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

Year Number of Results
1995 2
1997 1
1998 3
2000 1
2001 1
2002 1
2003 1
2006 2
2007 1
2008 4
2009 1
2010 2
2012 5
2013 6
2014 6
2015 10
2016 12
2017 6
2018 14
2019 12
2020 3
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2024 0

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Similar articles for PMID: 23819640

91 results

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SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes.
Mason AG, Slieker RC, Balog J, Lemmers RJLF, Wong CJ, Yao Z, Lim JW, Filippova GN, Ne E, Tawil R, Heijmans BT, Tapscott SJ, van der Maarel SM. Mason AG, et al. Skelet Muscle. 2017 Jun 6;7(1):12. doi: 10.1186/s13395-017-0129-7. Skelet Muscle. 2017. PMID: 28587678 Free PMC article.
Genome-wide binding and mechanistic analyses of Smchd1-mediated epigenetic regulation.
Chen K, Hu J, Moore DL, Liu R, Kessans SA, Breslin K, Lucet IS, Keniry A, Leong HS, Parish CL, Hilton DJ, Lemmers RJ, van der Maarel SM, Czabotar PE, Dobson RC, Ritchie ME, Kay GF, Murphy JM, Blewitt ME. Chen K, et al. Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):E3535-44. doi: 10.1073/pnas.1504232112. Epub 2015 Jun 19. Proc Natl Acad Sci U S A. 2015. PMID: 26091879 Free PMC article.
Smchd1 is a maternal effect gene required for genomic imprinting.
Wanigasuriya I, Gouil Q, Kinkel SA, Tapia Del Fierro A, Beck T, Roper EA, Breslin K, Stringer J, Hutt K, Lee HJ, Keniry A, Ritchie ME, Blewitt ME. Wanigasuriya I, et al. Elife. 2020 Nov 13;9:e55529. doi: 10.7554/eLife.55529. Elife. 2020. PMID: 33186096 Free PMC article.
Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in SMCHD1 in a Family With FSHD.
Cascella R, Strafella C, Caputo V, Galota RM, Errichiello V, Scutifero M, Petillo R, Marella GL, Arcangeli M, Colantoni L, Zampatti S, Ricci E, Deidda G, Politano L, Giardina E. Cascella R, et al. Front Neurol. 2018 Nov 28;9:1027. doi: 10.3389/fneur.2018.01027. eCollection 2018. Front Neurol. 2018. PMID: 30546343 Free PMC article.
91 results