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Genome-Wide Association Study
DNA methylome in human CD4+ T cells identifies transcriptionally repressive and non-repressive methylation peaks.
Genome-wide DNA methylation study suggests epigenetic accessibility and transcriptional poising of interferon-regulated genes in naïve CD4+ T cells from lupus patients.
DNA replication timing during development anticipates transcriptional programs and parallels enhancer activation.
CAGm: a repository of germline microsatellite variations in the 1000 genomes project.
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.
Cross-hybridization on PCR-spotted microarrays.
Identification and characterization of zebrafish ocular formation genes.
High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry.
GenomeRunner: automating genome exploration.
Epigenomic elements enriched in the promoters of autoimmunity susceptibility genes.
Systematic classification of non-coding RNAs by epigenomic similarity.
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study.
Hypomethylation coordinates antagonistically with hypermethylation in cancer development: a case study of leukemia.
Genome-wide DNA methylation patterns in CD4+ T cells from patients with systemic lupus erythematosus.
Oklahoma Nathan Shock Center of Excellence in Basic Biology of Aging