What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Molecular biology, Biochemistry, Adapter molecule crk, Cell biology and Phosphorylation.
His Molecular biology study integrates concerns from other disciplines, such as Complementary DNA, Murine leukemia virus, Signal transduction and Virology.
His Adapter molecule crk research integrates issues from SH3 domain, SH2 domain and Guanine nucleotide exchange factor.
His Cell biology study combines topics from a wide range of disciplines, such as Apoptosis and Cellular differentiation.
His Phosphorylation study frequently links to adjacent areas such as Kinase.
His research in the fields of Mitogen-activated protein kinase kinase overlaps with other disciplines such as Bcl-2-associated X protein.
His most cited work include:
- Human adult T-cell leukemia virus: complete nucleotide sequence of the provirus genome integrated in leukemia cell DNA. (1266 citations)
- JNK promotes Bax translocation to mitochondria through phosphorylation of 14‐3‐3 proteins (460 citations)
- C3G, a guanine nucleotide-releasing protein expressed ubiquitously, binds to the Src homology 3 domains of CRK and GRB2/ASH proteins. (346 citations)
What are the main themes of his work throughout his whole career to date?
Seisuke Hattori focuses on Cell biology, Molecular biology, Phosphorylation, Signal transduction and Biochemistry.
Many of his studies on Cell biology involve topics that are commonly interrelated, such as Ectodomain.
Seisuke Hattori combines subjects such as GTPase-activating protein, Virology, Mutant, Gene and Gene product with his study of Molecular biology.
His work on Phosphoproteomics as part of his general Phosphorylation study is frequently connected to Nephrin, thereby bridging the divide between different branches of science.
His studies deal with areas such as Epidermal growth factor, Kidney and Cell adhesion as well as Signal transduction.
Seisuke Hattori interconnects Guanine nucleotide exchange factor and Adapter molecule crk in the investigation of issues within SH2 domain.
He most often published in these fields:
- Cell biology (53.45%)
- Molecular biology (32.76%)
- Phosphorylation (27.59%)
What were the highlights of his more recent work (between 2015-2021)?
- Cell biology (53.45%)
- Cancer research (8.62%)
- Glycosylation (2.59%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Cell biology, Cancer research, Glycosylation, Alternative splicing and HEK 293 cells.
His work in Focal adhesion and Signal transduction is related to Cell biology.
His research integrates issues of Cancer and Colorectal cancer in his study of Signal transduction.
His HEK 293 cells study combines topics in areas such as Cell, Tyrosine, FYN, GTPase-activating protein and Molecular biology.
His Molecular biology research is multidisciplinary, incorporating perspectives in Mutation, Mutant and Zebrafish.
The Cell migration study combines topics in areas such as PI3K/AKT/mTOR pathway, Filamin, Phosphorylation and mTORC2.
Between 2015 and 2021, his most popular works were:
- STED super-resolution imaging of mitochondria labeled with TMRM in living cells. (23 citations)
- CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability. (20 citations)
- Mammalian target of rapamycin (mTOR) complex 2 regulates filamin A-dependent focal adhesion dynamics and cell migration (17 citations)
In his most recent research, the most cited papers focused on:
Seisuke Hattori spends much of his time researching Cell biology, HEK 293 cells, Phenotype, Signal transduction and Molecular biology.
In his works, Seisuke Hattori performs multidisciplinary study on Cell biology and Fluorescence.
His HEK 293 cells research incorporates elements of Translation, Ribosome biogenesis and Ribosomal RNA.
The concepts of his Phenotype study are interwoven with issues in Exon skipping, Protein function, FLNA and Mutation.
As part of his studies on Signal transduction, Seisuke Hattori often connects relevant subjects like Phosphorylation.
His Molecular biology research is multidisciplinary, incorporating elements of Mutation, Mutant and Gene knockdown.
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