leucine has been researched along with Dementias, Transmissible in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Agarwal, S; Gill, AC; Goldmann, W; Graham, JF; Kirby, L | 1 |
| Mizusawa, H; Shiraishi, A; Yamada, M | 1 |
| Ghetti, B; Harris, DA; Piccardo, P; Stewart, RS | 1 |
| Barrow, CJ; Beyreuther, K; Cappai, R; Collins, SJ; Jobling, MF; Masters, CL; Stewart, L; Thyer, JM; White, AR | 1 |
| Inaba, A; Itoh, Y; Kamata, T; Kayano, T; Kitamoto, T; Matsushita, M; Mizusawa, H; Okeda, R; Otomo, E; Satoh, S; Suematsu, N; Takashima, M; Wada, Y; Yamada, M | 1 |
1 review(s) available for leucine and Dementias, Transmissible
| Article | Year |
|---|---|
An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity.
Topics: Amino Acid Substitution; Brain; Codon; Female; Humans; Leucine; Male; Methionine; Middle Aged; Mutation, Missense; Nuclear Family; Pedigree; Polymorphism, Genetic; Prion Diseases; Prions; Proline; Valine | 1999 |
4 other study(ies) available for leucine and Dementias, Transmissible
| Article | Year |
|---|---|
Inverse correlation of thermal lability and conversion efficiency for five prion protein polymorphic variants.
Topics: Amino Acid Substitution; Animals; Cell-Free System; Deer; Genetic Predisposition to Disease; Genetic Variation; Immunity, Innate; Leucine; Mice; Peptide Fragments; Polymorphism, Genetic; Prion Diseases; Prions; Proline; Protein Conformation; Protein Denaturation; Protein Folding; Protein Stability; Sheep; Temperature | 2010 |
Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.
Topics: Female; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Prion Diseases; Prions; Proline | 2002 |
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 |
Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation.
Topics: Amino Acid Substitution; Animals; Circular Dichroism; Drug Resistance; Endopeptidase K; Escherichia coli; Leucine; Mice; Mice, Inbred BALB C; Prion Diseases; Prions; Proline; Protein Structure, Secondary; Recombinant Proteins | 1999 |