Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Por um escritor misterioso
Descrição
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library
Cornelia de Lange Syndrome (CdLS) is a cohesinopathy (changes in
Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library
Frontiers Cornelia de Lange Syndrome as Paradigm of Chromatinopathies
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
Ptn antagonizes Brd2 during neuronal differentiation in the developing
Rescue of Axon Pruning and Proliferation Defect by SMC1 transgene (A-B)
de
por adulto (o preço varia de acordo com o tamanho do grupo)