相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Repurposing of FDA-approved drugs as autophagy inhibitors in tumor cells
Kumari Prerna et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2022)
Nilotinib, A Tyrosine Kinase Inhibitor, Suppresses the Cell Growth and Triggers Autophagy in Papillary Thyroid Cancer
Lei Meng et al.
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY (2022)
Spatiotemporal analysis of soluble aggregates and autophagy markers in the R6/2 mouse model
M. J. Vijay Kumar et al.
SCIENTIFIC REPORTS (2021)
Intrastriatal Administration of AAV5-miHTT in Non-Human Primates and Rats Is Well Tolerated and Results in miHTT Transgene Expression in Key Areas of Huntington Disease Pathology
Elisabeth A. Spronck et al.
BRAIN SCIENCES (2021)
Huntington's Disease: New Frontiers in Therapeutics
Ling Pan et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2021)
Mitochondrial SIRT3 confers neuroprotection in Huntington's disease by regulation of oxidative challenges and mitochondrial dynamics
Luana Naia et al.
FREE RADICAL BIOLOGY AND MEDICINE (2021)
Exposure of R6/2 mice in an enriched environment augments P42 therapy efficacy on Huntington ? s disease progression
Simon Couly et al.
NEUROPHARMACOLOGY (2021)
Revisiting cell and gene therapies in Huntington's disease
Margarida Beatriz et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2021)
Promising drug for Huntington disease fails in major trial
Meredith Wadman
SCIENCE (2021)
Paving the way towards precise and safe CRISPR genome editing
Pawel Sledzinski et al.
BIOTECHNOLOGY ADVANCES (2021)
Lowering Mutant Huntingtin Levels and Toxicity: Autophagy-Endolysosome Pathways in Huntington's Disease
Evelina Valionyte et al.
JOURNAL OF MOLECULAR BIOLOGY (2020)
Potent and sustained huntingtin lowering via AAV5 encoding miRNA preserves striatal volume and cognitive function in a humanized mouse model of Huntington disease
Nicholas S. Caron et al.
NUCLEIC ACIDS RESEARCH (2020)
Recent Advances in the Treatment of Huntington's Disease: Targeting DNA and RNA
Kathleen M. Shannon
CNS DRUGS (2020)
Therapeutic Advances for Huntington's Disease
Ashok Kumar et al.
BRAIN SCIENCES (2020)
Medical, Surgical, and Genetic Treatment of Huntington Disease
Christine M. Stahl et al.
NEUROLOGIC CLINICS (2020)
Patient-reported impact of symptoms in Huntington disease: PRISM-HD
Alistair M. Glidden et al.
NEUROLOGY (2020)
Extending the Phenotypic Spectrum of Huntington Disease: Hypothermia
Sule Altiner et al.
MOLECULAR SYNDROMOLOGY (2020)
Early Downregulation of p75NTR by Genetic and Pharmacological Approaches Delays the Onset of Motor Deficits and Striatal Dysfunction in Huntington's Disease Mice
Nuria Suelves et al.
MOLECULAR NEUROBIOLOGY (2019)
TFEB dysregulation as a driver of autophagy dysfunction in neurodegenerative disease: Molecular mechanisms, cellular processes, and emerging therapeutic opportunities
Constanza J. Cortes et al.
NEUROBIOLOGY OF DISEASE (2019)
SIRT1 is increased in affected brain regions and hypothalamic metabolic pathways are altered in Huntington disease
B. Baldo et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2019)
Stem cells in animal models of Huntington disease: A systematic review
Gabriela Delevati Colpo et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2019)
Ubiquilins regulate autophagic flux through mTOR signalling and lysosomal acidification
Mumine Senturk et al.
NATURE CELL BIOLOGY (2019)
Huntingtin Lowering Strategies for Disease Modification in Huntington's Disease
Sarah J. Tabrizi et al.
NEURON (2019)
Killing Two Angry Birds with One Stone: Autophagy Activation by Inhibiting Calpains in Neurodegenerative Diseases and Beyond
Jonasz Jeremiasz Weber et al.
BIOMED RESEARCH INTERNATIONAL (2019)
AAV5-miHTT Gene Therapy Demonstrates Sustained Huntingtin Lowering and Functional Improvement in Huntington Disease Mouse Models
Elisabeth A. Spronck et al.
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT (2019)
Targeting Huntingtin Expression in Patients with Huntington's Disease
Sarah J. Tabrizi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2019)
Physical Activity and Exercise Outcomes in Huntington Disease (PACE-HD): Protocol for a 12-Month Trial Within Cohort Evaluation of a Physical Activity Intervention in People With Huntington Disease
Cheney J. G. Drew et al.
PHYSICAL THERAPY (2019)
Metformin treatment reduces motor and neuropsychiatric phenotypes in the zQ175 mouse model of Huntington disease
Ana Sanchis et al.
EXPERIMENTAL AND MOLECULAR MEDICINE (2019)
The effect of particle size on nanodiamond fluorescence and colloidal properties in biological media
Emma R. Wilson et al.
NANOTECHNOLOGY (2019)
Clinicopathological differences between the motor onset and psychiatric onset of Huntington's disease, focusing on the nucleus accumbens
Mitsuaki Hirano et al.
NEUROPATHOLOGY (2019)
Depression in neurodegenerative diseases: Common mechanisms and current treatment options
Ciaran P. C. Galts et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2019)
Mechanisms and disease implications of sirtuin-mediated autophagic regulation
In Hye Lee
EXPERIMENTAL AND MOLECULAR MEDICINE (2019)
Curcumin dietary supplementation ameliorates disease phenotype in an animal model of Huntington's disease
F. Elifani et al.
HUMAN MOLECULAR GENETICS (2019)
Cellular quality control by the ubiquitin-proteasome system and autophagy
Christian Pohl et al.
SCIENCE (2019)
The Role of Microglia and Astrocytes in Huntington's Disease
Thulani H. Palpagama et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2019)
Epigenetics in Neurodegenerative Diseases: The Role of Histone Deacetylases
Sorabh Sharma et al.
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS (2019)
Conditioned medium from amniotic cells protects striatal degeneration and ameliorates motor deficits in the R6/2 mouse model of Huntington's disease
Carmela Giampa et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2019)
Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease
Marta Garcia-Miralles et al.
MOLECULAR NEUROBIOLOGY (2019)
Recent advances in the therapeutic development for Huntington disease
Tiago A. Mestre
PARKINSONISM & RELATED DISORDERS (2019)
Nanocarriers as a powerful vehicle to overcome blood-brain barrier in treating neurodegenerative diseases: Focus on recent advances
Xiaoqian Niu et al.
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES (2019)
AAV5-miHTT Lowers Huntingtin mRNA and Protein without Off-Target Effects in Patient-Derived Neuronal Cultures and Astrocytes
Sonay Keskin et al.
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT (2019)
Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System
Sarah M. Carpanini et al.
