Hiroshi Kawamoto mostly deals with Immunology, Cell biology, Progenitor cell, Population and T cell. His study in Immunology is interdisciplinary in nature, drawing from both CD34, Haematopoiesis, Stromal cell and Green fluorescent protein. His Cell biology research incorporates themes from Cellular differentiation, Interleukin-7 receptor, Lymphocyte, Cytotoxic T cell and Cell type.
His study looks at the intersection of Cellular differentiation and topics like Transcription factor with Promoter and Regulation of gene expression. His Progenitor cell research integrates issues from Endothelial stem cell, Embryonic stem cell and B cell. Hiroshi Kawamoto works mostly in the field of T cell, limiting it down to topics relating to Molecular biology and, in certain cases, T-cell receptor.
Hiroshi Kawamoto focuses on Cell biology, Immunology, Progenitor cell, T cell and Molecular biology. His Cell biology study combines topics from a wide range of disciplines, such as Cellular differentiation, Enhancer, Transcription factor, Cell fate determination and Regulation of gene expression. Hiroshi Kawamoto performs multidisciplinary study in Immunology and Population in his work.
He has included themes like Lineage, Haematopoiesis and B cell in his Progenitor cell study. In his study, which falls under the umbrella issue of T cell, T-cell receptor, Cancer research and Antigen is strongly linked to Cytotoxic T cell. Hiroshi Kawamoto interconnects Cell, Gene rearrangement, Gene and Transplantation in the investigation of issues within Molecular biology.
The scientist’s investigation covers issues in Cancer research, Cell biology, T-cell receptor, Induced pluripotent stem cell and Cytotoxic T cell. His studies in Cancer research integrate themes in fields like Antibody, Gene, Major histocompatibility complex and Untranslated region. Hiroshi Kawamoto specializes in Cell biology, namely Progenitor cell.
His research integrates issues of Molecular biology, Human leukocyte antigen and Regeneration in his study of Induced pluripotent stem cell. His work deals with themes such as T cell, Leukemia, Cell culture and Antigen, which intersect with Cytotoxic T cell. His Transcription factor research is multidisciplinary, relying on both Cellular differentiation and B cell.
Hiroshi Kawamoto spends much of his time researching Cancer research, Cell biology, Molecular biology, Cellular differentiation and Progenitor cell. His Cancer research research is multidisciplinary, incorporating perspectives in Protein kinase B, Thymocyte, CD8, Cytotoxic T cell and Antibody. His studies deal with areas such as Endothelial stem cell, Adult stem cell and Enhancer, Transcription factor, Cell fate determination as well as Cell biology.
His work in Molecular biology addresses issues such as Induced pluripotent stem cell, which are connected to fields such as Human leukocyte antigen, CTL*, T cell and T-Cell Receptor Gene. His Progenitor cell research is within the category of Stem cell. His Innate lymphoid cell study is associated with Immunology.
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Innate production of T H 2 cytokines by adipose tissue-associated c-Kit + Sca-1 + lymphoid cells
Kazuyo Moro;Taketo Yamada;Masanobu Tanabe;Tsutomu Takeuchi.
A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Aberrant PD-L1 expression through 3′-UTR disruption in multiple cancers
Keisuke Kataoka;Yuichi Shiraishi;Yohei Takeda;Seiji Sakata.
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells
Erik Arner;Carsten O. Daub;Kristoffer Vitting-Seerup;Robin Andersson.
In Vitro Generation of Lymphohematopoietic Cells from Endothelial Cells Purified from Murine Embryos
Shin-Ichi Nishikawa;Satomi Nishikawa;Hiroshi Kawamoto;Hisahiro Yoshida.
Adult T-cell progenitors retain myeloid potential
Haruka Wada;Kyoko Masuda;Rumi Satoh;Kiyokazu Kakugawa.
An Essential Developmental Checkpoint for Production of the T Cell Lineage
Tomokatsu Ikawa;Satoshi Hirose;Kyoko Masuda;Kiyokazu Kakugawa.
Analyses of peripheral blood mononuclear cells in operational tolerance after pediatric living donor liver transplantation.
Ying Li;Takaaki Koshiba;Atsushi Yoshizawa;Yukihide Yonekawa.
American Journal of Transplantation (2004)
A cell-autonomous requirement for CXCR4 in long-term lymphoid and myeloid reconstitution
Kenji Kawabata;Miho Ujikawa;Takeshi Egawa;Hiroshi Kawamoto.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Development and Function of Invariant Natural Killer T Cells Producing TH2- and TH17-Cytokines
Hiroshi Watarai;Etsuko Sekine-Kondo;Tomokuni Shigeura;Yasutaka Motomura.
PLOS Biology (2012)
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