1 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.

2 wariant choroby creutzfeldta-jakoba: aktualny stan wiedzy

3 molecular modeling of prion transmission to humans

4 influence of the aqueous environment on protein structure—a plausible hypothesis concerning the mechanism of amyloidogenesis

5 polymorphism of amyloid-like fibrils can be defined by the concentration of seeds

6 the scrapie prevalence in a goat herd is underestimated by using a rapid diagnostic test

7 biochemical characterization of prion strains in bank voles

8 computational analysis of candidate prion-like proteins in bacteria and their role

9 protein folding activity of the ribosome (pfar) –– a target for antiprion compounds

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

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

12 heidenhain variant of creutzfeldt–jakob disease in a patient who had bovine bioprosthetic valve implantation

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

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

15 Reduced Genetic Diversity in the Clown Anemonefish Amphiprion ocellaris in Exploited Reefs of Spermonde Archipelago, Indonesia

16 Bacteria isolated from Bengal cat (Felis catus × Prionailurus bengalensis) anal sac secretions produce volatile compounds potentially associated with animal signaling.

17 All the Same? The Secret Life of Prion Strains within Their Target Cells

18 Inhibition of the pro-inflammatory mediators in rat neutrophils by shanzhiside methyl ester and its acetyl derivative isolated from Barleria prionitis.

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

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

21 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.

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

23 Underglycosylated prion protein modulates plaque formation in the brain.

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

25 Presence of the protein indoleamine 2,3-dioxygenase (IDO) in the maternal-fetal interface of the yolk sac placenta of blue shark, Prionace glauca.

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

27 Molecular characterization and expression patterns of glucocorticoid receptor (GR) genes in protandrous hermaphroditic yellowtail clownfish, Amphiprion clarkii.

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

29 Wreckfish (Polyprion americanus). New Knowledge About Reproduction, Larval Husbandry, and Nutrition. Promise as a New Species for Aquaculture

30 Induced Spawning of F1 Wreckfish (Hāpuku) Polyprion oxygeneios Using a Synthetic Agonist of Gonadotropin-Releasing Hormone

31 Transcriptomic Changes during Previtellogenic and Vitellogenic Stages of Ovarian Development in Wreckfish (Hāpuku), Polyprion oxygeneios (Perciformes)

32 Description of the Annual Reproductive Cycle of Wreckfish Polyprion americanus in Captivity

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

34 a medicinal herb scutellaria lateriflora inhibits prp replication in vitro and delays the onset of prion disease in mice

35 el silenciamiento de la proteína priónica celular (prpc) mediante rna de interferencia (sirna) reduce la infección por hsv-1 y hsv-2 en células sk-sy5y

36 age and environment influences on mouse prion disease progression: behavioral changes and morphometry and stereology of hippocampal astrocytes

37 seeking a new paradigm for alzheimer’s disease: considering the roles of inflammation, blood-brain barrier dysfunction, and prion disease

38 deficiency of prion protein induces impaired autophagic flux in neurons

39 prion disease risk perception in canadian medical laboratories

40 prion protein and aging

41 complete chloroplast genome sequence of barleria prionitis, comparative chloroplast genomics and phylogenetic relationships among acanthoideae

42 taxonomic revision of the genus prionopelta (hymenoptera, formicidae) in the malagasy region

43 ucai, novo gênero de anacolini (coleoptera, cerambycidae, prioninae) do brasil ucai, a new genus of anacolini (coleoptera, cerambycidae, prioninae) from brazil

44 brain prion amyloid imaging in gerstmann-straussler- scheinker disease using positron emisson tomography

45 synaptic dysfunction in prion diseases: a trafficking problem?

46 reduced genetic diversity in the clown anemonefish amphiprion ocellaris in exploited reefs of spermonde archipelago, indonesia

47 prion-like domains in phagobiota

48 the cellular prion protein: a player in immunological quiescence

49 prion diseases and the gastrointestinal tract

50 structural characterization and interaction with rca120 of a highly sulfated keratan sulfate from blue shark (prionace glauca) cartilage

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

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

53 from prion diseases to prion-like propagation mechanisms of neurodegenerative diseases

54 evidence for prion-like mechanisms in several neurodegenerative diseases: potential implications for immunotherapy

55 a review of the distribution and biology of the small carrion beetle prionochaeta opaca of north america (coleoptera; leiodidae; catopinae)

56 Alzheimer’s disease brain contains tau fractions with differential prion-like activities

57 Tau assemblies do not behave like independently acting prion-like particles in mouse neural tissue

58 DNA barcoding for bio-surveillance of emerging pests and species identification in Afrotropical Prioninae (Coleoptera, Cerambycidae)

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

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