Prion-like Propagation

Prion-Like Propagation is a pathogenic mechanism in neurodegenerative biophysics whereby misfolded protein aggregates catalyze the conformational conversion of their normally folded counterparts into toxic conformers, enabling cell-to-cell spread of proteinopathy along neural networks in a manner mechanistically analogous to prion diseases but typically without infectious transmission.

217

Publications

20K

Citations

1.3K

Authors

423

Institutions

Publications per year

2017–2026

120

Variants

Prion-like Spreading

Authors

1.3K

  1. MH
    Masato Hasegawa

    Tokyo Metropolitan Institute of Medical Science, Japan

    13 publications · 2.2K citations

    13

    h-index

  2. RM
    Ronald Melki

    Centre National de la Recherche Scientifique, France

    11 publications · 991 citations

    11

    h-index

  3. LB
    Luc Bousset

    Centre National de la Recherche Scientifique, France

    8 publications · 884 citations

    8

    h-index

  4. NR
    Neil R. Cashman

    University of British Columbia, Canada

    8 publications · 856 citations

    8

    h-index

  5. BI
    Benoit I. Giasson

    University of Pennsylvania, United States

    8 publications · 451 citations

    8

    h-index

1–5 of 1.3K

Venues

  1. Journal of Biological Chemistry

    JBC · 15 publications · 1.3K citations

    15

    h-index

  2. Proceedings of the National Academy of Sciences

    PNAS · 16 publications · 2.7K citations

    15

    h-index

  3. Acta Neuropathologica Communications

    15 publications · 1.5K citations

    14

    h-index

  4. Acta Neuropathologica

    9 publications · 1.4K citations

    9

    h-index

  5. Brain

    9 publications · 2.3K citations

    9

    h-index

1–5