Takashi Muramatsu spends much of his time researching Midkine, Molecular biology, Cell biology, Biochemistry and Growth factor. His work deals with themes such as Cancer research, Pleiotrophin, Immunology and Pathology, which intersect with Midkine. Takashi Muramatsu focuses mostly in the field of Pathology, narrowing it down to matters related to Gene expression and, in some cases, Epithelioma.
His Molecular biology research incorporates themes from Cellular differentiation, Transfection, Complementary DNA, High endothelial venules and Retinoic acid. His Cell biology study combines topics from a wide range of disciplines, such as Syndecan 1, Fetus, Basigin and Central nervous system. His research in Growth factor intersects with topics in Endocrinology, Neurotrophin, Astrocyte, Fibroblast growth factor and Wilms' tumor.
His primary areas of study are Midkine, Molecular biology, Biochemistry, Internal medicine and Cell biology. His studies in Midkine integrate themes in fields like Cancer research, Pleiotrophin, Immunology and Pathology. His Cancer research research is multidisciplinary, relying on both Cancer and Gene expression.
In his study, Teratocarcinoma is inextricably linked to Antigen, which falls within the broad field of Molecular biology. Takashi Muramatsu has researched Internal medicine in several fields, including Endocrinology and Cardiology. Takashi Muramatsu interconnects Neurite, Embryonic stem cell, Basigin and Receptor in the investigation of issues within Cell biology.
Takashi Muramatsu focuses on Internal medicine, Midkine, Cardiology, Endocrinology and Growth factor. His Midkine study incorporates themes from Cancer research, Pleiotrophin, Immunology, Cytokine and Pathology. He usually deals with Cancer research and limits it to topics linked to Cancer and Small interfering RNA.
His work carried out in the field of Pleiotrophin brings together such families of science as Basic fibroblast growth factor, Knockout mouse, Embryonic stem cell and Cell biology. His Growth factor research incorporates elements of Carcinoma, Tumor marker and In vivo. His work in Proteoglycan covers topics such as Molecular biology which are related to areas like Antibody.
Midkine, Internal medicine, Endocrinology, Pleiotrophin and Immunology are his primary areas of study. Midkine is a primary field of his research addressed under Growth factor. As a part of the same scientific study, Takashi Muramatsu usually deals with the Endocrinology, concentrating on Angiogenesis and frequently concerns with Umbilical vein, Hypoxia and Immunoelectron microscopy.
The concepts of his Pleiotrophin study are interwoven with issues in Basic fibroblast growth factor, Continuous ambulatory peritoneal dialysis, Peritoneum and Connective tissue. While the research belongs to areas of Basic fibroblast growth factor, Takashi Muramatsu spends his time largely on the problem of Cancer cell, intersecting his research to questions surrounding Molecular biology. His work in the fields of Proinflammatory cytokine overlaps with other areas such as Population.
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cDNA cloning and sequencing of a new gene intensely expressed in early differentiation stages of embryonal carcinoma cells and in mid-gestation period of mouse embryogenesis.
Kenji Kadomatsu;Mineko Tomomura;Takashi Muramatsu.
Biochemical and Biophysical Research Communications (1988)
A Small Interfering RNA Targeting Vascular Endothelial Growth Factor as Cancer Therapeutics
Yoshifumi Takei;Kenji Kadomatsu;Yukio Yuzawa;Seiichi Matsuo.
Cancer Research (2004)
Midkine and Pleiotrophin: Two Related Proteins Involved in Development, Survival, Inflammation and Tumorigenesis
Journal of Biochemistry (2002)
Midkine and pleiotrophin in neural development and cancer
Kenji Kadomatsu;Takashi Muramatsu.
Cancer Letters (2004)
A Receptor-like Protein-tyrosine Phosphatase PTPζ/RPTPβ Binds a Heparin-binding Growth Factor Midkine INVOLVEMENT OF ARGININE 78 OF MIDKINE IN THE HIGH AFFINITY BINDING TO PTPζ
Nobuaki Maeda;Keiko Ichihara-Tanaka;Terutoshi Kimura;Kenji Kadomatsu.
Journal of Biological Chemistry (1999)
Expression of the heparin-binding cytokines, midkine (MK) and HB-GAM (pleiotrophin) is associated with epithelial-mesenchymal interactions during fetal development and organogenesis
T.A. Mitsiadis;M. Salmivirta;T. Muramatsu;H. Muramatsu.
A New Family of Heparin-binding Growth/Differentiation Factors: Increased Midkine Expression in Wilms' Tumor and Other Human Carcinomas
Jun-ichiro Tsutsui;Kenji Kadomatsu;Shyuichiro Matsubara;Akira Nakagawara.
Cancer Research (1993)
A retinoic acid responsive gene MK found in the teratocarcinoma system is expressed in spatially and temporally controlled manner during mouse embryogenesis.
K. Kadomatsu;Ruo-Pan Huang;T. Suganuma;F. Murata.
Journal of Cell Biology (1990)
Basigin (CD147): a multifunctional transmembrane protein involved in reproduction, neural function, inflammation and tumor invasion
T Muramatsu;T Miyauchi.
Histology and Histopathology (2003)
A Null Mutation in Basigin, an Immunoglobulin Superfamily Member, Indicates Its Important Roles in Peri-implantation Development and Spermatogenesis
Tadahiko Igakura;Kenji Kadomatsu;Tadashi Kaname;Tadashi Kaname;Hisako Muramatsu.
Developmental Biology (1998)
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