176 related articles for article (PubMed ID: 19690880)
1. Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4.
Chadwick BP
Chromosoma; 2009 Dec; 118(6):675-81. PubMed ID: 19690880
[TBL] [Abstract][Full Text] [Related]
2. Emerging roles of macrosatellite repeats in genome organization and disease development.
Dumbovic G; Forcales SV; Perucho M
Epigenetics; 2017 Jul; 12(7):515-526. PubMed ID: 28426282
[TBL] [Abstract][Full Text] [Related]
3. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.
van Overveld PG; Lemmers RJ; Sandkuijl LA; Enthoven L; Winokur ST; Bakels F; Padberg GW; van Ommen GJ; Frants RR; van der Maarel SM
Nat Genet; 2003 Dec; 35(4):315-7. PubMed ID: 14634647
[TBL] [Abstract][Full Text] [Related]
4. In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.
Neguembor MV; Gabellini D
Epigenomics; 2010 Apr; 2(2):271-87. PubMed ID: 22121874
[TBL] [Abstract][Full Text] [Related]
5. 4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy.
Cortesi A; Pesant M; Sinha S; Marasca F; Sala E; Gregoretti F; Antonelli L; Oliva G; Chiereghin C; Soldà G; Bodega B
Genome Res; 2019 Jun; 29(6):883-895. PubMed ID: 31097473
[TBL] [Abstract][Full Text] [Related]
6. Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.
de Greef JC; Lemmers RJ; van Engelen BG; Sacconi S; Venance SL; Frants RR; Tawil R; van der Maarel SM
Hum Mutat; 2009 Oct; 30(10):1449-59. PubMed ID: 19728363
[TBL] [Abstract][Full Text] [Related]
7. Facioscapulohumeral muscular dystrophy.
Sacconi S; Salviati L; Desnuelle C
Biochim Biophys Acta; 2015 Apr; 1852(4):607-14. PubMed ID: 24882751
[TBL] [Abstract][Full Text] [Related]
8. Variation in array size, monomer composition and expression of the macrosatellite DXZ4.
Tremblay DC; Moseley S; Chadwick BP
PLoS One; 2011 Apr; 6(4):e18969. PubMed ID: 21544201
[TBL] [Abstract][Full Text] [Related]
9. Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers.
Tsumagari K; Qi L; Jackson K; Shao C; Lacey M; Sowden J; Tawil R; Vedanarayanan V; Ehrlich M
Nucleic Acids Res; 2008 Apr; 36(7):2196-207. PubMed ID: 18281700
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
van Overveld PG; Enthoven L; Ricci E; Rossi M; Felicetti L; Jeanpierre M; Winokur ST; Frants RR; Padberg GW; van der Maarel SM
Ann Neurol; 2005 Oct; 58(4):569-76. PubMed ID: 16178028
[TBL] [Abstract][Full Text] [Related]
12. Epigenetic mechanisms of facioscapulohumeral muscular dystrophy.
de Greef JC; Frants RR; van der Maarel SM
Mutat Res; 2008 Dec; 647(1-2):94-102. PubMed ID: 18723032
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy.
Buzhov BT; Lemmers RJ; Tournev I; van der Wielen MJ; Ishpekova B; Petkov R; Petrova J; Frants RR; Padberg GW; van der Maarel SM
Neuromuscul Disord; 2005 Jul; 15(7):471-5. PubMed ID: 15935668
[TBL] [Abstract][Full Text] [Related]
15. Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea.
Lee JH; Park HJ; Seong MW; Park SS; Choi YC
Yonsei Med J; 2021 Jan; 62(1):95-98. PubMed ID: 33381940
[TBL] [Abstract][Full Text] [Related]
16. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
[TBL] [Abstract][Full Text] [Related]
17. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
Zeng W; de Greef JC; Chen YY; Chien R; Kong X; Gregson HC; Winokur ST; Pyle A; Robertson KD; Schmiesing JA; Kimonis VE; Balog J; Frants RR; Ball AR; Lock LF; Donovan PJ; van der Maarel SM; Yokomori K
PLoS Genet; 2009 Jul; 5(7):e1000559. PubMed ID: 19593370
[TBL] [Abstract][Full Text] [Related]
18. Genomic analysis of facioscapulohumeral muscular dystrophy.
Clapp J; Bolland DJ; Hewitt JE
Brief Funct Genomic Proteomic; 2003 Oct; 2(3):213-23. PubMed ID: 15239924
[TBL] [Abstract][Full Text] [Related]
19. SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite.
Dion C; Roche S; Laberthonnière C; Broucqsault N; Mariot V; Xue S; Gurzau AD; Nowak A; Gordon CT; Gaillard MC; El-Yazidi C; Thomas M; Schlupp-Robaglia A; Missirian C; Malan V; Ratbi L; Sefiani A; Wollnik B; Binetruy B; Salort Campana E; Attarian S; Bernard R; Nguyen K; Amiel J; Dumonceaux J; Murphy JM; Déjardin J; Blewitt ME; Reversade B; Robin JD; Magdinier F
Nucleic Acids Res; 2019 Apr; 47(6):2822-2839. PubMed ID: 30698748
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
