig S McIntosh, Kristin A Ham, et al.Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouseC J Mann, K Honeyman, A J Cheng, et al.International Journal of Molecular Sciences|April 12, 2022
Antisense Oligonucleotide Induction of the hnRNPA1b Isoform Affects Pre-mRNA Splicing of SMN2 in SMA Type I FibroblastsJarichad Toosaranont, Sukanya Ruschadaariyachat, Warasinee Mujchariyakul, et al.Human Gene Therapy|January 24, 2013
A novel morpholino oligomer targeting ISS-N1 improves rescue of severe spinal muscular atrophy transgenic miceHaiyan Zhou, Narinder Janghra, Chalermchai Mitrpant, et al.Neuroscience|June 27, 2012
Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophyR S Anderton, L L Price, B J Turner, et al.Nature Genetics|January 1, 1995
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyN G Laing, S D Wilton, P A Akkari, et al.Pageof 19