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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