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Showing 1 to 20 of 133 for “"huntington"”.

  1. Verhaltensversuche bei Tiermodellen der Chorea Huntington

    Bellut, David2008

    aachen Repository record

  2. Faraldsfræði Huntington sjúkdóms á Íslandi. 2008-2022

    Saga Briem 2000-2023

    Inngangur: Huntington sjúkdómur (HS) er sjaldgæfur, ættlægur taugahrörnunarsjúkdómur sem einkennist af ofhreyfingum, geðröskun og heilabilun. Sjúkdómurinn erfist ríkjandi og stafar af cýtósín-adenín-gúanín þríkirnaþenslu í huntingtin geninu. Algengi er hæst í einstaklingum af evrópskum uppruna en …

    u-iceland Repository record

  3. Genetic and anthropometric studies of aging in Huntington disease

    Farrer, Lindsay Ames1985

    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

  4. A molecular approach to Huntington disease in Southern Africa

    Greenberg, Leslie J H LDivision of Human Genetics1990

    cape-town Repository record

  5. Partielle Resistenz Chorea Huntington transgener Mäuse gegen globale cerebrale Ischämie

    Alberty, Anke AlexandraPublikationsserver der RWTH Aachen University2004

    … as well as neurodegenerative diseases such as Huntington's disease (HD). Surprisingly it has been found that HD transgenic mice are resistant to intrastriatal injections of excitotoxic substances. We investigated whether HD transgenic mice are also resistant to global cerebral ischemia, …

    aachen Repository record

  6. Glutamatantagonisten zur Therapie der Chorea Huntington : Untersuchungen am transgenen Mausmodell

    Sprünken, Arne Wolfgang2004

    aachen Repository record

  7. American Machiavelli: Samuel P. Huntington the Author of Grand Strategy

    Fine, ToddThe Graduate School and University Center of The City University of New York2027

    <p>Samuel P. Huntington was one of the most influential political scientists of the 20th century, authoring a series of influential “concepts” and “paradigms” that have had tremendous impact on both scholarship and political practice. Historians have made great efforts to chart the anomalous, …

    cuny-grad Repository record

  8. Identification of Landscape Site Development Criteria and Compilation for Fossil Fuel Electric Power Plants Applied to a Critique of Huntington Canyon Power Plant, Huntington, Utah

    Manns, Thomas Franklin, II

    utahstate Repository record

  9. Transplantation neuraler Stammzellen im Quinolinsäuremodell der Chorea Huntington in der Maus

    Saß, Christian Franz Friedrich2008

    aachen Repository record

  10. The Huntington Library's early nineteenth-century sheet music and its publishers

    Rice, Albert R

    sjsu Repository record

  11. Marine Interstitial Tardigrades and Other Meiofauna of Huntington Beach, South Carolina.

    Gaugler, Michael Scott2002

    <p>At Huntington Beach, SC meiofauna distribution was investigated. The purpose of the study was to determine tardigrade species present and any significant differences in the distribution pattern. Meiofauna were analyzed to determine if there were significant differences in their distribution …

    etsu Repository record

  12. Therapiestudien zur Hemmung der glutamatergen Neurotransmission im transgenen Mausmodell der Chorea Huntington

    Schiefer, Johannes2006

    aachen Repository record

  13. Somatic instability in Huntington disease and its impact on transcription and translation

    Wagner, MaximilianUniversität Ulm

    ulm-diss Repository record

  14. Silencing mutant Huntingtin by RNA interference for the treatment of Huntington Disease

    Wagner, Laura A.University of British Columbia2008

    Huntington Disease (HD) is a dominantly inherited neurological disease attributed to a CAG expansion within the HD gene. The HD mutation gives rise to a polyglutamine expansion in exon 1 of the protein huntingtin (Htt). Since the discovery of the HD mutation in 1993, various HD gene mouse models …

    ubc Repository record

  15. Analysis of Huntington Disease Caregiver Quality of Life Using The Enroll-Hd Population

    Banfield, Emilyn2024

    <p>Huntington disease (HD) is a neurodegenerative condition inherited in an autosomal dominant manner caused by a CAG triplet repeat expansion within the <em>HTT</em> gene. Thus, HD is unique among neurodegenerative disorders with a caregiver population often burdened by both the caregiver role and …

    uthsc Repository record

  16. The role of a genetic counsellor in a support group for Huntington disease

    du Toit, MaxineDepartment of Clinical Laboratory Sciences2019

    … of a genetic counsellor in a support group for Huntington disease. This study examines the role of a genetic counsellor in a Huntington Disease support group, specifically the Huntington’s Association of South Africa (HASA). A qualitative research approach was used to interview 17 people who …

    cape-town Repository record

  17. Said-Huntington Discourse Analyzer : a machine-learning tool for classifying and analyzing discourse

    Hashmi, Muhammad Ali, S.M. Massachusetts Institute of TechnologyMassachusetts Institute of Technology2015

    … I have developed a prototype tool "Said-Huntington Discourse Analyzer" that machine classifies news articles on a normative scale -- a scale that measures "clash of civilization" polarization in an article on the basis of conflict. The tool also extracts semantically meaningful …

    mit Repository record

  18. Analyse von Polymorphismen als genetische Modifikatoren der Spinozerebellären Ataxie Typ 3 und Morbus Huntington

    Czisch, Leah Raphaela2027

    tuebingen

  19. Molecular investigation of the trinucleotide repeats within the Huntington disease gene in Southern Africa

    September, AlisonDepartment of Medicine1999

    Huntington disease (HD) is an autosom 1 dominant, progressive neurodegenerative condition, which usually presents in mid-life. The disease-causing mutation was identified in 1993 and entails the expansion of an unstable repeat (CAG)n within exon 1 of the, HD gene (IT-15). A polymorphic (CCG)n …

    cape-town Repository record

  20. Das R6/2-Mausmodell der Chorea Huntington : verhaltensbiologische Charakteristika und der Einfluss ihres Diabetes mellitus

    Puls, ChristianePublikationsserver der RWTH Aachen University2005

    R6/2 transgenic mice express exon 1 of the human Huntington`s disease (HD) gene with an increased CAG repeat length and develop a progressive neurological phenotype. Some of these mice were also found to develop a diabetes mellitus. The aim of this study was to search for behavioural tests that are …

    aachen Repository record

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