Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
BET Proteins in Chromatin Architecture, Transcription and Disease
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Cornelia de Lange syndrome mutations in NIPBL can impair cohesin-mediated DNA loop extrusion
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms - Kaur - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
The Drosophila melanogaster model for Cornelia de Lange syndrome: Implications for etiology and therapeutics - Dorsett - 2016 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
Generation of corrected hiPSC clones from a Cornelia de Lange Syndrome (CdLS) patient through CRISPR-Cas-based technology, Stem Cell Research & Therapy
Ptn antagonizes Brd2 during neuronal differentiation in the developing
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