Keyword Connections

prion protein

Journals

1

1 Biochemical and biophysical research communications

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Bibliographies

22

1 PrP (122-139) is a covert mitochondrial targeting signal of prion protein and it specifically triggers the perinuclear clustering of mitochondria in neuronal culture cells.

2 creutzfeldt-jakob disease: analysis of four cases

3 deficiency of prion protein induces impaired autophagic flux in neurons

4 subtype and regional-specific neuroinflammation in sporadic creutzfeldt-jakob disease

5 the cellular prion protein: a player in immunological quiescence

6 prion fragment peptides are digested with membrane type matrix metalloproteinases and acquire enzyme resistance through cu2+-binding

7 Monoacylated Cellular Prion Proteins Reduce Amyloid-β-Induced Activation of Cytoplasmic Phospholipase A2 and Synapse Damage

8 Cellular prion protein gene polymorphisms linked to differential scrapie susceptibility correlate with distinct residue connectivity between secondary structure elements.

9 Absence of single nucleotide polymorphisms (SNPs) in the open reading frame (ORF) of the prion protein gene (PRNP) in a large sampling of various chicken breeds.

10 Melatonin-stimulated exosomes enhance the regenerative potential of chronic kidney disease-derived mesenchymal stem/stromal cells via cellular prion proteins.

11 Prion protein glycans reduce intracerebral fibril formation and spongiosis in prion disease.

12 Underglycosylated prion protein modulates plaque formation in the brain.

13 Prion protein—Semisynthetic prion protein (PrP) variants with posttranslational modifications

14 Author Correction: Octa-repeat domain of the mammalian prion protein mRNA forms stable A-helical hairpin structure rather than G-quadruplexes.

15 Quantification of the vacuolation (spongiform change) and prion protein deposition in 11 patients with sporadic Creutzfeldt-Jakob disease

16 Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome

17 prion protein and aging

18 evolutionary implications of metal binding features in different species’ prion protein: an inorganic point of view

19 monoacylated cellular prion proteins reduce amyloid-β-induced activation of cytoplasmic phospholipase a2 and synapse damage

20 deposition pattern and subcellular distribution of disease-associated prion protein in cerebellar organotypic slice cultures infected with scrapie

21 molecular dynamics simulations capture the misfolding of the bovine prion protein at acidic ph

22 Prion-induced photoreceptor degeneration begins with misfolded prion protein accumulation in cones at two distinct sites: cilia and ribbon synapses