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Human Molecular Genetics|February 15, 2011
Absence of disturbed axonal transport in spinal and bulbar muscular atrophyBilal Malik, Niranjanan Nirmalananthan, Lynsey G Bilsland, et al.
Acta Neuropathologica Communications|June 2, 2023
X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular diseaseAnastasia Gromova, Byeonggu Cha, Erica M Robinson, et al.
Gene|February 18, 2005
A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosageStephen M Jackson, Alex J Whitworth, Jessica C Greene, et al.
Antioxidants & Redox Signaling|May 7, 2013
S-nitrosylation of dynamin-related protein 1 mediates mutant huntingtin-induced mitochondrial fragmentation and neuronal injury in Huntington's diseaseFlorian Haun, Tomohiro Nakamura, Alicia D Shiu, et al.
Molecular Neurobiology|November 25, 2025
The 4E-BPs as Translational Regulators in Neurological Disorders: Molecular Mechanisms and Therapeutic PotentialSindhu S Baskarapantula, Venkata Surya Kumar, Priyajit Changdar, et al.
Nature Medicine|March 6, 2018
Selective modulation of the androgen receptor AF2 domain rescues degeneration in spinal bulbar muscular atrophyNisha M Badders, Ane Korff, Helen C Miranda, et al.
Science (New York, N.Y.)|March 9, 2002
Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1Angeles Fernandez-Gonzalez, Albert R La Spada, Jason Treadaway, et al.
Human Molecular Genetics|May 2, 2007
Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicityIsabella Palazzolo, Barrington G Burnett, Jessica E Young, et al.
International Journal of Molecular Sciences|February 27, 2026
PPAR-Delta Agonist Therapies Did Not Rescue Hallmark Disease Phenotypes in Two Sets of Preclinical Trials in ALS TDP-43 and C9orf72 Model MiceDavid T Luong, Chenchen Niu, Eunice Kim, et al.
Nature Communications|February 3, 2023
Alternative polyadenylation transcriptome-wide association study identifies APA-linked susceptibility genes in brain disordersYa Cui, Frederick J Arnold, Fanglue Peng, et al.
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