- Recent advances in stem cell therapy: efficacy, ethics, safety concerns, and future directions focusing on neurodegenerative disorders - a review
- Clinical experience and treatment considerations with vesicular monoamine transport 2 inhibitors
- Hijacking intercellular trafficking for the spread of protein aggregates in neurodegenerative diseases: a focus on tunneling nanotubes (TNTs)
- Pharmacology, Signaling and Therapeutic Potential of Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators
- Mechanisms for plastic landmark anchoring in zebrafish compass neurons
- Ideal animal models according to multifaceted mechanisms and peculiarities in neurological disorders: present and challenges
- Docosahexaenoic Acid (DHA) Supplementation in a Triglyceride Form Prevents from Polyglutamine-Induced Dysfunctions in <em>Caenorhabditis elegans</em>
- Decoding Neurodegeneration: A Review of Molecular Mechanisms and Therapeutic Advances in Alzheimer's, Parkinson's, and ALS
- Potential Protective Effects of Pungent Flavor Components in Neurodegenerative Diseases
- Calcium Ions in the Physiology and Pathology of the Central Nervous System
- Advances and Challenges in Gene Therapy for Neurodegenerative Diseases: A Systematic Review
- Navigating triplet repeats sequencing: concepts, methodological challenges and perspective for Huntington's disease
- Isothiocyanates induce autophagy and inhibit protein synthesis in primary cells via modulation of AMPK-mTORC1-S6K1 signaling pathway, and protect against mutant huntingtin aggregation
- Traversing the epigenetic landscape: DNA methylation from retina to brain in development and disease
- When repetita no-longer iuvant: somatic instability of the CAG triplet in Huntington's disease
- Unlocking the neuroprotective potential of Ziziphora clinopodioides flavonoids in combating neurodegenerative diseases and other brain injuries
- Mechanism and Clinical Application Prospects of Mitochondrial DNA Single Nucleotide Polymorphism in Neurodegenerative Diseases
- Ascertainment of uninterrupted CAG repeat length and disease-modifying variants in fragment-based genetic testing for Huntington Disease
- Frequency and neuropathology of HTT repeat expansions in FTD/ALS: co-existence rather than causation
- Cognitive impairment predicts medication discrepancies in Huntington's Disease: patient self-report compared to pharmacy records
- Distinct roles of ascorbic acid in extracellular vesicles and free form: Implications for metabolism and oxidative stress in presymptomatic Huntington's Disease
- Mitochondria-targeted nanotherapeutics: A new Frontier in neurodegenerative disease treatment
- Glial response in the midcingulate cortex in Huntington's disease
- The kinase LRRK2 is required for the physiological function and expression of the glial glutamate transporter EAAT2 (SLC1A2)
- Advanced Glycation End Products in Neurodegenerative Diseases
- Insights into the causes and consequences of DNA repeat expansions from 700,000 biobank participants
- A tool to automate assessment of regional brain atrophy in mouse models of neurodegenerative disease
- Beyond Huntington's Disease - Late-Onset Chorea Caused by a Homozygous Variant in ERCC4
- The eye movement and gait variability analysis in Chinese patients with Huntington's disease
- Therapeutic targeting of the oxidative stress generated by pathological molecular pathways in the neurodegenerative diseases, ALS and Huntington's
- No Evidence of Early Developmental Delay in Juvenile-Onset Huntington's Disease Patients
- Corticostriatal maldevelopment in the R6/2 mouse model of juvenile Huntington's disease
- CAFE: An Integrated Web App for High-Dimensional Analysis and Visualization in Spectral Flow Cytometry
- Spontaneous Intracranial Hypotension as a Cause of Exacerbation in Huntington's Disease - ERRATUM
- Spontaneous Intracranial Hypotension as a Cause of Exacerbation in Huntington's Disease - ADDENDUM
- A novel cryptic splice donor due to synonymous variant in <em>VPS13A</em> as an underlying cause of a chorea-acanthocytosis in a large family
- Impact of somato-cognitive coordination therapy on activities of daily living in a patient with Huntington's disease
- Single prolonged stress induces behavior and transcriptomic changes in the medial prefrontal cortex to increase susceptibility to anxiety-like behavior in rats
- Role of Rho-associated kinases and their inhibitor fasudil in neurodegenerative diseases
- Extrachromosomal DNA: Molecular perspectives in aging and neurodegenerative diseases
- Cognitive engagement may slow clinical progression and brain atrophy in Huntington's disease
- CRISPR/Cas9-induced double-strand breaks in the huntingtin locus lead to CAG repeat contraction through DNA end resection and homology-mediated repair
- Evidence-Based Review on Symptomatic Management of Huntington's Disease
- Intrathecal baclofen pump for severe hypertonia in a patient with juvenile Huntington's disease: illustrative case
- beta-Blocker Use and Delayed Onset and Progression of Huntington Disease
- Protective Effects of Antcin H Isolated from Antrodia cinnamomea Against Neuroinflammation in Huntington's Disease via NLRP3 Inflammasome Inhibition
- Bioinformatics and Machine Learning-Based Identification of Critical Biomarkers and Immune Infiltration in Venous Thromboembolism
- C. elegans huntingtin, htt-1, promotes robust autophagy induction and survival under stress conditions
- How many people have a Huntington's Disease expansion: A population-based prevalence study in Northern Scotland
