YEAR
- 2012.02.02 Epigenetic regulation of osteoclast differentiation. Yasui T, Hirose J, Aburatani H, Tanaka S.Ann. N. Y. Acad. Sci. 2011 Dec;1240:7-13. doi: 10.1111/j.1749-6632.2011.06245.x
- 2012.01.29 G-protein-coupled receptor inactivation by an allosteric inverse-agonist antibody. Hino T, Arakawa T, Iwanari H, Yurugi-Kobayashi T, Ikeda-Suno C, Nakada-Nakura Y, Kusano-Arai O, Weyand S, Shimamura T, Nomura N, Cameron AD, Kobayashi T, Hamakubo T, Iwata S, Murata T.Nature. 2012 Jan 29;482(7384):237-40. doi: 10.1038/nature10750
- 2012.01.25 The proteomic profile of circulating pentraxin 3 (PTX3) complex in sepsis demonstrates the interaction with azurocidin 1 and other components of neutrophil extracellular traps. Daigo K, Yamaguchi N, Kawamura T, Matsubara K, Jiang S, Ohashi R, Sudou Y, Kodama T, Naito M, Inoue K, Hamakubo T.Mol. Cell Proteomics. 2012 Jun;11(6):M111.015073. doi: 10.1074/mcp.M111.015073
- 2012.01.22 Crystal structure of the channelrhodopsin light-gated cation channel. Kato HE, Zhang F, Yizhar O, Ramakrishnan C, Nishizawa T, Hirata K, Ito J, Aita Y, Tsukazaki T, Hayashi S, Hegemann P, Maturana AD, Ishitani R, Deisseroth K, Nureki O.Nature. 2012 Jan 22;482(7385):369-74. doi: 10.1038/nature10870
- 2012.01.06 Insights into the mechanism of proton transport in cytochrome c oxidase. Yamashita T, Voth GA.J. Am. Chem. Soc. 2012 Jan 18;134(2):1147-52. doi: 10.1021/ja209176e
- 2012.01.03 Severe dermatitis with loss of epidermal Langerhans cells in human and mouse zinc deficiency. Kawamura T, Ogawa Y, Nakamura Y, Nakamizo S, Ohta Y, Nakano H, Kabashima K, Katayama I, Koizumi S, Kodama T, Nakao A, Shimada S.J. Clin. Invest. 2012 Feb;122(2):722-32. doi: 10.1172/JCI58618
- 2012.01.01 Theoretical Study on the Photocyclization Mechanism of Diarylethenes with Transition Metal Substituents M. Hatakeyama, S. Yokojima, K. Shinoda, T. Koike, M. Akita, S. NakamuraJ. Am. Chem. Soc. 2004, 126, 38, 12112–12120 doi: 10.1021/ja035035o
- 2011.12.07 Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency. Wang L, Tsutsumi S, Kawaguchi T, Nagasaki K, Tatsuno K, Yamamoto S, Sang F, Sonoda K, Sugawara M, Saiura A, Hirono S, Yamaue H, Miki Y, Isomura M, Totoki Y, Nagae G, Isagawa T, Ueda H, Murayama-Hosokawa S, Shibata T, Sakamoto H, Kanai Y, Kaneda A, Noda T, Aburatani H.Genome Res. 2012 Feb;22(2):208-19. doi: 10.1101/gr.123109.111
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