These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
633 related articles for article (PubMed ID: 27816329)
1. A complex interplay of genetic and epigenetic events leads to abnormal expression of the DUX4 gene in facioscapulohumeral muscular dystrophy. Gatica LV; Rosa AL Neuromuscul Disord; 2016 Dec; 26(12):844-852. PubMed ID: 27816329 [TBL] [Abstract][Full Text] [Related]
3. Sporadic DUX4 expression in FSHD myocytes is associated with incomplete repression by the PRC2 complex and gain of H3K9 acetylation on the contracted D4Z4 allele. Haynes P; Bomsztyk K; Miller DG Epigenetics Chromatin; 2018 Aug; 11(1):47. PubMed ID: 30122154 [TBL] [Abstract][Full Text] [Related]
5. Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2. Lemmers RJLF; van der Vliet PJ; Vreijling JP; Henderson D; van der Stoep N; Voermans N; van Engelen B; Baas F; Sacconi S; Tawil R; van der Maarel SM Hum Mol Genet; 2018 Oct; 27(20):3488-3497. PubMed ID: 30281091 [TBL] [Abstract][Full Text] [Related]
6. Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4. Balog J; Thijssen PE; Shadle S; Straasheijm KR; van der Vliet PJ; Krom YD; van den Boogaard ML; de Jong A; F Lemmers RJ; Tawil R; Tapscott SJ; van der Maarel SM Epigenetics; 2015; 10(12):1133-42. PubMed ID: 26575099 [TBL] [Abstract][Full Text] [Related]
7. Genetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologs. Zeng W; Chen YY; Newkirk DA; Wu B; Balog J; Kong X; Ball AR; Zanotti S; Tawil R; Hashimoto N; Mortazavi A; van der Maarel SM; Yokomori K Hum Mutat; 2014 Aug; 35(8):998-1010. PubMed ID: 24838473 [TBL] [Abstract][Full Text] [Related]
9. Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy. Jones TI; King OD; Himeda CL; Homma S; Chen JC; Beermann ML; Yan C; Emerson CP; Miller JB; Wagner KR; Jones PL Clin Epigenetics; 2015; 7(1):37. PubMed ID: 25904990 [TBL] [Abstract][Full Text] [Related]
10. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. de Greef JC; Krom YD; den Hamer B; Snider L; Hiramuki Y; van den Akker RFP; Breslin K; Pakusch M; Salvatori DCF; Slütter B; Tawil R; Blewitt ME; Tapscott SJ; van der Maarel SM Hum Mol Genet; 2018 Feb; 27(4):716-731. PubMed ID: 29281018 [TBL] [Abstract][Full Text] [Related]
11. Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing. Jones TI; Yan C; Sapp PC; McKenna-Yasek D; Kang PB; Quinn C; Salameh JS; King OD; Jones PL Clin Epigenetics; 2014; 6(1):23. PubMed ID: 25400706 [TBL] [Abstract][Full Text] [Related]
15. Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2. Lemmers RJ; van der Vliet PJ; Balog J; Goeman JJ; Arindrarto W; Krom YD; Straasheijm KR; Debipersad RD; Özel G; Sowden J; Snider L; Mul K; Sacconi S; van Engelen B; Tapscott SJ; Tawil R; van der Maarel SM Eur J Hum Genet; 2018 Jan; 26(1):94-106. PubMed ID: 29162933 [TBL] [Abstract][Full Text] [Related]
16. Direct interplay between two candidate genes in FSHD muscular dystrophy. Ferri G; Huichalaf CH; Caccia R; Gabellini D Hum Mol Genet; 2015 Mar; 24(5):1256-66. PubMed ID: 25326393 [TBL] [Abstract][Full Text] [Related]
17. The FSHD2 gene SMCHD1 is a modifier of disease severity in families affected by FSHD1. Sacconi S; Lemmers RJ; Balog J; van der Vliet PJ; Lahaut P; van Nieuwenhuizen MP; Straasheijm KR; Debipersad RD; Vos-Versteeg M; Salviati L; Casarin A; Pegoraro E; Tawil R; Bakker E; Tapscott SJ; Desnuelle C; van der Maarel SM Am J Hum Genet; 2013 Oct; 93(4):744-51. PubMed ID: 24075187 [TBL] [Abstract][Full Text] [Related]
18. Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy. Greco A; Goossens R; van Engelen B; van der Maarel SM Clin Genet; 2020 Jun; 97(6):799-814. PubMed ID: 32086799 [TBL] [Abstract][Full Text] [Related]
19. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Richards M; Coppée F; Thomas N; Belayew A; Upadhyaya M Hum Genet; 2012 Mar; 131(3):325-40. PubMed ID: 21984394 [TBL] [Abstract][Full Text] [Related]