Microdeletions and mutations of CREBBP (CBP) gene can cause
Por um escritor misterioso
Descrição
Genes, Free Full-Text
Rubinstein Syndrome - an overview
The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migration, Acta Neuropathologica Communications
A) Location of the exon CREBBP mutations found in this study. Only
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4
Differences in Specificity and Selectivity Between CBP and p300 Acetylation of Histone H3 and H3/H4
Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients - Spena - 2015 - Clinical Genetics - Wiley Online Library
Frontiers Impaired Regulation of Histone Methylation and Acetylation Underlies Specific Neurodevelopmental Disorders
New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
de
por adulto (o preço varia de acordo com o tamanho do grupo)
