Genome occupancy of NIPBL in mouse P19 teratocarcinoma cells.. Genome occupancy of NIPBL in mouse P19 teratocarcinoma cells.
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA548964
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Mutations in NIPBL are the major cause of Cornelia de Lange Syndrome (CdLS). NIPBL is the cohesin loading factor and has recently been associated with the BET (Bromodomains and Extra Terminal (ET) domain) proteins BRD2 and BRD4. Related to this, a CdLS-like phenotype has been described associated to BRD4 mutations. We have study the genomic occupancy of NIPBL in mouse P19 teratocarcinoma cells. Overall design: Chi-seq of Nipbl and imput
创建时间：
2019-06-14
