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Genes involved in distinct diabetes types suggest shared disease mechanisms. We show that rare ONECUT1 coding variants cause monogenic recessive diabetes (neonatal or very early-onset, syndromic) in two unrelated patients, and monogenic dominant diabetes (early adult-onset) in heterozygous relatives...
ORGANISM(S): Homo sapiens (Human) 
2021-11-03 | PXD018887 | Pride
Mapping ONECUT1 TF binding with ChIP-exo
The aim of this project is to locate the precise binding of the ONECUT1 transcription factor. NOTE: This study was updated on 7th May 2014. All samples, experiments, runs and files were replaced. This was due to an incorrect reagent being used in the earlier version.
ORGANISM(S): Mus musculus 
A ONECUT1 regulatory, non-coding region in pancreatic development and diabetes [RNA-seq]
A ONECUT1 regulatory, non-coding region in pancreatic development and diabetes [Nanopore-seq]
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