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

Year Number of Results
1962 2
1964 1
1965 4
1966 7
1967 1
1968 1
1969 5
1970 3
1972 1
1974 2
1975 1
1976 11
1977 9
1978 8
1979 13
1980 10
1981 14
1982 7
1983 13
1984 21
1985 14
1986 12
1987 17
1988 14
1989 14
1990 14
1991 24
1992 26
1993 23
1994 17
1995 14
1996 23
1997 20
1998 14
1999 19
2000 11
2001 24
2002 13
2003 23
2004 29
2005 32
2006 42
2007 38
2008 36
2009 43
2010 39
2011 51
2012 37
2013 37
2014 34
2015 34
2016 34
2017 48
2018 38
2019 45
2020 24
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Article type
Publication date

Search Results

1,035 results
Results by year
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Page 1
Impact of Sarcopenia as a Prognostic Biomarker of Bladder Cancer.
Fukushima H, Takemura K, Suzuki H, Koga F. Fukushima H, et al. Int J Mol Sci. 2018 Oct 1;19(10):2999. doi: 10.3390/ijms19102999. Int J Mol Sci. 2018. PMID: 30275370 Free PMC article. Review.
Targeted in vivo epigenome editing of H3K27me3.
Fukushima HS, Takeda H, Nakamura R. Fukushima HS, et al. Epigenetics Chromatin. 2019 Mar 13;12(1):17. doi: 10.1186/s13072-019-0263-z. Epigenetics Chromatin. 2019. PMID: 30871638 Free PMC article.
IFT172 as the 19th gene causative of oral-facial-digital syndrome.
Yamada M, Uehara T, Suzuki H, Takenouchi T, Fukushima H, Morisada N, Tominaga K, Onoda M, Kosaki K. Yamada M, et al. Among authors: Fukushima H. Am J Med Genet A. 2019 Dec;179(12):2510-2513. doi: 10.1002/ajmg.a.61373. Epub 2019 Oct 6. Am J Med Genet A. 2019. PMID: 31587445 No abstract available.
Hippocampal clock regulates memory retrieval via Dopamine and PKA-induced GluA1 phosphorylation.
Hasegawa S, Fukushima H, Hosoda H, Serita T, Ishikawa R, Rokukawa T, Kawahara-Miki R, Zhang Y, Ohta M, Okada S, Tanimizu T, Josselyn SA, Frankland PW, Kida S. Hasegawa S, et al. Among authors: Fukushima H. Nat Commun. 2019 Dec 18;10(1):5766. doi: 10.1038/s41467-019-13554-y. Nat Commun. 2019. PMID: 31852900 Free PMC article.
Sweat retention anhidrosis associated with tubular aggregate myopathy.
Ishitsuka Y, Inoue S, Furuta J, Koguchi-Yoshioka H, Nakamura Y, Watanabe R, Okiyama N, Fujisawa Y, Enokizono T, Fukushima H, Suzuki H, Nishino I, Kosaki K, Fujimoto M. Ishitsuka Y, et al. Among authors: Fukushima H. Br J Dermatol. 2019 Nov;181(5):1104-1106. doi: 10.1111/bjd.18175. Epub 2019 Aug 21. Br J Dermatol. 2019. PMID: 31145807 No abstract available.
A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay.
Ueno Y, Enokizono T, Fukushima H, Ohto T, Imagawa K, Tanaka M, Sakai A, Suzuki H, Uehara T, Takenouchi T, Kosaki K, Takada H. Ueno Y, et al. Among authors: Fukushima H. Hum Genome Var. 2019 May 23;6:25. doi: 10.1038/s41439-019-0056-8. eCollection 2019. Hum Genome Var. 2019. PMID: 31149344 Free PMC article.
Schuurs-Hoeijmakers syndrome in two patients from Japan.
Hoshino Y, Enokizono T, Imagawa K, Tanaka R, Suzuki H, Fukushima H, Arai J, Sumazaki R, Uehara T, Takenouchi T, Kosaki K. Hoshino Y, et al. Among authors: Fukushima H. Am J Med Genet A. 2019 Mar;179(3):341-343. doi: 10.1002/ajmg.a.9. Epub 2018 Dec 27. Am J Med Genet A. 2019. PMID: 30588754
NOTCH2 Hajdu-Cheney Mutations Escape SCFFBW7-Dependent Proteolysis to Promote Osteoporosis.
Fukushima H, Shimizu K, Watahiki A, Hoshikawa S, Kosho T, Oba D, Sakano S, Arakaki M, Yamada A, Nagashima K, Okabe K, Fukumoto S, Jimi E, Bigas A, Nakayama KI, Nakayama K, Aoki Y, Wei W, Inuzuka H. Fukushima H, et al. Mol Cell. 2017 Nov 16;68(4):645-658.e5. doi: 10.1016/j.molcel.2017.10.018. Mol Cell. 2017. PMID: 29149593 Free PMC article.
Identification of a novel KLC1-ROS1 fusion in a case of pediatric low-grade localized glioma.
Nakano Y, Tomiyama A, Kohno T, Yoshida A, Yamasaki K, Ozawa T, Fukuoka K, Fukushima H, Inoue T, Hara J, Sakamoto H, Ichimura K. Nakano Y, et al. Among authors: Fukushima H. Brain Tumor Pathol. 2019 Jan;36(1):14-19. doi: 10.1007/s10014-018-0330-3. Epub 2018 Oct 22. Brain Tumor Pathol. 2019. PMID: 30350109 Review.
1,035 results
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