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glycine and TDP-43 Proteinopathies

glycine has been researched along with TDP-43 Proteinopathies in 2 studies

TDP-43 Proteinopathies: Diseases characterized by the presence of abnormally phosphorylated, ubiquitinated, and cleaved DNA-binding protein TDP-43 in affected brain and spinal cord. Inclusions of the pathologic protein in neurons and glia, without the presence of AMYLOID, is the major feature of these conditions, thus making these proteinopathies distinct from most other neurogenerative disorders in which protein misfolding leads to brain amyloidosis. Both frontotemporal lobar degeneration and AMYOTROPHIC LATERAL SCLEROSIS exhibit this common method of pathogenesis and thus they may represent two extremes of a continuous clinicopathological spectrum of one disease.

Research

Studies (2)

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

Authors

AuthorsStudies
An, S1
Zhang, X1
Shi, Y1
Zhang, J1
Wan, Y1
Wang, Y1
Zhang, Y1
Liu, Q1
Dammer, EB1
Fallini, C1
Gozal, YM1
Duong, DM1
Rossoll, W1
Xu, P1
Lah, JJ1
Levey, AI1
Peng, J1
Bassell, GJ1
Seyfried, NT1

Other Studies

2 other studies available for glycine and TDP-43 Proteinopathies

ArticleYear
High glycine content in TDP-43: a potential culprit in limbic-predominant age-related TDP-43 encephalopathy.
    The Journal of international medical research, 2020, Volume: 48, Issue:6

    Topics: Age Factors; Aged, 80 and over; Amino Acid Sequence; Brain; DNA-Binding Proteins; Glycine; Humans; P

2020
Coaggregation of RNA-binding proteins in a model of TDP-43 proteinopathy with selective RGG motif methylation and a role for RRM1 ubiquitination.
    PloS one, 2012, Volume: 7, Issue:6

    Topics: Amino Acid Motifs; Animals; Arginine; Blotting, Western; Cell Nucleus; Cytoplasm; DNA-Binding Protei

2012