Compounds > aspartic acid
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aspartic acid and Dementias, Transmissible

aspartic acid has been researched along with Dementias, Transmissible in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antonov, A; Bourgognon, JM; Bradley, SJ; Scheiblich, H; Spiers, JG; Steinert, JR; Tobin, AB1
Aguzzi, A; Bremer, J; Craveiro, M; Cudalbu, C; Gruetter, R; Mlynárik, V1
Brandel, JP; Faucheux, BA; Haïk, S; Hauw, JJ; Laplanche, JL; Peoc'h, K; Privat, N1
Beloeil, JC; Dormont, D; Gillet, B; Herzog, C; Lasmézas, C; Méric, P; Provost, F; Vidal, C1
Collinge, J; Cordery, RJ; Godbolt, A; MacManus, DG; Rossor, MN; Waldman, AD1
Anthony, DC; Blamire, AM; Broom, KA; Griffin, JL; Lowe, JP; Perry, VH; Scott, H; Sibson, NR; Styles, P1

Other Studies

6 other study(ies) available for aspartic acid and Dementias, Transmissible

ArticleYear
Alterations in neuronal metabolism contribute to the pathogenesis of prion disease.
    Cell death and differentiation, 2018, Volume: 25, Issue:8

    Topics: Aminobutyrates; Animals; Aspartic Acid; Cerebral Cortex; Down-Regulation; Glucose; Glucose Transporter Type 1; Hippocampus; Machine Learning; Metabolome; Mice; Mice, Transgenic; Nitric Oxide; Prion Diseases; Prostaglandins; Signal Transduction; Sphingolipids; Up-Regulation

2018
In Vivo Longitudinal (1)H MRS Study of Transgenic Mouse Models of Prion Disease in the Hippocampus and Cerebellum at 14.1 T.
    Neurochemical research, 2015, Volume: 40, Issue:12

    Topics: Animals; Aspartic Acid; Brain Chemistry; Cerebellum; Glutamic Acid; Hippocampus; Inositol; Lactic Acid; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred BALB C; Mice, Knockout; Mice, Transgenic; Prion Diseases; Prion Proteins; Prions

2015
Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation.
    Annals of neurology, 2004, Volume: 56, Issue:6

    Topics: Asparagine; Aspartic Acid; Brain; Humans; Mutation; Prion Diseases; PrPSc Proteins

2004
Preclinical metabolic changes in mouse prion diseases detected by 1H-nuclear magnetic resonance spectroscopy.
    Neuroreport, 2006, Jan-23, Volume: 17, Issue:1

    Topics: Animals; Aspartic Acid; Brain; Cattle; Disease Models, Animal; Female; Infections; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred C57BL; Prion Diseases; Scrapie; Time Factors

2006
Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopy.
    Neuroradiology, 2006, Volume: 48, Issue:6

    Topics: Adult; Aspartic Acid; Brain; Case-Control Studies; Creatine; Female; Heterozygote; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Prion Diseases; Prions

2006
MRI and MRS alterations in the preclinical phase of murine prion disease: association with neuropathological and behavioural changes.
    Neurobiology of disease, 2007, Volume: 26, Issue:3

    Topics: Animals; Aspartic Acid; Astrocytes; Body Water; Brain; Choline; Creatine; Diffusion; Disease Models, Animal; Disease Progression; Gliosis; Glucose; Glutamic Acid; Hyperkinesis; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred C57BL; Microglia; Prion Diseases

2007