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

Year Number of Results
1995 1
2000 5
2002 2
2003 2
2004 2
2005 2
2006 6
2007 5
2008 1
2009 1
2010 1
2011 1
2012 2
2013 6
2014 5
2015 2
2016 3
2017 5
2018 4
2019 4
2020 2
2021 4
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56 results
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Page 1
CTCF deletion syndrome: clinical features and epigenetic delineation.
Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S. Hori I, et al. Among authors: higashimoto k. J Med Genet. 2017 Dec;54(12):836-842. doi: 10.1136/jmedgenet-2017-104854. Epub 2017 Aug 28. J Med Genet. 2017. PMID: 28848059
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.
Rumbajan JM, Yamaguchi Y, Nakabayashi K, Higashimoto K, Yatsuki H, Nishioka K, Matsuoka K, Aoki S, Toda S, Takeda S, Seki H, Hatada I, Hata K, Soejima H, Joh K. Rumbajan JM, et al. Among authors: higashimoto k. Gene. 2016 Jun 1;583(2):141-146. doi: 10.1016/j.gene.2016.02.025. Epub 2016 Feb 18. Gene. 2016. PMID: 26911255
DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.
Watanabe H, Higashimoto K, Miyake N, Morita S, Horii T, Kimura M, Suzuki T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Uemura T, Hatada I, Matsumoto N, Soejima H. Watanabe H, et al. Among authors: higashimoto k. FASEB J. 2020 Jan;34(1):960-973. doi: 10.1096/fj.201901757R. Epub 2019 Nov 28. FASEB J. 2020. PMID: 31914674 Free PMC article.
56 results
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