FRONTIERS IN IMMUNOLOGY (2019)
Functional role of mesenchymal stem cells in the treatment of chronic neurodegenerative diseases
Debora Lo Furno et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2018)
Concise Review: The Use of Stem Cells for Understanding and Treating Huntington's Disease
Bronwen Connor
STEM CELLS (2018)
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population
Chris Kay et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2018)
Therapeutic effects of stem cells in rodent models of Huntington's disease: Review and electrophysiological findings
Sandra M. Holley et al.
CNS NEUROSCIENCE & THERAPEUTICS (2018)
Activation of NPY-Y2 receptors ameliorates disease pathology in the R6/2 mouse and PC12 cell models of Huntington's disease
Oluwaseun Fatoba et al.
EXPERIMENTAL NEUROLOGY (2018)
Human cellular models of medium spiny neuron development and Huntington disease
Monika M. Golas
LIFE SCIENCES (2018)
Thymoquinone loaded solid lipid nanoparticles counteracts 3-Nitropropionic acid induced motor impairments and neuroinflammation in rat model of Huntington's disease
Surekha Ramachandran et al.
METABOLIC BRAIN DISEASE (2018)
Brain-Derived Neurotrophic Factor Prevents Depressive-Like Behaviors in Early-Symptomatic YAC128 Huntington's Disease Mice
Victor Silva da Fonseca et al.
MOLECULAR NEUROBIOLOGY (2018)
Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) Enhances Hippocampal Synaptic Plasticity and Improves Memory Performance in Huntington's Disease
N. Cabezas-Llobet et al.
MOLECULAR NEUROBIOLOGY (2018)
AAV5-miHTT Gene Therapy Demonstrates Broad Distribution and Strong Human Mutant Huntingtin Lowering in a Huntington's Disease Minipig Model
Melvin M. Evers et al.
MOLECULAR THERAPY (2018)
Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements
Michael Kosicki et al.
NATURE BIOTECHNOLOGY (2018)
Amelioration of Huntington's disease phenotypes by Beta-Lapachone is associated with increases in Sirt1 expression, CREB phosphorylation and PGC-1 alpha deacetylation
Mijung Lee et al.
PLOS ONE (2018)
Mechanism of neuroprotection by trehalose: controversy surrounding autophagy induction
He-Jin Lee et al.
CELL DEATH & DISEASE (2018)
Precise Excision of the CAG Tract from the Huntingtin Gene by Cas9 Nickases
Magdalena Dabrowska et al.
FRONTIERS IN NEUROSCIENCE (2018)
Human Neural Stem Cell Transplantation Rescues Functional Deficits in R6/2 and Q140 Huntington's Disease Mice
Jack C. Reidling et al.
STEM CELL REPORTS (2018)
Therapeutic efficacy of regulable GDNF expression for Huntington's and Parkinson's disease by a high-induction, background-free GeneSwitch vector
Shi Cheng et al.
EXPERIMENTAL NEUROLOGY (2018)
Treatment of neurodegenerative disorders through the blood-brain barrier using nanocarriers
N. Poovaiah et al.
NANOSCALE (2018)
Huntingtin Aggregation Impairs Autophagy, Leading to Argonaute-2 Accumulation and Global MicroRNA Dysregulation
Karolina Pircs et al.
CELL REPORTS (2018)
Decreased BDNF Release in Cortical Neurons of a Knock-in Mouse Model of Huntington's Disease
Chenglong Yu et al.
SCIENTIFIC REPORTS (2018)
New directions in therapeutics for Huntington disease
Katya T. Potkin et al.
FUTURE NEUROLOGY (2018)
Current Pharmacological Approaches to Reduce Chorea in Huntington's Disease
Emma M. Coppen et al.
DRUGS (2017)
Comparative Mitochondrial-Based Protective Effects of Resveratrol and Nicotinamide in Huntington's Disease Models
Luana Naia et al.
MOLECULAR NEUROBIOLOGY (2017)
AAV5-miHTT gene therapy demonstrates suppression of mutant huntingtin aggregation and neuronal dysfunction in a rat model of Huntington's disease
J. Miniarikova et al.
GENE THERAPY (2017)
A novel humanizedmouse model of Huntington disease for preclinical development of therapeutics targeting mutant huntingtin alleles
Amber L. Southwell et al.
HUMAN MOLECULAR GENETICS (2017)
Nonclinical Development of ANX005: A Humanized Anti-C1q Antibody for Treatment of Autoimmune and Neurodegenerative Diseases
Janice A. Lansita et al.
INTERNATIONAL JOURNAL OF TOXICOLOGY (2017)
CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington's disease
Su Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2017)
An open-label study to assess the feasibility and tolerability of rilmenidine for the treatment of Huntington's disease
Benjamin R. Underwood et al.
JOURNAL OF NEUROLOGY (2017)
Histone Deacetylase Inhibitors Protect Against Pyruvate Dehydrogenase Dysfunction in Huntington's Disease
Luana Naia et al.
JOURNAL OF NEUROSCIENCE (2017)
Laquinimod treatment in the R6/2 mouse model
Gisa Ellrichmann et al.
SCIENTIFIC REPORTS (2017)
The Self-Inactivating KamiCas9 System for the Editing of CNS Disease Genes
Nicolas Merienne et al.
CELL REPORTS (2017)
Modeling Human Neurological and Neurodegenerative Diseases: From Induced Pluripotent Stem Cells to Neuronal Differentiation and Its Applications in Neurotrauma
Hisham Bahmad et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2017)
Induced Pluripotent Stem Cell-Derived Neural Stem Cell Transplantations Reduced Behavioral Deficits and Ameliorated Neuropathological Changes in YAC128 Mouse Model of Huntington's Disease
Abeer Al-Gharaibeh et al.
FRONTIERS IN NEUROSCIENCE (2017)
Safe and Efficient Silencing with a Pol II, but Not a Pol III, Promoter Expressing an Artificial miRNA Targeting Human Huntingtin
Edith L. Pfister et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2017)
RNAi mechanisms in Huntington's disease therapy: siRNA versus shRNA
Sebastian Aguiar et al.
TRANSLATIONAL NEURODEGENERATION (2017)
Metformin intake associates with better cognitive function in patients with Huntington's disease
David Hervas et al.
PLOS ONE (2017)
Physical Therapy and Exercise Interventions in Huntington's Disease: A Mixed Methods Systematic Review
Nora Fritz et al.
JOURNAL OF HUNTINGTONS DISEASE (2017)
Beneficial effects of glatiramer acetate in Huntington's disease mouse models: Evidence for BDNF-elevating and immunomodulatory mechanisms
Jody Corey-Bloom et al.
BRAIN RESEARCH (2017)
Nanotechnology and nanocarrier-based approaches on treatment of degenerative diseases
Anindita Chowdhury et al.
INTERNATIONAL NANO LETTERS (2017)
Crosstalk and Interplay between the Ubiquitin-Proteasome System and Autophagy
Chang Hoon Ji et al.
