Item Type | Name |
Academic Article
|
Expression of normal and mutant huntingtin in the developing brain.
|
Academic Article
|
Fast transport and retrograde movement of huntingtin and HAP 1 in axons.
|
Academic Article
|
Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
|
Academic Article
|
Wild-type and mutant huntingtins function in vesicle trafficking in the secretory and endocytic pathways.
|
Academic Article
|
Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease.
|
Academic Article
|
Forskolin and dopamine D1 receptor activation increase huntingtin's association with endosomes in immortalized neuronal cells of striatal origin.
|
Academic Article
|
Are there multiple pathways in the pathogenesis of Huntington's disease?
|
Academic Article
|
Huntingtin expression stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy.
|
Academic Article
|
Caspase 3-cleaved N-terminal fragments of wild-type and mutant huntingtin are present in normal and Huntington's disease brains, associate with membranes, and undergo calpain-dependent proteolysis.
|
Academic Article
|
Changes in cortical and striatal neurons predict behavioral and electrophysiological abnormalities in a transgenic murine model of Huntington's disease.
|
Academic Article
|
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain.
|
Academic Article
|
Huntingtin localization in brains of normal and Huntington's disease patients.
|
Academic Article
|
Huntingtin is present in the nucleus, interacts with the transcriptional corepressor C-terminal binding protein, and represses transcription.
|
Academic Article
|
Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition.
|
Academic Article
|
Huntingtin is degraded to small fragments by calpain after ischemic injury.
|
Academic Article
|
Lysosomal proteases are involved in generation of N-terminal huntingtin fragments.
|
Academic Article
|
Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits.
|
Academic Article
|
Five siRNAs targeting three SNPs may provide therapy for three-quarters of Huntington's disease patients.
|
Academic Article
|
Polyglutamine expansion in huntingtin alters its interaction with phospholipids.
|
Academic Article
|
Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease.
|
Academic Article
|
Mutant huntingtin impairs vesicle formation from recycling endosomes by interfering with Rab11 activity.
|
Academic Article
|
Aberrant Rab11-dependent trafficking of the neuronal glutamate transporter EAAC1 causes oxidative stress and cell death in Huntington's disease.
|
Academic Article
|
Oligonucleotide therapeutic approaches for Huntington disease.
|
Academic Article
|
Native mutant huntingtin in human brain: evidence for prevalence of full-length monomer.
|
Academic Article
|
Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease.
|
Academic Article
|
Hunting down huntingtin.
|
Academic Article
|
Autophagy regulates the processing of amino terminal huntingtin fragments.
|
Academic Article
|
Huntingtin bodies sequester vesicle-associated proteins by a polyproline-dependent interaction.
|
Academic Article
|
Huntingtin associates with acidic phospholipids at the plasma membrane.
|
Academic Article
|
CAG expansion affects the expression of mutant Huntingtin in the Huntington's disease brain.
|
Academic Article
|
Striatal synaptosomes from Hdh140Q/140Q knock-in mice have altered protein levels, novel sites of methionine oxidation, and excess glutamate release after stimulation.
|
Academic Article
|
HTT-lowering reverses Huntington's disease immune dysfunction caused by NF?B pathway dysregulation.
|
Academic Article
|
Increased Steady-State Mutant Huntingtin mRNA in Huntington's Disease Brain.
|
Academic Article
|
Assessment of chloroquine treatment for modulating autophagy flux in brain of WT and HD mice.
|
Academic Article
|
CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems.
|
Academic Article
|
Huntingtin-lowering strategies in Huntington's disease: antisense oligonucleotides, small RNAs, and gene editing.
|
Academic Article
|
Mass Spectrometry Analysis of Wild-Type and Knock-in Q140/Q140 Huntington's Disease Mouse Brains Reveals Changes in Glycerophospholipids Including Alterations in Phosphatidic Acid and Lyso-Phosphatidic Acid.
|
Academic Article
|
Does the Mutant CAG Expansion in Huntingtin mRNA Interfere with Exonucleolytic Cleavage of its First Exon?
|
Academic Article
|
Widespread Central Nervous System Gene Transfer and Silencing After Systemic Delivery of Novel AAV-AS Vector.
|
Academic Article
|
Effects of Exogenous NUB1 Expression in the Striatum of HDQ175/Q7 Mice.
|
Academic Article
|
Autophagy Activation by Transcription Factor EB (TFEB) in Striatum of HDQ175/Q7 Mice.
|
Academic Article
|
Cellular Analysis of Silencing the?Huntington's Disease Gene Using AAV9?Mediated Delivery of Artificial Micro?RNA into the Striatum of?Q140/Q140?Mice.
|
Academic Article
|
Exosome-mediated Delivery of Hydrophobically Modified siRNA for Huntingtin mRNA Silencing.
|
Academic Article
|
Allele-Selective Suppression of Mutant Huntingtin in Primary Human Blood Cells.
|
Academic Article
|
Synthesis and Evaluation of Parenchymal Retention and Efficacy of a Metabolically Stable O-Phosphocholine-N-docosahexaenoyl-l-serine siRNA Conjugate in Mouse Brain.
|
Academic Article
|
A Fresh Look at Huntingtin mRNA Processing in Huntington's Disease.
|
Academic Article
|
Optimized Cholesterol-siRNA Chemistry Improves Productive Loading onto Extracellular Vesicles.
|
Academic Article
|
Artificial miRNAs Reduce Human Mutant Huntingtin Throughout the Striatum in a Transgenic Sheep Model of Huntington's Disease.
|
Academic Article
|
Transvascular Delivery of Hydrophobically Modified siRNAs: Gene Silencing in the Rat Brain upon Disruption of the Blood-Brain Barrier.
|
Academic Article
|
Selective Neuronal Uptake and Distribution of AAVrh8, AAV9, and AAVrh10 in Sheep After Intra-Striatal Administration.
|
Academic Article
|
Rac1 Activity Is Modulated by Huntingtin and Dysregulated in Models of Huntington's Disease.
|
Academic Article
|
Huntingtin associates with the actin cytoskeleton and a-actinin isoforms to influence stimulus dependent morphology changes.
|
Academic Article
|
A divalent siRNA chemical scaffold for potent and sustained modulation of gene expression throughout the central nervous system.
|
Academic Article
|
Allele-Specific Knockdown of Mutant Huntingtin Protein via Editing at Coding Region Single Nucleotide Polymorphism Heterozygosities.
|
Concept
|
Huntingtin Protein
|
Academic Article
|
Chemical engineering of therapeutic siRNAs for allele-specific gene silencing in Huntington's disease models.
|
Academic Article
|
Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease.
|
Academic Article
|
A programmable dual-targeting siRNA scaffold supports potent two-gene modulation in the central nervous system.
|
Academic Article
|
mRNA Nuclear Clustering Leads to a Difference in Mutant Huntingtin mRNA and Protein Silencing by siRNAs In Vivo.
|