Microdeletions and mutations of CREBBP (CBP) gene can cause
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Human CREBBP acetyltransferase is impaired by etoposide quinone, an oxidative and leukemogenic metabolite of the anticancer drug etoposide through modification of redox-sensitive zinc-finger cysteine residues - ScienceDirect
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High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
Microdeletions and mutations of CREBBP (CBP) gene can cause
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
CBP and P300 regulate distinct gene networks required for human primary myoblast differentiation and muscle integrity
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Inhibition of histone acetyltransferase function radiosensitizes CREBBP/EP300 mutants via repression of homologous recombination, potentially targeting a gain of function
CREBBP (CREB binding protein)
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