MOLECULES AND CELLS (2017)
MicroRNA-27a reduces mutant hutingtin aggregation in an in vitro model of Huntington's disease
Jae-Jun Ban et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2017)
Is Huntingtin Dispensable in the Adult Brain?
Jeh-Ping Liu et al.
JOURNAL OF HUNTINGTONS DISEASE (2017)
Huntington's Disease-Update on Treatments
Kara J. Wyant et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2017)
AMPK activation protects from neuronal dysfunction and vulnerability across nematode, cellular and mouse models of Huntington's disease
Rafael P. Vazquez-Manrique et al.
HUMAN MOLECULAR GENETICS (2016)
Huntington's disease (HD): the neuropathology of a multisystem neurodegenerative disorder of the human brain
U. Rueb et al.
BRAIN PATHOLOGY (2016)
A novel therapeutic application of solid lipid nanoparticles encapsulated thymoquinone (TQ-SLNs) on 3-nitroproponic acid induced Huntington's disease-like symptoms in wistar rats
Surekha Ramachandran et al.
CHEMICO-BIOLOGICAL INTERACTIONS (2016)
Expression of brain-derived neurotrophic factor in astrocytes - Beneficial effects of glatiramer acetate in the R6/2 and YAC128 mouse models of Huntington's disease
Christiane Reick et al.
EXPERIMENTAL NEUROLOGY (2016)
Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9
Jun Wan Shin et al.
HUMAN MOLECULAR GENETICS (2016)
Effect of Deutetrabenazine on Chorea Among Patients With Huntington Disease A Randomized Clinical Trial
Samuel Frank et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2016)
Nanoparticle-mediated brain drug delivery: Overcoming blood-brain barrier to treat neurodegenerative diseases
Claudia Saraiva et al.
JOURNAL OF CONTROLLED RELEASE (2016)
Mechanisms of deep brain stimulation
Todd M. Herrington et al.
JOURNAL OF NEUROPHYSIOLOGY (2016)
Prostaglandin E2 EP2 activation reduces memory decline in R6/1 mouse model of Huntington's disease by the induction of BDNF-dependent synaptic plasticity
Marta Anglada-Huguet et al.
NEUROBIOLOGY OF DISEASE (2016)
Dopamine exacerbates mutant Huntingtin toxicity via oxidative mediated inhibition of autophagy in SH-SY5Y neuroblastoma cells: Beneficial effects of anti-oxidant therapeutics
Chiara Vidoni et al.
NEUROCHEMISTRY INTERNATIONAL (2016)
The Prevalence of Huntington's Disease
Michael D. Rawlins et al.
NEUROEPIDEMIOLOGY (2016)
Insulin and IGF-1 regularize energy metabolites in neural cells expressing full-length mutant huntingtin
Luana Naia et al.
NEUROPEPTIDES (2016)
GENE THERAPY BY PROTEASOME ACTIVATOR, PA28γ, IMPROVES MOTOR COORDINATION AND PROTEASOME FUNCTION IN HUNTINGTON'S DISEASE YAC128 MICE
J. Jeon et al.
NEUROSCIENCE (2016)
A randomized, controlled trial of a multi-modal exercise intervention in Huntington's disease
Lori Quinn et al.
PARKINSONISM & RELATED DISORDERS (2016)
Pharmacology of dextromethorphan: Relevance to dextromethorphan/quinidine (Nuedexta®) clinical use
Charles P. Taylor et al.
PHARMACOLOGY & THERAPEUTICS (2016)
Characterization of Behavioral, Neuropathological, Brain Metabolic and Key Molecular Changes in zQ175 Knock-In Mouse Model of Huntington's Disease
Qi Peng et al.
PLOS ONE (2016)
Nilotinib Effects in Parkinson's Disease and Dementia with Lewy Bodies
Fernando Pagan et al.
JOURNAL OF PARKINSONS DISEASE (2016)
The Effects of Pharmacological Inhibition of Histone Deacetylase 3 (HDAC3) in Huntington's Disease Mice
Haiqun Jia et al.
PLOS ONE (2016)
SIRT1 Activity Is Linked to Its Brain Region-Specific Phosphorylation and Is Impaired in Huntington's Disease Mice
Raffaella Tulino et al.
PLOS ONE (2016)
Cellular Analysis of Silencing the Huntington's Disease Gene Using AAV9 Mediated Delivery of Artificial Micro RNA into the Striatum of Q140/Q140 Mice
Allison M. Keeler et al.
JOURNAL OF HUNTINGTONS DISEASE (2016)
LBH589, A Hydroxamic Acid-Derived HDAC Inhibitor, is Neuroprotective in Mouse Models of Huntington's Disease
Vanita Chopra et al.
JOURNAL OF HUNTINGTONS DISEASE (2016)
Autophagy Activation by Transcription Factor EB (TFEB) in Striatum of HDQ175/Q7 Mice
Petr Vodicka et al.
JOURNAL OF HUNTINGTONS DISEASE (2016)
Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease
Jong-Min Lee et al.
CELL (2015)
Ciliary neurotrophic factor (CNTF): New facets of an old molecule for treating neurodegenerative and metabolic syndrome pathologies
Sarah Pasquin et al.
CYTOKINE & GROWTH FACTOR REVIEWS (2015)
Early white matter abnormalities, progressive brain pathology and motor deficits in a novel knock-in mouse model of Huntington's disease
Jing Jin et al.
HUMAN MOLECULAR GENETICS (2015)
Huntingtin functions as a scaffold for selective macroautophagy
Yan-Ning Rui et al.
NATURE CELL BIOLOGY (2015)
siRNA screen identifies QPCT as a druggable target for Huntington's disease
Maria Jimenez-Sanchez et al.
NATURE CHEMICAL BIOLOGY (2015)
Melatonin: Physiological effects in humans
B. Claustrat et al.
NEUROCHIRURGIE (2015)
Huntington Disease Pathogenesis and Treatment
Praveen Dayalu et al.
NEUROLOGIC CLINICS (2015)
Triheptanoin improves brain energy metabolism in patients with Huntington disease
Isaac Mawusi Adanyeguh et al.
NEUROLOGY (2015)
Transcriptional dysregulation in Huntington's disease: The role of histone deacetylases
Sorabh Sharma et al.
PHARMACOLOGICAL RESEARCH (2015)
Autophagy in neurodegenerative diseases: From pathogenic dysfunction to therapeutic modulation
Marta Martinez-Vicente
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2015)
Reductions in behavioral deficits and neuropathology in the R6/2 mouse model of Huntington's disease following transplantation of bone-marrow-derived mesenchymal stem cells is dependent on passage number
Julien Rossignol et al.
STEM CELL RESEARCH & THERAPY (2015)
Neural and mesenchymal stem cells in animal models of Huntington's disease: past experiences and future challenges
Irina Kerkis et al.
