The effect of genetically modified platelet-derived growth factor-BB over-expressing mesenchymal stromal cells during core decompression for steroid-associated osteonecrosis of the femoral head in rabbits is a research paper published in Stem Cell Research & Therapy (2021). On theSindex it has a DataRank of 0.619. It has been cited 61 times.
Scored on demand from live citation data
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph β no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full β never from an abstract alone.
Base Score Contribution
0.619
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 βNational institute of arthritis and musculoskeletal and skin diseases
Grant: R01AR057837
National institute of arthritis and musculoskeletal and skin diseases
Grant: R01AR063717
National institute of arthritis and musculoskeletal and skin diseases
Grant: R01AR072613
National institute of arthritis and musculoskeletal and skin diseases
Grant: R01AR073145
National institute of arthritis and musculoskeletal and skin diseases
Grant: R01AR074458
National institute of arthritis and musculoskeletal and skin diseases
Grant: U01AR069395
School of medicine, Stanford University
Grant: Stanford Medical Scholars Fellowship Program
National Institutes of Health
Grant: 5R01AR063717-02
Wear Particle Disease and NF-kappa B Signaling
National Institutes of Health
Grant: 1R01AR073145-01
Customized MSCs to Enhance Healing of Bone Defects
National Institutes of Health
Grant: 5R01AR057837-04
Microengineered Osteons for Bone Tissue Engineering
National Institutes of Health
Grant: 5R01AR074458-03
Vascularization in bone tissue engineering constructs
National Institutes of Health
Grant: 5R01AR072613-03
Tissue Engineering Approaches for Improved Treatment of Early Stage Osteonecrosis of the Hip
National Institutes of Health
Grant: 1U01AR069395-01A1
Systems Modeling Guided Bone regeneration
FWCI
12.27
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 1 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 2 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 2 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 5 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 5 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 6 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 6 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 7 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 7 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 8 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 8 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 9 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 9 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 10 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 10 of Preosteoclast plays a pathogenic role in syndesmophyte formation of ankylosing spondylitis through the secreted PDGFB β GRB2/ERK/RUNX2 pathway
Additional file 3 of Inhibition of insulin degrading enzyme suppresses osteoclast hyperactivity via enhancing Nrf2-dependent antioxidant response in glucocorticoid-induced osteonecrosis of the femoral head
Additional file 3 of Inhibition of insulin degrading enzyme suppresses osteoclast hyperactivity via enhancing Nrf2-dependent antioxidant response in glucocorticoid-induced osteonecrosis of the femoral head
Additional file 6 of Inhibition of insulin degrading enzyme suppresses osteoclast hyperactivity via enhancing Nrf2-dependent antioxidant response in glucocorticoid-induced osteonecrosis of the femoral head
Additional file 2 of Inhibition of insulin degrading enzyme suppresses osteoclast hyperactivity via enhancing Nrf2-dependent antioxidant response in glucocorticoid-induced osteonecrosis of the femoral head