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

Year Number of Results
1977 3
1978 7
1979 3
1980 4
1981 5
1982 7
1983 9
1984 8
1985 8
1986 7
1987 12
1988 15
1989 15
1990 26
1991 41
1992 45
1993 53
1994 51
1995 78
1996 106
1997 105
1998 128
1999 148
2000 197
2001 227
2002 265
2003 300
2004 377
2005 485
2006 641
2007 702
2008 870
2009 1051
2010 1126
2011 1300
2012 1536
2013 1752
2014 1795
2015 1807
2016 1837
2017 1928
2018 1904
2019 1032
2020 47
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Article type
Publication date

Search Results

19,747 results
Results by year
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Page 1
Hereditary SWI/SNF complex deficiency syndromes.
Agaimy A, Foulkes WD. Agaimy A, et al. Semin Diagn Pathol. 2018 May;35(3):193-198. doi: 10.1053/j.semdp.2018.01.002. Epub 2018 Feb 1. Semin Diagn Pathol. 2018. PMID: 29397238 Review.
Towards a Unified Model of SMC Complex Function.
Hassler M, Shaltiel IA, Haering CH. Hassler M, et al. Curr Biol. 2018 Nov 5;28(21):R1266-R1281. doi: 10.1016/j.cub.2018.08.034. Curr Biol. 2018. PMID: 30399354 Free PMC article. Review.
Polycomb and Trithorax Group Genes in Drosophila.
Kassis JA, Kennison JA, Tamkun JW. Kassis JA, et al. Genetics. 2017 Aug;206(4):1699-1725. doi: 10.1534/genetics.115.185116. Genetics. 2017. PMID: 28778878 Free PMC article. Review.
SOX9: A genomic view of tissue specific expression and action.
Symon A, Harley V. Symon A, et al. Int J Biochem Cell Biol. 2017 Jun;87:18-22. doi: 10.1016/j.biocel.2017.03.005. Epub 2017 Mar 16. Int J Biochem Cell Biol. 2017. PMID: 28323209 Review.
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types.
Zirkel A, Nikolic M, Sofiadis K, Mallm JP, Brackley CA, Gothe H, Drechsel O, Becker C, Altmüller J, Josipovic N, Georgomanolis T, Brant L, Franzen J, Koker M, Gusmao EG, Costa IG, Ullrich RT, Wagner W, Roukos V, Nürnberg P, Marenduzzo D, Rippe K, Papantonis A. Zirkel A, et al. Mol Cell. 2018 May 17;70(4):730-744.e6. doi: 10.1016/j.molcel.2018.03.030. Epub 2018 Apr 26. Mol Cell. 2018. PMID: 29706538 Free article.
SHLD2/FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choice.
Findlay S, Heath J, Luo VM, Malina A, Morin T, Coulombe Y, Djerir B, Li Z, Samiei A, Simo-Cheyou E, Karam M, Bagci H, Rahat D, Grapton D, Lavoie EG, Dove C, Khaled H, Kuasne H, Mann KK, Klein KO, Greenwood CM, Tabach Y, Park M, Côté JF, Masson JY, Maréchal A, Orthwein A. Findlay S, et al. EMBO J. 2018 Sep 14;37(18):e100158. doi: 10.15252/embj.2018100158. Epub 2018 Aug 28. EMBO J. 2018. PMID: 30154076 Free PMC article.
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