Kết quả tìm kiếm - Katsuhiro Hanada
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Molecular genetics of RecQ helicase disorders Bằng Katsuhiro Hanada, Ian D. Hickson
Được phát hành 2007Revisão -
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Mechanisms of interstrand DNA crosslink repair and human disorders Bằng Satoru Hashimoto, Hirofumi Anai, Katsuhiro Hanada
Được phát hành 2016Revisão -
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RecQ DNA helicase is a suppressor of illegitimate recombination in <i>Escherichia coli</i> Bằng Katsuhiro Hanada, T. UKITA, Yuko Kohno, Kazue Saito, Junichi Kato, Hideo Ikeda
Được phát hành 1997Artigo -
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FBH1 co-operates with MUS81 in inducing DNA double-strand breaks and cell death following replication stress Bằng Kasper Fugger, Wai Kit Chu, Peter Haahr, Arne Nedergaard Kousholt, Halfdan Beck, Miranda Payne, Katsuhiro Hanada, Ian D. Hickson, Claus Storgaard Sørensen
Được phát hành 2013Artigo -
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The relationship between Helicobacter pylori infection and Alzheimer’s disease in Japan Bằng Seiji Shiota, Kazunari Murakami, Aoi Yoshiiwa, Kyoko Yamamoto, S. Ohno, Akiko Kuroda, Kazuhiro Mizukami, Katsuhiro Hanada, Tadayoshi Okimoto, Masaaki Kodama, Kou Abe, Yoshio Yamaoka, Toshio Fujioka
Được phát hành 2011Artigo -
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FBH1 Helicase Disrupts RAD51 Filaments in Vitro and Modulates Homologous Recombination in Mammalian Cells Bằng Jitka Šimandlová, Jennifer Zagelbaum, Miranda Payne, Wai Kit Chu, I. A. Shevelev, Katsuhiro Hanada, Sujoy Chatterjee, Dylan A. Reid, Ying Liu, Pavel Janščák, Eli Rothenberg, Ian D. Hickson
Được phát hành 2013Artigo -
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Perturbations of Vascular Homeostasis and Aortic Valve Abnormalities in Fibulin-4 Deficient Mice Bằng Katsuhiro Hanada, Marcel Vermeij, George A. Garinis, Monique C. de Waard, Maurice G.S. Kunen, Loretha Myers, Alex Maas, Dirk J. Duncker, Carel Meijers, Harry C. Dietz, Roland Kanaar, Jeroen Essers
Được phát hành 2007Artigo -
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Transcriptome analysis reveals cyclobutane pyrimidine dimers as a major source of UV-induced DNA breaks Bằng George A. Garinis, James R. Mitchell, Michael Moorhouse, Katsuhiro Hanada, Harm de Waard, Dimitri Vandeputte, Judith Jans, Karl Brand, Marcel Smid, Peter J. van der Spek, Jan H.J. Hoeijmakers, Roland Kanaar, Gijsbertus T. J. van der Horst
Được phát hành 2005Artigo -
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Digenic mutations in <i>ALDH2</i> and <i>ADH5</i> impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome Bằng Yasuyoshi Oka, Motoharu Hamada, Yuka Nakazawa, Hideki Muramatsu, Yusuke Okuno, Koichiro Higasa, Mayuko Shimada, Honoka Takeshima, Katsuhiro Hanada, Taichi Hirano, Toshiro Kawakita, Hirotoshi Sakaguchi, Takuya Ichimura, Shuichi Ozono, Kotaro Yuge, Yoriko Watanabe, Yuko Kotani, Mutsumi Yamane, Yumiko Kasugai, Miyako Tanaka, Takayoshi Suganami, Shinichiro Nakada, Norisato Mitsutake, Yuichiro Hara, Kohji Kato, Seiji Mizuno, Noriko Miyake, Yosuke Kawai, Katsushi Tokunaga, Masao Nagasaki, Seiji Kito, Keiichi Isoyama, Masafumi Onodera, Hideo Kaneko, Naomichi Matsumoto, Fumihiko Matsuda, Keitaro Matsuo, Yoshiyuki Takahashi, Tomoji Mashimo, Seiji Kojima, Tomoo Ogi
Được phát hành 2020Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
DNA
Gene
Cell biology
DNA damage
DNA repair
Homologous recombination
Molecular biology
Biochemistry
DNA replication
Genome instability
Helicase
Helicobacter pylori
Homologous chromosome
Immunology
Medicine
Nucleotide excision repair
RNA
Chemistry
Fanconi anemia
Gastroenterology
Internal medicine
Odds ratio
RAD51
RecQ helicase
Recombination
Replication (statistics)
Virology
ALDH2