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

Year Number of Results
2006 1
2007 2
2011 3
2012 6
2013 7
2014 6
2015 7
2016 10
2017 10
2018 9
2019 6
2020 7
2021 4
2022 6
2023 2
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77 results
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Page 1
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome.
Niihori T, Nagai K, Fujita A, Ohashi H, Okamoto N, Okada S, Harada A, Kihara H, Arbogast T, Funayama R, Shirota M, Nakayama K, Abe T, Inoue SI, Tsai IC, Matsumoto N, Davis EE, Katsanis N, Aoki Y. Niihori T, et al. Among authors: funayama r. Am J Hum Genet. 2019 Jun 6;104(6):1233-1240. doi: 10.1016/j.ajhg.2019.04.014. Epub 2019 May 23. Am J Hum Genet. 2019. PMID: 31130285 Free PMC article.
Phenotypic heterogeneity in individuals with MECOM variants in 2 families.
Niihori T, Tanoshima R, Sasahara Y, Sato A, Irie M, Saito-Nanjo Y, Funayama R, Shirota M, Abe T, Okuyama Y, Ishii N, Nakayama K, Kure S, Imaizumi M, Aoki Y. Niihori T, et al. Among authors: funayama r. Blood Adv. 2022 Sep 27;6(18):5257-5261. doi: 10.1182/bloodadvances.2020003812. Blood Adv. 2022. PMID: 35020829 Free PMC article. No abstract available.
Cellular senescence and chromatin structure.
Funayama R, Ishikawa F. Funayama R, et al. Chromosoma. 2007 Oct;116(5):431-40. doi: 10.1007/s00412-007-0115-7. Epub 2007 Jun 20. Chromosoma. 2007. PMID: 17579878 Review.
Wnt5a in cancer-associated fibroblasts promotes colorectal cancer progression.
Hirashima T, Karasawa H, Aizawa T, Suzuki T, Yamamura A, Suzuki H, Kajiwara T, Musha H, Funayama R, Shirota M, Ohnuma S, Nakayama K, Unno M. Hirashima T, et al. Among authors: funayama r. Biochem Biophys Res Commun. 2021 Sep 3;568:37-42. doi: 10.1016/j.bbrc.2021.06.062. Epub 2021 Jun 25. Biochem Biophys Res Commun. 2021. PMID: 34175688
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: funayama r. Ann Neurol. 2019 Jun;85(6):927-933. doi: 10.1002/ana.25481. Epub 2019 Apr 25. Ann Neurol. 2019. PMID: 30945334
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations.
Mitsuzawa S, Suzuki N, Akiyama T, Ishikawa M, Sone T, Kawada J, Funayama R, Shirota M, Mitsuhashi H, Morimoto S, Ikeda K, Shijo T, Ohno A, Nakamura N, Ono H, Ono R, Osana S, Nakagawa T, Nishiyama A, Izumi R, Kaneda S, Ikeuchi Y, Nakayama K, Fujii T, Warita H, Okano H, Aoki M. Mitsuzawa S, et al. Among authors: funayama r. Stem Cell Reports. 2021 Jun 8;16(6):1527-1541. doi: 10.1016/j.stemcr.2021.04.021. Epub 2021 May 27. Stem Cell Reports. 2021. PMID: 34048688 Free PMC article.
Biallelic GALM pathogenic variants cause a novel type of galactosemia.
Wada Y, Kikuchi A, Arai-Ichinoi N, Sakamoto O, Takezawa Y, Iwasawa S, Niihori T, Nyuzuki H, Nakajima Y, Ogawa E, Ishige M, Hirai H, Sasai H, Fujiki R, Shirota M, Funayama R, Yamamoto M, Ito T, Ohara O, Nakayama K, Aoki Y, Koshiba S, Fukao T, Kure S. Wada Y, et al. Among authors: funayama r. Genet Med. 2019 Jun;21(6):1286-1294. doi: 10.1038/s41436-018-0340-x. Epub 2018 Oct 19. Genet Med. 2019. PMID: 30451973 Free article.
77 results