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

Year Number of Results
1963 1
1969 1
1970 1
1972 1
1973 2
1974 1
1976 2
1977 1
1979 1
1980 1
1982 1
1984 4
1985 4
1986 3
1987 3
1988 3
1989 1
1990 3
1991 4
1992 3
1993 4
1994 6
1995 12
1996 7
1997 8
1998 21
1999 13
2000 17
2001 18
2002 21
2003 25
2004 19
2005 18
2006 15
2007 19
2008 20
2009 23
2010 9
2011 26
2012 29
2013 37
2014 18
2015 31
2016 28
2017 26
2018 27
2019 38
2020 34
2021 49
2022 31
2023 23
2024 24

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672 results

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Page 1
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
Kuro-o M, Matsumura Y, Aizawa H, Kawaguchi H, Suga T, Utsugi T, Ohyama Y, Kurabayashi M, Kaname T, Kume E, Iwasaki H, Iida A, Shiraki-Iida T, Nishikawa S, Nagai R, Nabeshima YI. Kuro-o M, et al. Among authors: iida a. Nature. 1997 Nov 6;390(6655):45-51. doi: 10.1038/36285. Nature. 1997. PMID: 9363890
The Clinical Application of Hydrogen as a Medical Treatment.
Iida A, Nosaka N, Yumoto T, Knaup E, Naito H, Nishiyama C, Yamakawa Y, Tsukahara K, Terado M, Sato K, Ugawa T, Nakao A. Iida A, et al. Acta Med Okayama. 2016 Oct;70(5):331-337. doi: 10.18926/AMO/54590. Acta Med Okayama. 2016. PMID: 27777424 Free article. Review.
Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis.
Kawai Y, Watanabe Y, Omae Y, Miyahara R, Khor SS, Noiri E, Kitajima K, Shimanuki H, Gatanaga H, Hata K, Hattori K, Iida A, Ishibashi-Ueda H, Kaname T, Kanto T, Matsumura R, Miyo K, Noguchi M, Ozaki K, Sugiyama M, Takahashi A, Tokuda H, Tomita T, Umezawa A, Watanabe H, Yoshida S, Goto YI, Maruoka Y, Matsubara Y, Niida S, Mizokami M, Tokunaga K. Kawai Y, et al. Among authors: iida a. PLoS Genet. 2023 Dec 7;19(12):e1010625. doi: 10.1371/journal.pgen.1010625. eCollection 2023 Dec. PLoS Genet. 2023. PMID: 38060463 Free PMC article.
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling.
Guo L, Iida A, Bhavani GS, Gowrishankar K, Wang Z, Xue JY, Wang J, Miyake N, Matsumoto N, Hasegawa T, Iizuka Y, Matsuda M, Nakashima T, Takechi M, Iseki S, Yambe S, Nishimura G, Koseki H, Shukunami C, Girisha KM, Ikegawa S. Guo L, et al. Among authors: iida a. Nat Commun. 2021 Apr 6;12(1):2046. doi: 10.1038/s41467-021-22340-8. Nat Commun. 2021. PMID: 33824347 Free PMC article.
SLC4A2 Deficiency Causes a New Type of Osteopetrosis.
Xue JY, Grigelioniene G, Wang Z, Nishimura G, Iida A, Matsumoto N, Tham E, Miyake N, Ikegawa S, Guo L. Xue JY, et al. Among authors: iida a. J Bone Miner Res. 2022 Feb;37(2):226-235. doi: 10.1002/jbmr.4462. Epub 2021 Nov 11. J Bone Miner Res. 2022. PMID: 34668226 Free article.
Occult Sources of Bleeding in Blunt Trauma : A Narrative Review.
Yumoto T, Kosaki Y, Yamakawa Y, Iida A, Yamamoto H, Yamada T, Tsukahara K, Naito H, Osako T, Nakao A. Yumoto T, et al. Among authors: iida a. Acta Med Okayama. 2017 Oct;71(5):363-368. doi: 10.18926/AMO/55433. Acta Med Okayama. 2017. PMID: 29042693 Free article. Review.
RILPL1-related OPDM is absent in a Japanese cohort.
Eura N, Iida A, Ogasawara M, Hayashi S, Noguchi S, Nishino I. Eura N, et al. Among authors: iida a. Am J Hum Genet. 2022 Nov 3;109(11):2088-2089. doi: 10.1016/j.ajhg.2022.10.005. Am J Hum Genet. 2022. PMID: 36332612 Free PMC article. No abstract available.
672 results