lysine has been researched along with Dementias, Transmissible in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anson, KJ; Caughey, B; Dolan, MA; Dorward, DW; Groveman, BR; Kraus, A; Raymond, LD | 1 |
| Brajusković, G; Cadez, I; Dimitrijević, R; Dobricić, V; Keckarević, D; Keckarević-Marković, M; Kecmanović, M; Romac, S; Savić-Pavićević, D | 1 |
| Dvorakova, E; Holada, K; Janouskova, O; Panigaj, M; Prouza, M | 1 |
| Carp, RI; Choi, EK; Choi, YG; Jeon, YC; Kascsak, RJ; Kim, JI; Kim, YS; Park, SJ; Rubenstein, R | 1 |
| Lund, C; Olsen, CM; Tranulis, MA; Tveit, H | 1 |
| Aiken, JM; Bartz, JC; Bessen, RA; Marsh, RF; McKenzie, DI | 1 |
6 other study(ies) available for lysine and Dementias, Transmissible
| Article | Year |
|---|---|
Charge neutralization of the central lysine cluster in prion protein (PrP) promotes PrP(Sc)-like folding of recombinant PrP amyloids.
Topics: Amyloid; Animals; Humans; Lysine; Mesocricetus; Molecular Dynamics Simulation; Mutagenesis; Polyelectrolytes; Polymers; Prion Diseases; Protein Conformation; Protein Folding; Protein Multimerization; Protein Structure, Secondary; PrPSc Proteins; Recombinant Proteins; Static Electricity | 2015 |
Polymorphisms of the prion protein gene (PRNP) in a Serbian population.
Topics: Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Mutagenesis, Insertional; Oligopeptides; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Repetitive Sequences, Amino Acid; Sequence Deletion; Serbia | 2010 |
Development of monoclonal antibodies specific for glycated prion protein.
Topics: Animals; Antibodies, Monoclonal; Arginine; Brain; Glycosylation; Humans; Hybridomas; Lysine; Mice; Mice, Knockout; Mice, Transgenic; Peptides; Prion Diseases; Prions; Recombinant Proteins | 2011 |
Nonenzymatic glycation at the N terminus of pathogenic prion protein in transmissible spongiform encephalopathies.
Topics: Animals; Arginine; Astrocytes; Binding, Competitive; Blotting, Western; Brain; Cricetinae; Dose-Response Relationship, Drug; Enzyme-Linked Immunosorbent Assay; Glycosylation; Humans; Immunohistochemistry; Kinetics; Lysine; Mice; Mice, Inbred C57BL; Models, Biological; Oxygen; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase; Peptides; Precipitin Tests; Prion Diseases; Prions; Protein Isoforms; Protein Processing, Post-Translational; Protein Structure, Tertiary; PrPSc Proteins | 2004 |
Characterization of the prion protein 3F4 epitope and its use as a molecular tag.
Topics: Amino Acid Sequence; Animals; Antibodies, Monoclonal; Antibody Affinity; Binding Sites; Cell Line, Tumor; Cricetinae; Epitopes; Immunoassay; Lysine; Mice; Molecular Probe Techniques; Peptides; Prion Diseases; Prions; Protein Binding; Species Specificity | 2007 |
Transmissible mink encephalopathy species barrier effect between ferret and mink: PrP gene and protein analysis.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Brain; Codon; Disease Susceptibility; DNA Primers; Ferrets; Glutamine; Lysine; Mink; Molecular Sequence Data; Phenylalanine; Point Mutation; Polymerase Chain Reaction; Prion Diseases; Prions; Sequence Homology, Amino Acid; Sequence Homology, Nucleic Acid; Species Specificity | 1994 |