STEM CELL RESEARCH & THERAPY (2015)
G-protein-coupled receptors regulate autophagy by ZBTB16-mediated ubiquitination and proteasomal degradation of Atg14L
Tao Zhang et al.
ELIFE (2015)
Calpain inhibition mediates autophagy-dependent protection against polyglutamine toxicity
F. M. Menzies et al.
CELL DEATH AND DIFFERENTIATION (2015)
Development, characterization and nasal delivery of rosmarinic acid-loaded solid lipid nanoparticles for the effective management of Huntington's disease
Rahul Bhatt et al.
DRUG DELIVERY (2015)
Amitriptyline Improves Motor Function via Enhanced Neurotrophin Signaling and Mitochondrial Functions in the Murine N171-82Q Huntington Disease Model
Wei-Na Cong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
Activation of IGF-1 and Insulin Signaling Pathways Ameliorate Mitochondrial Function and Energy Metabolism in Huntington's Disease Human Lymphoblasts
Luana Naia et al.
MOLECULAR NEUROBIOLOGY (2015)
Therapeutic Effect of Berberine on Huntington's Disease Transgenic Mouse Model
Wenxiao Jiang et al.
PLOS ONE (2015)
Treadmill exercise improves short-term memory by enhancing hippocampal cell proliferation in quinolinic acid-induced Huntington's disease rats
You-Mi Kim et al.
JOURNAL OF EXERCISE REHABILITATION (2015)
Reassessing Models of Basal Ganglia Function and Dysfunction
Alexandra B. Nelson et al.
ANNUAL REVIEW OF NEUROSCIENCE, VOL 37 (2014)
Huntington's Disease (HD): Degeneration of Select Nuclei, Widespread Occurrence of Neuronal Nuclear and Axonal Inclusions in the Brainstem
Udo Rueb et al.
BRAIN PATHOLOGY (2014)
Autophagy of Mitochondria: A Promising Therapeutic Target for Neurodegenerative Disease
Pradip K. Kamat et al.
CELL BIOCHEMISTRY AND BIOPHYSICS (2014)
Mitochondrial Biogenesis: Pharmacological Approaches
Teresa Valero
CURRENT PHARMACEUTICAL DESIGN (2014)
The many faces of autophagy dysfunction in Huntington's disease: from mechanism to therapy
Constanza J. Cortes et al.
DRUG DISCOVERY TODAY (2014)
Insulin and IGF-1 improve mitochondrial function in a PI-3K/Akt-dependent manner and reduce mitochondrial generation of reactive oxygen species in Huntington's disease knock-in striatal cells
Marcio Ribeiro et al.
FREE RADICAL BIOLOGY AND MEDICINE (2014)
A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease
Marianne R. Smith et al.
HUMAN MOLECULAR GENETICS (2014)
Rhes, a Striatal-selective Protein Implicated in Huntington Disease, Binds Beclin-1 and Activates Autophagy
Robert G. Mealer et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Nilotinib-induced autophagic changes increase endogenous parkin level and ubiquitination, leading to amyloid clearance
Irina Lonskaya et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2014)
Quadruple deep brain stimulation in Huntington's disease, targeting pallidum and subthalamic nucleus: case report and review of the literature
D. Gruber et al.
JOURNAL OF NEURAL TRANSMISSION (2014)
Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY)
Erik van Duijn et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2014)
Deep brain stimulation for Huntington's disease: long-term results of a prospective open-label study
Victoria Gonzalez et al.
JOURNAL OF NEUROSURGERY (2014)
IGF-1 Intranasal Administration Rescues Huntington's Disease Phenotypes in YAC128 Mice
Carla Lopes et al.
MOLECULAR NEUROBIOLOGY (2014)
Multisource Ascertainment of Huntington Disease in Canada: Prevalence and Population at Risk
Emily R. Fisher et al.
MOVEMENT DISORDERS (2014)
Systematic Review of Pharmacological Treatments for Depressive Symptoms in Huntington's Disease
Calum D. Moulton et al.
MOVEMENT DISORDERS (2014)
The cognitive burden in Huntington's disease: Pathology, phenotype, and mechanisms of compensation
Marina Papoutsi et al.
MOVEMENT DISORDERS (2014)
Bilateral Globus Pallidus Stimulation in Westphal Variant of Huntington Disease
Giuliana Cislaghi et al.
NEUROMODULATION (2014)
Task-Specific Training in Huntington Disease: A Randomized Controlled Feasibility Trial
Lori Quinn et al.
PHYSICAL THERAPY (2014)
A 5-year follow-up of deep brain stimulation in Huntington's disease
Jose Luis Lopez-Sendon Moreno et al.
PARKINSONISM & RELATED DISORDERS (2014)
Ubiquilin-1 Overexpression Increases the Lifespan and Delays Accumulation of Huntingtin Aggregates in the R6/2 Mouse Model of Huntington's Disease
Nathaniel Safren et al.
PLOS ONE (2014)
Allele-Specific Silencing of Mutant Huntingtin in Rodent Brain and Human Stem Cells
Valerie Drouet et al.
PLOS ONE (2014)
Transplantation of Induced Pluripotent Stem Cells Improves Functional Recovery in Huntington's Disease Rat Model
Shuhua Mu et al.
PLOS ONE (2014)
Potential function for the Huntingtin protein as a scaffold for selective autophagy
Joseph Ochaba et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Sirtuin 1 activator SRT2104 protects Huntington's disease mice
Mali Jiang et al.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2014)
Degeneration of the Cerebellum in Huntington's Disease (HD): Possible Relevance for the Clinical Picture and Potential Gateway to Pathological Mechanisms of the Disease Process
Udo Rueb et al.
BRAIN PATHOLOGY (2013)
Histone deacetylase class II and acetylated core histone immunohistochemistry in human brains with Huntington's disease
Hsin Hsien Yeh et al.
BRAIN RESEARCH (2013)
What effect does a structured home-based exercise programme have on people with Huntington's disease? A randomized, controlled pilot study
Hanan Khalil et al.
CLINICAL REHABILITATION (2013)
Video game play (Dance Dance Revolution) as a potential exercise therapy in Huntington's disease: a controlled clinical trial
Anne D. Kloos et al.
CLINICAL REHABILITATION (2013)
Targeting Sirtuin-1 in Huntington's Disease: Rationale and Current Status
Wenzhen Duan
CNS DRUGS (2013)
PGC-1α, mitochondrial dysfunction, and Huntington's disease
Ashu Johri et al.
FREE RADICAL BIOLOGY AND MEDICINE (2013)
A fully humanized transgenic mouse model of Huntington disease
Amber L. Southwell et al.
HUMAN MOLECULAR GENETICS (2013)
Nilotinib reverses loss of dopamine neurons and improves motor behavior via autophagic degradation of -synuclein in Parkinsons disease models
Michaeline L. Hebron et al.
