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Nucleic Acids Research|January 21, 2011
Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interferenceMateusz de Mezer, Marzena Wojciechowska, Marek Napierala, et al.
Stem Cell Research|August 26, 2019
Excision of the expanded GAA repeats corrects cardiomyopathy phenotypes of iPSC-derived Friedreich's ataxia cardiomyocytesJixue Li, Natalia Rozwadowska, Amanda Clark, et al.
Annals of Clinical and Translational Neurology|August 17, 2017
Selected missense mutations impair frataxin processing in Friedreich ataxiaElisia Clark, Jill S Butler, Charles J Isaacs, et al.
Biofactors (Oxford, England)|December 13, 2012
Expanded complexity of unstable repeat diseasesUrszula Polak, Elizabeth McIvor, Sharon Y R Dent, et al.
Annals of Clinical and Translational Neurology|July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxiaAngela D Bhalla, Alireza Khodadadi-Jamayran, Yanjie Li, et al.
Nucleic Acids Research|July 12, 2005
Advances in mechanisms of genetic instability related to hereditary neurological diseasesRobert D Wells, Ruhee Dere, Micheal L Hebert, et al.
Antioxidants & Redox Signaling|May 23, 2025
Sulforaphane Targets Multiple Pathological Processes in Friedreich Ataxia Patient-Induced Pluripotent Stem Cell-Derived Sensory NeuronsWenyao Yang, Bruce Thompson, Sara Miellet, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
R loops stimulate genetic instability of CTG.CAG repeatsYunfu Lin, Sharon Y R Dent, John H Wilson, et al.
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