Differential Regulation of Mouse Hippocampal Gene Expression Sex Differences by Chromosomal Content and Gonadal Sex is a research paper published in Molecular Neurobiology (2022). On theSindex it has a DataRank of 0. It has been cited 30 times.
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NIA NIH HHS
Grant: T32 AG052363
BLRD VA
Grant: I01 BX005592
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Grant: P30 AG050886
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Grant: R01 AG057434
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Grant: R56 AG067754
NEI NIH HHS
Grant: P30 EY021725
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Grant: R01 AG059430
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Grant: F31 AG064861
BLRD VA
Grant: I01 BX003906
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Grant: P30 AG050911
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Grant: R00 AG059920
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Grant: R01 AG069742
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Grant: R01 AG070035
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Grant: R21 AG058811
BLRD VA
Grant: IK6 BX006033
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Grant: K99 AG059920
National Institutes of Health
Grant: 1P30AG050911-01
Integrative Redox Biology Core
National Institutes of Health
Grant: 3P30AG050886-06S1
Comparative Bioenergetics of Aging
National Institutes of Health
Grant: 5R01AG069742-04
Cellular senescence and epigenomic remodeling in ovarian aging
National Institutes of Health
Grant: 5R21AG058811-02
A Four Core Genotype (FCG) Approach to Investigating Sex Differences in Health and Longevity
National Institutes of Health
Grant: 1K99AG059920-01A1
The metabolomic consequences of small size and long life
National Institutes of Health
Grant: 5R01AG070035-05
Role of estrogen receptor-a in aging and sex-specific responses to 17a-estradiol
National Institutes of Health
Grant: 1R56AG067754-01A1
A novel approach to understand a mechanism of proteostatic decline with aging
National Institutes of Health
Grant: 5R01AG057434-03
A sex difference approach to evaluating resilience as a predictor of healthspan in mice
National Institutes of Health
Grant: 1I01BX003906-01A2
Dynamics of the brain epigenome with aging
National Institutes of Health
Grant: 2P30EY021725-06
P30-Center Core Grant for Vision Research
National Institutes of Health
Grant: 5R01AG059430-05
Sex divergence and cell specificity of age-related hippocampal DNA modifications
National Institutes of Health
Grant: 5F31AG064861-03
Epigenetic regulation of sexually divergent neuroinflammation with brain aging and Alzheimer's disease
National Institutes of Health
Grant: 5T32AG052363-04
GEROSCIENCE TRAINING PROGRAM IN OKLAHOMA
FWCI
3.40
Citation Percentile
0.9%
Citation Trend
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Keywords
Sustainable Development Goals
Additional file 4 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 2 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 3 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 11 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 10 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 8 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 1 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 9 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 3 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 10 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 6 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 1 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 4 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 7 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 11 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 5 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 2 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 9 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 7 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease
Additional file 5 of Microglial senescence contributes to female-biased neuroinflammation in the aging mouse hippocampus: implications for Alzheimer’s disease