Page last updated: 2024-08-17

lysine and DDPAC

lysine has been researched along with DDPAC 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's1 (25.00)24.3611
2020's2 (50.00)2.80

Authors

AuthorsStudies
Bell, BM; Giasson, BI; Xia, Y1
Arenas, A; Barnett, KR; Chen, J; Gal, J; Kasarskis, EJ; Kuang, L; Zhu, H1
Hirata, K; Kitamoto, T; Nakamura, T; Satoh, K; Suzuki, K; Takayanagi, M1
Budka, H; Ghetti, B; Haraszti, L; Horvath, S; Kovacs, GG; Majtenyi, K; Molnar, MJ; Murrell, JR; Spina, S1

Other Studies

4 other study(ies) available for lysine and DDPAC

ArticleYear
Tau Lysine Pseudomethylation Regulates Microtubule Binding and Enhances Prion-like Tau Aggregation.
    International journal of molecular sciences, 2023, May-05, Volume: 24, Issue:9

    Topics: Alzheimer Disease; Frontotemporal Dementia; Humans; Lysine; Microtubules; Pick Disease of the Brain; Prions; tau Proteins; Tauopathies

2023
Lysine acetylation regulates the RNA binding, subcellular localization and inclusion formation of FUS.
    Human molecular genetics, 2020, 09-29, Volume: 29, Issue:16

    Topics: Acetylation; Adult; Amyotrophic Lateral Sclerosis; beta Karyopherins; Female; Frontotemporal Dementia; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Lysine; Male; Middle Aged; Nuclear Localization Signals; Protein Domains; RNA-Binding Protein FUS; RNA-Binding Proteins; Sirtuins; Young Adult

2020
[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].
    Rinsho shinkeigaku = Clinical neurology, 2018, Nov-28, Volume: 58, Issue:11

    Topics: 14-3-3 Proteins; Alleles; Amino Acid Substitution; Biomarkers; Brain; Codon; Creutzfeldt-Jakob Syndrome; Diffusion Magnetic Resonance Imaging; Disease Progression; Electroencephalography; Frontotemporal Dementia; Glutamates; Humans; Lysine; Male; Middle Aged; Mutation; Polymorphism, Genetic; Prion Proteins; tau Proteins

2018
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Sep-15, Volume: 24, Issue:12

    Topics: Chorea; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Female; Frontotemporal Dementia; Genetic Predisposition to Disease; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neuropsychological Tests; Supranuclear Palsy, Progressive; Tomography Scanners, X-Ray Computed

2009