Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Tsukasa Matsunaga"'
Autor:
Masataka Tsuda, Saki Ogawa, Masato Ooka, Kaori Kobayashi, Kouji Hirota, Mitsuo Wakasugi, Tsukasa Matsunaga, Tetsushi Sakuma, Takashi Yamamoto, Shunsuke Chikuma, Hiroyuki Sasanuma, Michelle Debatisse, Aidan J Doherty, Robert P Fuchs, Shunichi Takeda
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0213383 (2019)
Replicative DNA polymerases are frequently stalled at damaged template strands. Stalled replication forks are restored by the DNA damage tolerance (DDT) pathways, error-prone translesion DNA synthesis (TLS) to cope with excessive DNA damage, and erro
Externí odkaz:
https://doaj.org/article/19f99db9044847b2a3d180b42b4ea026
Publikováno v:
Asian Pacific Journal of Allergy & Immunology; Sep2024, Vol. 42 Issue 3, p298-304, 7p
Autor:
Katsumi Yamashita, Randy Y.C. Poon, Yukihito Ishizaka, Tsukasa Matsunaga, Hitoshi Nakagama, Ryoichi Kizu, Katsuji Yoshioka, Sanae Uchida
Cdc25 dual specificity phosphatases positively regulate the cell cycle by activating cyclin-dependent kinase/cyclin complexes. Of the three mammalian Cdc25 isoforms, Cdc25A is phosphorylated by genotoxic stress–activated Chk1 or Chk2, which trigger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a503bd220db7506f5a76367aa31fdbee
https://doi.org/10.1158/0008-5472.c.6499226.v1
https://doi.org/10.1158/0008-5472.c.6499226.v1
Autor:
Katsumi Yamashita, Randy Y.C. Poon, Yukihito Ishizaka, Tsukasa Matsunaga, Hitoshi Nakagama, Ryoichi Kizu, Katsuji Yoshioka, Sanae Uchida
Supplementary Figure 1 from Stress-Activated Mitogen-Activated Protein Kinases c-Jun NH2-Terminal Kinase and p38 Target Cdc25B for Degradation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a60da604da6f5569bbd0f201049e641
https://doi.org/10.1158/0008-5472.22379351
https://doi.org/10.1158/0008-5472.22379351
Autor:
Katsumi Yamashita, Randy Y.C. Poon, Yukihito Ishizaka, Tsukasa Matsunaga, Hitoshi Nakagama, Ryoichi Kizu, Katsuji Yoshioka, Sanae Uchida
Supplementary Materials from Stress-Activated Mitogen-Activated Protein Kinases c-Jun NH2-Terminal Kinase and p38 Target Cdc25B for Degradation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31fdc770b23bedd7126591f9bb6ce070
https://doi.org/10.1158/0008-5472.22379348.v1
https://doi.org/10.1158/0008-5472.22379348.v1
Autor:
Saki Horie, Kenji Mishiro, Mio Nishino, Inori Domae, Mitsuo Wakasugi, Tsukasa Matsunaga, Munetaka Kunishima
Modified antibodies play essential roles in various fields, such as analysis, diagnosis, and therapy, which require modified antibodies with optimal physical and biological properties. To this aim, the development of methods for site-selective antibo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3223f5b6cdac4d46c4a5a6cdbb4728
https://doi.org/10.26434/chemrxiv-2023-c0k4n
https://doi.org/10.26434/chemrxiv-2023-c0k4n
Publikováno v:
Genes to Cells. 27:356-367
The structure-specific endonuclease XPF-ERCC1 is a multi-functional heterodimer that participates in a variety of DNA repair mechanisms for maintaining genome integrity. Both subunits contain C-terminal tandem helix-hairpin-helix (HhH
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 887:503616
Autor:
Salma Akter, Samuel H. Wilson, Mitsuo Wakasugi, Tomoo Ogi, Keli Agama, Tsukasa Matsunaga, Yves Pommier, Rajendra Prasad, Shigenori Iwai, Naoto Shimizu, Hiroyuki Sasanuma, Liton Kumar Saha, Kouji Hirota, Yuka Nakazawa, Shunichi Takeda, Shar-yin Naomi Huang
Publikováno v:
Proc Natl Acad Sci U S A
Nucleotide excision repair (NER) removes helix-destabilizing adducts including ultraviolet (UV) lesions, cyclobutane pyrimidine dimers (CPDs), and pyrimidine (6-4) pyrimidone photoproducts (6-4PPs). In comparison with CPDs, 6-4PPs have greater cytoto
Publikováno v:
Biochem Biophys Res Commun
The ERCC1-XPF heterodimer is a structure-specific endonuclease and plays multiple roles in various DNA repair pathways including nucleotide excision repair and also telomere maintenance. The dimer formation, which is mediated by their C-terminal heli