Search Results - "Bates, G P"
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1
Fluid losses and hydration status of industrial workers under thermal stress working extended shifts
Published in Occupational and environmental medicine (London, England) (01-02-2003)“…Aims: To assess whether workers under significant thermal stress necessarily dehydrated during their exposure and whether “involuntary dehydration” was…”
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2
Formation of Polyglutamine Inclusions in Non-CNS Tissue
Published in Human molecular genetics (01-05-1999)“…Huntington's disease (HD) is one of a class of inherited progressive neurodegenerative disorders that are caused by a CAG/polyglutamine repeat expansion. We…”
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3
Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain
Published in Science (American Association for the Advancement of Science) (26-09-1997)“…The cause of neurodegeneration in Huntington's disease (HD) is unknown. Patients with HD have an expanded NH$_2$-terminal polyglutamine region in huntingtin…”
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4
Impaired Glutamate Uptake in the R6 Huntington's Disease Transgenic Mice
Published in Neurobiology of disease (01-10-2001)“…Huntington's disease (HD) is a late-onset neurodegenerative disease for which the mutation is CAG/polyglutamine repeat expansion. The R6 mouse lines expressing…”
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5
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
Published in Nature genetics (01-04-1998)“…Nephropathic cystinosis, an autosomal recessive disorder resulting from defective lysosomal transport of cystine, is the most common inherited cause of renal…”
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6
Inclusion formation in Huntington's disease R6/2 mouse muscle cultures
Published in Journal of neurochemistry (01-10-2003)“…Huntington's disease (HD) is an autosomal dominant disorder caused by an expansion in the number of glutamine repeats in the N‐terminal region of the…”
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7
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
Published in Nature genetics (01-02-1997)“…Six inherited neurodegenerative diseases are caused by a CAG/polyglutamine expansion, including spinal and bulbar muscular atrophy (SBMA), Huntington's disease…”
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8
Ultrastructural Localization and Progressive Formation of Neuropil Aggregates in Huntington's Disease Transgenic Mice
Published in Human molecular genetics (01-07-1999)“…How aggregates of polyglutamine proteins are involved in the neurological symptoms of glutamine repeat diseases is unknown. We show that huntingtin aggregates…”
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9
Sequence Comparison of Human and Yeast Telomeres Identifies Structurally Distinct Subtelomeric Domains
Published in Human molecular genetics (01-08-1997)“…We have sequenced and compared DNA from the ends of three human chromosomes: 4p, 16p and 22q. In all cases the pro-terminal regions are subdivided by…”
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10
Heat exhaustion in a deep underground metalliferous mine
Published in Occupational and environmental medicine (London, England) (01-03-2000)“…OBJECTIVES To examine the incidence, clinical state, personal risk factors, haematology, and biochemistry of heat exhaustion occurring at a deep underground…”
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11
Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
Published in The Lancet (British edition) (10-01-1998)“…Neuronal intranuclear inclusions have been found in the brain of a transgenic mouse model of Huntington's disease and in necropsy brain tissue of patients with…”
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12
Inter- and intra-specific variation within the genus Psoroptes (Acari: Psoroptidae)
Published in Veterinary parasitology (30-06-1999)“…In this paper the taxonomy and relative importance of various species within the genus Psoroptes are reviewed with respect to inter- and intra-specific…”
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13
Fatigue in industrial workers under thermal stress on extended shift lengths
Published in Occupational medicine (Oxford) (01-10-2001)“…A field investigation to examine the fatigue levels in industrial workers working extended (10, 12 and 12.5 h) shifts under significant levels of thermal…”
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14
Amyloid-like inclusions in Huntington’s disease
Published in Neuroscience (01-01-2000)“…Huntington’s disease is a progressive, autosomal dominantly inherited, neurodegenerative disease that is characterized by involuntary movements (chorea),…”
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15
Transgenic Models of Huntington's Disease
Published in Human molecular genetics (01-01-1997)“…CAG/polyglutamine expansion has been shown to form the molecular basis of an increasing number of inherited neurodegenerative diseases. The mutation is likely…”
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16
Brain Neurotransmitter Deficits in Mice Transgenic for the Huntington’s Disease Mutation
Published in Journal of neurochemistry (01-04-1999)“…: Huntington’s disease (HD) is associated with an expansion in the CAG repeat sequence of a gene on chromosome 4, resulting in a neurodegenerative process…”
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17
The risk of heat exhaustion at a deep underground metalliferous mine in relation to body-mass index and predicted VO2max
Published in Occupational medicine (Oxford) (01-05-2000)“…The risk of heat exhaustion at a deep underground metalliferous mine was assessed in relation to the body-mass index (BMI) and predicted maximal oxygen uptake…”
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The Risk of Heat Exhaustion at a Deep Underground Metalliferous Mine in Relation to Surface Temperatures
Published in Occupational medicine (Oxford) (01-07-2000)“…The risk of heat exhaustion at a deep underground metalliferous mine was assessed in relation to thermal conditions prevailing on the surface. For each day of…”
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Suberoylanilide Hydroxamic Acid, a Histone Deacetylase Inhibitor, Ameliorates Motor Deficits in a Mouse Model of Huntington's Disease
Published in Proceedings of the National Academy of Sciences - PNAS (18-02-2003)“…Huntington's disease (HD) is an inherited, progressive neurological disorder that is caused by a CAG/polyglutamine repeat expansion and for which there is no…”
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The Huntington's Disease Protein Interacts with p53 and CREB-Binding Protein and Represses Transcription
Published in Proceedings of the National Academy of Sciences - PNAS (06-06-2000)“…Huntington's Disease (HD) is caused by an expansion of a polyglutamine tract within the huntingtin (htt) protein. Pathogenesis in HD appears to include the…”
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