- Unveiling the structural proteome of an Alzheimer's disease rat brain model
- A tool to automate assessment of regional brain atrophy in mouse models of neurodegenerative disease
- Shifting focus from ideality to reality: a qualitative study on how quality of life is defined by premanifest and manifest Huntington's disease gene expansion carriers
- Brain-derived neurotrophic factor plays with TRiC: focus on synaptic dysfunction in Huntington's disease
- Emerging biophysical techniques for probing synaptic transmission in neurodegenerative disorders
- Unveiling biomarker detection in Alzheimer's disease: a computational approach to microarray analysis
- Insights into RNA-mediated pathology in new mouse models of Huntington's disease
- Corrigendum: An automatic measure for speech intelligibility in dysarthrias-validation across multiple languages and neurological disorders
- Roscovitine, a CDK Inhibitor, Reduced Neuronal Toxicity of mHTT by Targeting HTT Phosphorylation at S1181 and S1201 In Vitro
- Advancements in Targeting Ion Channels for the Treatment of Neurodegenerative Diseases
- Erucin, a Natural Isothiocyanate, Prevents Polyglutamine-Induced Toxicity in <em>Caenorhabditis elegans</em> via <em>aak-2</em>/AMPK and <em>daf-16</em>/FOXO Signaling
- Co-Aggregation of TDP-43 with Other Pathogenic Proteins and Their Co-Pathologies in Neurodegenerative Diseases
- Exosome Cargo in Neurodegenerative Diseases: Leveraging Their Intercellular Communication Capabilities for Biomarker Discovery and Therapeutic Delivery
- Exploring the Connection Between Nanomaterials and Neurodegenerative Disorders
- Quantitative and Computational Spinal Imaging in Neurodegenerative Conditions and Acquired Spinal Disorders: Academic Advances and Clinical Prospects
- Calcium bridges built by mitochondria-associated endoplasmic reticulum membranes: potential targets for neural repair in neurological diseases
- Global analysis of endogenous protein disorder in cells
- Copper homeostasis and neurodegenerative diseases
- Small molecule modulation of p75(NTR) engages the autophagy-lysosomal pathway and reduces huntingtin aggregates in cellular and mouse models of Huntington's disease
- Insights into the causes and consequences of DNA repeat expansions from 700,000 biobank participants
- Exploring the role of vault complex in the nervous system: a literature review
- Neuroacanthocytosis: Case report and neuroimaging findings
- Striatum-enriched protein, arginase 2 localizes to medium spiny neurons and controls striatal metabolic profile
- Purinergic-associated immune responses in neurodegenerative diseases
- Reprogrammed human lateral ganglionic eminence precursors generate striatal neurons and restore motor function in a rat model of Huntington's disease
- Saffron and its major constituents against neurodegenerative diseases: A mechanistic review
- Unknown roles of tau pathology in neurological disorders. Challenges and new perspectives
- Critical role of hydrogen sulfide in the management of neurodegenerative disease
- Damage of the Phospholipid Bilayer by Aβ42 at Physiologically Relevant Peptide Concentrations
- Myelin Lipid Alterations in Neurodegenerative Diseases: Landscape and Pathogenic Implications
- Suppression of Huntington's Disease Somatic Instability by Transcriptional Repression and Direct CAG Repeat Binding
- F2,6BP restores mitochondrial genome integrity in Huntington's Disease
- Exploration of the Role of Vitamins in Preventing Neurodegenerative Diseases: Comprehensive Review on Preclinical and Clinical Findings
- Interplay between Sex and Disease Burden in Huntington's Disease: Clinical and Neuroimaging Perspectives
- Huntingtin CAG repeat size variations below the Huntington's disease threshold: associations with depression, anxiety and basal ganglia structure
- The Impact of Aging on Neurological Diseases in the Elderly: Molecular Mechanisms and Therapeutic Perspectives
- Correction: Huntington Disease Health Related Quality of Life, Function and Well Being: The Patient's Perspective
- Exploring the role of Cdk5 on striatal synaptic plasticity in a 3-NP-induced model of early stages of Huntington's disease
- Data-driven Huntington's disease progression modelling and estimation of societal cost in the UK
- More than just a number: the gut microbiota and brain function across the extremes of life
- Copper homeostasis and cuproptosis in central nervous system diseases
- Apathy and Functional Status in Early-Stage Huntington's Disease
- Mitochondrial DAMPs: Key Mediators in Neuroinflammation and Neurodegenerative Disease Pathogenesis
- Break-up and recovery of harmony between direct and indirect pathways in the basal ganglia: Huntington's disease and treatment
- Preventing acute neurotoxicity of CNS therapeutic oligonucleotides with the addition of Ca<sup>2+</sup> and Mg<sup>2+</sup> in the formulation
- Nanopore Identification of Polyglutamine Length via Cross-Slit Sensing
- A special focus on polyadenylation and alternative polyadenylation in neurodegenerative diseases: A systematic review
- Fueling neurodegeneration: metabolic insights into microglia functions
- Comprehensive Analysis of the Gene Expression Profiles of Rat Brain Tissues under Environmental Exposure to Nicotine
- Visual training induced occipital fast sleep spindle clustering in humans revealed by full-night HD-EEG recordings
- New MiniPromoter Ple389 (ADORA2A) drives selective expression in medium spiny neurons in mice and non-human primates
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