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1 - 6 of 6 results found for GAL3ST1.

  1. Emmanuelle Viré | MRC Prion Unit and Institute of Prion diseases -...

    Emmanuelle Viré. e.vire@prion.ucl.ac.uk. Tel: 020 7679 5094. Courtauld Building, Room G01. • PubMed•.  .  . Research Synopsis. We explore if epigenetics is a hallmark of protein-based inheritance in neurodegeneration. Our research

    https://www.ucl.ac.uk/prion/emmanuelle-vire

  2. Programme 1 | MRC Prion Unit and Institute of Prion diseases - UCL –...

    Recently we identified STX6 and GAL3ST1 as risk factors for CJD. ... At the UCL Institute of Prion Diseases (IoPD) we discovered that a common amino acid variant (V29M) of the sole enzyme involved in the synthesis of sulfatide (GAL3ST1 gene) confers a

    https://www.ucl.ac.uk/prion/programme-1

  3. Genome-wide association study identifies risk variants for sporadic Creutzfeldt-Jakob...

    Mammalian prions are lethal pathogens composed of fibrillar assemblies of misfolded prion protein. Human prion diseases are rare and usually rapidly fatal neurodegenerative disorders, the most common being sporadic Creutzfeldt-Jakob disease (sCJD).

    http://iris.ucl.ac.uk/iris/publication/1788919/18

  4. Genetic risk factors for Creutzfeldt-Jakob disease

    © 2020 Prion diseases are a group of fatal neurodegenerative disorders of mammals that share a central role for prion protein (PrP, gene PRNP) in their pathogenesis. Prions are infectious agents that account for the observed transmission of prion

    http://iris.ucl.ac.uk/iris/publication/1794191/1

  5. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob...

    BACKGROUND: Human prion diseases are rare and usually rapidly fatal neurodegenerative disorders, the most common being sporadic Creutzfeldt-Jakob disease (sCJD). Variants in the PRNP gene that encodes prion protein are strong risk factors for sCJD

    http://iris.ucl.ac.uk/iris/publication/1814630/1

  6. local://serve-db-document.tcgi?collection=iris-researchers&record_...

    local://serve-db-document.tcgi?collection=iris-researchers&record_id=SMEAD68

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