Toshitsugu Fujita

Identification of a tissue-non-specific homologue of axonal fasciculation and elongation protein zeta-1.

Identification of FEZ1 as a protein that interacts with JC virus agnoprotein and microtubules: role of agnoprotein-induced dissociation of FEZ1 from microtubules in viral propagation.

The rate of c-fos transcription in vivo is continuously regulated at the level of elongation by dynamic stimulus-coupled recruitment of positive transcription elongation factor b.

Fasciculation and elongation protein zeta-1 (FEZ1) participates in the polarization of hippocampal neuron by controlling the mitochondrial motility.

Gene-specific recruitment of positive and negative elongation factors during stimulated transcription of the MKP-1 gene in neuroendocrine cells.

Axonal guidance protein FEZ1 associates with tubulin and kinesin motor protein to transport mitochondria in neurites of NGF-stimulated PC12 cells.

Up-regulation of P-TEFb by the MEK1-extracellular signal-regulated kinase signaling pathway contributes to stimulated transcription elongation of immediate early genes in neuroendocrine cells.

Negative elongation factor NELF controls transcription of immediate early genes in a stimulus-specific manner.

A functional NF-kappaB enhancer element in the first intron contributes to the control of c-fos transcription.

The transcription elongation factors NELF, DSIF and P-TEFb control constitutive transcription in a gene-specific manner.

Transcription elongation factors are involved in programming hormone production in pituitary neuroendocrine GH4C1 cells.

Splice variants of enigma homolog, differentially expressed during heart development, promote or prevent hypertrophy.

Promoter-proximal pausing of RNA polymerase II: an opportunity to regulate gene transcription.

Functions of fasciculation and elongation protein zeta-1 (FEZ1) in the brain.

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

Direct identification of insulator components by insertional chromatin immunoprecipitation.

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

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.