PUBLICATIONS

2018

  1. Fratta P, Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Brito-Armas JM, Kalmar B, Ule A, Yu Y, Birsa N, Bodo C, Collins T, Conicella AE, Mejia Maza A, Marrero-Gagliardi A, Stewart M, Mianne J, Corrochano S, Emmett W, Codner G, Groves M, Fukumura R, Gondo Y, Lythgoe M, Pauws E, Peskett E, Stanier P, Teboul L, Hallegger M, Calvo A, Chiò A, Isaacs AM, Fawzi NL, Wang E, Housman DE, Baralle F, Greensmith L, Buratti E, Plagnol V, Fisher EM, Acevedo-Arozena A: Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. EMBO J. 2018 Jun 1;37(11). pii: e98684. doi: 10.15252/embj.201798684. Epub 2018 May 15.

2017年

  1. Li B, Qing T, Zhu J, Wen Z, Yu Y, Fukumura R, Zheng Y, Gondo Y, Shi L: A Comprehensive Mouse Transcriptomic BodyMap across 17 Tissues by RNA-seq. Sci Rep. 2017 Jun 23;7(1):4200. doi: 10.1038/s41598-017-04520-z.

2016年

  1. Makino S, Fukumura R, Gondo Y: Illegitimate translation causes unexpected gene expression from on-target out-of-frame alleles created by CRISPR-Cas9. Sci Rep. 2016 Dec 21;6:39608. doi: 10.1038/srep39608. [プレスリリース：http://www.riken.jp/pr/press/2016/20161226_2/]
  2. Ichimura S, Sasaki S, Murata T, Fukumura R, Gondo Y, Ikegawa S, Furuichi T: An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes. Exp Anim. 2017 May 3;66(2):137-144. doi: 10.1538/expanim.16-0085. Epub 2016 Dec 8.
  3. Masumura K, Toyoda-Hokaiwado N, Ukai A, Gondo Y, Honma M, Nohmi T: Dose-dependent de novo germline mutations detected by whole-exome sequencing in progeny of ENU-treated male gpt delta mice. Mutat Res. 2016 Nov 1;810:30-39. doi: 10.1016/j.mrgentox.2016.09.009. Epub 2016 Sep 28.
  4. Masumura K, Toyoda-Hokaiwado N, Ukai A, Gondo Y, Honma M, Nohmi T: Estimation of the frequency of inherited germline mutations by whole exome sequencing in ethyl nitrosourea-treated and untreated gpt delta mice. Genes Environ. 2016 Apr 1;38:10. doi: 10.1186/s41021-016-0035-y. eCollection 2016.
  5. Toki H, Minowa O, Inoue M, Motegi H, Karashima Y, Ikeda A, Kaneda H, Sakuraba Y, Saiki Y, Wakana S, Suzuki H, Gondo Y, Shiroishi T, Noda T: Novel allelic mutations in murine Serca2 induce differential development of squamous cell tumors. Biochem Biophys Res Commun. 2016 Aug 5;476(4):175-182. doi: 10.1016/j.bbrc.2016.04.136. Epub 2016 Apr 27.
  6. Inoue M, Toki H, Matsui J, Togashi Y, Dobashi A, Fukumura R, Gondo Y, Minowa O, Tanaka N, Mori S, Takeuchi K, Noda T: Mouse models for ROS1-fusion-positive lung cancers and their application to the analysis of multikinase inhibitor efficiency. Carcinogenesis. 2016 May;37(5):452-60. doi: 10.1093/carcin/bgw028. Epub 2016 Mar 10.
  7. Kim YJ, Kang Y, Park HY, Lee JR, Yu DY, Murata T, Gondo Y, Hwang JH, Kim YH, Lee CH, Rhee M, Han PL, Chung BH, Lee HJ, Kim KS: STEP signaling pathway mediates psychomotor stimulation and morphine withdrawal symptoms, but not for reward, analgesia and tolerance. Exp Mol Med. 2016 Feb 26;48:e212. doi: 10.1038/emm.2016.1.

