M. Saijo

发表

XAB2, a Novel Tetratricopeptide Repeat Protein Involved in Transcription-coupled DNA Repair and Transcription*

J. Hoeijmakers, Y. Nakatsu, W. Vermeulen, 2000, The Journal of Biological Chemistry.

BRCA1 contributes to transcription‐coupled repair of DNA damage through polyubiquitination and degradation of Cockayne syndrome B protein

A. Yasui, J. Parvin, C. Ishioka, 2011, Cancer science.

DDB2 Complex-Mediated Ubiquitylation around DNA Damage Is Oppositely Regulated by XPC and Ku and Contributes to the Recruitment of XPA

A. Takedachi, Kiyoji Tanaka, M. Saijo, 2010, Molecular and Cellular Biology.

High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

T. Ishikawa, Y. Nakatsu, H. Nakane, 1995, Nature.

Two E3 ubiquitin ligases, SCF‐Skp2 and DDB1‐Cul4, target human Cdt1 for proteolysis

K. Nakayama, K. Nakayama, C. Obuse, 2006, The EMBO journal.

DDB2, the xeroderma pigmentosum group E gene product, is directly ubiquitylated by Cullin 4A-based ubiquitin ligase complex.

Keiji Tanaka, T. Chiba, T. Natsume, 2005, DNA repair.

Functional TFIIH Is Required for UV-Induced Translocation of CSA to the Nuclear Matrix

Kiyoji Tanaka, S. Kamiuchi, M. Saijo, 2007, Molecular and Cellular Biology.

Mutations in the XPD gene leading to xeroderma pigmentosum symptoms

Y. Nakatsu, I. Kuraoka, Kiyoji Tanaka, 1997, Human mutation.

Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair

A. Yasui, M. Honma, E. Neilan, 2012, Nature Genetics.

Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome

A. Takedachi, Kiyoji Tanaka, M. Saijo, 2015, Molecular and Cellular Biology.

The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair*

Kiyoji Tanaka, M. Saijo, Yooksil Sin, 2015, The Journal of Biological Chemistry.

DNA Repair Protein XPA Binds Replication Protein A (RPA) (*)

A. Yasui, Y. Nakatsu, K. Sugasawa, 1995, The Journal of Biological Chemistry.

Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein in strand-specific DNA repair.

K. Tanaka, Y. Nakatsu, S. Takeuchi, 1998, Nucleic acids research.

A Japanese trichothiodystrophy patient with XPD mutations

M. Uchiyama, Kiyoji Tanaka, M. Saijo, 2011, Journal of Human Genetics.

Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS

R. Kosaki, Chie Ishigami, Kiyoji Tanaka, 2015, Journal of Human Genetics.

Inhibition of UVSSA ubiquitination suppresses transcription‐coupled nucleotide excision repair deficiency caused by dissociation from USP7

Mitsuru Higa, Kiyoji Tanaka, M. Saijo, 2018, The FEBS journal.

Stabilization of Ultraviolet (UV)-stimulated Scaffold Protein A by Interaction with Ubiquitin-specific Peptidase 7 Is Essential for Transcription-coupled Nucleotide Excision Repair*

Mitsuru Higa, Kiyoji Tanaka, M. Saijo, 2016, The Journal of Biological Chemistry.

Xeroderma pigmentosum A homolog from Hydra partially complements DNA repair defect in human XPA-deficient cells

A. A. Galande, M. Saijo, S. Ghaskadbi, 2021, Journal of Biosciences.

Growth state and cell cycle dependent phosphorylation of DNA topoisomerase II in Swiss 3T3 cells.

M. Ui, M. Saijo, T. Enomoto, 1992, Biochemistry.

Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA

T. Ikegami, M. Shirakawa, Y. Kyōgoku, 1998, Nature Structural &Molecular Biology.

Phosphorylation-independent Stimulation of DNA Topoisomerase II Activity (*)

K. Kimura, M. Saijo, T. Enomoto, 1996, The Journal of Biological Chemistry.

Purification and characterization of type II DNA topoisomerase from mouse FM3A cells: phosphorylation of topoisomerase II and modification of its activity.

F. Hanaoka, M. Ui, M. Saijo, 1990, Biochemistry.

RPAP3 interacts with Reptin to regulate UV‐induced phosphorylation of H2AX and DNA damage

Li Xu, Kiyoji Tanaka, M. Saijo, 2009, Journal of cellular biochemistry.

A novel cytoplasmic GTPase XAB1 interacts with DNA repair protein XPA.

K. Tanaka, Y. Nakatsu, Kiyoji Tanaka, 2000, Nucleic acids research.

Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I‐DNA covalent complex

A. Yasui, M. Honma, P. J. Brooks, 2011, Genes to cells : devoted to molecular & cellular mechanisms.

DGCR8 Mediates Repair of UV-Induced DNA Damage Independently of RNA Processing.

Philip R. Gafken, B. Clurman, K. Sugasawa, 2017, Cell reports.

Expression of a transfected DNA repair gene (XPA) in xeroderma pigmentosum group A cells restores normal DNA repair and mutagenesis of UV-treated plasmids.

