Results 251 to 260 of about 56,657 (298)

Prion protein fragment (106-126) activates NLRP3 inflammasome and promotes platelet-monocyte/neutrophil interactions, potentially contributing to an inflammatory state. [PDF]

Front Cell Dev Biol
Verma R, Kailashiya J, Mukherjee A, Chaurasia RN, Dash D.   +4 more
europepmc   +1 more source

Prion protein gene (PRNP) variation in German and Danish cervids. [PDF]

Vet Res
Ernst S, Piestrzyńska-Kajtoch A, Gethmann J, Natonek-Wiśniewska M, Sadeghi B, Polak MP, Keller M, Gavier-Widén D, Moazami-Goudarzi K, Houston F, Groschup MH, Fast C.   +11 more
europepmc   +1 more source

NMR spectroscopy with prion proteins and prion protein fragments

, 1999
openaire   +2 more sources

Oral Presentation

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

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Aptamers against prion proteins and prions

Cellular and Molecular Life Sciences, 2009
Prion diseases are fatal neurodegenerative and infectious disorders of humans and animals, characterized by structural transition of the host-encoded cellular prion protein (PrP(c)) into the aberrantly folded pathologic isoform PrP(Sc). RNA, DNA or peptide aptamers are classes of molecules which can be selected from complex combinatorial libraries for ...
Sabine, Gilch, Hermann M, Schätzl
openaire   +2 more sources

The fate of the prion protein in the prion/plasminogen complex

Biochemical and Biophysical Research Communications, 2003
The cellular prion protein (PrP(c)) forms complexes with plasminogen. Here, we show that the PrP(c) in this complex is cleaved to yield fragments of PrP(c). The cleavage is accelerated by plasmin but does not appear to be dependent on it.
Kornblatt, Jack A., Marchal, Stéphane, Rezaei, Human, Kornblatt, M. Judith, Balny, Claude, Lange, Reinhard, Debey, Marie-Pascale, Hui Bon Hoa, Gaston, Marden, Michael C., Grosclaude, Jeanne   +9 more
openaire   +3 more sources

Structural Studies of Prion Proteins and Prions

2011
Prion diseases are a group of fatal and incurable neurodegenerative ­disorders of mammals. They uniquely manifest as sporadic, genetic, and infectious maladies. The agent responsible for prion diseases is the prion. A prion is defined as a proteinaceous infectious particle, which is solely constituted by an alternately folded form of the prion protein (
Legname, Giuseppe, GIACHIN G, BENETTI F.
openaire   +1 more source

Human prion diseases with variant prion protein

Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 1994
Abstract Recent molecular genetic studies revealed that the human prion protein (PrP) gene has a large repertoire of polymorphisms and mutations. Each variant PrP seems to correspond to a distinct type of prion diseases. W e report herein that it is useful to classify prion diseases into plaque type or non-plaque type, based on the ...
T, Kitamoto, J, Tateishi
openaire   +2 more sources