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

Year Number of Results
2002 3
2004 2
2005 1
2006 2
2007 2
2012 3
2013 3
2014 3
2017 5
2018 6
2019 9
2020 10
2021 15
2022 11
2023 7
2024 6

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75 results

Results by year

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Page 1
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: yanagi k. 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
Four pedigrees with aminoacyl-tRNA synthetase abnormalities.
Okamoto N, Miya F, Tsunoda T, Kanemura Y, Saitoh S, Kato M, Yanagi K, Kaname T, Kosaki K. Okamoto N, et al. Among authors: yanagi k. Neurol Sci. 2022 Apr;43(4):2765-2774. doi: 10.1007/s10072-021-05626-z. Epub 2021 Sep 28. Neurol Sci. 2022. PMID: 34585293
HECW2-related disorder in four Japanese patients.
Yanagishita T, Hirade T, Shimojima Yamamoto K, Funatsuka M, Miyamoto Y, Maeda M, Yanagi K, Kaname T, Nagata S, Nagata M, Ishihara Y, Miyashita Y, Asano Y, Sakata Y, Kosaki K, Yamamoto T. Yanagishita T, et al. Among authors: yanagi k. Am J Med Genet A. 2021 Oct;185(10):2895-2902. doi: 10.1002/ajmg.a.62363. Epub 2021 May 28. Am J Med Genet A. 2021. PMID: 34047014
HIST1H1E syndrome with deficiency in multiple pituitary hormones.
Tanabe Y, Nomura N, Minami M, Takaya J, Okamoto N, Yanagi K, Kaname T, Fujii Y, Kaneko K. Tanabe Y, et al. Among authors: yanagi k. Clin Pediatr Endocrinol. 2023;32(3):195-198. doi: 10.1297/cpe.2023-0002. Epub 2023 Mar 7. Clin Pediatr Endocrinol. 2023. PMID: 37362168 Free PMC article. No abstract available.
Imaging immune surveillance by T cells and NK cells.
McCann FE, Suhling K, Carlin LM, Eleme K, Taner SB, Yanagi K, Vanherberghen B, French PM, Davis DM. McCann FE, et al. Among authors: yanagi k. Immunol Rev. 2002 Nov;189:179-92. doi: 10.1034/j.1600-065x.2002.18915.x. Immunol Rev. 2002. PMID: 12445274 Review.
Recurrent de novo MAPK8IP3 variants cause neurological phenotypes.
Iwasawa S, Yanagi K, Kikuchi A, Kobayashi Y, Haginoya K, Matsumoto H, Kurosawa K, Ochiai M, Sakai Y, Fujita A, Miyake N, Niihori T, Shirota M, Funayama R, Nonoyama S, Ohga S, Kawame H, Nakayama K, Aoki Y, Matsumoto N, Kaname T, Matsubara Y, Shoji W, Kure S. Iwasawa S, et al. Among authors: yanagi k. Ann Neurol. 2019 Jun;85(6):927-933. doi: 10.1002/ana.25481. Epub 2019 Apr 25. Ann Neurol. 2019. PMID: 30945334
Novel NARS2 variant causing leigh syndrome with normal lactate levels.
Tanaka R, Takeguchi R, Kuroda M, Suzuki N, Makita Y, Yanagi K, Kaname T, Takahashi S. Tanaka R, et al. Among authors: yanagi k. Hum Genome Var. 2022 May 4;9(1):12. doi: 10.1038/s41439-022-00191-z. Hum Genome Var. 2022. PMID: 35508527 Free PMC article.
75 results