Microdeletions and mutations of CREBBP (CBP) gene can cause
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Microdeletions and mutations of CREBBP (CBP) gene can cause
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4
Roles of CREB-binding protein (CBP)/p300 in respiratory epithelium tumorigenesis
Schematic representation of mouse CBP. Amino acid residues 1 and 2441
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients
Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
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