Skip to main navigation
Skip to search
Skip to main content
Penn State Home
Help & FAQ
Link opens in a new tab
Search content at Penn State
Home
Researchers
Research output
Research units
Equipment
Grants & Projects
Prizes
Activities
HUS1 regulates in vivo responses to genotoxic chemotherapies
G. Balmus
, P. X. Lim
, A. Oswald
, K. R. Hume
, A. Cassano
, J. Pierre
, A. Hill
, W. Huang
, A. August
, T. Stokol
, T. Southard
, R. S. Weiss
Veterinary and Biomedical Sciences
Research output
:
Contribution to journal
›
Article
›
peer-review
10
Link opens in a new tab
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'HUS1 regulates in vivo responses to genotoxic chemotherapies'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Hus1
100%
In Vivo Response
100%
Mitomycin C
70%
DNA Damage Response
40%
DNA Double-strand Breaks
30%
Replication Stress
30%
Mutant Mice
20%
Double mutant
20%
ATM Pathway
20%
Phosphorylation
10%
Interdependency
10%
Cell Proliferation
10%
Inducer
10%
Cell Apoptosis
10%
Genomic Instability
10%
Ionizing Radiation
10%
Signaling Factors
10%
DNA Replication
10%
Hypomorphic mutation
10%
Embryonic Lethality
10%
Type-specific
10%
Adult Mice
10%
Crosslinking Agent
10%
Genome Integrity
10%
Specific Action
10%
Response Mechanism
10%
Hydroxyurea
10%
Rad1
10%
Severe Damage
10%
Tissue Morphology
10%
Checkpoint Kinase 1 (CHK1)
10%
Response Network
10%
Genotoxin
10%
Replication Inhibitor
10%
ATM Kinase
10%
ATR Kinase
10%
Type Control
10%
Immunology and Microbiology
DNA Damage Response
100%
Replication
100%
Hypersensitivity
75%
Double-Strand DNA Break
75%
Mouse Mutant
50%
Wild Type
25%
Cross Linking
25%
Allele
25%
Cell Proliferation
25%
Genomic Instability
25%
Low Drug Dose
25%
Programmed Cell Death
25%
Phosphotransferase
25%
phosphorylation
25%
Kinase
25%
Biochemistry, Genetics and Molecular Biology
DNA Damage Response
100%
Erethism
75%
Double-Strand DNA Break
75%
Mouse Mutant
50%
Allele
25%
Kinase
25%
Phosphotransferase
25%
Wild Type
25%
Cell Proliferation
25%
Cross-Link
25%
Genome Instability
25%
Low Drug Dose
25%
Hydroxycarbamide
25%
Genomics
25%
Programmed Cell Death
25%
phosphorylation
25%