Chromatin dysfunction in Huntington's disease

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Towards AI-driven prediction of <i>HTT</i> CAG size in super-expanded human spiny projection neurons from Huntington disease donors.

Journal of Huntington's disease·2026

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Longitudinal and combined assessment of 24(S)-hydroxycholesterol and Neurofilament light chain in the early stages of Huntington's disease.

Neurobiology of disease·2026

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Corrigendum to "Transplanted human striatal progenitors exhibit functional integration and modulate host circuitry in a Huntington's disease animal model" [Pharmacol. Res. 219 (2025) 107905].

Pharmacological research·2026

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Introduction to special issue: neurodevelopment in huntington's disease.

Journal of Huntington's disease·2026

Same author

A human CAGinSTEM platform for decoding HTT repeats' somatic instability links CAG interruption to HD pathology in neurons.

Cell reports·2025

Same author

Corrigendum to 'Insights into kinetics, release, and behavioral effects of brain-targeted hybrid nanoparticles for cholesterol delivery in Huntington's disease' J Control Release. 2021 Feb 10;330:587-598.

Journal of controlled release : official journal of the Controlled Release Society·2025

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Deletion of Fbxo25 causes excessive repetitive behavior, impaired recognition memory, reduced dendritic complexity, and aberrant protein expression in mice.

Progress in neurobiology·2026

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Neuropsychiatric Disease Mechanisms and Interventions. from 22q11.2 Deletion Syndrome Experimental Studies.

Progress in neurobiology·2026

Same journal

REM sleep as a dummy-model of the world: A theoretical framework.

Progress in neurobiology·2026

Same journal

CA3 transiently modulates spatial representation in CA1.

Progress in neurobiology·2026

Same journal

Love, death, and oxytocin: In memory of Larry Young.

Progress in neurobiology·2026

Same journal

Assessing peripheral oxytocin and cortisol levels and epigenetic variations of oxytocin receptor and glucocorticoid receptor genes in school-aged preterm-born children.

Progress in neurobiology·2026

Related Experiment Videos

Chromatin dysfunction in Huntington's disease

Related Concept Videos

Towards AI-driven prediction of <i>HTT</i> CAG size in super-expanded human spiny projection neurons from Huntington disease donors.

Longitudinal and combined assessment of 24(S)-hydroxycholesterol and Neurofilament light chain in the early stages of Huntington's disease.

Corrigendum to "Transplanted human striatal progenitors exhibit functional integration and modulate host circuitry in a Huntington's disease animal model" [Pharmacol. Res. 219 (2025) 107905].

Introduction to special issue: neurodevelopment in huntington's disease.

A human CAGinSTEM platform for decoding HTT repeats' somatic instability links CAG interruption to HD pathology in neurons.

Corrigendum to 'Insights into kinetics, release, and behavioral effects of brain-targeted hybrid nanoparticles for cholesterol delivery in Huntington's disease' J Control Release. 2021 Feb 10;330:587-598.

Deletion of Fbxo25 causes excessive repetitive behavior, impaired recognition memory, reduced dendritic complexity, and aberrant protein expression in mice.

Neuropsychiatric Disease Mechanisms and Interventions. from 22q11.2 Deletion Syndrome Experimental Studies.

REM sleep as a dummy-model of the world: A theoretical framework.

CA3 transiently modulates spatial representation in CA1.

Love, death, and oxytocin: In memory of Larry Young.

Assessing peripheral oxytocin and cortisol levels and epigenetic variations of oxytocin receptor and glucocorticoid receptor genes in school-aged preterm-born children.

Related Experiment Videos

Chromatin dysfunction in Huntington's disease

Related Concept Videos

Related Articles

Towards AI-driven prediction of <i>HTT</i> CAG size in super-expanded human spiny projection neurons from Huntington disease donors.

Longitudinal and combined assessment of 24(S)-hydroxycholesterol and Neurofilament light chain in the early stages of Huntington's disease.

Corrigendum to "Transplanted human striatal progenitors exhibit functional integration and modulate host circuitry in a Huntington's disease animal model" [Pharmacol. Res. 219 (2025) 107905].

Introduction to special issue: neurodevelopment in huntington's disease.

A human CAGinSTEM platform for decoding HTT repeats' somatic instability links CAG interruption to HD pathology in neurons.

Corrigendum to 'Insights into kinetics, release, and behavioral effects of brain-targeted hybrid nanoparticles for cholesterol delivery in Huntington's disease' J Control Release. 2021 Feb 10;330:587-598.

Deletion of Fbxo25 causes excessive repetitive behavior, impaired recognition memory, reduced dendritic complexity, and aberrant protein expression in mice.

Neuropsychiatric Disease Mechanisms and Interventions. from 22q11.2 Deletion Syndrome Experimental Studies.

REM sleep as a dummy-model of the world: A theoretical framework.

CA3 transiently modulates spatial representation in CA1.

Love, death, and oxytocin: In memory of Larry Young.

Assessing peripheral oxytocin and cortisol levels and epigenetic variations of oxytocin receptor and glucocorticoid receptor genes in school-aged preterm-born children.