Casa
rubinstein taybi omim

Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

Por um escritor misterioso

Descrição
Frontiers 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
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome, Orphanet Journal of Rare Diseases
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome in diverse populations - Dowsett - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
de por adulto (o preço varia de acordo com o tamanho do grupo)