Compounds > valine

valine and Amyloid Deposits

valine has been researched along with Amyloid Deposits in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Allegri, RF; Bartoloni, L; Pletnikova, O; Riudavets, MA; Schultz, M; Sevlever, G; St George-Hyslop, P; Troncoso, JC1
Capellari, S; Cras, P; Ghetti, B; Giese, A; Kretzschmar, H; Ladogana, A; Langeveld, JP; Notari, S; Parchi, P; Pocchiari, M; Roncaroli, F; Strammiello, R; Zerr, I1
Behl, M; Du, Y; Farlow, MR; Fontanilla, CV; Gu, H; Monnot, AD; Wei, X; Zheng, W1
Almkvist, O; Bogdanovic, N; Långström, B; Nordberg, A; Schöll, M; Viitanen, M; Wall, A1
Alpérovitch, A; Amant, C; Amouyel, P; Berr, C; Hauw, JJ; Helbecque, N; Mohr, M; Sazdovitch, V1
Andreoletti, O; Basset-Leobon, C; Delisle, MB; Haik, S; Hauw, JJ; Peoc'h, K; Rigal, M; Sazdovitch, V; Uro-Coste, E1
Kamitani, T; Kawauchi, Y; Kishida, H; Kitamoto, T; Yagishita, S1

Other Studies

7 other study(ies) available for valine and Amyloid Deposits

ArticleYear
Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation.
    Brain pathology (Zurich, Switzerland), 2013, Volume: 23, Issue:5

    Topics: Adult; Dementia; DNA Mutational Analysis; Electroencephalography; Family Health; Female; Frontal Lobe; Humans; Inclusion Bodies; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Neuropsychological Tests; Plaque, Amyloid; Presenilin-1; Temporal Lobe; Tomography Scanners, X-Ray Computed; Valine

2013
Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification.
    Acta neuropathologica, 2009, Volume: 118, Issue:5

    Topics: Aged; Aged, 80 and over; Brain; Creutzfeldt-Jakob Syndrome; DNA Mutational Analysis; Female; Humans; Incidence; Male; Methionine; Middle Aged; Neurologic Examination; Phenotype; Plaque, Amyloid; PrPSc Proteins; Retrospective Studies; Valine

2009
Lead exposure increases levels of β-amyloid in the brain and CSF and inhibits LRP1 expression in APP transgenic mice.
    Neuroscience letters, 2011, Feb-18, Volume: 490, Issue:1

    Topics: Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Animals; Brain; Cells, Cultured; Choroid Plexus; Enzyme-Linked Immunosorbent Assay; Gene Expression Regulation; Humans; Lead; Low Density Lipoprotein Receptor-Related Protein-1; Mass Spectrometry; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurons; Phenylalanine; Plaque, Amyloid; Receptors, LDL; Tumor Suppressor Proteins; Valine

2011
Time course of glucose metabolism in relation to cognitive performance and postmortem neuropathology in Met146Val PSEN1 mutation carriers.
    Journal of Alzheimer's disease : JAD, 2011, Volume: 24, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Alzheimer Disease; Brain; Brain Mapping; Cognition Disorders; Female; Fluorodeoxyglucose F18; Glucose; Humans; Male; Mental Status Schedule; Methionine; Middle Aged; Mutation; Neuropsychological Tests; Plaque, Amyloid; Positron-Emission Tomography; Postmortem Changes; Presenilin-1; Statistics as Topic; Time Factors; Valine

2011
Polymorphism of the codon 129 of the prion protein (PrP) gene and neuropathology of cerebral ageing.
    Acta neuropathologica, 2003, Volume: 106, Issue:1

    Topics: Aged; Aged, 80 and over; Aging; Amyloid beta-Peptides; Analysis of Variance; Brain; Chi-Square Distribution; Codon; DNA Mutational Analysis; Female; Genotype; Humans; Male; Methionine; Neurofibrillary Tangles; Plaque, Amyloid; Polymorphism, Genetic; Prions; tau Proteins; Valine

2003
Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques.
    Archives of neurology, 2006, Volume: 63, Issue:3

    Topics: Amyloid; Arginine; Blotting, Western; Brain; Creutzfeldt-Jakob Syndrome; Haplotypes; Histidine; Humans; Immunohistochemistry; Male; Middle Aged; Mutation; Plaque, Amyloid; Prion Proteins; Prions; Protein Precursors; Valine

2006
Autopsy case of Creutzfeldt-Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum.
    Neuropathology : official journal of the Japanese Society of Neuropathology, 2006, Volume: 26, Issue:4

    Topics: Autopsy; Blotting, Western; Cerebellum; Creutzfeldt-Jakob Syndrome; Female; Genotype; Humans; Kuru; Methionine; Middle Aged; Peptide Hydrolases; Plaque, Amyloid; Polymerase Chain Reaction; Polymorphism, Genetic; Prions; Valine

2006