K. Tanaka, K. Kraemer, M. Saijo, 1995, Carcinogenesis.

Isolation of XAB2 Complex Involved in Pre-mRNA Splicing, Transcription, and Transcription-coupled Repair*

J. Qin, H. Handa, Y. Nakatsu, 2008, Journal of Biological Chemistry.

Generation of splice switching oligonucleotides targeting the Cockayne syndrome group B gene product in order to change the diseased cell state.

S. Obika, M. Saijo, Yooksil Sin, 2018, Biochemical and biophysical research communications.

The Ubiquitin Ligase Activity in the DDB2 and CSA Complexes Is Differentially Regulated by the COP9 Signalosome in Response to DNA Damage

Jun-ichi Sawada, Alexei F. Kisselev, R. Drapkin, 2003, Cell.

Translocation of Cockayne syndrome group A protein to the nuclear matrix: Possible relevance to transcription-coupled DNA repair

J. Hoeijmakers, E. Citterio, Kiyoji Tanaka, 2002, Proceedings of the National Academy of Sciences of the United States of America.

UV-Induced Ubiquitylation of XPC Protein Mediated by UV-DDB-Ubiquitin Ligase Complex

Keiji Tanaka, K. Sugasawa, G. Chu, 2005, Cell.

Identification of the nature of modification that causes the shift of DNA topoisomerase II beta to apparent higher molecular weight forms in the M phase.

K. Kimura, M. Ui, M. Saijo, 1994, The Journal of biological chemistry.

UV-induced skin carcinogenesis in xeroderma pigmentosum group A (XPA) gene-knockout mice with nucleotide excision repair-deficiency.

K. Tanaka, Y. Nakatsu, S. Takeuchi, 2001, Mutation research.

Analysis of the conserved NER helicases (XPB and XPD) and UV-induced DNA damage in Hydra.

A. A. Galande, M. Saijo, S. Ghaskadbi, 2018, Biochimica et biophysica acta. General subjects.

Identification of a damaged-DNA binding domain of the XPA protein.

K. Tanaka, M. Shirakawa, K. Morikawa, 1996, Mutation research.

High mobility of flap endonuclease 1 and DNA polymerase eta associated with replication foci in mammalian S-phase nucleus.

L. Solovjeva, M. Svetlova, L. Sasina, 2005, Molecular biology of the cell.

The role of Cockayne syndrome group A (CSA) protein in transcription-coupled nucleotide excision repair

M. Saijo, 2013, Mechanisms of Ageing and Development.

Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase.

K. Kimura, M. Ui, M. Saijo, 1994, The Journal of biological chemistry.

DNA Damage Recognition by XPA Protein Promotes Efficient Recruitment of Transcription Factor II H*

J. Egly, F. Coin, Kiyoji Tanaka, 1997, The Journal of Biological Chemistry.

Inactivation of oncoprotein binding by a single Cys706‐to‐Tyr substitution in the retinoblastoma protein

Y. Taya, K. Ishizaki, M. Sasaki, 1994, FEBS letters.

Three novel mutations responsible for Cockayne syndrome group A.

Y. Nakatsu, M. Yamaizumi, Kiyoji Tanaka, 2003, Genes & genetic systems.

Structural basis of ubiquitin recognition by the winged-helix domain of Cockayne syndrome group B protein

S. Fukai, M. Saijo, A. Yamagata, 2019, Nucleic acids research.

Sequential binding of DNA repair proteins RPA and ERCC1 to XPA in vitro.

K. Tanaka, F. Hanaoka, C. Masutani, 1996, Nucleic acids research.

Enhancement of damage-specific DNA binding of XPA by interaction with the ERCC1 DNA repair protein.

R. Wood, Y. Nakatsu, I. Kuraoka, 1995, Biochemical and biophysical research communications.

Truncated XPA protein detected in atypical group A xeroderma pigmentosum

K. Tanaka, N. Tachi, M. Saijo, 1996, Acta paediatrica.

Nucleotide Excision Repair by Mutant Xeroderma Pigmentosum Group A (XPA) Proteins with Deficiency in Interaction with RPA*

A. Takedachi, Kiyoji Tanaka, M. Saijo, 2010, The Journal of Biological Chemistry.

Inhibition of nucleotide excision repair by anti-XPA monoclonal antibodies which interfere with binding to RPA, ERCC1, and TFIIH.

I. Kuraoka, Kiyoji Tanaka, M. Saijo, 2004, Biochemical and biophysical research communications.

Resonance assignments, solution structure, and backbone dynamics of the DNA- and RPA-binding domain of human repair factor XPA.

T. Ikegami, M. Shirakawa, Y. Kyōgoku, 1999, Journal of Biochemistry (Tokyo).

70-kDa Heat Shock Cognate Protein Interacts Directly with the N-terminal Region of the Retinoblastoma Gene Product pRb

Shuji Takahashi, K. Kamiguchi, Y. Taya, 1995, The Journal of Biological Chemistry.

Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP‐F and XFE

S. Iwai, I. Kuraoka, Kiyoji Tanaka, 2012, Genes to cells : devoted to molecular & cellular mechanisms.

Camptothecin compromises transcription recovery and cell survival against cisplatin and ultraviolet irradiation regardless of transcription-coupled nucleotide excision repair.

Kuniyoshi Iwabuchi, T. Matsunaga, M. Wakasugi, 2022, DNA repair.