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Items: 1 to 20 of 22

1.

[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].

Pikó H, Molnár MJ, Herczegfalvi A, Mayer P, Karcagi V.

Orv Hetil. 2011 Sep 25;152(39):1576-85. doi: 10.1556/OH.2011.29179. Hungarian.

PMID:
21920844
2.

Facioscapulohumeral muscular dystrophy.

Tawil R, Van Der Maarel SM.

Muscle Nerve. 2006 Jul;34(1):1-15. Review.

PMID:
16508966
3.

Genomic analysis of facioscapulohumeral muscular dystrophy.

Clapp J, Bolland DJ, Hewitt JE.

Brief Funct Genomic Proteomic. 2003 Oct;2(3):213-23. Review.

PMID:
15239924
4.

Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).

Fisher J, Upadhyaya M.

Neuromuscul Disord. 1997 Jan;7(1):55-62. Review.

PMID:
9132141
5.

In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.

Neguembor MV, Gabellini D.

Epigenomics. 2010 Apr;2(2):271-87. doi: 10.2217/epi.10.8. Review.

PMID:
22121874
6.

Facioscapulohumeral muscular dystrophy.

Sacconi S, Salviati L, Desnuelle C.

Biochim Biophys Acta. 2015 Apr;1852(4):607-14. doi: 10.1016/j.bbadis.2014.05.021. Epub 2014 May 29. Review.

7.

Molecular diagnosis of facioscapulohumeral muscular dystrophy.

Upadhyaya M, Cooper DN.

Expert Rev Mol Diagn. 2002 Mar;2(2):160-71. Review.

PMID:
11962336
8.

Facioscapulohumeral Muscular Dystrophy.

DeSimone AM, Pakula A, Lek A, Emerson CP Jr.

Compr Physiol. 2017 Sep 12;7(4):1229-1279. doi: 10.1002/cphy.c160039. Review.

PMID:
28915324
9.

[Facioscapulohumeral muscular dystrophy (FSHD)].

Funakoshi M, Goto K, Kim BY, Arahata K.

Nihon Rinsho. 1997 Dec;55(12):3181-5. Review. Japanese.

PMID:
9436432
10.

Genetic and epigenetic contributors to FSHD.

Daxinger L, Tapscott SJ, 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. Review.

11.

The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy.

van der Maarel SM, Frants RR.

Am J Hum Genet. 2005 Mar;76(3):375-86. Epub 2005 Jan 24. Review. No abstract available.

12.

Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions.

Statland JM, Tawil R.

Curr Opin Neurol. 2011 Oct;24(5):423-8. doi: 10.1097/WCO.0b013e32834959af. Review.

PMID:
21734574
13.

Epigenetic mechanisms of facioscapulohumeral muscular dystrophy.

de Greef JC, Frants RR, van der Maarel SM.

Mutat Res. 2008 Dec 1;647(1-2):94-102. doi: 10.1016/j.mrfmmm.2008.07.011. Epub 2008 Aug 3. Review.

14.

[Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].

Goto K, Song MD, Lee JH, Arahata K.

Rinsho Shinkeigaku. 1995 Dec;35(12):1416-8. Review. Japanese.

PMID:
8752415
15.

[Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy].

Su Q, Zhang C.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Oct;18(5):398-401. Review. Chinese.

PMID:
11592052
16.

Molecular basis of facioscapulohumeral muscular dystrophy.

Tupler R, Gabellini D.

Cell Mol Life Sci. 2004 Mar;61(5):557-566. doi: 10.1007/s00018-003-3285-3. Review.

PMID:
15004695
17.

The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy.

Cabianca DS, Gabellini D.

J Cell Biol. 2010 Dec 13;191(6):1049-60. doi: 10.1083/jcb.201007028. Review.

18.

Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and disease.

Himeda CL, Jones TI, Jones PL.

Antioxid Redox Signal. 2015 Jun 1;22(16):1463-82. doi: 10.1089/ars.2014.6090. Epub 2014 Dec 4. Review.

19.

Facioscapulohumeral muscular dystrophy.

van der Maarel SM, Frants RR, Padberg GW.

Biochim Biophys Acta. 2007 Feb;1772(2):186-94. Epub 2006 Jun 6. Review.

20.

Emerging roles of macrosatellite repeats in genome organization and disease development.

Dumbovic G, Forcales SV, Perucho M.

Epigenetics. 2017 Jul 3;12(7):515-526. doi: 10.1080/15592294.2017.1318235. Epub 2017 Apr 20. Review.

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