Search Results - "Hayden, Michael R"
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1
The GALAH+ survey: Third data release
Published in Monthly notices of the Royal Astronomical Society (2021)“…ABSTRACT The ensemble of chemical element abundance measurements for stars, along with precision distances and orbit properties, provides high-dimensional data…”
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2
BDNF overexpression in the forebrain rescues Huntington's disease phenotypes in YAC128 mice
Published in The Journal of neuroscience (03-11-2010)“…Huntington's disease (HD) is caused by an expansion of the polyglutamine tract at the N terminus of huntingtin. This mutation reduces levels of BDNF in the…”
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3
Autophagy in Huntington disease and huntingtin in autophagy
Published in Trends in neurosciences (Regular ed.) (01-01-2015)“…Highlights • HTT is an important regulator of autophagy that is, in turn, degraded by autophagy. • Genes regulating protein clearance show altered expression…”
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4
Sigma-1 Receptor (S1R) Interaction with Cholesterol: Mechanisms of S1R Activation and Its Role in Neurodegenerative Diseases
Published in International journal of molecular sciences (15-04-2021)“…The sigma-1 receptor (S1R) is a 223 amino acid-long transmembrane endoplasmic reticulum (ER) protein. The S1R modulates the activity of multiple effector…”
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5
More codeine fatalities after tonsillectomy in North American children
Published in Pediatrics (Evanston) (01-05-2012)“…In 2009 we reported the fatal case of a toddler who had received codeine after adenotonsillectomy for obstructive sleep apnea syndrome. The child was an…”
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6
Pridopidine protects neurons from mutant-huntingtin toxicity via the sigma-1 receptor
Published in Neurobiology of disease (01-09-2019)“…Huntington's disease (HD) is a neurodegenerative disease caused by a CAG repeat expansion in the Huntingtin gene (HTT), translated into a Huntingtin protein…”
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7
The GALAH survey: effective temperature calibration from the InfraRed Flux Method in the Gaia system
Published in Monthly notices of the Royal Astronomical Society (01-10-2021)“…ABSTRACT In order to accurately determine stellar properties, knowledge of the effective temperature of stars is vital. We implement Gaia and 2MASS photometry…”
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8
Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity
Published in Nature medicine (01-03-2011)“…Huntington's disease is an inherited and incurable neurodegenerative disorder caused by an abnormal polyglutamine (polyQ) expansion in huntingtin (encoded by…”
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9
Interrupting sequence variants and age of onset in Huntington's disease: clinical implications and emerging therapies
Published in Lancet neurology (01-11-2020)“…Huntington's disease is a fatal neurodegenerative disorder that is caused by CAG-CAA repeat expansion, encoding polyglutamine, in the huntingtin (HTT) gene…”
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10
Recommendations for genetic testing to reduce the incidence of anthracycline‐induced cardiotoxicity
Published in British journal of clinical pharmacology (01-09-2016)“…Aims Anthracycline‐induced cardiotoxicity (ACT) occurs in 57% of treated patients and remains an important limitation of anthracycline‐based chemotherapy. In…”
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Curation of the Mammalian Palmitoylome Indicates a Pivotal Role for Palmitoylation in Diseases and Disorders of the Nervous System and Cancers
Published in PLoS computational biology (01-08-2015)“…Palmitoylation involves the reversible posttranslational addition of palmitate to cysteines and promotes membrane binding and subcellular localization. Recent…”
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12
Modeling Doxorubicin-Induced Cardiotoxicity in Human Pluripotent Stem Cell Derived-Cardiomyocytes
Published in Scientific reports (04-05-2016)“…Doxorubicin is a highly efficacious anti-cancer drug but causes cardiotoxicity in many patients. The mechanisms of doxorubicin-induced cardiotoxicity (DIC)…”
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13
Fundamental relations for the velocity dispersion of stars in the Milky Way
Published in Monthly notices of the Royal Astronomical Society (01-09-2021)“…ABSTRACT We explore the fundamental relations governing the radial and vertical velocity dispersions of stars in the Milky Way, from combined studies of…”
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14
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease
Published in American journal of human genetics (06-06-2019)“…Huntington disease (HD) is caused by a CAG repeat expansion in the huntingtin (HTT) gene. Although the length of this repeat is inversely correlated with age…”
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15
Laquinimod arrests experimental autoimmune encephalomyelitis by activating the aryl hydrocarbon receptor
Published in Proceedings of the National Academy of Sciences - PNAS (11-10-2016)“…Laquinimod is an oral drug currently being evaluated for the treatment of relapsing, remitting, and primary progressive multiple sclerosis and Huntington’s…”
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Comparative Mitochondrial-Based Protective Effects of Resveratrol and Nicotinamide in Huntington’s Disease Models
Published in Molecular neurobiology (01-09-2017)“…Sirtuin 1 (SIRT1) is a nicotinamide adenine dinucleotide (NAD + )-dependent lysine deacetylase that regulates longevity and enhances mitochondrial metabolism…”
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Pridopidine rescues BDNF/TrkB trafficking dynamics and synapse homeostasis in a Huntington disease brain-on-a-chip model
Published in Neurobiology of disease (15-10-2022)“…Huntington disease (HD) is a neurodegenerative disorder caused by polyglutamine-encoding CAG repeat expansion in the huntingtin (HTT) gene. HTT is involved in…”
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Early Increase in Extrasynaptic NMDA Receptor Signaling and Expression Contributes to Phenotype Onset in Huntington's Disease Mice
Published in Neuron (Cambridge, Mass.) (28-01-2010)“…N-methyl-D-aspartate receptor (NMDAR) excitotoxicity is implicated in the pathogenesis of Huntington's disease (HD), a late-onset neurodegenerative disorder…”
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19
ABCA1 in adipocytes regulates adipose tissue lipid content, glucose tolerance, and insulin sensitivity[S]
Published in Journal of lipid research (01-03-2014)“…Adipose tissue contains one of the largest reservoirs of cholesterol in the body. Adipocyte dysfunction in obesity is associated with intracellular cholesterol…”
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CAG-repeat length and the age of onset in Huntington disease (HD): A review and validation study of statistical approaches
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01-03-2010)“…CAG‐repeat length in the gene for HD is inversely correlated with age of onset (AOO). A number of statistical models elucidating the relationship between CAG…”
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