HUMAN MOLECULAR GENETICS (2013)
A study of molecular changes relating to energy metabolism and cellular stress in people with Huntington's disease: looking for biomarkers
Jolanta Krzyszton-Russjan et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2013)
Nilotinib Induces Autophagy in Hepatocellular Carcinoma through AMPK Activation
Hui-Chuan Yu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease
Alicia Semaka et al.
JOURNAL OF MEDICAL GENETICS (2013)
Dose-dependent Neuroprotection of VEGF165 in Huntington's Disease Striatum
Stuart M. Ellison et al.
MOLECULAR THERAPY (2013)
Enhanced Ca2+-dependent glutamate release from astrocytes of the BACHD Huntington's disease mouse model
William Lee et al.
NEUROBIOLOGY OF DISEASE (2013)
DYSREGULATION OF SYNAPTIC PROTEINS, DENDRITIC SPINE ABNORMALITIES AND PATHOLOGICAL PLASTICITY OF SYNAPSES AS EXPERIENCE-DEPENDENT MEDIATORS OF COGNITIVE AND PSYCHIATRIC SYMPTOMS IN HUNTINGTON'S DISEASE
J. Nithianantharajah et al.
NEUROSCIENCE (2013)
Monitoring Autophagy in the Treatment of Protein Aggregate Diseases: Steps Toward Identifying Autophagic Biomarkers
Conrad C. Weihl
NEUROTHERAPEUTICS (2013)
GDNF, NGF and BDNF as therapeutic options for neurodegeneration
Shelley J. Allen et al.
PHARMACOLOGY & THERAPEUTICS (2013)
Transplantation of umbilical cord-derived mesenchymal stem cells into the striata of R6/2 mice: behavioral and neuropathological analysis
Kyle D. Fink et al.
STEM CELL RESEARCH & THERAPY (2013)
A Randomized Feasibility Study of a 12-Week Community-Based Exercise Program for People With Huntington's Disease
Monica Busse et al.
JOURNAL OF NEUROLOGIC PHYSICAL THERAPY (2013)
Natural History of Huntington Disease
E. Ray Dorsey et al.
JAMA NEUROLOGY (2013)
Longitudinal analysis of the behavioural phenotype in YAC128 (C57BL/6J) Huntington's disease transgenic mice
Simon Brooks et al.
BRAIN RESEARCH BULLETIN (2012)
Light and electron microscopic characterization of the evolution of cellular pathology in YAC128 Huntington's disease transgenic mice
Zubeyde Bayram-Weston et al.
BRAIN RESEARCH BULLETIN (2012)
Screening of Therapeutic Strategies for Huntington's Disease in YAC128 Transgenic Mice
Joana M. Gil-Mohapel
CNS NEUROSCIENCE & THERAPEUTICS (2012)
Mitochondrial-Associated Metabolic Changes and Neurodegeneration in Huntingtons Disease - from Clinical Features to the Bench
Tatiana R. Rosenstock et al.
CURRENT DRUG TARGETS (2012)
α-Synuclein levels modulate Huntington's disease in mice
Silvia Corrochano et al.
HUMAN MOLECULAR GENETICS (2012)
Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice
Mahmoud A. Pouladi et al.
HUMAN MOLECULAR GENETICS (2012)
Selective histone deacetylase (HDAC) inhibition imparts beneficial effects in Huntingtons disease mice: implications for the ubiquitinproteasomal and autophagy systems
Haiqun Jia et al.
HUMAN MOLECULAR GENETICS (2012)
Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
Julie C. Stout et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
Deep brain stimulation in Huntington's disease: A 4-year follow-up case report
Sabine Spielberger et al.
MOVEMENT DISORDERS (2012)
The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis
Tamara Pringsheim et al.
MOVEMENT DISORDERS (2012)
Neuroprotective role of Sirt1 in mammalian models of Huntington's disease through activation of multiple Sirt1 targets
Mali Jiang et al.
NATURE MEDICINE (2012)
Sirt1 mediates neuroprotection from mutant huntingtin by activation of the TORC1 and CREB transcriptional pathway
Hyunkyung Jeong et al.
NATURE MEDICINE (2012)
Evidence-based guideline: Pharmacologic treatment of chorea in Huntington disease Report of the Guideline Development Subcommittee of the American Academy of Neurology
Melissa J. Armstrong et al.
NEUROLOGY (2012)
Huntington's Disease and the Striatal Medium Spiny Neuron: Cell-Autonomous and Non-Cell-Autonomous Mechanisms of Disease
Michelle E. Ehrlich
NEUROTHERAPEUTICS (2012)
Deep brain stimulation in disabling involuntary vocalization associated with Huntington's disease
Pedro J. Garcia-Ruiz et al.
PARKINSONISM & RELATED DISORDERS (2012)
Comprehensive Behavioral and Molecular Characterization of a New Knock-In Mouse Model of Huntington's Disease: zQ175
Liliana B. Menalled et al.
PLOS ONE (2012)
A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
SCIENCE (2012)
The Sirtuin 2 Inhibitor AK-7 Is Neuroprotective in Huntington's Disease Mouse Models
Vanita Chopra et al.
CELL REPORTS (2012)
Adenoviral Astrocyte-Specific Expression of BDNF in the Striata of Mice Transgenic for Huntington's Disease Delays the Onset of the Motor Phenotype
Leticia Arregui et al.
CELLULAR AND MOLECULAR NEUROBIOLOGY (2011)
IGF-1 protects against diabetic features in an in vivo model of Huntington's disease
A. I. Duarte et al.
EXPERIMENTAL NEUROLOGY (2011)
Long-term follow-up of pallidal deep brain stimulation in two cases of Huntington's disease
Gail A. Kang et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Constitutive Upregulation of Chaperone-Mediated Autophagy in Huntington's Disease
Hiroshi Koga et al.
JOURNAL OF NEUROSCIENCE (2011)
Novel Regulation of Parkin Function through c-Abl-Mediated Tyrosine Phosphorylation: Implications for Parkinson's Disease
Syed Z. Imam et al.
JOURNAL OF NEUROSCIENCE (2011)
Conditional BDNF release under pathological conditions improves Huntington's disease pathology by delaying neuronal dysfunction
Albert Giralt et al.
MOLECULAR NEURODEGENERATION (2011)
Preclinical Safety of RNAi-Mediated HTT Suppression in the Rhesus Macaque as a Potential Therapy for Huntington's Disease
Jodi L. McBride et al.
MOLECULAR THERAPY (2011)
Milestones in Movement Disorders Clinical Trials: Advances and Landmark Studies
C. Warren Olanow et al.
MOVEMENT DISORDERS (2011)
Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity
Wenjun Song et al.
NATURE MEDICINE (2011)
Nicotinamide improves motor deficits and upregulates PGC-1 alpha and BDNF gene expression in a mouse model of Huntington's disease
Tyisha Hathorn et al.
NEUROBIOLOGY OF DISEASE (2011)
FK506 ameliorates cell death features in Huntington's disease striatal cell models
Tatiana R. Rosenstock et al.
