Ogi T - Search Results

1

Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.

Matsumoto Y, Miyamoto T, Sakamoto H, Izumi H, Nakazawa Y, Ogi T, Tahara H, Oku S, Hiramoto A, Shiiki T, Fujisawa Y, Ohashi H, Sakemi Y, Matsuura S. Matsumoto Y, et al. Among authors: ogi t. DNA Repair (Amst). 2011 Mar 7;10(3):314-21. doi: 10.1016/j.dnarep.2010.12.002. Epub 2011 Jan 12. DNA Repair (Amst). 2011. PMID: 21227757

2

A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives.

Nakazawa Y, Yamashita S, Lehmann AR, Ogi T. Nakazawa Y, et al. Among authors: ogi t. DNA Repair (Amst). 2010 May 4;9(5):506-16. doi: 10.1016/j.dnarep.2010.01.015. Epub 2010 Feb 18. DNA Repair (Amst). 2010. PMID: 20171149 Free article.

3

Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome.

Ogi T, Walker S, Stiff T, Hobson E, Limsirichaikul S, Carpenter G, Prescott K, Suri M, Byrd PJ, Matsuse M, Mitsutake N, Nakazawa Y, Vasudevan P, Barrow M, Stewart GS, Taylor AM, O'Driscoll M, Jeggo PA. Ogi T, et al. PLoS Genet. 2012;8(11):e1002945. doi: 10.1371/journal.pgen.1002945. Epub 2012 Nov 8. PLoS Genet. 2012. PMID: 23144622 Free PMC article.

4

[Molecular cloning and characterisation of UVSSA, the responsible gene for UV-sensitive syndrome].

Ogi T, Nakazawa Y, Sasaki K, Guo C, Yoshiura K, Utani A, Nagayama Y. Ogi T, et al. Seikagaku. 2013 Mar;85(3):133-44. Seikagaku. 2013. PMID: 23631307 Review. Japanese. No abstract available.

5

Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency.

Tamura S, Higuchi K, Tamaki M, Inoue C, Awazawa R, Mitsuki N, Nakazawa Y, Mishima H, Takahashi K, Kondo O, Imai K, Morio T, Ohara O, Ogi T, Furukawa F, Inoue M, Yoshiura K, Kanazawa N. Tamura S, et al. Among authors: ogi t. Clin Immunol. 2015 Oct;160(2):255-60. doi: 10.1016/j.clim.2015.07.004. Epub 2015 Jul 11. Clin Immunol. 2015. PMID: 26172957

6

XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.

Guo C, Nakazawa Y, Woodbine L, Björkman A, Shimada M, Fawcett H, Jia N, Ohyama K, Li TS, Nagayama Y, Mitsutake N, Pan-Hammarström Q, Gennery AR, Lehmann AR, Jeggo PA, Ogi T. Guo C, et al. Among authors: ogi t. J Allergy Clin Immunol. 2015 Oct;136(4):1007-17. doi: 10.1016/j.jaci.2015.06.007. Epub 2015 Aug 5. J Allergy Clin Immunol. 2015. PMID: 26255102

7

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

Niida H, Matsunuma R, Horiguchi R, Uchida C, Nakazawa Y, Motegi A, Nishimoto K, Sakai S, Ohhata T, Kitagawa K, Moriwaki S, Nishitani H, Ui A, Ogi T, Kitagawa M. Niida H, et al. Among authors: ogi t. Nat Commun. 2017 Jul 18;8:16102. doi: 10.1038/ncomms16102. Nat Commun. 2017. PMID: 28719581 Free PMC article.

8

Common TFIIH recruitment mechanism in global genome and transcription-coupled repair subpathways.

Okuda M, Nakazawa Y, Guo C, Ogi T, Nishimura Y. Okuda M, et al. Among authors: ogi t. Nucleic Acids Res. 2017 Dec 15;45(22):13043-13055. doi: 10.1093/nar/gkx970. Nucleic Acids Res. 2017. PMID: 29069470 Free PMC article.

9

ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repair.

Tsuda M, Cho K, Ooka M, Shimizu N, Watanabe R, Yasui A, Nakazawa Y, Ogi T, Harada H, Agama K, Nakamura J, Asada R, Fujiike H, Sakuma T, Yamamoto T, Murai J, Hiraoka M, Koike K, Pommier Y, Takeda S, Hirota K. Tsuda M, et al. Among authors: ogi t. PLoS One. 2017 Nov 17;12(11):e0188320. doi: 10.1371/journal.pone.0188320. eCollection 2017. PLoS One. 2017. PMID: 29149203 Free PMC article.

10

Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations.

Doi H, Koyano S, Miyatake S, Nakajima S, Nakazawa Y, Kunii M, Tomita-Katsumoto A, Oda K, Yamaguchi Y, Fukai R, Ikeda S, Kato R, Ogata K, Kubota S, Hayashi N, Takahashi K, Tada M, Tanaka K, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Ogi T, Aihara M, Takeuchi H, Matsumoto N, Tanaka F. Doi H, et al. Among authors: ogi t. J Hum Genet. 2018 Apr;63(4):417-423. doi: 10.1038/s10038-017-0408-5. Epub 2018 Feb 5. J Hum Genet. 2018. PMID: 29403087

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