methionine has been researched along with Familial Fatal Insomnia in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 5 (55.56) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Bolakhrif, N; Gohlke, H; Gremer, L; Kaiser, J; Nagel-Steger, L; Pauly, T; Willbold, D | 1 |
| Axer, H; Grimm, A; Karvouniari, P; Rupprecht, S; Schultze, T; Schwab, M; Witte, OW; Zinke, J | 1 |
| Beekes, M; Ebert, E; Lüllmann, K; Mitrova, E; Oikonomou, P; Schlomm, M; Schmitz, M; Wohlhage, M; Zafar, S; Zerr, I | 1 |
| Feng, B; Jin, R; Liu, T; Wang, S; Wang, W; Wang, Z; Xiao, G; Zhou, Z | 1 |
| Chen, K; Li, X; Lin, X; Sun, L; Xiao, S; Yan, F | 1 |
| Dong, XP; Gong, HS; Guo, Y; Liu, Y; Shi, Q; Tian, C; Wang, SB; Xia, SL; Xie, WL; Xu, BL; Xu, Y; Zhang, BY; Zhang, J | 1 |
| Amthauer, H; Braas, R; Gregor, A; Hahne, HH; Harder, A; Jendroska, K; Kretzschmar, HA; Kreuz, F; Kuhlmann, T; Neukirch, K; Plotkin, M; Schulz-Schaeffer, WJ; Windl, O; Wirth, T | 1 |
| Chrétien, F; Créminon, C; Delisle, MB; Dormont, D; Gambetti, P; Gras, G; Gray, F; Ironside, JW; Le Pavec, G; Mikol, J; Parchi, P; Uro-Coste, E; Vallat-Decouvelaere, AV | 1 |
| Ayache, N; Brandel, JP; Dormont, D; Faucheux, BA; Galanaud, D; Haïk, S; Hauw, JJ; Linguraru, MG; Peoc'h, K; Privat, N | 1 |
9 other study(ies) available for methionine and Familial Fatal Insomnia
| Article | Year |
|---|---|
Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation.
Topics: Amyloid; Amyloidosis; Creutzfeldt-Jakob Syndrome; Humans; Insomnia, Fatal Familial; Methionine; Polymorphism, Genetic; Prion Proteins; Protein Folding; Valine | 2022 |
Does the clinical phenotype of fatal familial insomnia depend on PRNP codon 129 methionine-valine polymorphism?
Topics: Adult; Brain; Codon; Diagnosis, Differential; Fatal Outcome; Female; Fluorodeoxyglucose F18; Humans; Insomnia, Fatal Familial; Methionine; Phenotype; Polymorphism, Genetic; Polysomnography; Positron-Emission Tomography; Prion Proteins; Prions; Radiopharmaceuticals; Tomography, X-Ray Computed; Valine; Young Adult | 2013 |
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Topics: Adult; Aged; Aged, 80 and over; Codon; Creutzfeldt-Jakob Syndrome; Female; Genotype; Humans; Immunoblotting; Insomnia, Fatal Familial; Male; Methionine; Middle Aged; Mutation; Phosphorylation; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Protein Isoforms; Protein Processing, Post-Translational; PrPC Proteins; PrPSc Proteins; Valine | 2014 |
Methionine oxidation accelerates the aggregation and enhances the neurotoxicity of the D178N variant of the human prion protein.
Topics: Animals; Apoptosis; Cell Line, Tumor; Chromatography, High Pressure Liquid; Circular Dichroism; Endopeptidase K; Genetic Predisposition to Disease; Humans; Hydrogen Peroxide; Insomnia, Fatal Familial; Mass Spectrometry; Methionine; Microscopy, Confocal; Mutation, Missense; Neurotoxicity Syndromes; Oxidants; Oxidation-Reduction; Prions; Protein Conformation; Protein Structure, Secondary | 2014 |
Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.
Topics: Base Sequence; Brain; Codon; Electroencephalography; Female; Homozygote; Humans; Insomnia, Fatal Familial; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Prions | 2015 |
Comparison of the pathologic and pathogenic features in six different regions of postmortem brains of three patients with fatal familial insomnia.
Topics: Adult; Animals; Autopsy; Blotting, Western; Chromosomes, Human, Pair 20; Codon; Creutzfeldt-Jakob Syndrome; Endopeptidase K; Female; Glial Fibrillary Acidic Protein; Gyrus Cinguli; Humans; Immunohistochemistry; Insomnia, Fatal Familial; Male; Methionine; Mice; Mice, Inbred C57BL; Middle Aged; Mutation; Pedigree; Phosphopyruvate Hydratase; Prefrontal Cortex; Prion Proteins; Prions; Real-Time Polymerase Chain Reaction; RNA, Messenger; Specimen Handling; Thalamus; Transcription Factors | 2013 |
Early age of onset in fatal familial insomnia. Two novel cases and review of the literature.
Topics: Adult; Age of Onset; Asparagine; Aspartic Acid; DNA Mutational Analysis; Family Health; Genetic Counseling; Glucose; Humans; Immunohistochemistry; Insomnia, Fatal Familial; Male; Methionine; Middle Aged; Neurologic Examination; Pedigree; Postmortem Changes; Prions; Review Literature as Topic; Thalamus; Tomography, Emission-Computed | 2004 |
Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases.
Topics: Adult; Aged; Amyloid; Brain; Case-Control Studies; Child; Codon; Creutzfeldt-Jakob Syndrome; Excitatory Amino Acid Transporter 1; Female; Heterozygote; Humans; Insomnia, Fatal Familial; Macrophages; Male; Methionine; Microglia; Middle Aged; Prion Proteins; Prions; Protein Precursors; Severity of Illness Index; Time Factors; Valine | 2004 |
In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.
Topics: Alleles; Brain; Codon; Dementia; Diffusion Magnetic Resonance Imaging; DNA Mutational Analysis; Gliosis; Homozygote; Humans; Insomnia, Fatal Familial; Magnetic Resonance Spectroscopy; Male; Methionine; Middle Aged; Neurologic Examination; Neuropsychological Tests; Polysomnography; Prion Proteins; Prions; Thalamic Diseases; Thalamus | 2008 |