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Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 4, 2015
Chromosome substitution strain assessment of a Huntington's disease modifier locusEliana Marisa Ramos, Marina Kovalenko, Jolene R Guide, et al.
Nucleic Acids Research|March 22, 2021
Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirectionJennie C L Roy, Antonia Vitalo, Marissa A Andrew, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Somatic CRISPR editing of Msh3 mitigates Huntington's disease pathology in miceEsaria Oliver, Marina Kovalenko, Mathilde Louçã, et al.
Journal of Huntington'S Disease|February 27, 2018
HttQ111/+ Huntington's Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic DysfunctionMarina Kovalenko, Austen Milnerwood, James Giordano, et al.
Plos Genetics|October 13, 2023
CAG repeat expansion in the Huntington's disease gene shapes linear and circular RNAs biogenesisDilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, et al.
Elife|September 29, 2020
Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease miceMarina Kovalenko, Serkan Erdin, Marissa A Andrew, et al.
Human Molecular Genetics|September 3, 2020
Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-outJacob M Loupe, Ricardo Mouro Pinto, Kyung-Hee Kim, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2024
Identification of genetic modifiers of Huntington's disease somatic CAG repeat instability by in vivo CRISPR-Cas9 genome editingRicardo Mouro Pinto, Ryan Murtha, António Azevedo, et al.
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