Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P16104 (
H2AX
)
3,930
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Functional impairment of DNA damage response pathways leads to increased genomic instability. Here we describe the centrosomal protein
CEP152
as a new regulator of genomic integrity and cellular response to DNA damage. Using homozygosity mapping and exome sequencing, we identified
CEP152
mutations in Seckel syndrome and showed that impaired
CEP152
function leads to accumulation of genomic defects resulting from replicative stress through enhanced activation of ATM signaling and increased
H2AX
phosphorylation.
...
PMID:CEP152 is a genome maintenance protein disrupted in Seckel syndrome. 2139 65