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Publications by Rebecca A. Henseler
Diverse Chemicals Including Aryl Hydrocarbon Receptor Ligands Modulate Transcriptional Activity of the 3′immunoglobulin Heavy Chain Regulatory Region
Toxicology
Toxicology
Related publications
Dynamic Changes in Binding of Immunoglobulin Heavy Chain 3′ Regulatory Region to Protein Factors During Class Switching
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Role of Mediator in Transcriptional Activation by the Aryl Hydrocarbon Receptor
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Pax5 and Linker Histone H1 Coordinate DNA Methylation and Histone Modifications in the 3' Regulatory Region of the Immunoglobulin Heavy Chain Locus
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Gene Co-Regulation and Co-Expression in the Aryl Hydrocarbon Receptor-Mediated Transcriptional Regulatory Network in the Mouse Liver
Archives of Toxicology
Mutagenesis
Toxicology
Health
Medicine
In a Model of Immunoglobulin Heavy-Chain (IGH)/MYC Translocation, theIgh 3′ Regulatory Region inducesMYC Expression at the Immature Stage of B Cell Development
Genes Chromosomes and Cancer
Cancer Research
Genetics
Induction of Colonic Regulatory T Cells by Mesalamine by Activating the Aryl Hydrocarbon Receptor
Cellular and Molecular Gastroenterology and Hepatology
Hepatology
Gastroenterology
Homologous Elements Hs3a and Hs3b in the 3′ Regulatory Region of the Murine Immunoglobulin Heavy Chain (Igh) Locus Are Both Dispensable for Class-Switch Recombination.
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Aryl Hydrocarbon Receptor Repressor Methylation
Circulation: Cardiovascular Genetics
Does the Aryl Hydrocarbon Receptor Regulate Pluripotency?
Current Opinion in Toxicology
Toxicology