Masato Kasuga mainly focuses on Internal medicine, Endocrinology, Cell biology, Biochemistry and Insulin. His Internal medicine research includes elements of Diabetes mellitus and Type 2 diabetes. His Endocrinology study combines topics in areas such as Receptor and Gastric emptying.
In his research, Gene expression and Protein kinase B is intimately related to Molecular biology, which falls under the overarching field of Cell biology. His Biochemistry study combines topics from a wide range of disciplines, such as Cell culture and GRB10. His Insulin research is multidisciplinary, incorporating elements of Arteriosclerosis, Metabolic disorder, Asymptomatic and Coma.
His primary areas of investigation include Internal medicine, Endocrinology, Insulin, Cell biology and Diabetes mellitus. The study incorporates disciplines such as Gastroenterology, Immunology and Type 2 diabetes in addition to Internal medicine. His Type 2 diabetes research integrates issues from Single-nucleotide polymorphism and Type 2 Diabetes Mellitus.
His work in Endocrinology is not limited to one particular discipline; it also encompasses Cholecystokinin. His Cell biology study frequently draws connections to adjacent fields such as Biochemistry. His Protein tyrosine phosphatase study integrates concerns from other disciplines, such as Proto-oncogene tyrosine-protein kinase Src and Tyrosine phosphorylation.
Internal medicine, Endocrinology, Diabetes mellitus, Insulin and Insulin resistance are his primary areas of study. His study in Internal medicine focuses on Receptor in particular. Masato Kasuga has included themes like Inflammation and Downregulation and upregulation in his Endocrinology study.
He combines subjects such as Cancer, Obesity and Epidemiology with his study of Diabetes mellitus. The concepts of his Insulin study are interwoven with issues in Arteriosclerosis, Asymptomatic, Coma and Cell biology. His study explores the link between Gene expression and topics such as Pancreatic islets that cross with problems in Molecular biology.
Internal medicine, Endocrinology, Insulin, Diabetes mellitus and Cell biology are his primary areas of study. Masato Kasuga studies Internal medicine, namely Receptor. The concepts of his Endocrinology study are interwoven with issues in Inflammation and Downregulation and upregulation.
Masato Kasuga has researched Insulin in several fields, including Metabolic disorder, Transgene, Pathogenesis, Arteriosclerosis and FOXO1. Masato Kasuga interconnects Asymptomatic, Epidemiology and Coma in the investigation of issues within Diabetes mellitus. The study incorporates disciplines such as Cytotoxic T cell and ZAP70, T-cell receptor in addition to Cell biology.
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MCP-1 contributes to macrophage infiltration into adipose tissue, insulin resistance, and hepatic steatosis in obesity
Hajime Kanda;Sanshiro Tateya;Yoshikazu Tamori;Ko Kotani;Ko Kotani.
Journal of Clinical Investigation (2006)
Report of the Committee on the Classification and Diagnostic Criteria of Diabetes Mellitus
Yutaka Seino;Kishio Nanjo;Naoko Tajima;Takashi Kadowaki.
Journal of Diabetes Investigation (2010)
Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin.
Akihiro Asakawa;Akio Inui;Oshihiro Kaga;Hideki Yuzuriha.
Gastroenterology (2001)
Insulin resistance and growth retardation in mice lacking insulin receptor substrate-1.
Hiroyuki Tamemoto;Takashi Kadowaki;Kazuyuki Tobe;Takeshi Yagi.
Nature (1994)
Report of the Committee on the classification and diagnostic criteria of diabetes mellitus : The Committee of the Japan Diabetes Society on the diagnostic criteria of diabetes mellitus
Yutaka Seino;Kishio Nanjo;Naoko Tajima;Takashi Kadowaki.
Diabetology international (2010)
International clinical harmonization of glycated hemoglobin in Japan: From Japan Diabetes Society to National Glycohemoglobin Standardization Program values.
Atsunori Kashiwagi;Masato Kasuga;Eiichi Araki;Yoshitomo Oka.
Journal of Diabetes Investigation (2012)
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
Kazuki Yasuda;Kazuaki Miyake;Yukio Horikawa;Kazuo Hara.
Nature Genetics (2008)
Induction of cyclooxygenase 2 in gastric mucosal lesions and its inhibition by the specific antagonist delays healing in mice
Hisashi Mizuno;Choitsu Sakamoto;Kohei Matsuda;Ken Wada.
Gastroenterology (1997)
Insulin/Foxo1 Pathway Regulates Expression Levels of Adiponectin Receptors and Adiponectin Sensitivity
Atsushi Tsuchida;Toshimasa Yamauchi;Yusuke Ito;Yusuke Hada.
Journal of Biological Chemistry (2004)
Antagonism of ghrelin receptor reduces food intake and body weight gain in mice
A Asakawa;A Inui;T Kaga;G Katsuura.
Gut (2003)
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