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SAHA decreases HDAC 2 and 4 levels in vivo and improves molecular phenotypes in the R6/2 mouse model of Huntington's disease

PloS one, 2011-11, Vol.6 (11), p.e27746

2011

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Physiology of Hyperuricemia and Urate-Lowering Treatments

Frontiers in medicine, 2018-05, Vol.5, p.160-160

2018

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Clinically Precedented Protein Kinases: Rationale for Their Use in Neurodegenerative Disease

Frontiers in aging neuroscience, 2020-09, Vol.12, p.242-242

2020

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A Review of Welfare Assessment Methods in Reptiles, and Preliminary Application of the Welfare Quality ® Protocol to the Pygmy Blue-Tongue Skink, Tiliqua adelaidensis , Using Animal-Based Measures

Animals (Basel), 2019-01, Vol.9 (1), p.27

2019

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A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease

The Journal of experimental medicine, 2008-08, Vol.205 (8), p.1869-1877

2008

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Identifying priorities for balance interventions through a participatory co-design approach with end-users

BMC neurology, 2023-07, Vol.23 (1), p.266-266, Article 266

2023

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Comparing Effectiveness of a Generic Oral Nutritional Supplement With Specialized Formula in the Treatment of Active Pediatric Crohn's Disease

Inflammatory bowel diseases, 2022-12, Vol.28 (12), p.1859-1864

2022

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Genetic knock-down of HDAC7 does not ameliorate disease pathogenesis in the R6/2 mouse model of Huntington's disease

PloS one, 2009-06, Vol.4 (6), p.e5747-e5747

2009

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Glutamate receptor abnormalities in the YAC128 transgenic mouse model of Huntington’s disease

Neuroscience, 2007-06, Vol.147 (2), p.354-372

2007

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Sp1 Is Up-regulated in Cellular and Transgenic Models of Huntington Disease, and Its Reduction Is Neuroprotective

The Journal of biological chemistry, 2006-06, Vol.281 (24), p.16672-16680

2006

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Balance Interventions to Improve Upright Balance Control and Balance Confidence in People With Motor-Incomplete Spinal Cord Injury or Disease: A Systematic Review and Meta-analysis

Archives of physical medicine and rehabilitation, 2024-08

2024

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Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease

Human molecular genetics, 2005-10, Vol.14 (20), p.3065-3078

2005

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Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease

Molecular neurodegeneration, 2008-10, Vol.3 (1), p.17-17, Article 17

2008

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Oleic acid is an endogenous ligand of TLX/NR2E1 that triggers hippocampal neurogenesis

Proceedings of the National Academy of Sciences - PNAS, 2022-03, Vol.119 (13), p.e2023784119-e2023784119

2022

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Unintentional longline insertion into the descending aorta in a neonate with left congenital diaphragmatic hernia

Archives of disease in childhood. Fetal and neonatal edition, 2021-07, Vol.106 (4), p.430-430

2021

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Decreased association of the transcription factor Sp1 with genes downregulated in Huntington's disease

Neurobiology of disease, 2006-05, Vol.22 (2), p.233-241

2006

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(R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells

Proceedings of the National Academy of Sciences - PNAS, 2014-09, Vol.111 (35), p.12853-12858

2014

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Physical and occupational therapists' learning needs and preferences for education on functional electrical stimulation: A qualitative descriptive study

Artificial organs, 2024-09, Vol.48 (9), p.1018-1030

2024

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Characterizing Human Stem Cell–derived Sensory Neurons at the Single-cell Level Reveals Their Ion Channel Expression and Utility in Pain Research

Molecular therapy, 2014-08, Vol.22 (8), p.1530-1543

2014

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A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease

Brain (London, England : 1878), 2024-05, Vol.147 (5), p.1784-1798

2024

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The design, synthesis and evaluation of low molecular weight acidic sulfonamides as URAT1 inhibitors for the treatment of gout

MedChemComm, 2016-01, Vol.7 (8), p.1572-1579

2016

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Environmental Enrichment Reduces Neuronal Intranuclear Inclusion Load But Has No Effect on Messenger RNA Expression in a Mouse Model of Huntington Disease

Journal of neuropathology and experimental neurology, 2010-08, Vol.69 (8), p.817-827

2010

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Drugging DNA Damage Repair Pathways for Trinucleotide Repeat Expansion Diseases

Journal of Huntington's disease, 2021-01, Vol.10 (1), p.203-220

2021

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Huntingtin Modulates Transcription, Occupies Gene Promoters In Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manner

The Journal of neuroscience, 2008-10, Vol.28 (42), p.10720-10733

2008

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Adductor magnus: An EMG investigation into proximal and distal portions and direction specific action

Clinical anatomy (New York, N.Y.), 2018-05, Vol.31 (4), p.535-543

2018

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SAHA decreases HDAC 2 and 4 levels in vivo and improves molecular phenotypes in the R6/2 mouse model of Huntington's disease

Physiology of Hyperuricemia and Urate-Lowering Treatments

Clinically Precedented Protein Kinases: Rationale for Their Use in Neurodegenerative Disease

A Review of Welfare Assessment Methods in Reptiles, and Preliminary Application of the Welfare Quality ® Protocol to the Pygmy Blue-Tongue Skink, Tiliqua adelaidensis , Using Animal-Based Measures

A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease

Identifying priorities for balance interventions through a participatory co-design approach with end-users

Comparing Effectiveness of a Generic Oral Nutritional Supplement With Specialized Formula in the Treatment of Active Pediatric Crohn's Disease

Genetic knock-down of HDAC7 does not ameliorate disease pathogenesis in the R6/2 mouse model of Huntington's disease

Glutamate receptor abnormalities in the YAC128 transgenic mouse model of Huntington’s disease

Sp1 Is Up-regulated in Cellular and Transgenic Models of Huntington Disease, and Its Reduction Is Neuroprotective

Balance Interventions to Improve Upright Balance Control and Balance Confidence in People With Motor-Incomplete Spinal Cord Injury or Disease: A Systematic Review and Meta-analysis

Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease

Optimisation of region-specific reference gene selection and relative gene expression analysis methods for pre-clinical trials of Huntington's disease

Oleic acid is an endogenous ligand of TLX/NR2E1 that triggers hippocampal neurogenesis

Unintentional longline insertion into the descending aorta in a neonate with left congenital diaphragmatic hernia

Decreased association of the transcription factor Sp1 with genes downregulated in Huntington's disease

(R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells

Physical and occupational therapists' learning needs and preferences for education on functional electrical stimulation: A qualitative descriptive study

Characterizing Human Stem Cell–derived Sensory Neurons at the Single-cell Level Reveals Their Ion Channel Expression and Utility in Pain Research

A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease

The design, synthesis and evaluation of low molecular weight acidic sulfonamides as URAT1 inhibitors for the treatment of gout

Environmental Enrichment Reduces Neuronal Intranuclear Inclusion Load But Has No Effect on Messenger RNA Expression in a Mouse Model of Huntington Disease

Drugging DNA Damage Repair Pathways for Trinucleotide Repeat Expansion Diseases

Huntingtin Modulates Transcription, Occupies Gene Promoters In Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manner

Adductor magnus: An EMG investigation into proximal and distal portions and direction specific action

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