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Publications by Joan S. Steffan
PIAS1 Regulates Mutant Huntingtin Accumulation and Huntington’s Disease-Associated Phenotypes in Vivo
Neuron
Neuroscience
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Genistein Induces Degradation of Mutant Huntingtin in Fibroblasts From Huntington’s Disease Patients
Metabolic Brain Disease
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Huntingtin Lowering Strategies for Disease Modification in Huntington’s Disease
Neuron
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Inhibition of Aggregation of Mutant Huntingtin by Nucleic Acid Aptamers in Vitro and in a Yeast Model of Huntington’s Disease
Huntington’s Disease: From the Physiological Function of Huntingtin to the Disease
Caspase-6-Resistant Mutant Huntingtin Does Not Rescue the Toxic Effects of Caspase-Cleavable Mutant Huntingtin in Vivo
Journal of Huntington's disease
Molecular Neuroscience
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Control of Huntington’s Disease-Associated Phenotypes by the Striatum-Enriched Transcription Factor Foxp2
Cell Reports
Biochemistry
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Molecular Biology
Silencing of the Mutant Huntingtin Gene Through CRISPR-Cas9 Improves the Mitochondrial Biomarkers in an in Vitro Model of Huntington’s Disease
Cell Transplantation
Transplantation
Biomedical Engineering
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Mutant Huntingtin Impairs Axonal Trafficking in Mammalian Neurons in Vivo and in Vitro
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Compartment-Dependent Degradation of Mutant Huntingtin Accounts for Its Preferential Accumulation in Neuronal Processes
Journal of Neuroscience
Neuroscience