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significance
5 studies tagged significance, dated 1995-03-01 to 2022-06-03. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Expression relationship and significance of NEAT1 and miR-27a-3p in serum and cerebrospinal fluid of patients with Alzheimer's disease 2022-06-03
- Alzheimer's Disease Variants with the Genome-Wide Significance are Significantly Enriched in Immune Pathways and Active in Immune Cells 2016-01-09
- Cerebral Microbleeds, CSF p-Tau, and Cognitive Decline: Significance of Anatomic Distribution 2015-07-30
Studies
5 studies carry this tag.
Date range
1995 to 2022
Top journals
- AJNR. American journal of neuroradiology 1
- BMC neurology 1
- Journal of neuropathology and experimental neurology 1
- Molecular neurobiology 1
- Neuroscience letters 1
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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The MMSE score, MoCA score, serum miR-27a-3p level, cerebrospinal fluid miR-27a-3p, Aβ42 levels and Aβ42/Aβ40 ratio of AD patients in mild group and moderate-to-severe group were all lower than those in the control group, and the moderate-to-severe group were lower than the mild group (all P < 0.05);the serum NEAT1 level, SUVR, and cerebrospinal fluid NEAT1 and BACE1 levels were higher than those in the control group, and the moderate-to-severe group were higher than the mild group (all P < 0.05).
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The existing large-scale genome-wide association studies (GWAS) datasets provide strong support for investigating the mechanisms of Alzheimer's disease (AD) by applying multiple methods of pathway analysis.
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60/100
The distribution of microbleeds revealed different associations with amyloid-β and phosphorylated tau 181 protein levels and cognition.
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DJ-1 and alpha-synuclein are leading biomarkers for Parkinson's disease diagnosis and/or monitoring disease progression.
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The histologically apparent polymorphism of plaques containing beta-amyloid in Alzheimer's disease is thought to represent different stages in plaque evolution. beta-amyloid-immunopositive plaques were classified according to the pattern of beta-amyloid distribution (diffuse vs dense-core) and the presence or absence of dystrophic beta-amyloid precursor protein-immunopositive (beta-APP+) neurites (neuritic vs non-neuritic).