2015年

  1. Mun HS, Saab BJ, Ng E, McGirr A, Lipina TV, Gondo Y, Georgiou J, Roder JC: Self-directed exploration provides a Ncs1-dependent learning bonus. Sci Rep. 2015 Dec 7;5:17697. doi: 10.1038/srep17697.
  2. Shibata N, Ohoka N, Sugaki Y, Onodera C, Inoue M, Sakuraba Y, Takakura D, Hashii N, Kawasaki N, Gondo Y, Naito M: Degradation of Stop Codon Read-through Mutant Proteins via the Ubiquitin-Proteasome System Causes Hereditary Disorders. J Biol Chem. 2015 Nov 20;290(47):28428-37. doi: 10.1074/jbc.M115.670901. Epub 2015 Oct 6.
  3. Sakamaki A, Katsuragi Y, Otsuka K, Tomita M, Obata M, Iwasaki T, Abe M, Sato T, Ochiai M, Sakuraba Y, Aoyagi Y, Gondo Y, Sakimura K, Nakagama H, Mishima Y, Kominami R: Bcl11b SWI/SNF-complex subunit modulates intestinal adenoma and regeneration after γ-irradiation through Wnt/β-catenin pathway. Carcinogenesis. 2015 Jun;36(6):622-31. doi: 10.1093/carcin/bgv044. Epub 2015 Mar 31.
  4. Makino S, Zhulyn O, Mo R, Puviindran V, Zhang X, Murata T, Fukumura R, Ishitsuka Y, Kotaki H, Matsumaru D, Ishii S, Hui CC, Gondo Y: T396I mutation of mouse Sufu reduces the stability and activity of Gli3 repressor. PLoS One. 2015 Mar 11;10(3):e0119455. doi: 10.1371/journal.pone.0119455. eCollection 2015.[プレスリリース http://www.riken.jp/pr/press/2015/20150312_1/]
  5. Hirose S, Touma M, Go R, Katsuragi Y, Sakuraba Y, Gondo Y, Abe M, Sakimura K, Mishima Y, Kominami R: Bcl11b prevents the intrathymic development of innate CD8 T cells in a cell intrinsic manner. Int Immunol. 2015 Apr;27(4):205-15. doi: 10.1093/intimm/dxu104. Epub 2014 Nov 24.

2014年

  1. Arime Y, Fukumura R, Miura I, Mekada K, Yoshiki A, Wakana S, Gondo Y, Akiyama K: Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice. Behav Brain Funct. 2014 Dec 8;10:45. doi: 10.1186/1744-9081-10-45.
  2. Murata T, Ishitsuka Y, Karouji K, Kaneda H, Toki H, Nakai Y, Makino S, Fukumura R, Kotaki H, Wakana S, Noda T, Gondo Y: β-CateninC429S mice exhibit sterility consequent to spatiotemporally sustained Wnt signalling in the internal genitalia. Sci Rep. 2014 Nov 7;4:6959. doi: 10.1038/srep06959.
  3. SEQC/MAQC-III Consortium: A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. Nat Biotechnol. 2014 Sep;32(9):903-14. doi: 10.1038/nbt.2957. Epub 2014 Aug 24.
  4. Toki H, Inoue M, Minowa O, Motegi H, Saiki Y, Wakana S, Masuya H, Gondo Y, Shiroishi T, Yao R, Noda T: Novel retinoblastoma mutation abrogating the interaction to E2F2/3, but not E2F1, led to selective suppression of thyroid tumors. Cancer Sci. 2014 Oct;105(10):1360-8. doi: 10.1111/cas.12495. Epub 2014 Sep 29.
  5. Ohno M, Sakumi K, Fukumura R, Furuichi M, Iwasaki Y, Hokama M, Ikemura T, Tsuzuki T, Gondo Y, Nakabeppu Y: 8-oxoguanine causes spontaneous de novo germline mutations in mice. Sci Rep. 2014 Apr 15;4:4689. doi: 10.1038/srep04689.[プレスリリース http://ja.brc.riken.jp/news/guide_20140416_02.html][http://www.bioreg.kyushu-u.ac.jp/mib/topics/pressrelease/2014_04_14.pdf][ https://www.nagahama-i-bio.ac.jp/research/池村淑道客員教授・名誉教授らの研究成果が国際/]
  6. Ohnishi T, Murata T, Watanabe A, Hida A, Ohba H, Iwayama Y, Mishima K, Gondo Y, Yoshikawa T: Defective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis. J Biol Chem. 2014 Apr 11;289(15):10785-96. doi: 10.1074/jbc.M113.536706. Epub 2014 Feb 19.

2013年

  1. more to come, shortly...