NEUROCHEMISTRY INTERNATIONAL (2011)
Structural MRI detects progressive regional brain atrophy and neuroprotective effects in N171-82Q Huntington's disease mouse model
Yong Cheng et al.
NEUROIMAGE (2011)
Hdac6 Knock-Out Increases Tubulin Acetylation but Does Not Modify Disease Progression in the R6/2 Mouse Model of Huntington's Disease
Anna Bobrowska et al.
PLOS ONE (2011)
Mitochondrial Turnover and Aging of Long-Lived Postmitotic Cells: The Mitochondrial-Lysosomal Axis Theory of Aging
Alexei Terman et al.
ANTIOXIDANTS & REDOX SIGNALING (2010)
Genetically engineered mesenchymal stem cells reduce behavioral deficits in the YAC 128 mouse model of Huntington's disease
Nicholas D. Dey et al.
BEHAVIOURAL BRAIN RESEARCH (2010)
Dopamine and Glutamate in Huntington's Disease: A Balancing Act
Veronique M. Andre et al.
CNS NEUROSCIENCE & THERAPEUTICS (2010)
Wheel Running and Environmental Enrichment Differentially Modify Exon-Specific BDNF Expression in the Hippocampus of Wild-Type and Pre-motor Symptomatic Male and Female Huntington's Disease Mice
M. S. Zajac et al.
HIPPOCAMPUS (2010)
Rilmenidine attenuates toxicity of polyglutamine expansions in a mouse model of Huntington's disease
Claudia Rose et al.
HUMAN MOLECULAR GENETICS (2010)
Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease
Jinho Kim et al.
HUMAN MOLECULAR GENETICS (2010)
Insulin and Insulin-like Growth Factor-1 Receptors Act as Ligand-specific Amplitude Modulators of a Common Pathway Regulating Gene Transcription
Jeremie Boucher et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
The Clinical and Genetic Features of Huntington Disease
Aaron Sturrock et al.
JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY (2010)
Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease
Marta Martinez-Vicente et al.
NATURE NEUROSCIENCE (2010)
Neural stem cell systems: physiological players or in vitro entities?
Luciano Conti et al.
NATURE REVIEWS NEUROSCIENCE (2010)
Huntington's disease: a clinical review
Raymund A. C. Roos
ORPHANET JOURNAL OF RARE DISEASES (2010)
SIRT2 inhibition achieves neuroprotection by decreasing sterol biosynthesis
Ruth Luthi-Carter et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Phosphorylation by the c-Abl protein tyrosine kinase inhibits parkin's ubiquitination and protective function
Han Seok Ko et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Of mice, rats and men: Revisiting the quinolinic acid hypothesis of Huntington's disease
Robert Schwarcz et al.
PROGRESS IN NEUROBIOLOGY (2010)
Prevention of depressive behaviour in the YAC128 mouse model of Huntington disease by mutation at residue 586 of huntingtin
Mahmoud A. Pouladi et al.
BRAIN (2009)
The R6 lines of transgenic mice: A model for screening new therapies for Huntington's disease
Joana M. Gil et al.
BRAIN RESEARCH REVIEWS (2009)
Riluzole protects Huntington disease patients from brain glucose hypometabolism and grey matter volume loss and increases production of neurotrophins
Ferdinando Squitieri et al.
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING (2009)
A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference
Maria Stella Lombardi et al.
EXPERIMENTAL NEUROLOGY (2009)
Intrabody Gene Therapy Ameliorates Motor, Cognitive, and Neuropathological Symptoms in Multiple Mouse Models of Huntington's Disease
Amber L. Southwell et al.
JOURNAL OF NEUROSCIENCE (2009)
In Vivo Evidence for NMDA Receptor-Mediated Excitotoxicity in a Murine Genetic Model of Huntington Disease
Mary Y. Heng et al.
JOURNAL OF NEUROSCIENCE (2009)
Intracerebral Transplantation of Neural Stem Cells Combined With Trehalose Ingestion Alleviates Pathology in a Mouse Model of Huntington's Disease
Chia-Ron Yang et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2009)
Nonallele-specific Silencing of Mutant and Wild-type Huntingtin Demonstrates Therapeutic Efficacy in Huntington's Disease Mice
Ryan L. Boudreau et al.
MOLECULAR THERAPY (2009)
Treatment of the Symptoms of Huntington's Disease: Preliminary Results Comparing Aripiprazole and Tetrabenazine
Livia Brusa et al.
MOVEMENT DISORDERS (2009)
Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin
Shu-ichi Okamoto et al.
NATURE MEDICINE (2009)
Brain-derived neurotrophic factor in neurodegenerative diseases
Chiara Zuccato et al.
NATURE REVIEWS NEUROLOGY (2009)
Approaches to Prevent Dopamine Quinone-Induced Neurotoxicity
Ikuko Miyazaki et al.
NEUROCHEMICAL RESEARCH (2009)
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease
N. A. Aziz et al.
NEUROLOGY (2009)
Risperidone and the Treatment of Psychiatric, Motor, and Cognitive Symptoms in Huntington's Disease
Kevin Duff et al.
ANNALS OF CLINICAL PSYCHIATRY (2008)
Impairing the Mitochondrial Fission and Fusion Balance: A New Mechanism of Neurodegeneration
Andrew B. Knott et al.
MITOCHONDRIA AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISORDERS (2008)
Modulation of vascular endothelial growth factor (VEGF) expression in motor neurons and its electrophysiological effects
Daniel P. McCloskey et al.
BRAIN RESEARCH BULLETIN (2008)
A study of chorea after tetrabenazine withdrawal in patients with Huntington disease
Samuel Frank et al.
CLINICAL NEUROPHARMACOLOGY (2008)
Mechanisms of neurodegeneration in Huntington's disease
Joana M. Gil et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2008)
The antidepressant sertraline improves the phenotype, promotes neurogenesis and increases BDNF levels in the R6/2 Huntington's disease mouse model
Qi Peng et al.
EXPERIMENTAL NEUROLOGY (2008)
The metabolic profile of early Huntington's disease - a combined human and transgenic mouse study
Anna O. G. Goodman et al.
EXPERIMENTAL NEUROLOGY (2008)
Identification and allele-specific silencing of the mutant huntingtin allele in Huntington's disease patient-derived fibroblasts
P. H. J. van Bilsen et al.
HUMAN GENE THERAPY (2008)
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1
Salima Hacein-Bey-Abina et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice
Michelle Gray et al.
JOURNAL OF NEUROSCIENCE (2008)
Long-term follow-up of Huntington disease treated by bilateral deep brain stimulation of the internal globus pallidus
Brigitte Biolsi et al.
JOURNAL OF NEUROSURGERY (2008)
The relationship between CAG repeat length and clinical progression in Huntington's disease
Bernard Ravina et al.
