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

Year Number of Results
1981 4
1982 1
1983 1
1984 1
1988 1
1989 3
1990 2
1991 3
1992 5
1993 3
1994 1
1995 2
1996 5
1997 6
1998 6
1999 2
2000 5
2001 8
2002 5
2003 4
2004 6
2005 8
2006 7
2007 9
2008 5
2009 7
2010 11
2011 12
2012 17
2013 16
2014 9
2015 12
2016 6
2017 7
2018 8
2019 10
2020 2
2021 5
2022 6
2023 7
2024 3

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223 results

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Page 1
Facioscapulohumeral muscular dystrophy: the road to targeted therapies.
Tihaya MS, Mul K, Balog J, de Greef JC, Tapscott SJ, Tawil R, Statland JM, van der Maarel SM. Tihaya MS, et al. Among authors: tapscott sj. Nat Rev Neurol. 2023 Feb;19(2):91-108. doi: 10.1038/s41582-022-00762-2. Epub 2023 Jan 10. Nat Rev Neurol. 2023. PMID: 36627512 Review.
Deconstructing myotonic dystrophy.
Tapscott SJ. Tapscott SJ. Science. 2000 Sep 8;289(5485):1701-2. doi: 10.1126/science.289.5485.1701. Science. 2000. PMID: 11001736
Networking the nucleus.
Rajapakse I, Scalzo D, Tapscott SJ, Kosak ST, Groudine M. Rajapakse I, et al. Among authors: tapscott sj. Mol Syst Biol. 2010 Jul;6:395. doi: 10.1038/msb.2010.48. Mol Syst Biol. 2010. PMID: 20664641 Free PMC article. Review.
Genetic and epigenetic contributors to FSHD.
Daxinger L, Tapscott SJ, van der Maarel SM. Daxinger L, et al. Among authors: tapscott sj. 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.
Skeletal muscle programming and re-programming.
Fong AP, Tapscott SJ. Fong AP, et al. Among authors: tapscott sj. Curr Opin Genet Dev. 2013 Oct;23(5):568-73. doi: 10.1016/j.gde.2013.05.002. Epub 2013 Jun 4. Curr Opin Genet Dev. 2013. PMID: 23756045 Free PMC article. Review.
Insights into pediatric rhabdomyosarcoma research: Challenges and goals.
Yohe ME, Heske CM, Stewart E, Adamson PC, Ahmed N, Antonescu CR, Chen E, Collins N, Ehrlich A, Galindo RL, Gryder BE, Hahn H, Hammond S, Hatley ME, Hawkins DS, Hayes MN, Hayes-Jordan A, Helman LJ, Hettmer S, Ignatius MS, Keller C, Khan J, Kirsch DG, Linardic CM, Lupo PJ, Rota R, Shern JF, Shipley J, Sindiri S, Tapscott SJ, Vakoc CR, Wexler LH, Langenau DM. Yohe ME, et al. Among authors: tapscott sj. Pediatr Blood Cancer. 2019 Oct;66(10):e27869. doi: 10.1002/pbc.27869. Epub 2019 Jun 21. Pediatr Blood Cancer. 2019. PMID: 31222885 Free PMC article. Review.
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.
van den Heuvel A, Lassche S, Mul K, Greco A, San León Granado D, Heerschap A, Küsters B, Tapscott SJ, Voermans NC, van Engelen BGM, van der Maarel SM. van den Heuvel A, et al. Among authors: tapscott sj. Sci Rep. 2022 Jan 26;12(1):1426. doi: 10.1038/s41598-022-04817-8. Sci Rep. 2022. PMID: 35082321 Free PMC article.
Elevated plasma complement components in facioscapulohumeral dystrophy.
Wong CJ, Wang L, Holers VM, Frazer-Abel A, van der Maarel SM, Tawil R, Statland JM, Tapscott SJ; ReSolve Network. Wong CJ, et al. Among authors: tapscott sj. Hum Mol Genet. 2022 Jun 4;31(11):1821-1829. doi: 10.1093/hmg/ddab364. Hum Mol Genet. 2022. PMID: 34919696 Free PMC article.
223 results