Skip to Main Content

Paper Details

Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the <i>RUNX3</i> Promoter.
Front Genet
5
2022
-, 13kb, 50bp DNA probe, AS, Ankylosing Spondylitis, Genetic Variants, Jurkat, NE, Promoter, RUNT-related transcription factor, RUNX3 promoter, SNPs, T cell line, U937 NE, c-MYC, c-MYC TF binding-site, c-MYC binding-site, c-MYC protein, enhancer-like region, human, inflammatory spinal arthritis, monocyte, monocyte-like U937 cells, primary human CD14 monocytes, primary human T-cells, promoter, regulatory elements, risk allele, single nucleotide polymorphisms
Author NameAffiliation
Julian C KnightUniversity of Oxford
Bryan Paul WordsworthUniversity of Oxford
Bryan Paul WordsworthNational Institute for Health Research Oxford Comprehensive Biomedical Research Centre, Botnar Research Centre
  • 1 - 3

Datasets

Release 1.2