Reducing Senescent Cell Burden in Aging and Disease is a research paper published in Trends in Molecular Medicine (2020). On theSindex it has a DataRank of 0.787. It has been cited 189 times.
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Base Score Contribution
0.787
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →NIA NIH HHS
Grant: P01 AG004875
NIA NIH HHS
Grant: R01 AG048792
NIA NIH HHS
Grant: R33 AG061456
NIA NIH HHS
Grant: P01 AG062413
NIA NIH HHS
Grant: R37 AG013925
National Institutes of Health
Grant: 5P01AG004875-34
Physiology of Bone Metabolism in an Aging Population
National Institutes of Health
Grant: 3P01AG062413-02S1
Targeting Cellular Senescence to Extend Healthspan
National Institutes of Health
Grant: 5R01AG048792-03
Estrogen receptor regulation of bone metabolism in adult mice
National Institutes of Health
FWCI
14.62
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file of Mild exacerbation of obesity- and age-dependent liver disease progression by senolytic cocktail dasatinib + quercetin
Additional file of Mild exacerbation of obesity- and age-dependent liver disease progression by senolytic cocktail dasatinib + quercetin
Additional file 4 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 4 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 5 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 5 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 2 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 3 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 3 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 2 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 1 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
Additional file 1 of Identification of potential cell death-related biomarkers for diagnosis and treatment of osteoporosis
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 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