FANCD2 limits acetaldehyde‐induced genomic instability during DNA replication in esophageal keratinocytes is a research paper published in Molecular Oncology (2021). On theSindex it has a DataRank of 0. It has been cited 22 times.
Scored on demand from live citation data
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph — 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 — never from an abstract alone.
W. W. Smith Charitable Trust
Grant: C1706
NCI NIH HHS
Grant: P01 CA098101
NCI NIH HHS
Grant: P30 CA013696
National Cancer Institute
Grant: P30‐CA013696
NIAAA NIH HHS
Grant: R01 AA026297
National Institute on Alcohol Abuse and Alcoholism
Grant: R01‐AA026297
W. W. Smith Charitable Trust
Grant: C2007
NIEHS NIH HHS
Grant: 27307C2007
NIAAA NIH HHS
Grant: F31 AA027133
National Institute on Alcohol Abuse and Alcoholism
Grant: F31‐AA027133
National Institutes of Health
Grant: 3P30CA013696-21S1
CANCER CENTER CORE SUPPORT GRANT
National Institutes of Health
Grant: 2R01AA026297-07A1
Aldh2 and epithelial homeostasis and pathobiology
National Institutes of Health
Grant: 5F31AA027133-02
Roles of the Fanconi Anemia DNA Repair Pathway in Managing Acetaldehyde-induced Replicative Damage and Fork Stability in Esophageal Keratinocytes
College of Medicine, Drexel University
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 2 of Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report
Additional file 2 of Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report
Additional file 1 of Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report
Additional file 1 of Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report