Compounds > valine

valine and Familial Fatal Insomnia

valine has been researched along with Familial Fatal Insomnia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Bolakhrif, N; Gohlke, H; Gremer, L; Kaiser, J; Nagel-Steger, L; Pauly, T; Willbold, D1
Axer, H; Grimm, A; Karvouniari, P; Rupprecht, S; Schultze, T; Schwab, M; Witte, OW; Zinke, J1
Beekes, M; Ebert, E; Lüllmann, K; Mitrova, E; Oikonomou, P; Schlomm, M; Schmitz, M; Wohlhage, M; Zafar, S; Zerr, I1
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, AV1

Other Studies

4 other study(ies) available for valine and Familial Fatal Insomnia

ArticleYear
Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation.
    The Journal of biological chemistry, 2022, Volume: 298, Issue:10

    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?
    Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 2013, Dec-15, Volume: 9, Issue:12

    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.
    Neurobiology of aging, 2014, Volume: 35, Issue:5

    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
Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases.
    Journal of neuropathology and experimental neurology, 2004, Volume: 63, Issue:10

    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