MOVEMENT DISORDERS (2008)
GPi-DBS in Huntington's disease: Results on motor function and cognition in a 72-year-old case
Alfonso Fasano et al.
MOVEMENT DISORDERS (2008)
Mitochondrial fragmentation in neurodegeneration
Andrew B. Knott et al.
NATURE REVIEWS NEUROSCIENCE (2008)
Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease
Wenzhen Duan et al.
NEUROBIOLOGY OF DISEASE (2008)
PROGRESSIVE SYNAPTIC PATHOLOGY OF MOTOR CORTICAL NEURONS IN A BAC TRANSGENIC MOUSE MODEL OF HUNTINGTON'S DISEASE
J. Spampanato et al.
NEUROSCIENCE (2008)
Artificial miRNAs mitigate shRNA-mediated toxicity in the brain: Implications for the therapeutic development of RNAi
Jodi L. McBride et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice
Elizabeth A. Thomas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Systematic assessment of BDNF and its receptor levels in human cortices affected by Huntington's disease
Chiara Zuccato et al.
BRAIN PATHOLOGY (2008)
Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits
M. DiFiglia et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Induction of neostriatal neurogenesis slows disease progression in a transgenic murine model of Huntington disease
Sung-Rae Cho et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Riluzole in Huntington's disease: A 3-year, randomized controlled study
G. Bernhard Landwehrmeyer et al.
ANNALS OF NEUROLOGY (2007)
Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington's disease patients
Chiung-Mei Chen et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Low brain-derived neurotrophic factor (BDNF) levels in serum of Huntington's disease patients
A. Ciammola et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2007)
Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease
Jean-Pyo Lee et al.
NATURE MEDICINE (2007)
Metformin therapy in a transgenic mouse model of Huntington's disease
Thong C. Ma et al.
NEUROSCIENCE LETTERS (2007)
High-capacity adenoviral vector-mediated reduction of Huntingtin aggregate load in vitro and in vivo
Bin Huang et al.
HUMAN GENE THERAPY (2007)
A pilot study of the clinical efficacy and safety of memantine for Huntington's disease
William G. Ondo et al.
PARKINSONISM & RELATED DISORDERS (2007)
Role of brain-derived neurotrophic factor in Huntington's disease
Chiara Zuccato et al.
PROGRESS IN NEUROBIOLOGY (2007)
Patients with Huntington's disease have impaired awareness of cognitive, emotional, and functional abilities
Karin F. Hoth et al.
JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY (2007)
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1α in Huntington's disease neurodegeneration
Patrick Weydt et al.
CELL METABOLISM (2006)
Mitochondrial-dependent Ca2+ handling in Huntington's disease striatal cells:: Effect of histone deacetylase inhibitors
Jorge M. A. Oliveira et al.
JOURNAL OF NEUROSCIENCE (2006)
Transcriptional repression of PGC-α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration
Libin Cui et al.
CELL (2006)
Hypothalamic-endocrine aspects in Huntington's disease
Asa Petersen et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2006)
Viral delivery of glial cell line-derived neurotrophic factor improves behavior and protects striatal neurons in a mouse model of Huntington's disease
Jodi L. McBride et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Fatality in mice due to oversaturation of cellular microRNA/short hairpin RNA pathways
Dirk Grimm et al.
NATURE (2006)
Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase
M Borrell-Pagès et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
Effective gene therapy with nonintegrating lentiviral vectors
RJ Yáñez-Muñoz et al.
NATURE MEDICINE (2006)
Tetrabenazine as antichorea therapy in Huntington disease - A randomized controlled trial
FJ Marshall et al.
NEUROLOGY (2006)
Quetiapine in the treatment of behavioral disturbances in patients with Huntington's disease
M Alpay et al.
PSYCHOSOMATICS (2006)
Pharmacological management of Huntington's disease: An evidence-based review
Raphael M. Bonelli et al.
CURRENT PHARMACEUTICAL DESIGN (2006)
Differential effects of voluntary physical exercise on behavioral and brain-derived neurotrophic factor expression deficits in Huntington's disease transgenic mice
T. Y. C. Pang et al.
NEUROSCIENCE (2006)
Evaluation of the benzothiazole aggregation inhibitors riluzole and PGL-135 as therapeutics for Huntington's disease
E Hockly et al.
NEUROBIOLOGY OF DISEASE (2006)
Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity
JY Shin et al.
JOURNAL OF CELL BIOLOGY (2005)
Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease
JM Van Raamsdonk et al.
HUMAN MOLECULAR GENETICS (2005)
Proteomic analysis of protein expression and oxidative modification in R6/2 transgenic mice
M Perluigi et al.
MOLECULAR & CELLULAR PROTEOMICS (2005)
Normal huntingtin function: An alternative approach to Huntington's disease
E Cattaneo et al.
NATURE REVIEWS NEUROSCIENCE (2005)
Clinico-pathological rescue of a model mouse of Huntington's disease by siRNA
YL Wang et al.
NEUROSCIENCE RESEARCH (2005)
Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic mice
EC Stack et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2005)
Gene therapy of storage disorders by retroviral and lentiviral vectors
A Biffi et al.
HUMAN GENE THERAPY (2005)
Cognitive disorders and neurogenesis deficits in Huntington's disease mice are rescued by fluoxetine
HE Grote et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2005)
Unraveling a role for dopamine in Huntington's disease:: The dual role of reactive oxygen species and D2 receptor stimulation
D Charvin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
ProBDNF induces neuronal apoptosis via activation of a receptor complex of p75NTR and sortilin
HK Teng et al.
JOURNAL OF NEUROSCIENCE (2005)
Metabolic control through the PGC-1 family of transcription coactivators
JD Lin et al.
CELL METABOLISM (2005)
Lentiviral gene delivery of GDNF into the striatum of R6/2 Huntington mice fails to attenuate behavioral and neuropathological changes
N Popovic et al.
EXPERIMENTAL NEUROLOGY (2005)
Critical periods of suicide risk in Huntington's disease
JS Paulsen et al.
AMERICAN JOURNAL OF PSYCHIATRY (2005)
Pallidal deep brain stimulation influences both reflexive and voluntary saccades in Huntington's disease
AP Fawcett et al.
MOVEMENT DISORDERS (2005)
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease
L Arning et al.
NEUROGENETICS (2005)
Orexin loss in Huntington's disease
A Petersen et al.
HUMAN MOLECULAR GENETICS (2005)
AAV-mediated gene delivery of BDNF or GDNF is neuroprotective in a model of Huntington disease
AP Kells et al.
MOLECULAR THERAPY (2004)
Early striatal dendrite deficits followed by neuron loss with advanced age in the absence of anterograde cortical brain-derived neurotrophic factor
ZC Baquet et al.
JOURNAL OF NEUROSCIENCE (2004)
Paroxetine retards disease onset and progression in huntingtin mutant mice
WZ Duan et al.
