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Showing 1 to 20 of 96 for “"Huntington's"”.

  1. Investigating toxicity in Drosophila models of Huntington's Disease and Huntington's Disease-Like 2

    … the most well-known polyglutamine disorders is Huntington's disease (HD), which results from a CAG repeat expansion in the huntingtin (Htt) gene. HD is characterized by psychiatric symptoms, cognitive decline, and movement disturbances, especially chorea. Interestingly, some presumed HD patients …

    mit Repository record for Investigating toxicity in Drosophila models of Huntington's Disease and Huntington's Disease-Like 2 (opens in a new tab)

  2. Decision-making in Huntington's Disease

    Huntington’s disease (HD) is a neurodegenerative disorder caused by an expansion mutation in the huntingtin gene. Gene carriers are currently diagnosed with manifest HD when a movement disorder becomes apparent although such problems are often preceded by cognitive and psychiatric features which …

    cambridge Repository record for Decision-making in Huntington's Disease (opens in a new tab)

  3. Excitotoxic mechanisms in Huntington's disease

    Thesis (Ph. D.)--Massachusetts Institute of Technology, Whitaker College of Health Sciences and Technology, 1992.

    mit Repository record for Excitotoxic mechanisms in Huntington's disease (opens in a new tab)

  4. β-cell dysfunction in Huntington's disease

    Huntington's disease (HD), a fatal neurodegenerative disorder, is associated with an increased risk of diabetes mellitus. The reason for this is unknown, but considering the functional similarities of neurons and the insulin secreting pancreatic β-cell, pathological mechanisms may be shared by both …

    lund Repository record for β-cell dysfunction in Huntington's disease (opens in a new tab)

  5. Genetic linkage studies in Huntington's disease

    This document only includes an excerpt of the corresponding thesis or dissertation. To request a digital scan of the full text, please contact the Ruth Lilly Medical Library's Interlibrary Loan Department (rlmlill@iu.edu).

    iupui Repository record for Genetic linkage studies in Huntington's disease (opens in a new tab)

  6. Genetic and social aspects of Huntington's chorea

    The thesis is concerned with the investigation of Huntington's chorea in South East Scotland. It outlines the difficulties encountered in such an investigation and provides a history of the study of heredity to facilitate an understanding of problems concerning the inheritance of the disease.

    edinburgh Repository record for Genetic and social aspects of Huntington's chorea (opens in a new tab)

  7. Psychological distress in the context of Huntington's disease

    … and psychological therapy in the context of Huntington’s disease (HD). The literature review is a scoping review of 29 papers looking at different aspects of irritability in the context of HD. The review examines the validity of irritability as a meaningful construct in HD. Clinical and …

    lancaster Repository record for Psychological distress in the context of Huntington's disease (opens in a new tab)

  8. Characterization of a Drosophila model of Huntington's disease

    Huntington's disease (HD) is an autosomal dominant neurological disorder caused by a polyglutamine (polyQ) repeat expansion in the huntingtin (Htt) protein. The disease is characterized by neurodegeneration and formation of neuronal intracellular inclusions primarily in the striatum and cortex, …

    mit Repository record for Characterization of a Drosophila model of Huntington's disease (opens in a new tab)

  9. Cortical thinning and neuropsychological changes in presymptomatic Huntington's Disease

    … the neuropsychological symptoms experienced in Huntington‘s Disease (HD). Advances in cortical thickness mapping (an automated MRI method for precisely measuring the cortical thickness across the entire cortex) provide a new technique for examining changes in the brain in HD. Recent studies …

    auckland-ms Repository record for Cortical thinning and neuropsychological changes in presymptomatic Huntington's Disease (opens in a new tab)

  10. Understanding Huntington's Disease pathogenesis using next generation sequencing analyses

    Huntington's disease is one of nine expanded (CAG) repeat disorders. The expansion in Huntington's disease lies in the first exon of the huntingtin (HTT) gene and is pathogenic when (CAG)>/= 40 . Individuals with Huntington's disease develop motor, cognitive, and psychiatric symptoms in adulthood. …

    mit Repository record for Understanding Huntington's Disease pathogenesis using next generation sequencing analyses (opens in a new tab)

