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Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2022
Repeat-Associated Non-AUG Translation of AGAGGG Repeats that Cause X-Linked Dystonia-ParkinsonismCharles Jourdan Reyes, Katsura Asano, Peter K Todd, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|July 12, 2017
Matrin3 binds directly to intronic pyrimidine-rich sequences and controls alternative splicingYuri Uemura, Takuya Oshima, Munetaka Yamamoto, et al.
Cell Reports|August 31, 2023
iPSC motor neurons, but not other derived cell types, capture gene expression changes in postmortem sporadic ALS motor neuronsAaron Held, Michelle Adler, Christine Marques, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 2, 2022
Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor PhenotypeJulia Steinhardt, Henrike Hanssen, Marcus Heldmann, et al.
Neurology. Genetics|July 12, 2021
Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore SequencingCharles Jourdan Reyes, Björn-Hergen Laabs, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 11, 2020
DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-ParkinsonismChristin Krause, Susen Schaake, Karen Grütz, et al.
Genes|January 21, 2022
Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in <i>TAF1</i> with Nanopore SequencingTheresa Lüth, Joshua Laβ, Susen Schaake, et al.
Annals of Neurology|January 16, 2023
Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-ParkinsonismHenrike Hanssen, Cid C E Diesta, Marcus Heldmann, et al.
Annals of Neurology|April 12, 2019
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonismAna Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
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