Papers - OGI Tomoo
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Congenital mutations in the WDR4 gene cause severe microcephaly associated with genome instability Reviewed
Tomoo Ogi
GENES & GENETIC SYSTEMS Vol. 91 ( 6 ) page： 319 - 319 2016.12
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A 10-year follow-up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole-genome sequencing. Reviewed
Ono R, Masaki T, Mayca Pozo F, Nakazawa Y, Swagemakers SM, Nakano E, Sakai W, Takeuchi S, Kanda F, Ogi T, van der Spek PJ, Sugasawa K, Nishigori C
Photodermatology, photoimmunology & photomedicine Vol. 32 ( 4 ) page： 174-80 2016.7
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OkaYasuyoshi, OgiTomoo, Bekker-JensenSimon, MailandNiels
page： 98 2015.11
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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
Clinical immunology (Orlando, Fla.) Vol. 160 ( 2 ) page： 255-60 2015.10
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XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency. Open Access
The Journal of allergy and clinical immunology Vol. 136 ( 4 ) page： 1007-17 2015.10
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SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells. Open Access
Alagoz M, Katsuki Y, Ogiwara H, Ogi T, Shibata A, Kakarougkas A, Jeggo P
Nucleic acids research Vol. 43 ( 16 ) page： 7931-44 2015.9
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Sensitivity and dose dependency of radiation-induced injury in hematopoietic stem/progenitor cells in mice. Open Access
Guo CY, Luo L, Urata Y, Goto S, Huang WJ, Takamura S, Hayashi F, Doi H, Kitajima Y, Ono Y, Ogi T, Li TS
Scientific reports Vol. 5 page： 8055 2015.1
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A rapid, comprehensive system for assaying DNA repair activity and cytotoxic effects of DNA-damaging reagents.
Jia N, Nakazawa Y, Guo C, Shimada M, Sethi M, Takahashi Y, Ueda H, Nagayama Y, Ogi T
Nature protocols Vol. 10 ( 1 ) page： 12-24 2015.1
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Hypomorphic PCNA mutation underlies a human DNA repair disorder. Open Access
Baple EL, Chambers H, Cross HE, Fawcett H, Nakazawa Y, Chioza BA, Harlalka GV, Mansour S, Sreekantan-Nair A, Patton MA, Muggenthaler M, Rich P, Wagner K, Coblentz R, Stein CK, Last JI, Taylor AM, Jackson AP, Ogi T, Lehmann AR, Green CM, Crosby AH
The Journal of clinical investigation Vol. 124 ( 7 ) page： 3137-46 2014.7
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PRKDC mutations in a SCID patient with profound neurological abnormalities. Open Access
Woodbine L, Neal JA, Sasi NK, Shimada M, Deem K, Coleman H, Dobyns WB, Ogi T, Meek K, Davies EG, Jeggo PA
The Journal of clinical investigation Vol. 123 ( 7 ) page： 2969-80 2013.7
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Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia. Open Access
Kashiyama K, Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T
American journal of human genetics Vol. 92 ( 5 ) page： 807-19 2013.5
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[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
Seikagaku. The Journal of Japanese Biochemical Society Vol. 85 ( 3 ) page： 133-44 2013.3
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Functional characterization of the novel BRAF complex mutation, BRAF(V600delinsYM) , identified in papillary thyroid carcinoma. Open Access
Matsuse M, Mitsutake N, Tanimura S, Ogi T, Nishihara E, Hirokawa M, Fuziwara CS, Saenko VA, Suzuki K, Miyauchi A, Yamashita S
International journal of cancer. Journal international du cancer Vol. 132 ( 3 ) page： 738-43 2013.2
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miR-196a downregulation increases the expression of type I and III collagens in keloid fibroblasts. Open Access
Kashiyama K, Mitsutake N, Matsuse M, Ogi T, Saenko VA, Ujifuku K, Utani A, Hirano A, Yamashita S
The Journal of investigative dermatology Vol. 132 ( 6 ) page： 1597-604 2012.6
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Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair. Open Access
Nakazawa Y, Sasaki K, Mitsutake N, Matsuse M, Shimada M, Nardo T, Takahashi Y, Ohyama K, Ito K, Mishima H, Nomura M, Kinoshita A, Ono S, Takenaka K, Masuyama R, Kudo T, Slor H, Utani A, Tateishi S, Yamashita S, Stefanini M, Lehmann AR, Yoshiura K, Ogi T
Nature genetics Vol. 44 ( 5 ) page： 586-92 2012.5
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Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome. Open Access
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
PLoS genetics Vol. 8 ( 11 ) page： e1002945 2012
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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
DNA repair Vol. 10 ( 3 ) page： 314-21 2011.3
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A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives. Open Access
Nakazawa Y, Yamashita S, Lehmann AR, Ogi T
DNA repair Vol. 9 ( 5 ) page： 506-16 2010.5
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Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cells. Open Access
Ogi T, Limsirichaikul S, Overmeer RM, Volker M, Takenaka K, Cloney R, Nakazawa Y, Niimi A, Miki Y, Jaspers NG, Mullenders LH, Yamashita S, Fousteri MI, Lehmann AR
Molecular cell Vol. 37 ( 5 ) page： 714-27 2010.3
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Collaborative action of Brca1 and CtIP in elimination of covalent modifications from double-strand breaks to facilitate subsequent break repair. Open Access
Nakamura K, Kogame T, Oshiumi H, Shinohara A, Sumitomo Y, Agama K, Pommier Y, Tsutsui KM, Tsutsui K, Hartsuiker E, Ogi T, Takeda S, Taniguchi Y
PLoS genetics Vol. 6 ( 1 ) page： e1000828 2010.1