  11. CHROMATIN DISRUPTION IN HUNTINGTON'S DISEASE ALTERS DEVELOPMENT AND PRECEDES NEUROPATHOLOGY

    La Corea di Huntington (MH) è una malattia neurodegenerativa causata da un’espansione del tratto CAG nel gene Huntingtina (HTT), che porta alla formazione di un tratto di glutammine eccessivamente lungo nell’HTT mutata (mHTT). Sebbene la manifestazione clinica si osservi generalmente in età …

    milano Repository record for CHROMATIN DISRUPTION IN HUNTINGTON'S DISEASE ALTERS DEVELOPMENT AND PRECEDES NEUROPATHOLOGY (opens in a new tab)

  12. Cell-Type Specific Translational Profiling in Huntington's Disease Mouse Models

    … among the most vulnerable cell populations in Huntington's Disease (HD). Within this population, striatopallidal MSNs are more vulnerable than striatonigral MSNs, which may explain the typical progression in HD of chorea to hypokinesis. The biological basis for this differential vulnerability …

    rockefeller Repository record for Cell-Type Specific Translational Profiling in Huntington's Disease Mouse Models (opens in a new tab)

  13. The Social Construction of Huntington's Disease Caregivers in Colombia, South America

    … intensive, in-depth qualitative study of Huntington's disease (HD) caregivers (HDCs) in Colombia. I explored the Colombia HDCs' experience through the Hispanic culture of caring. I develop the theory of the subrogate agency based on 5 functional stages of HD from Shoulson and Fanh (1979). …

    unt Repository record for The Social Construction of Huntington's Disease Caregivers in Colombia, South America (opens in a new tab)

  14. Cognitive and synaptic dysfunction in a mouse model of Huntington's disease

    Huntington’s disease (HD) is a neurodegenerative disorder characterised by an unstable polyglutamine repeat expansion within the Huntingtin gene. Although clinical diagnosis of HD relies on the manifestation of a motor phenotype, cognitive symptoms often appear prior to diagnosis. This study has …

    dundee Repository record for Cognitive and synaptic dysfunction in a mouse model of Huntington's disease (opens in a new tab)

  15. Studies of Huntington's disease associated motor domain phosphorylation of kinesin-1

    … in impaired axonal transport associated with Huntington’s disease. Phosphorylation adds both negative charge and bulk to a protein. The mechanism by which S175 modification is related to impaired transport is not very well understood. It is not known whether phosphorylation of kinesin alone is …

    uiuc Repository record for Studies of Huntington's disease associated motor domain phosphorylation of kinesin-1 (opens in a new tab)

  16. Stress-activated protein kinase 1 and fast axonal transport in Huntington's disease.

    … protein kinase 1 and fast axonal transport in Huntington's disease.

    uic

  17. DNA Repair Deficiency in Huntington's Disease Fibroblasts and Induced Pluripotent Stem Cells

    … protein responsible for cellular dysfunction in Huntington’s disease (HD) –is a product of an expanded trinucleotide repeat (TNR) cytosine-adenine-guanine (CAG) sequence in exon 1 of the <em>huntingtin</em> <em>(HTT)</em> gene. The pathology of HD has been extensively researched; however, the …

    odu Repository record for DNA Repair Deficiency in Huntington's Disease Fibroblasts and Induced Pluripotent Stem Cells (opens in a new tab)

  18. The relationship of microRNAs to clinical features of Huntington's and Parkinson's disease

    … reported in neurodegenerative disorders, such as Huntington’s disease (HD) and Parkinson’s disease (PD), which may impact gene expression and modify disease progression and/or severity. To assess the relationship of miRNA levels to HD, small RNA sequence analysis was performed for 26 HD and 36 …

    bu Repository record for The relationship of microRNAs to clinical features of Huntington's and Parkinson's disease (opens in a new tab)

  19. Effects of Depression and Demographics On Word Generation In People With Huntington'S Disease

    … subjects as well as people with a diagnosis of Huntington's disease (HD). Participants were administered a battery of tests including the word generation test (FAS), and the supermarket portion of the Dementia Rating Scale (DRS) which assesses category fluency. </p><p>Participant's scores were …

    south-carolina Repository record for Effects of Depression and Demographics On Word Generation In People With Huntington'S Disease (opens in a new tab)

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