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ingtons-disease/2021-03-29T13:44:43-04:00https://www.chdifoundation.org/scientific-publications/functional-magnetic-resonance-imaging-of-working-memory-in-huntingtons-disease-cross-sectional-data-from-the-image-hd-study/2021-03-29T15:42:49-04:00https://www.chdifoundation.org/scientific-publications/movement-sequencing-in-huntington-disease/2021-03-30T14:00:32-04:00https://www.chdifoundation.org/scientific-publications/aberrantly-spliced-htt-a-new-player-in-huntingtons-disease-pathogenesis/2021-03-30T14:26:36-04:00https://www.chdifoundation.org/scientific-publications/identifying-sleep-disturbances-in-huntingtons-disease-using-a-simple-disease-focused-questionnaire/2021-03-30T16:05:03-04:00https://www.chdifoundation.org/scientific-publications/elevated-brain-3-hydroxykynurenine-and-quinolinate-levels-in-huntington-disease-mice/2021-03-31T13:15:22-04:00https://www.chdifoundation.org/scientific-publications/motor-dysfunction-influence-on-executive-functioning-in-manifest-and-premanifest-huntingtons-disease/2021-03-31T14:29:34-04:00https://www.chdifoundation.org/scientific-publications/huntingtin-gene-cag-repeat-numbers-in-chinese-patients-with-huntingtons-disease-and-controls/2021-04-01T12:43:29-04:00https://www.chdifoundation.org/scientific-publications/small-molecule-trkb-receptor-agonists-improve-motor-function-and-extend-survival-in-a-mouse-model-of-huntingtons-disease/2021-04-01T16:08:58-04:00https://www.chdifoundation.org/scientific-publications/striatal-synaptic-dysfunction-and-hippocampal-plasticity-deficits-in-the-hu97-18-mouse-model-of-huntington-disease/2021-04-05T14:44:14-04:00https://www.chdifoundation.org/scientific-publications/disposition-of-proteins-and-lipids-in-synaptic-membrane-compartments-is-altered-in-q175-q7-huntingtons-disease-mouse-striatum/2021-04-05T15:46:26-04:00https://www.chdifoundation.org/scientific-publications/structure-based-exploration-of-selectivity-for-atm-inhibitors-in-huntingtons-disease/2021-04-23T08:39:51-04:00https://www.chdifoundation.org/scientific-publications/activated-microglia-proliferate-at-neurites-of-mutant-huntingtin-expressing-neurons/2021-04-06T10:12:45-04:00https://www.chdifoundation.org/scientific-publications/dysfunctions-in-circadian-behavior-and-physiology-in-mouse-models-of-huntingtons-disease/2021-04-06T14:07:50-04:00https://www.chdifoundation.org/scientific-publications/dopamine-dependent-long-term-potentiation-in-the-dorsal-striatum-is-reduced-in-the-r6-2-mouse-model-of-huntingtons-disease/2021-04-06T15:04:12-04:00https://www.chdifoundation.org/scientific-publications/genetic-manipulations-of-mutant-huntingtin-in-mice-new-insights-into-huntingtons-disease-pathogenesis/2021-04-06T15:49:59-04:00https://www.chdifoundation.org/scientific-publications/tracking-motor-impairments-in-the-progression-of-huntingtons-disease/2021-04-07T15:16:44-04:00https://www.chdifoundation.org/scientific-publications/widespread-and-sustained-target-engagement-in-huntingtons-disease-minipigs-upon-intrastriatal-microrna-based-gene-therapy/2021-04-08T09:31:30-04:00https://www.chdifoundation.org/scientific-publications/pitfalls-in-the-detection-of-cholesterol-in-huntingtons-disease-models/2021-04-09T15:41:44-04:00https://www.chdifoundation.org/scientific-publications/a-genome-scale-rna-interference-screen-identifies-rras-signaling-as-a-pathologic-feature-of-huntingtons-disease/2021-04-12T14:09:14-04:00https://www.chdifoundation.org/scientific-publications/formation-of-polyglutamine-inclusions-in-a-wide-range-of-non-cns-tissues-in-the-hdhq150-knock-in-mouse-model-of-huntingtons-disease/2021-04-12T15:42:49-04:00https://www.chdifoundation.org/scientific-publications/early-and-progressive-circadian-abnormalities-in-huntingtons-disease-sheep-are-unmasked-by-social-environment/2021-04-13T15:31:28-04:00https://www.chdifoundation.org/scientific-publications/changes-in-cognitive-control-in-pre-manifest-huntingtons-disease-examined-using-pre-saccadic-eeg-potentials-a-longitudinal-study/2021-04-14T14:58:24-04:00https://www.chdifoundation.org/scientific-publications/neurochemical-correlates-of-caudate-atrophy-in-huntingtons-disease/2021-04-15T14:04:56-04:00https://www.chdifoundation.org/scientific-publications/correlative-light-and-electron-microscopy-suggests-that-mutant-huntingtin-dysregulates-the-endolysosomal-pathway-in-presymptomatic-huntingtons-disease/2021-04-16T08:49:31-04:00https://www.chdifoundation.org/scientific-publications/management-of-sleep-wake-cycles-improves-cognitive-function-in-a-transgenic-mouse-model-of-huntingtons-disease/2021-04-16T11:50:36-04:00https://www.chdifoundation.org/scientific-publications/integration-of-%ce%b2-catenin-sirtuin-and-foxo-signaling-protects-from-mutant-huntingtin-toxicity/2021-04-16T11:56:20-04:00https://www.chdifoundation.org/scientific-publications/pathways-to-decoding-the-clinical-potential-of-stress-response-foxo-interaction-networks-for-huntingtons-disease-of-gene-prioritization-and-context-dependence/2021-04-19T12:35:42-04:00https:/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