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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2004 2
2005 7
2006 6
2007 8
2008 8
2009 7
2010 3
2012 3
2013 5
2014 9
2015 7
2016 11
2017 8
2018 5
2019 10
2020 5
2021 7
2022 9
2023 11
2024 9
2025 7
2026 1

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131 results

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Page 1
Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer.
Soda M, Choi YL, Enomoto M, Takada S, Yamashita Y, Ishikawa S, Fujiwara S, Watanabe H, Kurashina K, Hatanaka H, Bando M, Ohno S, Ishikawa Y, Aburatani H, Niki T, Sohara Y, Sugiyama Y, Mano H. Soda M, et al. Among authors: takada s. Nature. 2007 Aug 2;448(7153):561-6. doi: 10.1038/nature05945. Epub 2007 Jul 11. Nature. 2007. PMID: 17625570
RNA-Based Therapeutic Technology.
Mashima R, Takada S, Miyamoto Y. Mashima R, et al. Among authors: takada s. Int J Mol Sci. 2023 Oct 16;24(20):15230. doi: 10.3390/ijms242015230. Int J Mol Sci. 2023. PMID: 37894911 Free PMC article. Review.
STAT6 gain-of-function variant exacerbates multiple allergic symptoms.
Takeuchi I, Yanagi K, Takada S, Uchiyama T, Igarashi A, Motomura K, Hayashi Y, Nagano N, Matsuoka R, Sugiyama H, Yoshioka T, Saito H, Kawai T, Miyaji Y, Inuzuka Y, Matsubara Y, Ohya Y, Shimizu T, Matsumoto K, Arai K, Nomura I, Kaname T, Morita H. Takeuchi I, et al. Among authors: takada s. J Allergy Clin Immunol. 2023 May;151(5):1402-1409.e6. doi: 10.1016/j.jaci.2022.12.802. Epub 2022 Dec 17. J Allergy Clin Immunol. 2023. PMID: 36538978
TEAD1 trapping by the Q353R-Lamin A/C causes dilated cardiomyopathy.
Yamada S, Ko T, Ito M, Sassa T, Nomura S, Okuma H, Sato M, Imasaki T, Kikkawa S, Zhang B, Yamada T, Seki Y, Fujita K, Katoh M, Kubota M, Hatsuse S, Katagiri M, Hayashi H, Hamano M, Takeda N, Morita H, Takada S, Toyoda M, Uchiyama M, Ikeuchi M, Toyooka K, Umezawa A, Yamanishi Y, Nitta R, Aburatani H, Komuro I. Yamada S, et al. Among authors: takada s. Sci Adv. 2023 Apr 14;9(15):eade7047. doi: 10.1126/sciadv.ade7047. Epub 2023 Apr 14. Sci Adv. 2023. PMID: 37058558 Free PMC article.
LMNA Q353R Mutation Causes Dilated Cardiomyopathy Through Impaired Vitamin D Signaling.
Ito M, Katoh M, Sassa T, Ko T, Fujita K, Yamada S, Miura K, Toyoda M, Takada S, Tobita T, Katagiri M, Kubota M, Yamada T, Hatsuse S, Morita H, Ikeuchi M, Matsuura K, Umezawa A, Nomura S, Aburatani H, Komuro I. Ito M, et al. Among authors: takada s. Circulation. 2024 Sep 17;150(12):971-974. doi: 10.1161/CIRCULATIONAHA.124.069972. Epub 2024 Sep 16. Circulation. 2024. PMID: 39283931 No abstract available.
JAK1 gain-of-function variant causes alopecia areata, atopic dermatitis, and autoimmune thyroid disease.
Fujita S, Kabashima S, Yanagi K, Toyokuni K, Yoshida K, Miyaji Y, Takada S, Motomura K, Tamari M, Nakazaki H, Hayashi Y, Nagano N, Uchiyama T, Oishi K, Yokoya S, Yoshioka T, Tanase-Nakao K, Yamamoto-Hanada K, Fukuie T, Horikawa R, Saito H, Matsubara Y, Ohya Y, Kaname T, Matsumoto K, Morita H. Fujita S, et al. Among authors: takada s. J Allergy Clin Immunol. 2025 Dec;156(6):1769-1771. doi: 10.1016/j.jaci.2025.09.012. Epub 2025 Oct 14. J Allergy Clin Immunol. 2025. PMID: 41085498 No abstract available.
Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome.
Kawai T, Kinoshita S, Takayama Y, Ohnishi E, Kamura H, Kojima K, Kikuchi H, Terao M, Sugawara T, Migita O, Kagami M, Isojima T, Yamaguchi Y, Wakui K, Ohashi H, Shimizu K, Mizuno S, Okamoto N, Fukushima Y, Takada F, Kosaki K, Takada S, Akutsu H, Ura K, Nakabayashi K, Hata K. Kawai T, et al. Among authors: takada s. Genet Med Open. 2024 Mar 14;2:101838. doi: 10.1016/j.gimo.2024.101838. eCollection 2024. Genet Med Open. 2024. PMID: 39669601 Free PMC article.
Correction of the Murine Model of Congenital Heart Disease Associated With the Nkx2-5 Mutation Using Prime Editing.
Ko T, Nishijo D, Tsuji-Hosokawa A, Tsuchiya I, Nomura S, Zhang B, Jiang Y, Fujimori K, Hiruma T, Abe R, Jimba T, Inoue S, Dai Z, Katoh M, Katagiri M, Ito M, Morita H, Takada S, Takeda N, Umezawa A, Komuro I. Ko T, et al. Among authors: takada s. Circ Genom Precis Med. 2025 Aug;18(4):e005194. doi: 10.1161/CIRCGEN.124.005194. Epub 2025 Jun 9. Circ Genom Precis Med. 2025. PMID: 40485469 No abstract available.
131 results