proline has been researched along with Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, X; Long, L; Lu, Z; Shu, Y | 1 |
| Cortes, CJ; Dearmond, SJ; Mallik, S; Mastrianni, JA; Tunnell, E; Wollman, R | 1 |
| Ciano, C; Di Fede, G; Fancellu, R; Mariotti, C; Nanetti, L; Pareyson, D; Politi, LS; Salsano, E; Scaioli, V; Tagliavini, F | 1 |
| Doh-ura, K; Furuta, A; Iwaki, T; Morisada, Y; Nakashima, S; Sasaki, K; Tateishi, J | 1 |
| Hope, J; Manson, JC; Melton, DW; Moore, RC; Redhead, NJ; Selfridge, J | 1 |
| Hsiao, K; Prusiner, SB | 1 |
| DeArmond, SJ; Foster, D; Groth, D; Hsiao, K; Prusiner, SB; Scott, M; Serban, H | 1 |
1 review(s) available for proline and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
| Article | Year |
|---|---|
Molecular genetics and transgenic model of Gertsmann-Sträussler-Scheinker disease.
Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Brain; Codon; Genetic Markers; Gerstmann-Straussler-Scheinker Disease; Humans; Leucine; Mice; Mice, Transgenic; Models, Genetic; Prions; Proline; PrPSc Proteins | 1991 |
6 other study(ies) available for proline and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
| Article | Year |
|---|---|
A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
Topics: Cerebellar Ataxia; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Lysine; Magnetic Resonance Imaging; Middle Aged; Mutation; Prion Proteins; Proline | 2017 |
A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation.
Topics: Adult; Amino Acid Substitution; Brain; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Male; Middle Aged; Mutation; Prion Diseases; Prion Proteins; Prions; Proline; Protein Conformation; PrPSc Proteins; Serine | 2008 |
Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.
Topics: Adult; Brain; Electroencephalography; Electrophysiological Phenomena; Evoked Potentials, Motor; Evoked Potentials, Somatosensory; Family; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Italy; Leucine; Lower Extremity; Magnetic Resonance Imaging; Male; Middle Aged; Neural Conduction; Neurologic Examination; Prions; Proline; Reflex, Abnormal | 2011 |
Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
Topics: Amyloid beta-Peptides; Astrocytes; Brain; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Glial Fibrillary Acidic Protein; Humans; Immunohistochemistry; Inclusion Bodies; Leucine; Microscopy, Electron; Middle Aged; Mutation; Organ Size; Pedigree; Prions; Proline; S100 Proteins; Schizophrenia; Staining and Labeling; Ubiquitin | 2003 |
Double replacement gene targeting for the production of a series of mouse strains with different prion protein gene alterations.
Topics: Alleles; Animals; Cell Line; Codon; Embryo, Mammalian; Gene Targeting; Genetic Vectors; Gerstmann-Straussler-Scheinker Disease; Humans; Leucine; Mice; Mice, Knockout; Mutagenesis, Site-Directed; Polymerase Chain Reaction; Prions; Proline; Protein Engineering; Stem Cells | 1995 |
Spontaneous neurodegeneration in transgenic mice with prion protein codon 101 proline----leucine substitution.
Topics: Amino Acid Sequence; Animals; Brain; Codon; Gene Expression; Gerstmann-Straussler-Scheinker Disease; Leucine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Molecular Sequence Data; Prions; Proline; PrPSc Proteins | 1991 |