Suppression of toxicity of the mutant huntingtin protein by its interacting compound, desonide | PNAS
Mitochondrial Abnormalities and Synaptic Damage in Huntington's Disease: a Focus on Defective Mitophagy and Mitochondria-Targeted Therapeutics | SpringerLink
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TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS | Scientific Reports
Absence of perilipin results in leanness and reverses obesity in Leprdb/db mice | Nature Genetics
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RNA toxicity in non‐coding repeat expansion disorders | The EMBO Journal
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IJMS | Free Full-Text | A Novel Huntington’s Disease Assessment Platform to Support Future Drug Discovery and Development
Insects | Free Full-Text | CRISPR/Cas9-Mediated Mutagenesis of Abdominal-A and Ultrabithorax in the Asian Corn Borer, Ostrinia furnacalis
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients | The EMBO Journal
Biomolecules | Free Full-Text | Oxidative Stress in DNA Repeat Expansion Disorders: A Focus on NRF2 Signaling Involvement
HAP40 is a conserved central regulator of Huntingtin and a potential modulator of Huntington's disease pathogenesis | PLOS Genetics
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4) Researchers sought to understand the genetic basis | Chegg.com
