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Huntington's Disease-An Outlook on the Interplay of the HTT Protein, Microtubules and Actin Cytoskeletal Components

Cells (Basel, Switzerland), 2020-06, Vol.9 (6), p.1514

2020

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The Tiny Drosophila Melanogaster for the Biggest Answers in Huntington's Disease

International journal of molecular sciences, 2018-08, Vol.19 (8), p.2398

2018

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Is Huntingtin Dispensable in the Adult Brain?

Journal of Huntington's disease, 2017-01, Vol.6 (1), p.1

2017

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Taming the Huntington's Disease Proteome: What Have We Learned?

Journal of Huntington's disease, 2021-01, Vol.10 (2), p.239

2021

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Induced Pluripotent Stem Cells in Huntington's Disease Research: Progress and Opportunity

Journal of Huntington's disease, 2016-01, Vol.5 (2), p.99

2016

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Translation of MicroRNA-Based Huntingtin-Lowering Therapies from Preclinical Studies to the Clinic

Molecular therapy, 2018-04, Vol.26 (4), p.947-962

2018

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The P42 peptide and Peptide-based therapies for Huntington's disease

Orphanet journal of rare diseases, 2016-03, Vol.11 (24), p.24, Article 24

2016

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A Fresh Look at Huntingtin mRNA Processing in Huntington's Disease

Journal of Huntington's disease, 2018-01, Vol.7 (2), p.101

2018

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Non-Cell Autonomous and Epigenetic Mechanisms of Huntington's Disease

International journal of molecular sciences, 2021-11, Vol.22 (22), p.12499

2021

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Primary cilia and autophagic dysfunction in Huntington's disease

Cell death and differentiation, 2015-09, Vol.22 (9), p.1413-1424

2015

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Large animal models for Huntington's disease research

Zoological research, 2024-03, Vol.45 (2), p.275

2024

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The importance of integrating basic and clinical research toward the development of new therapies for Huntington disease

The Journal of clinical investigation, 2011-02, Vol.121 (2), p.476-483

2011

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Modulating Neurotrophin Receptor Signaling as a Therapeutic Strategy for Huntington's Disease

Journal of Huntington's disease, 2017-01, Vol.6 (4), p.303

Simmons, Danielle A

2017

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Huntingtin and Its Role in Mechanisms of RNA-Mediated Toxicity

Toxins, 2021-07, Vol.13 (7), p.487

2021

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Energy dysfunction in Huntington’s disease: insights from PGC-1α, AMPK, and CKB

Cellular and molecular life sciences : CMLS, 2012-12, Vol.69 (24), p.4107-4120

2012

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The Role of the Immune System in Huntington’s Disease

Clinical & developmental immunology, 2013-01, Vol.2013, p.541259-11

2013

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Astrocytes and microglia in neurodegenerative diseases: Lessons from human in vitro models

Progress in neurobiology, 2021-05, Vol.200, p.101973-101973, Article 101973

2021

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Potassium channel dysfunction in neurons and astrocytes in Huntington's disease

CNS neuroscience & therapeutics, 2018-04, Vol.24 (4), p.311-318

2018

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Biological Aging and the Cellular Pathogenesis of Huntington's Disease

Journal of Huntington's disease, 2020-01, Vol.9 (2), p.115

2020

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Dietary fasting and time-restricted eating in Huntington's disease: therapeutic potential and underlying mechanisms

Translational neurodegeneration, 2024-04, Vol.13 (1), p.17-17

2024

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Transgenic animal models for study of the pathogenesis of Huntington's disease and therapy

Drug design, development and therapy, 2015-01, Vol.9 (default), p.2179-2188

2015

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Huntington’s Disease and Mitochondria

Neurotoxicity research, 2017-10, Vol.32 (3), p.518-529

2017

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Cell-Autonomous and Non-cell-Autonomous Pathogenic Mechanisms in Huntington’s Disease: Insights from In Vitro and In Vivo Models

Neurotherapeutics, 2019-10, Vol.16 (4), p.957-978

2019

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Protective Effect of Antioxidants on Neuronal Dysfunction and Plasticity in Huntington’s Disease

Oxidative medicine and cellular longevity, 2017-01, Vol.2017, p.3279061-15

2017

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Huntingtin Lowering Strategies

International journal of molecular sciences, 2020-03, Vol.21 (6), p.2146

2020

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Huntington's Disease-An Outlook on the Interplay of the HTT Protein, Microtubules and Actin Cytoskeletal Components

The Tiny Drosophila Melanogaster for the Biggest Answers in Huntington's Disease

Is Huntingtin Dispensable in the Adult Brain?

Taming the Huntington's Disease Proteome: What Have We Learned?

Induced Pluripotent Stem Cells in Huntington's Disease Research: Progress and Opportunity

Translation of MicroRNA-Based Huntingtin-Lowering Therapies from Preclinical Studies to the Clinic

The P42 peptide and Peptide-based therapies for Huntington's disease

A Fresh Look at Huntingtin mRNA Processing in Huntington's Disease

Non-Cell Autonomous and Epigenetic Mechanisms of Huntington's Disease

Primary cilia and autophagic dysfunction in Huntington's disease

Large animal models for Huntington's disease research

The importance of integrating basic and clinical research toward the development of new therapies for Huntington disease

Modulating Neurotrophin Receptor Signaling as a Therapeutic Strategy for Huntington's Disease

Huntingtin and Its Role in Mechanisms of RNA-Mediated Toxicity

Energy dysfunction in Huntington’s disease: insights from PGC-1α, AMPK, and CKB

The Role of the Immune System in Huntington’s Disease

Astrocytes and microglia in neurodegenerative diseases: Lessons from human in vitro models

Potassium channel dysfunction in neurons and astrocytes in Huntington's disease

Biological Aging and the Cellular Pathogenesis of Huntington's Disease

Dietary fasting and time-restricted eating in Huntington's disease: therapeutic potential and underlying mechanisms

Transgenic animal models for study of the pathogenesis of Huntington's disease and therapy

Huntington’s Disease and Mitochondria

Cell-Autonomous and Non-cell-Autonomous Pathogenic Mechanisms in Huntington’s Disease: Insights from In Vitro and In Vivo Models

Protective Effect of Antioxidants on Neuronal Dysfunction and Plasticity in Huntington’s Disease

Huntingtin Lowering Strategies

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