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Paper Details

Single-Nucleus RNA-Seq Reveals Dysregulation of Striatal Cell Identity Due to Huntington's Disease Mutations.
J Neurosci
24
2021
4524 cells, DEGs, HD, HD mutation, HTT, Htt, Huntington's Disease, Huntington's disease, MSN subtypes, MSNs, PRC, PRC2, Single, Striatal Cell, cell type identity genes, cell type-specific genes, differentially expressed genes, dominantly inherited neurodegenerative disorder, exon 1, genes, glial populations, huntingtin, huntingtin (HTT) gene, medium spiny neurons, mice, mouse, nuclear transcriptomes, polycomb repressive complex, polycomb repressive complex 2, striatal, striatal cell types, striatal medium spiny neurons, trinucleotide, wild
Author NameAffiliation
Brian R HerbInstitute for Genome Sciences, University of Maryland School of Medicine
Brian R HerbInstitute for Genome Sciences, University of Maryland School of Medicine
Seth A AmentInstitute for Genome Sciences, University of Maryland School of Medicine
Seth A AmentUniversity of Maryland School of Medicine
Seth A AmentInstitute for Genome Sciences, University of Maryland School of Medicine
Seth A AmentUniversity of Maryland School of Medicine
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