Microdeletions and mutations of CREBBP (CBP) gene can cause

Genes, Free Full-Text

Inhibition of histone acetyltransferase function radiosensitizes CREBBP/EP300 mutants via repression of homologous recombination, potentially targeting a gain of function

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein-Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia – topic of research paper in Clinical medicine. Download scholarly article PDF

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics

Microdeletions and mutations of CREBBP (CBP) gene can cause

Schematic representation of mouse CBP. Amino acid residues 1 and 2441

Microdeletions and mutations of CREBBP (CBP) gene can cause

Genes, Free Full-Text

PHD fi nger mutations in CBP in Rubinstein – Taybi patients. ( A ) DGGE

CREBBP (CREB binding protein)

KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia

Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome

The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migration, Acta Neuropathologica Communications

Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC