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

Year Number of Results
2002 3
2003 5
2004 14
2005 6
2006 8
2007 7
2008 7
2009 1
2010 4
2011 7
2012 14
2013 28
2014 31
2015 34
2016 32
2017 27
2018 32
2019 22
2020 31
2021 42
2022 33
2023 10
2024 7

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336 results

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Page 1
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity.
Moriya K, Nakano T, Honda Y, Tsumura M, Ogishi M, Sonoda M, Nishitani-Isa M, Uchida T, Hbibi M, Mizoguchi Y, Ishimura M, Izawa K, Asano T, Kakuta F, Abukawa D, Rinchai D, Zhang P, Kambe N, Bousfiha A, Yasumi T, Boisson B, Puel A, Casanova JL, Nishikomori R, Ohga S, Okada S, Sasahara Y, Kure S. Moriya K, et al. Among authors: kure s. J Exp Med. 2023 Sep 4;220(9):e20212276. doi: 10.1084/jem.20212276. Epub 2023 Jun 5. J Exp Med. 2023. PMID: 37273177 Free PMC article.
Gut microbiome-derived phenyl sulfate contributes to albuminuria in diabetic kidney disease.
Kikuchi K, Saigusa D, Kanemitsu Y, Matsumoto Y, Thanai P, Suzuki N, Mise K, Yamaguchi H, Nakamura T, Asaji K, Mukawa C, Tsukamoto H, Sato T, Oikawa Y, Iwasaki T, Oe Y, Tsukimi T, Fukuda NN, Ho HJ, Nanto-Hara F, Ogura J, Saito R, Nagao S, Ohsaki Y, Shimada S, Suzuki T, Toyohara T, Mishima E, Shima H, Akiyama Y, Akiyama Y, Ichijo M, Matsuhashi T, Matsuo A, Ogata Y, Yang CC, Suzuki C, Breeggemann MC, Heymann J, Shimizu M, Ogawa S, Takahashi N, Suzuki T, Owada Y, Kure S, Mano N, Soga T, Wada T, Kopp JB, Fukuda S, Hozawa A, Yamamoto M, Ito S, Wada J, Tomioka Y, Abe T. Kikuchi K, et al. Among authors: kure s. Nat Commun. 2019 Apr 23;10(1):1835. doi: 10.1038/s41467-019-09735-4. Nat Commun. 2019. PMID: 31015435 Free PMC article.
Infantile tullio phenomenon.
Kakisaka Y, Hino-Fukuyo N, Miyazaki H, Kure S. Kakisaka Y, et al. Among authors: kure s. J Pediatr. 2013 Apr;162(4):880. doi: 10.1016/j.jpeds.2012.10.049. Epub 2012 Dec 7. J Pediatr. 2013. PMID: 23219447 No abstract available.
Tohoku Medical Megabank Brain Magnetic Resonance Imaging Study: Rationale, Design, and Background.
Taira M, Mugikura S, Mori N, Hozawa A, Saito T, Nakamura T, Kiyomoto H, Kobayashi T, Ogishima S, Nagami F, Uruno A, Shimizu R, Kobayashi T, Yasuda J, Kure S, Sakurai M, Motoike IN, Kumada K, Nakaya N, Obara T, Oba K, Sekiguchi A, Thyreau B, Mutoh T, Takano Y, Abe M, Maikusa N, Tatewaki Y, Taki Y, Yaegashi N, Tomita H, Kinoshita K, Kuriyama S, Fuse N, Yamamoto M. Taira M, et al. Among authors: kure s. JMA J. 2023 Jul 14;6(3):246-264. doi: 10.31662/jmaj.2022-0220. Epub 2023 Jun 30. JMA J. 2023. PMID: 37560377 Free PMC article. Review.
Gingival Pigmentation in a Boy.
Nakagawa T, Wada Y, Miura A, Numata-Uematsu Y, Niizuma H, Kure S. Nakagawa T, et al. Among authors: kure s. J Pediatr. 2021 Jul;234:274-275. doi: 10.1016/j.jpeds.2021.03.052. Epub 2021 Mar 29. J Pediatr. 2021. PMID: 33794216 No abstract available.
GATA2 haploinsufficiency accelerates EVI1-driven leukemogenesis.
Katayama S, Suzuki M, Yamaoka A, Keleku-Lukwete N, Katsuoka F, Otsuki A, Kure S, Engel JD, Yamamoto M. Katayama S, et al. Among authors: kure s. Blood. 2017 Aug 17;130(7):908-919. doi: 10.1182/blood-2016-12-756767. Epub 2017 Jun 19. Blood. 2017. PMID: 28630119 Free article.
COVID-19 Transmission at Schools in Japan.
Akaishi T, Kushimoto S, Katori Y, Sugawara N, Igarashi K, Fujita M, Kure S, Takayama S, Abe M, Tanaka J, Kikuchi A, Abe Y, Imai H, Inaba Y, Iwamatsu-Kobayashi Y, Nishioka T, Onodera K, Ishii T. Akaishi T, et al. Among authors: kure s. Tohoku J Exp Med. 2021 Nov;255(3):239-246. doi: 10.1620/tjem.255.239. Tohoku J Exp Med. 2021. PMID: 34803121 Free article.
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.
Kamada F, Aoki Y, Narisawa A, Abe Y, Komatsuzaki S, Kikuchi A, Kanno J, Niihori T, Ono M, Ishii N, Owada Y, Fujimura M, Mashimo Y, Suzuki Y, Hata A, Tsuchiya S, Tominaga T, Matsubara Y, Kure S. Kamada F, et al. Among authors: kure s. J Hum Genet. 2011 Jan;56(1):34-40. doi: 10.1038/jhg.2010.132. Epub 2010 Nov 4. J Hum Genet. 2011. PMID: 21048783
336 results