Kota Tamada - Publications

Affiliations: 
Hiroshima University, Higashihiroshima-shi, Hiroshima-ken, Japan 
Area:
mental illness, autism

19 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Takumi T, Tamada K, Hatanaka F, Nakai N, Bolton PF. Behavioral neuroscience of autism. Neuroscience and Biobehavioral Reviews. PMID 31059731 DOI: 10.1016/j.neubiorev.2019.04.012  0.96
2019 Mori K, Tamada K, Kurooka H, Matsui M, Takumi T, Yokota Y. Gene expression profile data of the developing small intestine of -deficient mice. Data in Brief. 24: 103717. PMID 30984807 DOI: 10.1016/j.dib.2019.103717  0.96
2019 Furumai R, Tamada K, Liu X, Takumi T. UBE3A regulates the transcription of IRF, an anti-viral immunity. Human Molecular Genetics. PMID 30690483 DOI: 10.1093/hmg/ddz019  0.96
2018 Mori K, Nakamura H, Kurooka H, Miyachi H, Tamada K, Sugai M, Takumi T, Yokota Y. Id2 determines intestinal identity through repression of the foregut transcription factor, Irx5. Molecular and Cellular Biology. PMID 29463648 DOI: 10.1128/MCB.00250-17  0.96
2018 Takumi T, Tamada K. CNV biology in neurodevelopmental disorders. Current Opinion in Neurobiology. 48: 183-192. PMID 29331932 DOI: 10.1016/j.conb.2017.12.004  0.96
2017 Fukumoto K, Tamada K, Toya T, Nishino T, Yanagawa Y, Takumi T. Identification of genes regulating GABAergic interneuron maturation. Neuroscience Research. PMID 29203264 DOI: 10.1016/j.neures.2017.11.010  0.96
2017 Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T. Correction: Functional significance of rare neuroligin 1 variants found in autism. Plos Genetics. 13: e1007035. PMID 28972980 DOI: 10.1371/journal.pgen.1007035  0.96
2017 Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T. Functional significance of rare neuroligin 1 variants found in autism. Plos Genetics. 13: e1006940. PMID 28841651 DOI: 10.1371/journal.pgen.1006940  0.96
2017 Nakai N, Nagano M, Saitow F, Watanabe Y, Kawamura Y, Kawamoto A, Tamada K, Mizuma H, Onoe H, Watanabe Y, Monai H, Hirase H, Nakatani J, Inagaki H, Kawada T, et al. Serotonin rebalances cortical tuning and behavior linked to autism symptoms in 15q11-13 CNV mice. Science Advances. 3: e1603001. PMID 28691086 DOI: 10.1126/sciadv.1603001  0.96
2017 Kishimoto K, Nomura J, Ellegood J, Fukumoto K, Lerch JP, Moreno-De-Luca D, Bourgeron T, Tamada K, Takumi T. Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. PMID 28370817 DOI: 10.1111/gtc.12487  0.96
2017 Nishita M, Park SY, Nishio T, Kamizaki K, Wang Z, Tamada K, Takumi T, Hashimoto R, Otani H, Pazour GJ, Hsu VW, Minami Y. Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness. Scientific Reports. 7: 1. PMID 28127051 DOI: 10.1038/s41598-016-0028-x  0.96
2015 Liu X, Tamada K, Kishimoto R, Okubo H, Ise S, Ohta H, Ruf S, Nakatani J, Kohno N, Spitz F, Takumi T. Transcriptome profiling of white adipose tissue in a mouse model for 15q duplication syndrome. Genomics Data. 5: 394-6. PMID 26484295 DOI: 10.1016/j.gdata.2015.06.035  0.52
2015 Kishimoto R, Tamada K, Liu X, Okubo H, Ise S, Ohta H, Ruf S, Nakatani J, Kohno N, Spitz F, Takumi T. Model mice for 15q11-13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism. Human Molecular Genetics. PMID 26002101 DOI: 10.1093/hmg/ddv187  0.52
2015 Tamada K, Takumi T. Serotonin disturbance in mouse models of autism spectrum disorders Neuromethods. 100: 239-262. DOI: 10.1007/978-1-4939-2250-5_9  0.96
2011 Tamada K, Nakai N, Takumi T. [Humanized mouse model of autism]. Seikagaku. the Journal of Japanese Biochemical Society. 83: 841-5. PMID 22111376  0.52
2011 Kim W, Matsui T, Yamao M, Ishibashi M, Tamada K, Takumi T, Kohno K, Oba S, Ishii S, Sakumura Y, Bessho Y. The period of the somite segmentation clock is sensitive to Notch activity. Molecular Biology of the Cell. 22: 3541-9. PMID 21795391 DOI: 10.1091/mbc.E11-02-0139  0.52
2010 Tamada K, Tomonaga S, Hatanaka F, Nakai N, Takao K, Miyakawa T, Nakatani J, Takumi T. Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling. Plos One. 5: e15126. PMID 21179543 DOI: 10.1371/journal.pone.0015126  0.52
2009 Nakatani J, Tamada K, Hatanaka F, Ise S, Ohta H, Inoue K, Tomonaga S, Watanabe Y, Chung YJ, Banerjee R, Iwamoto K, Kato T, Okazawa M, Yamauchi K, Tanda K, et al. Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism. Cell. 137: 1235-46. PMID 19563756 DOI: 10.1016/j.cell.2009.04.024  0.52
2009 Enomoto M, Hayakawa S, Itsukushima S, Ren DY, Matsuo M, Tamada K, Oneyama C, Okada M, Takumi T, Nishita M, Minami Y. Autonomous regulation of osteosarcoma cell invasiveness by Wnt5a/Ror2 signaling. Oncogene. 28: 3197-208. PMID 19561643 DOI: 10.1038/onc.2009.175  0.52
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