ANNALS OF NEUROLOGY (2004)
Environmental enrichment rescues protein deficits in a mouse model of Huntington's disease, indicating a possible disease mechanism
TL Spires et al.
JOURNAL OF NEUROSCIENCE (2004)
The energetics of Huntington's disease
SE Browne et al.
NEUROCHEMICAL RESEARCH (2004)
Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease
M Tanaka et al.
NATURE MEDICINE (2004)
Cystamine increases L-cysteine levels in Huntington's disease transgenic mouse brain and in a PC12 model of polyglutamine aggregation
JH Fox et al.
JOURNAL OF NEUROCHEMISTRY (2004)
Generalized brain and skin proteasome inhibition in Huntington's disease
H Seo et al.
ANNALS OF NEUROLOGY (2004)
Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease
JM Canals et al.
JOURNAL OF NEUROSCIENCE (2004)
Bilateral globus pallidus stimulation for Huntington's disease
E Moro et al.
ANNALS OF NEUROLOGY (2004)
Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules
LR Gauthier et al.
CELL (2004)
Neurotransmitters and substances of abuse: Effects on adult neurogenesis
TA Powrozek et al.
CURRENT NEUROVASCULAR RESEARCH (2004)
Effects of rivastigmine on motor and cognitive impairment in Huntington's disease
M de Tommaso et al.
MOVEMENT DISORDERS (2004)
Quetiapine in the Management of Psychosis Secondary to Huntington's Disease: A Case Report
Dallas P. Seitz et al.
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE (2004)
Proactive transplantation of human neural stem cells prevents degeneration of striatal neurons in a rat model of Huntington disease
JK Ryu et al.
NEUROBIOLOGY OF DISEASE (2004)
Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease
B Ravikumar et al.
NATURE GENETICS (2004)
Genetic mouse models of Huntington's and Parkinson's diseases: illuminating but imperfect
MS Levine et al.
TRENDS IN NEUROSCIENCES (2004)
Treatment of Huntington's disease with galantamine
P Petrikis et al.
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY (2004)
Dendritic spine pathology and deficits in experience-dependent dendritic plasticity in R6/1 Huntington's disease transgenic mice
TL Spires et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
Analysis of cellular, transgenic and human models of Huntington's disease reveals tyrosine hydroxylase alterations and substantia nigra neuropathology
GJ Yohrling et al.
MOLECULAR BRAIN RESEARCH (2003)
Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease
EJ Slow et al.
HUMAN MOLECULAR GENETICS (2003)
A Randomized trial of amantadine in Huntington disease
P O'Suilleabhain et al.
ARCHIVES OF NEUROLOGY (2003)
IV amantadine improves chorea in Huntington's disease - An acute randomized, controlled study
C Lucetti et al.
NEUROLOGY (2003)
Structural and functional neuroprotection in a rat model of Huntington's disease by viral gene transfer of GDNF
JL McBride et al.
EXPERIMENTAL NEUROLOGY (2003)
Direct brain infusion of glial cell line-derived neurotrophic factor in Parkinson disease
SS Gill et al.
NATURE MEDICINE (2003)
Dietary restriction normalizes glucose metabolism and BDNF levels, slows disease progression, and increases survival in huntingtin mutant mice
WZ Duan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice
S Gines et al.
HUMAN MOLECULAR GENETICS (2003)
Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease
E Hockly et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Cystamine inhibits caspase activity - Implications for the treatment of polyglutamine disorders
M Lesort et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
The use of transgenic and knock-in mice to study Huntington's disease
MA Hickey et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
Rivastigmine in the treatment of Huntington's disease
U Rot et al.
EUROPEAN JOURNAL OF NEUROLOGY (2002)
Olanzapine for Huntington's disease: An open label study
RM Bonelli et al.
CLINICAL NEUROPHARMACOLOGY (2002)
Amantadine in Huntington's disease: open-label video-blinded study
C Lucetti et al.
NEUROLOGICAL SCIENCES (2002)
Modulation of DOI-induced increases in cortical BDNF expression by group II mGlu receptors
JC Gewirtz et al.
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR (2002)
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines
AV Panov et al.
NATURE NEUROSCIENCE (2002)
Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease
J Schiefer et al.
MOVEMENT DISORDERS (2002)
Neurotrophin signaling through the p75 neurotrophin receptor
PP Roux et al.
PROGRESS IN NEUROBIOLOGY (2002)
Olanzapine in Huntington's disease
D Paleacu et al.
ACTA NEUROLOGICA SCANDINAVICA (2002)
Opinion - Neural stem cell therapy for neurological diseases: dreams and reality
F Rossi et al.
NATURE REVIEWS NEUROSCIENCE (2002)
Regional and progressive thinning of the cortical ribbon in Huntington's disease
HD Rosas et al.
NEUROLOGY (2002)
Risperidone in chorea and psychosis of Huntington's disease
AK Erdemoglu et al.
EUROPEAN JOURNAL OF NEUROLOGY (2002)
Mouse models of Huntington's disease
LB Menalled et al.
TRENDS IN PHARMACOLOGICAL SCIENCES (2002)
Anterior cingulate cortical transplantation in transgenic Huntington's disease mice
A van Dellen et al.
BRAIN RESEARCH BULLETIN (2001)
Impaired glutamate uptake in the R6 Huntington's disease transgenic mice
JC Liévens et al.
NEUROBIOLOGY OF DISEASE (2001)
Neuropsychiatric aspects of Huntington's disease
JS Paulsen et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2001)
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato et al.
SCIENCE (2001)
Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease
LP de Almeida et al.
NEUROBIOLOGY OF DISEASE (2001)
Open interconnected model of basal ganglia-thalamocortical circuitry and its relevance to the clinical syndrome of Huntington's disease
D Joel
MOVEMENT DISORDERS (2001)
Signal transduction pathways through TRK-A and TRK-B receptors in human neuroblastoma cells
T Sugimoto et al.
JAPANESE JOURNAL OF CANCER RESEARCH (2001)
The selective vulnerability of nerve cells in Huntington's disease
KA Sieradzan et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2001)
Neurological abnormalities in a knock-in mouse model of Huntington's disease
CH Lin et al.
HUMAN MOLECULAR GENETICS (2001)
Mutant huntingtin enhances excitotoxic cell death
MM Zeron et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2001)
Regulation of cell death by the Abl tyrosine kinase
JYJ Wang
ONCOGENE (2000)
Brain-derived neurotrophic factor, neurotrophin-3, and neurotrophin-4/5 prevent the death of striatal projection neurons in a rodent model of Huntington's disease
E Pérez-Navarro et al.
JOURNAL OF NEUROCHEMISTRY (2000)
Chemical anatomy of striatal interneurons in normal individuals and in patients with Huntington's disease
F Cicchetti et al.
BRAIN RESEARCH REVIEWS (2000)
Brain-derived neurotrophic factor in Huntington disease
I Ferrer et al.
BRAIN RESEARCH (2000)