arginine has been researched along with Dementias, Transmissible in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alibhai, J; Blanco, AR; Campbell, L; de Wolf, C; Gill, AC; Gonzalez, L; Houston, EF; Hunter, N; Langeveld, JP; Martin, S; McCutcheon, S; Tan, BC | 1 |
| Pinheiro, TJ; Robinson, PJ | 1 |
| Cali, I; DeArmond, SJ; Geschwind, MD; Harbaugh, R; Kuo, A; Raudabaugh, B; Sanchez, H; Sattavat, M; See, T; Tartaglia, MC; Thai, JN | 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 |
| Ghetti, B; Harris, DA; Piccardo, P; Stewart, RS | 1 |
| Aiken, JM; Bartz, JC; Bessen, RA; Marsh, RF; McKenzie, DI | 1 |
7 other study(ies) available for arginine and Dementias, Transmissible
| Article | Year |
|---|---|
Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity.
Topics: Amino Acid Sequence; Animals; Antibodies, Monoclonal; Antibody Specificity; Arginine; Binding Sites; Codon; Immunoglobulin Isotypes; Immunohistochemistry; Mice; Molecular Sequence Data; Prion Diseases; Prions; Protein Binding; Protein Kinases; PrPSc Proteins; Recombinant Proteins; Sequence Alignment; Sheep | 2014 |
The unfolding of the prion protein sheds light on the mechanisms of prion susceptibility and species barrier.
Topics: Animals; Arginine; Cricetinae; Genetic Predisposition to Disease; Glutamine; Mice; Mutagenesis, Site-Directed; Prion Diseases; Prion Proteins; Prions; Protein Denaturation; Protein Folding; Species Specificity; Thermodynamics; Tryptophan | 2009 |
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease.
Topics: Arginine; Creutzfeldt-Jakob Syndrome; Dementia; Fatal Outcome; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Prion Diseases; Prion Proteins; Prions; Threonine | 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 |
Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.
Topics: Animals; Animals, Newborn; Arginine; Blotting, Western; Brain; Cells, Cultured; Cerebellum; Cricetinae; Cricetulus; Detergents; Disease Models, Animal; Electrophoresis, Polyacrylamide Gel; Fluorescent Antibody Technique; Gene Expression; Glial Fibrillary Acidic Protein; Golgi Apparatus; Golgi Matrix Proteins; Immunoprecipitation; Leucine; Membrane Proteins; Methionine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurodegenerative Diseases; Neurons; Octoxynol; Prion Diseases; Protein Structure, Tertiary; PrPSc Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sulfur Isotopes; Time Factors; Type C Phospholipases; Valine | 2005 |
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 |