In his articles, Yoichi Shinkai combines various disciplines, including Gene and Mutant. While working in this field, Yoichi Shinkai studies both Mutant and Gene. Yoichi Shinkai performs integrative Genetics and Germline research in his work. Many of his studies on Cell biology involve topics that are commonly interrelated, such as Stem cell. His study connects Cell biology and Stem cell. Yoichi Shinkai integrates many fields, such as Molecular biology and Genome, in his works. In his papers, Yoichi Shinkai integrates diverse fields, such as Genome and Molecular biology. In his study, Yoichi Shinkai carries out multidisciplinary DNA methylation and Reprogramming research. Yoichi Shinkai incorporates Reprogramming and DNA methylation in his studies.
Yoichi Shinkai undertakes interdisciplinary study in the fields of Gene and Embryonic stem cell through his works. By researching both Embryonic stem cell and Gene, he produces research that crosses academic boundaries. Yoichi Shinkai incorporates Genetics and Epigenetics in his studies. In his papers, Yoichi Shinkai integrates diverse fields, such as Epigenetics and Histone. His work often combines Histone and Methyltransferase studies. In his works, Yoichi Shinkai conducts interdisciplinary research on Methyltransferase and Histone H3. His Histone H3 study frequently draws parallels with other fields, such as Gene expression. Yoichi Shinkai performs integrative study on Gene expression and DNA in his works. In his work, he performs multidisciplinary research in DNA and Molecular biology.
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Class Switch Recombination and Hypermutation Require Activation-Induced Cytidine Deaminase (AID), a Potential RNA Editing Enzyme
Masamichi Muramatsu;Kazuo Kinoshita;Sidonia Fagarasan;Shuichi Yamada.
G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis
Makoto Tachibana;Kenji Sugimoto;Masami Nozaki;Jun Ueda.
Genes & Development (2002)
Partitioning and Plasticity of Repressive Histone Methylation States in Mammalian Chromatin
Antoine H.F.M. Peters;Stefan Kubicek;Karl Mechtler;Roderick J. O'Sullivan.
Molecular Cell (2003)
SET Domain-containing Protein, G9a, Is a Novel Lysine-preferring Mammalian Histone Methyltransferase with Hyperactivity and Specific Selectivity to Lysines 9 and 27 of Histone H3
Makoto Tachibana;Kenji Sugimoto;Tatsunobu Fukushima;Yoichi Shinkai.
Journal of Biological Chemistry (2001)
Histone Methyltransferases Direct Different Degrees of Methylation to Define Distinct Chromatin Domains.
Judd C. Rice;Scott D. Briggs;Beatrix Ueberheide;Cynthia M. Barber.
Molecular Cell (2003)
Histone methyltransferases G9a and GLP form heteromeric complexes and are both crucial for methylation of euchromatin at H3-K9.
Makoto Tachibana;Jun Ueda;Mikiko Fukuda;Naoki Takeda.
Genes & Development (2005)
G9a-mediated irreversible epigenetic inactivation of Oct-3/4 during early embryogenesis.
Nirit Feldman;Ariela Gerson;Jia Fang;En Li.
Nature Cell Biology (2006)
Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET
Toshiyuki Matsui;Danny Leung;Hiroki Miyashita;Irina A. Maksakova.
H3K9 methyltransferase G9a and the related molecule GLP
Yoichi Shinkai;Makoto Tachibana.
Genes & Development (2011)
Large histone H3 lysine 9 dimethylated chromatin blocks distinguish differentiated from embryonic stem cells
Bo Wen;Hao Wu;Hao Wu;Yoichi Shinkai;Rafael A Irizarry;Rafael A Irizarry.
Nature Genetics (2009)
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