Regional chromatin decompaction in cornelia de lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF

Human Molecular Genetics

Volumn 22, Issue 20, 2013, Pages 4180-4193

  Nolen, Leisha D ^a   Boyle, Shelagh ^a   Ansari, Morad ^a   Pritchard, Emily ^a   Bickmore, Wendy A ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COHESIN; PROTEIN; PROTEIN NIPBL; SMALL INTERFERING RNA; TRANSCRIPTION FACTOR CTCF; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CHROMATIN; CHROMATIN STRUCTURE; CHROMOSOME; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CPG ISLAND; DE LANGE SYNDROME; DNA DAMAGE; EXON; FLUORESCENCE ACTIVATED CELL SORTING; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE MUTATION; HISTONE MODIFICATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; NUCLEAR SIZE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN INTERACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; START CODON; TRANSCRIPTION INITIATION SITE; WESTERN BLOTTING;

CELL CYCLE PROTEINS; CELL LINE; CELL NUCLEUS; CHONDROITIN SULFATE PROTEOGLYCANS; CHROMATIN; CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOMES, HUMAN; DE LANGE SYNDROME; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE KNOCKDOWN TECHNIQUES; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MUTATION; PHENOTYPE; PROTEINS; REPRESSOR PROTEINS;

EID: 84884730929     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt265     Document Type: Article

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