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Porcine Model of Huntington´s Disease

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985904%3A_____%2F17%3A00483018" target="_blank" >RIV/67985904:_____/17:00483018 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.intechopen.com/books/huntington-s-disease-molecular-pathogenesis-and-current-models/porcine-model-of-huntington-s-disease" target="_blank" >https://www.intechopen.com/books/huntington-s-disease-molecular-pathogenesis-and-current-models/porcine-model-of-huntington-s-disease</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5772/66353" target="_blank" >10.5772/66353</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Porcine Model of Huntington´s Disease

  • Original language description

    At present, we are probably the only research facility to be breeding transgenic Huntington's disease minipigs (TgHD). These minipigs express N‐terminal part of human mutated huntingtin including 124Q under the control of human huntingtin promoter. The founder animal, born in 2009, gave birth to four subsequent generations with an equal contribution of wild‐type (WT) and transgenic (TgHD) piglets in all litters. We take different approaches, some of which are unique for large animal models, to study the phenotype development comparing WT and TgHD siblings. In this chapter, we review these approaches and the phenotype progression in the minipigs. Additionally, we outline perspectives in generation of new models using novel methodology and the potential of pig models in preclinical HD studies.

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

  • OECD FORD branch

    30403 - Technologies involving identifying the functioning of DNA, proteins and enzymes and how they influence the onset of disease and maintenance of well-being (gene-based diagnostics and therapeutic interventions [pharmacogenomics, gene-based therapeutics])

Result continuities

  • Project

    <a href="/en/project/LO1609" target="_blank" >LO1609: Models of the Serious Human Diseases: Traumatic Spinal Cord Injury, Huntington’s Disease, Melanoma and Infertility</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Book/collection name

    Huntington´s Disease - Molecular Pathogenesis and Current Models

  • ISBN

    978-953-51-3050-5

  • Number of pages of the result

    20

  • Pages from-to

    75-94

  • Number of pages of the book

    150

  • Publisher name

    Intech

  • Place of publication

    London

  • UT code for WoS chapter