Molecular biology, Aryl hydrocarbon receptor nuclear translocator, Transcription factor, Reporter gene and Complementary DNA are his primary areas of study. Masatsugu Ema conducted interdisciplinary study in his works that combined Molecular biology and Kinase insert domain receptor. His Aryl hydrocarbon receptor nuclear translocator research incorporates themes from Basic helix-loop-helix and Gene expression.
His work in the fields of Transcription factor, such as Aryl hydrocarbon receptor repressor, overlaps with other areas such as G alpha subunit. His research investigates the connection between Reporter gene and topics such as Messenger RNA that intersect with problems in Open reading frame, Retinoic acid, Transcription, P19 cell and HEK 293 cells. The study incorporates disciplines such as Amino acid and SIM2 in addition to Complementary DNA.
Masatsugu Ema mainly focuses on Cell biology, Embryonic stem cell, Molecular biology, Angiogenesis and Transgene. His Cell biology study integrates concerns from other disciplines, such as Transcription factor, Gene expression and Cellular differentiation. His work carried out in the field of Embryonic stem cell brings together such families of science as Cancer research and Embryogenesis.
His Molecular biology research integrates issues from Complementary DNA, cDNA library, Gene, Reporter gene and Aryl hydrocarbon receptor nuclear translocator. As part of one scientific family, Masatsugu Ema deals mainly with the area of Gene, narrowing it down to issues related to the Embryo, and often Phenotype. His work deals with themes such as Primitive streak and Mesoderm, which intersect with Vasculogenesis.
Masatsugu Ema mainly investigates Cell biology, Embryonic stem cell, Cellular differentiation, Angiogenesis and Transgene. His Cell biology research includes themes of Syncytium, Gene expression and Induced pluripotent stem cell. His Gene expression research focuses on Locus and how it connects with Lethality, P53 pathway, Embryo and Phenotype.
His Embryonic stem cell study often links to related topics such as Embryogenesis. His studies deal with areas such as MAPK/ERK pathway and Green fluorescent protein as well as Cellular differentiation. The Angiogenesis study combines topics in areas such as Neurogenesis, Lymphatic Endothelium, Neocortex and Progenitor cell.
His primary areas of study are Cell biology, Cellular differentiation, Transgene, Angiogenesis and Embryonic stem cell. His work on Inner cell mass as part of his general Cell biology study is frequently connected to Mechanism, thereby bridging the divide between different branches of science. His Cellular differentiation research is multidisciplinary, incorporating elements of Hedgehog signaling pathway, Homeobox protein NANOG, Blastocyst, Epiblast and MAPK/ERK pathway.
His Angiogenesis study incorporates themes from Neocortex, Neural development and Progenitor cell, Progenitor. His Embryonic stem cell study combines topics from a wide range of disciplines, such as Enhancer, Promoter, Ubiquitin C and Green fluorescent protein. The various areas that he examines in his Lymphatic Endothelium study include Niche, Regeneration and Fibroblast growth factor.
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A novel bHLH-PAS factor with close sequence similarity to hypoxia-inducible factor 1α regulates the VEGF expression and is potentially involved in lung and vascular development
Masatsugu Ema;Shinichiro Taya;Noboru Yokotani;Kazuhiro Sogawa.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Loss of teratogenic response to 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) in mice lacking the Ah (dioxin) receptor
Junsei Mimura;Keisuke Yamashita;Kenji Nakamura;Masanobu Morita.
Genes to Cells (2003)
Molecular mechanisms of transcription activation by HLF and HIF1α in response to hypoxia: their stabilization and redox signal-induced interaction with CBP/p300
Masatsugu Ema;Kiichi Hirota;Junsei Mimura;Hisaku Abe.
The EMBO Journal (1999)
Identification of a novel mechanism of regulation of Ah (dioxin) receptor function
Junsei Mimura;Masatsugu Ema;Kazuhiro Sogawa;Yoshiaki Fujii-Kuriyama.
Genes & Development (1999)
cDNA cloning and structure of mouse putative Ah receptor
M. Ema;K. Sogawa;N. Watanabe;Y. Chujoh.
Biochemical and Biophysical Research Communications (1992)
Dioxin binding activities of polymorphic forms of mouse and human arylhydrocarbon receptors.
Masatsugu Ema;Norihisa Ohe;Michiko Suzuki;Junsei Mimura.
Journal of Biological Chemistry (1994)
cDNA cloning and tissue-specific expression of a novel basic helix-loop-helix/PAS factor (Arnt2) with close sequence similarity to the aryl hydrocarbon receptor nuclear translocator (Arnt).
Ken Hirose;Masanobu Morita;Masatsugu Ema;Junsei Mimura.
Molecular and Cellular Biology (1996)
Subventricular Zone-Derived Neural Progenitor Cells Migrate Along a Blood Vessel Scaffold Toward the Post-stroke Striatum
Takuro Kojima;Takuro Kojima;Yuki Hirota;Masatsugu Ema;Satoru Takahashi.
Stem Cells (2010)
Combinatorial effects of Flk1 and Tal1 on vascular and hematopoietic development in the mouse.
Masatsugu Ema;Patrick Faloon;Wen Jie Zhang;Masanori Hirashima.
Genes & Development (2003)
Deletion of the selection cassette, but not cis-acting elements, in targeted Flk1-lacZ allele reveals Flk1 expression in multipotent mesodermal progenitors.
Masatsugu Ema;Masatsugu Ema;Masatsugu Ema;Satoru Takahashi;Satoru Takahashi;Satoru Takahashi;Janet Rossant;Janet Rossant;Janet Rossant.
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