REVIEW
Published on 30 Mar 2022
Alzheimer’s Disease: An Update and Insights Into Pathophysiology
doi 10.3389/fnagi.2022.742408
- 41,654 views
- 142 citations
- Frontiers in Aging Neuroscience
- Alzheimer's Disease and Related Dementias
- Research Topics
- Genes and Aging: From Bench Side to Bed side
Genes and Aging: From Bench Side to Bed side
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Articles
EDITORIAL
Published on 30 Mar 2022
Editorial: Genes and Aging: From Bench-to-Bedside
doi 10.3389/fnagi.2022.886967
- 1,496 views
- 1 citation
ORIGINAL RESEARCH
Published on 25 Feb 2022
Associations of Alcohol Dehydrogenase and Aldehyde Dehydrogenase Polymorphism With Cognitive Impairment Among the Oldest-Old in China
doi 10.3389/fnagi.2021.710966
- 5,874 views
- 7 citations
ORIGINAL RESEARCH
Published on 21 Dec 2021
Does Chronic Sleep Fragmentation Lead to Alzheimer's Disease in Young Wild-Type Mice?
doi 10.3389/fnagi.2021.759983
- 7,032 views
- 15 citations
SYSTEMATIC REVIEW
Published on 25 Nov 2021
Molecular Insight Into the Therapeutic Potential of Long Non-coding RNA-Associated Competing Endogenous RNA Axes in Alzheimer’s Disease: A Systematic Scoping Review
doi 10.3389/fnagi.2021.742242
- 3,604 views
- 19 citations
REVIEW
Published on 25 Nov 2021
Replenishing the Aged Brains: Targeting Oligodendrocytes and Myelination?
doi 10.3389/fnagi.2021.760200
- 4,945 views
- 19 citations
ORIGINAL RESEARCH
Published on 14 Oct 2021
Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing
doi 10.3389/fnagi.2021.745407
- 3,540 views
- 3 citations
REVIEW
Published on 12 Oct 2021
MicroRNAs as Potential Orchestrators of Alzheimer's Disease-Related Pathologies: Insights on Current Status and Future Possibilities
doi 10.3389/fnagi.2021.743573
- 6,930 views
- 39 citations
ORIGINAL RESEARCH
Published on 08 Jul 2021
The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han Patients
doi 10.3389/fnagi.2021.699836
- 3,649 views
- 18 citations
CASE REPORT
Published on 29 Jun 2021
Case Report: A Homozygous Mutation (p.Y62X) of Phospholipase D3 May Lead to a New Leukoencephalopathy Syndrome
doi 10.3389/fnagi.2021.671296
- 2,321 views
- 4 citations
