論文 - 中沢 由華
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Hailey-Hailey disease with oesophageal involvement due to a previously unreported ATP2C1 mutation.
Kono M, Kodera M, Inasaka Y, Hasegawa I, Muro Y, Nakazawa Y, Ogi T, Akiyama M
European journal of dermatology : EJD 2019年8月
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JAK/STAT3 and NF-κB Signaling Pathways Regulate Cancer Stem-Cell Properties in Anaplastic Thyroid Cancer Cells. 査読有り
29 巻 ( 5 ) 頁： 674-682 2019年5月
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A Japanese Case of Galli-Galli Disease due to a Previously Unreported POGLUT1 Mutation. 査読有り
Kono M, Sawada M, Nakazawa Y, Ogi T, Muro Y, Akiyama M
Acta dermato-venereologica 99 巻 ( 4 ) 頁： 458 - 459 2019年1月
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Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome 査読有り 国際共著
Calmels Nadege, Botta Elena, Jia Nan, Fawcett Heather, Nardo Tiziana, Nakazawa Yuka, Lanzafame Manuela, Moriwaki Shinichi, Sugita Katsuo, Kubota Masaya, Obringer Cathy, Spitz Marie-Aude, Stefanini Miria, Laugel Vincent, Orioli Donata, Ogi Tomoo, Lehmann Alan Robert
JOURNAL OF MEDICAL GENETICS 55 巻 ( 5 ) 頁： 329-343 2018年5月
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Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations
Doi Hiroshi, Koyano Shigeru, Miyatake Satoko, Nakajima Shinji, Nakazawa Yuka, Kunii Misako, Tomita-Katsumoto Atsuko, Oda Kayoko, Yamaguchi Yukie, Fukai Ryoko, Ikeda Shingo, Kato Rumiko, Ogata Katsuhisa, Kubota Shun, Hayashi Noriko, Takahashi Keita, Tada Mikiko, Tanaka Kenichi, Nakashima Mitsuko, Tsurusaki Yoshinori, Miyake Noriko, Saitsu Hirotomo, Ogi Tomoo, Aihara Michiko, Takeuchi Hideyuki, Matsumoto Naomichi, Tanaka Fumiaki
JOURNAL OF HUMAN GENETICS 63 巻 ( 4 ) 頁： 417-423 2018年4月
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An adolescent case of xeroderma pigmentosum variant confirmed by the onset of sun exposure-related skin cancer during Crohn's disease treatment
Terada Aoi, Aoshima Masahiro, Tanizaki Hideaki, Nakazawa Yuka, Ogi Tomoo, Tokura Yoshiki, Moriwaki Shinichi
JOURNAL OF CUTANEOUS IMMUNOLOGY AND ALLERGY 1 巻 ( 1 ) 頁： 23-26 2018年4月
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Yasuda Takeshi, Kagawa Wataru, Ogi Tomoo, Kato Takamitsu A., Suzuki Takehiro, Dohmae Naoshi, Takizawa Kazuya, Nakazawa Yuka, Genet Matthew D., Saotome Mika, Hama Michio, Konishi Teruaki, Nakajima Nakako Izumi, Hazawa Masaharu, Tomita Masanori, Koike Manabu, Noshiro Katsuko, Tomiyama Kenichi, Obara Chizuka, Gotoh Takaya, Ui Ayako, Fujimori Akira, Nakayama Fumiaki, Hanaoka Fumio, Sugasawa Kaoru, Okayasu Ryuichi, Jeggo Penny A., Tajima Katsushi
PLOS GENETICS 14 巻 ( 3 ) 頁： e1007277 2018年3月
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Common TFIIH recruitment mechanism in global genome and transcription-coupled repair subpathways 査読有り
Okuda Masahiko, Nakazawa Yuka, Guo Chaowan, Ogi Tomoo, Nishimura Yoshifumi
NUCLEIC ACIDS RESEARCH 45 巻 ( 22 ) 頁： 13043-13055 2017年12月
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ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repair 査読有り
Tsuda Masataka, Cho Kosai, Ooka Masato, Shimizu Naoto, Watanabe Reiko, Yasui Akira, Nakazawa Yuka, Ogi Tomoo, Harada Hiroshi, Agama Keli, Nakamura Jun, Asada Ryuta, Fujiike Haruna, Sakuma Tetsushi, Yamamoto Takashi, Murai Junko, Hiraoka Masahiro, Koike Kaoru, Pommier Yves, Takeda Shunichi, Hirota Kouji
PLOS ONE 12 巻 ( 11 ) 頁： e0188320 2017年11月
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Doi Ryoichiro, Tsuchiya Tomoshi, Mitsutake Norisato, Nishimura Satoshi, Matsuu-Matsuyama Mutsumi, Nakazawa Yuka, Ogi Tomoo, Akita Sadanori, Yukawa Hiroshi, Baba Yoshinobu, Yamasaki Naoya, Matsumoto Keitaro, Miyazaki Takuro, Kamohara Ryotaro, Hatachi Go, Sengyoku Hideyori, Watanabe Hironosuke, Obata Tomohiro, Niklason Laura E., Nagayasu Takeshi
SCIENTIFIC REPORTS 7 巻 ( 1 ) 頁： 8447 2017年8月
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An XPA gene splicing mutation resulting in trace protein expression in an elderly patient with xeroderma pigmentosum group A without neurological abnormalities. 査読有り
Takahashi Y, Endo Y, Kusaka-Kikushima A, Nakamaura S, Nakazawa Y, Ogi T, Uryu M, Tsuji G, Furue M, Moriwaki S.
Br J Dermatol 177 巻 ( 1 ) 頁： 253-257 2017年5月
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PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast. 査読有り 国際共著
Daigaku Y, Etheridge TJ, Nakazawa Y, Nakayama M, Watson AT, Miyabe I, Ogi T, Osborne MA, Carr AM.
PLoS Genetics 13 巻 ( 5 ) 頁： e1006789 2017年5月
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A ten-year follow up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole genome sequencing. 査読有り
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 32 巻 頁： 174-180 2016年7月
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Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly- progressing radiosensitive-severe combined immunodeficiency. 査読有り
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§.
Journal of Clinical Immunology 160 巻 頁： 255-260 2015年10月
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Hypomorphic PCNA mutation underlies a human DNA repair disorder. 査読有り 国際共著
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§.
Journal of Clinical Investigation 124 巻 頁： 3137-3146 2014年7月
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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. 査読有り 国際共著
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 AMR§, O'Driscoll M§, Jeggo PA§.
PLoS Genetics 8 巻 頁： e1002945 2012年11月
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Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly. 査読有り
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 10 巻 頁： 314-321 2011年3月
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A semi-automated non-radioactive system for measuring recovery of RNA synthesis and unscheduled DNA synthesis using ethynyluracil derivatives. 査読有り 国際共著
Nakazawa Y, Yamashita S, Lehmann AR, Ogi T§.
DNA Repair 9 巻 頁： 506-516 2010年5月
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Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cells. 査読有り 国際共著
Ogi T§, Limsirichaikul S*, Overmeer R*, Volker M*, Takenaka K*, Cloney R*, Nakazawa Y*, Niimi A, Miki Y, Jaspers N, Mullenders L*, Yamashita S*, Fousteri M*, Lehmann AR§.
Molecular Cell 37 巻 頁： 714-727 2010年3月