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

Year Number of Results
1992 1
1994 2
1995 4
1996 1
1998 1
1999 2
2000 2
2001 3
2002 3
2003 8
2004 10
2005 7
2006 9
2007 8
2008 4
2009 8
2010 11
2011 16
2012 17
2013 16
2014 12
2015 19
2016 14
2017 8
2018 17
2019 14
2020 13
2021 11
2022 5
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Search Results

220 results
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Page 1
p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models.
Grow EJ, Weaver BD, Smith CM, Guo J, Stein P, Shadle SC, Hendrickson PG, Johnson NE, Butterfield RJ, Menafra R, Kloet SL, van der Maarel SM, Williams CJ, Cairns BR. Grow EJ, et al. Among authors: van der maarel sm. Nat Genet. 2021 Aug;53(8):1207-1220. doi: 10.1038/s41588-021-00893-0. Epub 2021 Jul 15. Nat Genet. 2021. PMID: 34267371 Free PMC article.
Identical twins carry a persistent epigenetic signature of early genome programming.
van Dongen J, Gordon SD, McRae AF, Odintsova VV, Mbarek H, Breeze CE, Sugden K, Lundgren S, Castillo-Fernandez JE, Hannon E, Moffitt TE, Hagenbeek FA, van Beijsterveldt CEM, Jan Hottenga J, Tsai PC; BIOS Consortium; Genetics of DNA Methylation Consortium, Min JL, Hemani G, Ehli EA, Paul F, Stern CD, Heijmans BT, Slagboom PE, Daxinger L, van der Maarel SM, de Geus EJC, Willemsen G, Montgomery GW, Reversade B, Ollikainen M, Kaprio J, Spector TD, Bell JT, Mill J, Caspi A, Martin NG, Boomsma DI. van Dongen J, et al. Among authors: van der maarel sm. Nat Commun. 2021 Sep 28;12(1):5618. doi: 10.1038/s41467-021-25583-7. Nat Commun. 2021. PMID: 34584077 Free PMC article.
Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.
Beijer D, Kim HJ, Guo L, O'Donovan K, Mademan I, Deconinck T, Van Schil K, Fare CM, Drake LE, Ford AF, Kochański A, Kabzińska D, Dubuisson N, Van den Bergh P, Voermans NC, Lemmers RJ, van der Maarel SM, Bonner D, Sampson JB, Wheeler MT, Mehrabyan A, Palmer S, De Jonghe P, Shorter J, Taylor JP, Baets J. Beijer D, et al. Among authors: van der maarel sm. JCI Insight. 2021 Jul 22;6(14):e148363. doi: 10.1172/jci.insight.148363. JCI Insight. 2021. PMID: 34291734 Free PMC article.
Facioscapulohumeral muscular dystrophy.
van der Maarel SM, Frants RR, Padberg GW. van der Maarel SM, et al. Biochim Biophys Acta. 2007 Feb;1772(2):186-94. doi: 10.1016/j.bbadis.2006.05.009. Epub 2006 Jun 6. Biochim Biophys Acta. 2007. PMID: 16837171 Free article. Review.
[Facioscapulohumeral muscular dystrophy].
Wilbers J, Frants RR, van Engelen BG, Padberg GW, van der Maarel SM. Wilbers J, et al. Among authors: van der maarel sm. Ned Tijdschr Tandheelkd. 2010 Jan;117(1):11-4. Ned Tijdschr Tandheelkd. 2010. PMID: 20180344 Free article. Review. Dutch.
Facioscapulohumeral muscular dystrophy.
Tawil R, Van Der Maarel SM. Tawil R, et al. Among authors: van der maarel sm. Muscle Nerve. 2006 Jul;34(1):1-15. doi: 10.1002/mus.20522. Muscle Nerve. 2006. PMID: 16508966 Review.
Multiscale 3D-printing of microfluidic AFM cantilevers.
Kramer RCLN, Verlinden EJ, Angeloni L, van den Heuvel A, Fratila-Apachitei LE, van der Maarel SM, Ghatkesar MK. Kramer RCLN, et al. Among authors: van der maarel sm. Lab Chip. 2020 Jan 21;20(2):311-319. doi: 10.1039/c9lc00668k. Epub 2019 Dec 6. Lab Chip. 2020. PMID: 31808485
Genetic and epigenetic contributors to FSHD.
Daxinger L, Tapscott SJ, van der Maarel SM. Daxinger L, et al. Among authors: van der maarel sm. Curr Opin Genet Dev. 2015 Aug;33:56-61. doi: 10.1016/j.gde.2015.08.007. Epub 2015 Sep 7. Curr Opin Genet Dev. 2015. PMID: 26356006 Free PMC article. Review.
220 results