Masahide Takahashi mainly focuses on Molecular biology, Cancer research, Proto-Oncogene Proteins c-ret, Cell biology and Tyrosine kinase. His Molecular biology research is multidisciplinary, incorporating elements of Mutation, Biochemistry, Gene, Complementary DNA and RET proto-oncogene. Masahide Takahashi has researched Cancer research in several fields, including Transcription factor, Kinase activity, Pheochromocytoma, Thyroid carcinoma and Multiple endocrine neoplasia.
His Proto-Oncogene Proteins c-ret research incorporates elements of Morphogenesis, GDNF family of ligands and Kidney development. His Cell biology study combines topics from a wide range of disciplines, such as Gene targeting and Immunology. His studies in Tyrosine kinase integrate themes in fields like Proto-oncogene tyrosine-protein kinase Src and Oncogene RET.
His scientific interests lie mostly in Cancer research, Cell biology, Molecular biology, Pathology and Internal medicine. The Cancer research study combines topics in areas such as Carcinogenesis, Cancer, Tyrosine kinase, Proto-Oncogene Proteins c-ret and Genetically modified mouse. His Tyrosine kinase study combines topics in areas such as Receptor tyrosine kinase and Tyrosine phosphorylation.
His work carried out in the field of Cell biology brings together such families of science as Glial cell line-derived neurotrophic factor, Neurotrophic factors and Cell migration. Masahide Takahashi usually deals with Molecular biology and limits it to topics linked to Mutation and Multiple endocrine neoplasia. His Internal medicine research includes elements of Endocrinology and Oncology.
His primary areas of investigation include Cancer research, Cell biology, Pathology, Cancer and Internal medicine. His study focuses on the intersection of Cancer research and fields such as Carcinogenesis with connections in the field of In vivo. His Cell biology research is multidisciplinary, relying on both Cell and Cell migration.
His Cell migration study integrates concerns from other disciplines, such as Cancer cell and Protein kinase B. The study incorporates disciplines such as Gastroenterology, Endocrinology and Oncology in addition to Internal medicine. His Phosphorylation research is multidisciplinary, incorporating perspectives in Receptor, Tyrosine and Glutamine.
Masahide Takahashi mostly deals with Cell biology, Pathology, Cancer research, Cancer cell and Cell migration. His Cell biology research incorporates themes from Cell and Endocytosis. He combines subjects such as In vitro, Immunoprecipitation, Molecular biology, Glycoprotein and HEK 293 cells with his study of Cell.
His work in Pathology addresses subjects such as Stem cell, which are connected to disciplines such as Cellular differentiation, Fibroblast growth factor, Neurotrophic factors, Glial cell line-derived neurotrophic factor and Proto-Oncogene Proteins c-ret. His research integrates issues of Carcinogenesis, Cleavage and Autocrine signalling in his study of Cancer research. His Protein kinase B study deals with the bigger picture of Phosphorylation.
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Characterization of a multicomponent receptor for GDNF
James J. S. Treanor;Laurie Goodman;Frederic de Sauvage;Donna M. Stone.
Nature (1996)
Activation of a novel human transforming gene, ret, by DNA rearrangement
Masahide Takahashi;Jerome Ritz;Geoffrey M. Cooper.
Cell (1985)
Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains.
M Takahashi;Y Buma;T Iwamoto;Y Inaguma.
Oncogene (1988)
The GDNF/RET signaling pathway and human diseases.
Masahide Takahashi.
Cytokine & Growth Factor Reviews (2001)
Akt/PKB Regulates Actin Organization and Cell Motility via Girdin/APE
Atsushi Enomoto;Hideki Murakami;Naoya Asai;Nobuhiro Morone.
Developmental Cell (2005)
A GPI-linked Protein That Interacts With Ret to Form a Candidate Neurturin Receptor
Robert D. Klein;Robert D. Klein;Daniel Sherman;Wei-Hsien Ho;Donna Stone.
Nature (1997)
MECHANISM OF ACTIVATION OF THE RET PROTO-ONCOGENE BY MULTIPLE ENDOCRINE NEOPLASIA 2A MUTATIONS
Naoya Asai;T. Iwashita;M. Matsuyama;M. Takahashi.
Molecular and Cellular Biology (1995)
HPC-1 is associated with synaptotagmin and omega-conotoxin receptor.
A Yoshida;C Oho;A Omori;R Kuwahara.
Journal of Biological Chemistry (1992)
Tau protein kinase I converts normal tau protein into A68-like component of paired helical filaments.
K Ishiguro;M Takamatsu;K Tomizawa;A Omori.
Journal of Biological Chemistry (1992)
Incommensurate Spin Dynamics of Underdoped Superconductor YBa 2 Cu 3 O 6.7
M. Arai;T. Nishijima;Y. Endoh;T. Egami.
Physical Review Letters (1999)
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