valine 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 |
|---|---|
| Boyd, A; Collins, SJ; Johanssen, V; Klug, G; Lewis, V; Li, QX; Masters, CL; McLean, C; Pamphlett, R; Simpson, M | 1 |
| Capellari, S; Dopper, EG; Jansen, C; Kamphorst, W; Parchi, P; Rozemuller, AJ; Strammiello, R; van Swieten, JC | 1 |
| Clark, HB; Dlouhy, SR; Ghetti, B; Piccardo, P; Young, K | 1 |
| Beavis, RC; Bugiani, O; Frangione, B; Ghetti, B; Giaccone, G; Lievens, PM; Mohr, M; Perini, F; Piccardo, P; Prelli, F; Rossi, G; Salmona, M; Tagliavini, F; Tranchant, C; Warter, JM | 1 |
| Hata, M; Hoshino, T; Okimoto, N; Suenaga, A; Yamanaka, K | 1 |
| Doh-ura, K; Iwaki, T; Kitamoto, T; Miyazono, M; Tateishi, J | 1 |
| Bird, T; Cass, C; Devine-Gage, E; Hsiao, KK; Prusiner, SB; Schellenberg, GD; Wisniewski, H | 1 |
7 other study(ies) available for valine and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
| Article | Year |
|---|---|
Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
Topics: Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Gerstmann-Straussler-Scheinker Disease; Glycine; Humans; Middle Aged; Mutation; Neurofibrillary Tangles; Pedigree; Phenotype; Prion Proteins; Prions; Valine | 2013 |
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
Topics: Adult; Brain; Genetic Predisposition to Disease; Genome-Wide Association Study; Gerstmann-Straussler-Scheinker Disease; Glycine; Humans; Male; Netherlands; Polymorphism, Genetic; Prions; Valine | 2011 |
Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.
Topics: Adult; Gerstmann-Straussler-Scheinker Disease; Humans; Male; Mutation; Polymerase Chain Reaction; Prions; Valine | 1997 |
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
Topics: Adult; Alleles; Amyloid; Cerebral Cortex; Gerstmann-Straussler-Scheinker Disease; Heterozygote; Humans; Male; Methionine; Peptide Fragments; Prion Proteins; Prions; Protein Precursors; Sequence Analysis, Protein; Syndrome; Valine | 2001 |
Computational studies on prion proteins: effect of Ala(117)-->Val mutation.
Topics: Alanine; Amino Acid Sequence; Amino Acid Substitution; Computer Simulation; Gerstmann-Straussler-Scheinker Disease; Humans; Magnetic Resonance Spectroscopy; Mathematics; Models, Molecular; Models, Theoretical; Molecular Sequence Data; Mutagenesis, Site-Directed; Prions; Protein Conformation; Protein Structure, Secondary; Static Electricity; Valine | 2002 |
Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.
Topics: Adult; Aged; Brain Chemistry; Codon; Creutzfeldt-Jakob Syndrome; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Immunohistochemistry; Japan; Male; Middle Aged; Point Mutation; Polymorphism, Genetic; Prions; PrPSc Proteins; Valine | 1992 |
A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome.
Topics: Alanine; Base Sequence; Codon; DNA, Viral; Female; Genetic Variation; Germany; Gerstmann-Straussler-Scheinker Disease; Humans; Male; Molecular Sequence Data; Oligonucleotide Probes; Open Reading Frames; Prions; PrPSc Proteins; Telencephalon; United States; Valine; Viral Proteins | 1991 |