Issei Imoto spends much of his time researching Cancer research, Carcinogenesis, Molecular biology, Cancer and Comparative genomic hybridization. His Cancer research research is multidisciplinary, relying on both Cell culture, Epidermoid carcinoma, Cell growth, DNA methylation and Gene silencing. His work deals with themes such as Methylation and microRNA, which intersect with DNA methylation.
His study in Molecular biology is interdisciplinary in nature, drawing from both Gene expression, Gene and HNF1B. His work focuses on many connections between Cancer and other disciplines, such as Pathology, that overlap with his field of interest in Internal medicine, Gene knockdown, Digital polymerase chain reaction and Reference gene. His Comparative genomic hybridization research is included under the broader classification of Genetics.
His primary areas of study are Genetics, Cancer research, Molecular biology, Gene and Cancer. While the research belongs to areas of Cancer research, Issei Imoto spends his time largely on the problem of Carcinogenesis, intersecting his research to questions surrounding DNA methylation. His study on DNA methylation also encompasses disciplines like
Issei Imoto has researched Molecular biology in several fields, including Fluorescence in situ hybridization, Gene expression and Chromosomal translocation. Many of his studies on Cancer apply to Pathology as well. His Comparative genomic hybridization study combines topics in areas such as Gene dosage and Candidate gene.
The scientist’s investigation covers issues in Genetics, Gene, Genome-wide association study, Cancer research and Internal medicine. Issei Imoto combines subjects such as Schizophrenia, Computational biology, Genetic testing and Precision oncology with his study of Gene. His Cancer research research integrates issues from Cell culture, Carcinogenesis, Cancer, Fallopian tube and Gene silencing.
His Cancer study incorporates themes from Epstein–Barr virus, Intensive care medicine and Pathology. His work carried out in the field of Gene silencing brings together such families of science as Epigenetics, Cell growth and Candidate gene. The concepts of his Internal medicine study are interwoven with issues in Endocrinology and Oncology.
Issei Imoto mainly investigates Genetics, Gene, Genome-wide association study, Internal medicine and DNA methylation. His Genetics study frequently links to other fields, such as Developmental disorder. His Gene research is multidisciplinary, incorporating elements of Genetic counseling, Schizophrenia, Ovarian cancer and Family history.
His research integrates issues of Reference gene and Digital polymerase chain reaction in his study of Internal medicine. He is studying CpG site, which is a component of DNA methylation. The Methylation study combines topics in areas such as Gene silencing and Epigenetics.
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.
Exploration of tumor-suppressive microRNAs silenced by DNA hypermethylation in oral cancer.
Ken Ichi Kozaki;Issei Imoto;Seiki Mogi;Ken Omura.
Cancer Research (2008)
miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma
Mayuko Furuta;Ken Ich Kozaki;Shinji Tanaka;Shigeki Arii.
Carcinogenesis (2010)
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease
Kenya Nishioka;Shin Hayashi;Matthew J. Farrer;Andrew B. Singleton.
Annals of Neurology (2006)
PPM1D is a potential target for 17q gain in neuroblastoma
Fumiko Saito-Ohara;Issei Imoto;Jun Inoue;Hajime Hosoi.
Cancer Research (2003)
Alteration in copy numbers of genes as a mechanism for acquired drug resistance.
Kohichiroh Yasui;Saori Mihara;Chen Zhao;Hiroyuki Okamoto.
Cancer Research (2004)
miR-152 is a tumor suppressor microRNA that is silenced by DNA hypermethylation in endometrial cancer
Tomohiko Tsuruta;Ken Ichi Kozaki;Atsushi Uesugi;Mayuko Furuta.
Cancer Research (2011)
The tumor suppressive microRNA miR-218 targets the mTOR component rictor and inhibits AKT phosphorylation in oral cancer
Atsushi Uesugi;Ken Ichi Kozaki;Tomohiko Tsuruta;Mayuko Furuta.
Cancer Research (2011)
Identification of cIAP1 as a candidate target gene within an amplicon at 11q22 in esophageal squamous cell carcinomas.
Issei Imoto;Zeng-Quan Yang;Atiphan Pimkhaokham;Hitoshi Tsuda.
Cancer Research (2001)
Sex hormone-dependent tRNA halves enhance cell proliferation in breast and prostate cancers
Shozo Honda;Phillipe Loher;Megumi Shigematsu;Juan P. Palazzo.
Proceedings of the National Academy of Sciences of the United States of America (2015)
Identification of a Novel Gene, GASC1, within an Amplicon at 9p23–24 Frequently Detected in Esophageal Cancer Cell Lines
Zeng-Quan Yang;Issei Imoto;Yoji Fukuda;Atiphan Pimkhaokham.
Cancer Research (2000)
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