Hodaka Fujii

Enforced expression of the Ikaros isoform IK5 decreases the numbers of extrathymic intraepithelial lymphocytes and natural killer 1.1+ T cells.

Inducible translocation trap: a system for detecting inducible nuclear translocation.

Regulation of Stat1 protein expression by phenylalanine 172 in the coiled-coil domain.

Cell type-specific roles of Jak3 in IL-2-induced proliferative signal transduction.

Redundant promoter elements mediate IL-3-induced expression of a novel cytokine-inducible gene, cyclon.

Regulation of cell proliferation by interleukin-3-induced nuclear translocation of pyruvate kinase.

Temporal regulation of Stat5 activity in determination of cell differentiation program.

Nuclear translocation of 2-amino-3-ketobutyrate coenzyme A ligase by cold and osmotic stress.

Plasmodium circumsporozoite protein promotes the development of the liver stages of the parasite.

Cytokine-induced nuclear translocation of signaling proteins and their analysis using the inducible translocation trap system.

Receptor expression is essential for proliferation induced by dimerized Jak kinases.

Identification of a regulatory T cell specific cell surface molecule that mediates suppressive signals and induces Foxp3 expression.

Mechanisms of Signal Transduction from Receptors of Type I and Type II Cytokines.

Lack of nuclear translocation of cytoplasmic domains of IL-2/IL-15 receptor subunits.

Regulation of Fas-mediated immune homeostasis by an activation-induced protein, Cyclon.

Expression of GARP selectively identifies activated human FOXP3+ regulatory T cells.

Novel reporter cell line to analyze cytokine-mediated expression regulation of c-myc gene.

Insertional chromatin immunoprecipitation: a method for isolating specific genomic regions.

Species-specific 5'-genomic structure and multiple transcription start sites in the chicken Pax5 gene.

Direct identification of insulator components by insertional chromatin immunoprecipitation.

Apurinic/apyrimidinic endonuclease1/redox factor-1 (Ape1/Ref-1) is essential for IL-21-induced signal transduction through ERK1/2 pathway.

Transcription start sites and usage of the first exon of mouse Foxp3 gene.

Discovery and characterization of new transcripts from RNA-seq data in mouse CD4(+) T cells.

GARP-TGF-β complexes negatively regulate regulatory T cell development and maintenance of peripheral CD4+ T cells in vivo.

Regulation of the expression of GARP/latent TGF-β1 complexes on mouse T cells and their role in regulatory T cell and Th17 differentiation.

Efficient isolation of specific genomic regions and identification of associated proteins by engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP) using CRISPR.

Identification of telomere-associated molecules by engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP).

Identification of proteins associated with an IFNγ-responsive promoter by a retroviral expression system for enChIP using CRISPR.

Oligoribonucleotide (ORN) interference-PCR (ORNi-PCR): a simple method for suppressing PCR amplification of specific DNA sequences using ORNs.

Efficient isolation of specific genomic regions retaining molecular interactions by the iChIP system using recombinant exogenous DNA-binding proteins.

A critical role of the Thy28-MYH9 axis in B cell-specific expression of the Pax5 gene in chicken B cells.

Isolation of specific genomic regions and identification of associated molecules by engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP) using CRISPR.

Identification of non-coding RNAs associated with telomeres using a combination of enChIP and RNA sequencing.

Locus-specific biochemical epigenetics/chromatin biochemistry by insertional chromatin immunoprecipitation.

Isolation of Specific Genomic Regions and Identification of Their Associated Molecules by Engineered DNA-Binding Molecule-Mediated Chromatin Immunoprecipitation (enChIP) Using the CRISPR System and TAL Proteins.

Applications of Engineered DNA-Binding Molecules Such as TAL Proteins and the CRISPR/Cas System in Biology Research.