A. Ui

发表

Histone acetylation by CBP and p300 at double-strand break sites facilitates SWI/SNF chromatin remodeling and the recruitment of non-homologous end joining factors

J. Yokota, H. Ogiwara, A. Ui, 2011, Oncogene.

Histone acetylation by CBP and p300 at double-strand break sites facilitates SWI/SNF chromatin remodeling and the recruitment of non-homologous end joining factors.

J. Yokota, H. Ogiwara, A. Ui, 2011, Oncogene.

Phosphorylated HBO1 at UV irradiated sites is essential for nucleotide excision repair

R. Matsunuma, M. Kitagawa, T. Ohhata, 2017, Nature Communications.

The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants

A. Ui, F. Onoda, M. Seki, 2001, Molecular Genetics and Genomics.

Chl1 and Ctf4 are required for damage-induced recombinations.

H. Ogiwara, A. Ui, M. Seki, 2007, Biochemical and biophysical research communications.

Rad50 is involved in MMS-induced recombination between homologous chromosomes in mitotic cells.

H. Ogiwara, A. Ui, F. Onoda, 2007, Genes & genetic systems.

CHAMP1-POGZ counteracts the inhibitory effect of 53BP1 on homologous recombination and affects PARP inhibitor resistance

A. Ui, A. Yasui, Kozo Tanaka, 2022, Oncogene.

Transcriptional elongation factor ENL phosphorylated by ATM recruits polycomb and switches off transcription for DSB repair.

A. Ui, A. Yasui, Yuko Nagaura, 2015, Molecular cell.

Relationship among DNA double‐strand break (DSB), DSB repair, and transcription prevents genome instability and cancer

A. Ui, A. Yasui, N. Chiba, 2020, Cancer science.

Collaboration of MLLT1/ENL, Polycomb and ATM for transcription and genome integrity

A. Ui, A. Yasui, 2016, Nucleus.

Loss of heterozygosity in yeast can occur by ultraviolet irradiation during the S phase of the cell cycle.

A. Ui, S. Mashiko, K. Mishiba, 2006, Mutation research.

Dpb11, the budding yeast homolog of TopBP1, functions with the checkpoint clamp in recombination repair

H. Ogiwara, A. Ui, F. Onoda, 2006, Nucleic acids research.

Possible involvement of LKB1-AMPK signaling in non-homologous end joining

J. Yokota, C. Harris, H. Ogiwara, 2014, Oncogene.

Nucleosome remodelling, DNA repair and transcriptional regulation build negative feedback loops in cancer and cellular ageing

A. Ui, A. Yasui, S. Kanno, 2017, Philosophical Transactions of the Royal Society B: Biological Sciences.

SWI/SNF factors required for cellular resistance to DNA damage include ARID1A and ARID1B and show interdependent protein stability.

T. Nagase, H. Ogiwara, A. Ui, 2014, Cancer research.

Curcumin suppresses multiple DNA damage response pathways and has potency as a sensitizer to PARP inhibitor.

H. Ogiwara, A. Ui, A. Yasui, 2013, Carcinogenesis.

The ACF1 complex is required for DNA double-strand break repair in human cells.

Satoshi Nakajima, Takashi Kohno, H. Ogiwara, 2010, Molecular cell.

H. Ogiwara, A. Ui, K. Ohta, 2007, Nucleic acids research.

Ctf18 is required for homologous recombination-mediated double-strand break repair

H. Ogiwara, A. Ui, M. Seki, 2007, Nucleic acids research.

Ctf 18 is required for homologous recombination-mediated double-strand break repair

H. Ogiwara, A. Ui, M. Seki, 2007 .

Rad52 sumoylation and its involvement in the efficient induction of homologous recombination.

H. Ogiwara, A. Ui, D. Branzei, 2008, DNA repair.

Human SIRT2 and SIRT3 deacetylases function in DNA homologous recombinational repair

A. Ui, K. Sugasawa, Takeshi Yasuda, 2021, Genes to Cells.

Rmi1, a member of the Sgs1–Top3 complex in budding yeast, contributes to sister chromatid cohesion

A. Ui, M. Seki, T. Enomoto, 2007, EMBO reports.

Role of Elg1 protein in double strand break repair

H. Ogiwara, A. Ui, M. Seki, 2006, Nucleic acids research.

Activation of a novel pathway involving Mms1 and Rad59 in sgs1 cells.

H. Ogiwara, A. Ui, M. Seki, 2007, Biochemical and biophysical research communications.

SMC6 is required for MMS-induced interchromosomal and sister chromatid recombinations in Saccharomyces cerevisiae.

A. Ui, F. Onoda, M. Seki, 2004, DNA repair.

Novel function of HATs and HDACs in homologous recombination through acetylation of human RAD52 at double-strand break sites

P. Jeggo, A. Ui, Takamitsu A Kato, 2018, PLoS genetics.

Fine-tuning of DNA damage-dependent ubiquitination by OTUB2 supports the DNA repair pathway choice.

H. Ogiwara, A. Ui, Kiyoko Kato, 2014, Molecular cell.

Different domains of Sgs1 are required for mitotic and meiotic functions.

A. Ui, Y. Ohno, F. Onoda, 2000, Genes & genetic systems.

The ability of Sgs1 to interact with DNA topoisomerase III is essential for damage-induced recombination.

H. Ogiwara, A. Ui, S. Fukushige, 2005, DNA repair.

Functional and physical interaction between Sgs1 and Top3 and Sgs1-independent function of Top3 in DNA recombination repair.

A. Ui, F. Onoda, M. Seki, 2002, Genes & genetic systems.

Ames test-negative carcinogen, ortho-phenyl phenol, binds tubulin and causes aneuploidy in budding yeast.

A. Ui, T. Nunoshiba, S. Ishikawa, 2007, Mutation research.

BRCA1 transports the DNA damage signal for CDDP‐induced centrosome amplification through the centrosomal Aurora A

Y. Miki, A. Ui, C. Ishioka, 2022, Cancer science.

Novel Calcium-Binding Ablating Mutations Induce Constitutive RET Activity and Drive Tumorigenesis

A. Okamoto, A. Ui, A. Otsuka, 2022, Cancer research.

Phosphorylated HBO1 at UV irradiated sites is essential for nucleotide excision repair

R. Matsunuma, M. Kitagawa, T. Ohhata, 2018 .

Collaboration of MLLT1/ENL, Polycomb and ATM for transcription and genome integrity

A. Ui, A. Yasui, 2016, Nucleus.

Rad52 sumoylation and its involvement in the efficient induction of homologous recombination.

H. Ogiwara, A. Ui, M. Seki, 2008, DNA repair.