His primary areas of investigation include Endocrinology, Internal medicine, Cell biology, Apoptosis and Aromatase. His research in Endocrinology intersects with topics in Estrogen receptor and Steroidogenic factor 1. He regularly ties together related areas like Palmitic acid in his Internal medicine studies.
His work on Mitochondrion, Mitochondrial fission and Nucleus as part of general Cell biology research is frequently linked to Confocal, thereby connecting diverse disciplines of science. His study in Apoptosis is interdisciplinary in nature, drawing from both Mammalian embryology and Mitochondrial fission factor. The concepts of his Aromatase study are interwoven with issues in Cell growth, Dorsomedial hypothalamic nucleus, Messenger RNA, Gene targeting and Estrogen.
His primary scientific interests are in Internal medicine, Endocrinology, Cell biology, Molecular biology and Mitochondrion. Masatoshi Nomura interconnects Gastroenterology and Diabetes mellitus in the investigation of issues within Internal medicine. His work carried out in the field of Endocrinology brings together such families of science as Receptor, Aromatase and Androgen receptor.
His Cell biology research incorporates themes from Autophagy and Inflammation. The Molecular biology study combines topics in areas such as Transcription factor and Gene. His Mitochondrion study incorporates themes from mitochondrial fusion, Mitochondrial fission factor and Endoplasmic reticulum.
Masatoshi Nomura focuses on Internal medicine, Cell biology, Endocrinology, Gastroenterology and Mitochondrion. His work in Internal medicine covers topics such as Diabetes mellitus which are related to areas like Hypercortisolemia. His work deals with themes such as Inflammation, Transporter and Cell type, which intersect with Cell biology.
The various areas that Masatoshi Nomura examines in his Endocrinology study include Fibrosis and GNAS complex locus. His Gastroenterology research is multidisciplinary, incorporating perspectives in Clinical trial, Refractory, Human leukocyte antigen, Beta and Subclinical infection. His Mitochondrion research is multidisciplinary, relying on both Nuclear receptor, Endoplasmic reticulum, Mediator and Metabolic pathway.
Masatoshi Nomura spends much of his time researching Internal medicine, Cell biology, Mitochondrion, Nivolumab and Transporter. His Cell biology research includes elements of Glycolysis, Nuclear receptor and Metabolic pathway. His work on DNM1L as part of general Mitochondrion study is frequently linked to Thickening, therefore connecting diverse disciplines of science.
His Transporter study combines topics in areas such as Purinergic receptor, Pregabalin and Pharmacology. His Insulin study is focused on Endocrinology in general. His Endocrinology research incorporates themes from Downregulation and upregulation, LRP6 and LRP5.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice
Naotada Ishihara;Masatoshi Nomura;Akihiro Jofuku;Hiroki Kato.
Nature Cell Biology (2009)
Establishment and characterization of a steroidogenic human granulosa-like tumor cell line, KGN, that expresses functional follicle-stimulating hormone receptor.
Yoshihiro Nishi;Toshihiko Yanase;Yi Ming Mu;Koichi Oba.
Endocrinology (2001)
Hedgehog signaling pathway is a new therapeutic target for patients with breast cancer.
Makoto Kubo;Masafumi Nakamura;Akira Tasaki;Naoki Yamanaka.
Cancer Research (2004)
Ad4BP regulating steroidogenic P-450 gene is a member of steroid hormone receptor superfamily.
Shin Ichiro Honda;Ken-Ichirou Morohashi;Masatoshi Nomura;Hiroyuki Takeya.
Journal of Biological Chemistry (1993)
Developmental defects of the ventromedial hypothalamic nucleus and pituitary gonadotroph in the Ftz‐F1 disrupted mice
Koh Shinoda;Hong Lei;Hironori Yoshii;Masatoshi Nomura.
Developmental Dynamics (1995)
Endogenous Drp1 Mediates Mitochondrial Autophagy and Protects the Heart Against Energy Stress
Yoshiyuki Ikeda;Akihiro Shirakabe;Yasuhiro Maejima;Peiyong Zhai.
Circulation Research (2015)
Identical origin of adrenal cortex and gonad revealed by expression profiles of Ad4BP/SF-1.
Osamu Hatano;Akira Takakusu;Masatoshi Nomura;Ken Ichirou Morohashi.
Genes to Cells (1996)
Drp1-Dependent Mitochondrial Autophagy Plays a Protective Role Against Pressure Overload-Induced Mitochondrial Dysfunction and Heart Failure.
Akihiro Shirakabe;Peiyong Zhai;Yoshiyuki Ikeda;Yoshiyuki Ikeda;Toshiro Saito.
Circulation (2016)
Smad2 and Smad3 Are Redundantly Essential for the TGF-β–Mediated Regulation of Regulatory T Plasticity and Th1 Development
Tomohito Takimoto;Tomohito Takimoto;Yu Wakabayashi;Takashi Sekiya;Naoko Inoue.
Journal of Immunology (2010)
Saturated FFAs, palmitic acid and stearic acid, induce apoptosis in human granulosa cells.
Yi Ming Mu;Yi Ming Mu;Toshihiko Yanase;Yoshihiro Nishi;Atsushi Tanaka.
Endocrinology (2001)
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