His primary scientific interests are in Molecular biology, Genetics, Telomerase, Cell biology and EZH2. In the subject of general Genetics, his work in Histone code and Histone is often linked to Chromodomain, thereby combining diverse domains of study. His Telomerase study integrates concerns from other disciplines, such as Carcinogenesis and Cancer cell.
His Cell biology study combines topics from a wide range of disciplines, such as Heterochromatin, Heterochromatin protein 1 and Histone H3, Epigenetics. His biological study spans a wide range of topics, including Histone methyltransferase and Epigenetics of physical exercise, DNA methylation. His Histone methyltransferase research includes themes of Epigenomics and Histone methylation.
Jun-ichi Nakayama focuses on Cell biology, Heterochromatin, Chromatin, Genetics and Molecular biology. His Cell biology research is multidisciplinary, incorporating elements of Histone H3, Histone, Nucleosome, HDAC11 and Histone methylation. His Histone methylation research is multidisciplinary, incorporating perspectives in Histone methyltransferase, Histone code, Histone H2A, Histone H1 and Methyltransferase complex.
His work carried out in the field of Heterochromatin brings together such families of science as RNA interference and Gene silencing. His Molecular biology study combines topics in areas such as Gene expression, RNA, Gene, Telomerase and Telomerase reverse transcriptase. His research in Heterochromatin protein 1 tackles topics such as EZH2 which are related to areas like DNA methylation.
His primary scientific interests are in Cell biology, Chromatin, Heterochromatin, Chromodomain and Heterochromatin protein 1. His Cell biology research incorporates themes from Histone H3, Epigenetics, Histone, Nucleosome and Histone methylation. His work in Histone methylation addresses issues such as Methyltransferase complex, which are connected to fields such as Chromatin immunoprecipitation.
His work deals with themes such as RNA, Nuclear protein and Proteomics, which intersect with Chromatin. Heterochromatin is a subfield of Genetics that Jun-ichi Nakayama explores. Jun-ichi Nakayama works mostly in the field of Euchromatin, limiting it down to topics relating to EZH2 and, in certain cases, Non-histone protein, RNA-induced transcriptional silencing and SUV39H1, as a part of the same area of interest.
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.
Role of Histone H3 Lysine 9 Methylation in Epigenetic Control of Heterochromatin Assembly
Jun-ichi Nakayama;Judd C. Rice;Brian D. Strahl;C. David Allis.
Science (2001)
Telomerase activation by hTRT in human normal fibroblasts and hepatocellular carcinomas.
J.-I. Nakayama;H. Tahara;E. Tahara;M. Saito.
Nature Genetics (1998)
Maintenance of self-renewal ability of mouse embryonic stem cells in the absence of DNA methyltransferases Dnmt1, Dnmt3a and Dnmt3b.
Akiko Tsumura;Tomohiro Hayakawa;Yuichi Kumaki;Shin-ichiro Takebayashi.
Genes to Cells (2006)
TLP1: A Gene Encoding a Protein Component of Mammalian Telomerase Is a Novel Member of WD Repeats Family
Jun-ichi Nakayama;Motoki Saito;Hideo Nakamura;Akira Matsuura.
Cell (1997)
Trimethylated lysine 9 of histone H3 is a mark for DNA methylation in Neurospora crassa.
Hisashi Tamaru;Xing Zhang;Debra McMillen;Prim B. Singh.
Nature Genetics (2003)
Immuno-histochemical detection of human telomerase catalytic component, hTERT, in human colorectal tumor and non-tumor tissue sections.
Hidetoshi Tahara;Wataru Yasui;Eiji Tahara;Junya Fujimoto.
Oncogene (1999)
A chromodomain protein, Chp1, is required for the establishment of heterochromatin in fission yeast
Mahito Sadaie;Tetsushi Iida;Takeshi Urano;Jun-ichi Nakayama.
The EMBO Journal (2004)
A chromodomain protein, Swi6, performs imprinting functions in fission yeast during mitosis and meiosis.
Jun-ichi Nakayama;Amar J.S Klar;Shiv I.S Grewal.
Cell (2000)
Physiological Roles of Class I HDAC Complex and Histone Demethylase
Tomohiro Hayakawa;Jun-ichi Nakayama.
BioMed Research International (2011)
A novel quantitative 'stretch PCR assay', that detects a dramatic increase in telomerase activity during the progression of myeloid leukemias.
K.-I. Tatematsu;J.-I. Nakayama;M. Danbara;S. Shionoya.
Oncogene (1996)
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