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Items: 1 to 20 of 89

1.

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. doi: 10.1093/nar/gkn055.

2.
3.

Covalent modifications of histones during development and disease pathogenesis.

Bhaumik SR, Smith E, Shilatifard A.

Nat Struct Mol Biol. 2007 Nov;14(11):1008-16. Review.

PMID:
17984963
4.

DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1.

Dixit M, Ansseau E, Tassin A, Winokur S, Shi R, Qian H, Sauvage S, Mattéotti C, van Acker AM, Leo O, Figlewicz D, Barro M, Laoudj-Chenivesse D, Belayew A, Coppée F, Chen YW.

Proc Natl Acad Sci U S A. 2007 Nov 13;104(46):18157-62.

5.

Evidence that homologous X-chromosome pairing requires transcription and Ctcf protein.

Xu N, Donohoe ME, Silva SS, Lee JT.

Nat Genet. 2007 Nov;39(11):1390-6.

PMID:
17952071
6.

Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.

Lemmers RJ, Wohlgemuth M, van der Gaag KJ, van der Vliet PJ, van Teijlingen CM, de Knijff P, Padberg GW, Frants RR, van der Maarel SM.

Am J Hum Genet. 2007 Nov;81(5):884-94.

7.

Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.

de Greef JC, Wohlgemuth M, Chan OA, Hansson KB, Smeets D, Frants RR, Weemaes CM, Padberg GW, van der Maarel SM.

Neurology. 2007 Sep 4;69(10):1018-26.

PMID:
17785671
8.

Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy.

Clapp J, Mitchell LM, Bolland DJ, Fantes J, Corcoran AE, Scotting PJ, Armour JA, Hewitt JE.

Am J Hum Genet. 2007 Aug;81(2):264-79.

9.

The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein.

Kowaljow V, Marcowycz A, Ansseau E, Conde CB, Sauvage S, Mattéotti C, Arias C, Corona ED, Nuñez NG, Leo O, Wattiez R, Figlewicz D, Laoudj-Chenivesse D, Belayew A, Coppée F, Rosa AL.

Neuromuscul Disord. 2007 Aug;17(8):611-23.

PMID:
17588759
10.
11.

"Laminopathies": a wide spectrum of human diseases.

Worman HJ, Bonne G.

Exp Cell Res. 2007 Jun 10;313(10):2121-33. Review.

12.

Chromatin domains and regulation of transcription.

Razin SV, Iarovaia OV, Sjakste N, Sjakste T, Bagdoniene L, Rynditch AV, Eivazova ER, Lipinski M, Vassetzky YS.

J Mol Biol. 2007 Jun 8;369(3):597-607. Review.

PMID:
17466329
13.

RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA.

Alexiadis V, Ballestas ME, Sanchez C, Winokur S, Vedanarayanan V, Warren M, Ehrlich M.

Biochim Biophys Acta. 2007 Jan;1769(1):29-40.

14.

Dynamic genome architecture in the nuclear space: regulation of gene expression in three dimensions.

Lanctôt C, Cheutin T, Cremer M, Cavalli G, Cremer T.

Nat Rev Genet. 2007 Feb;8(2):104-15. Review.

PMID:
17230197
15.

Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.

Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR.

Neurology. 2007 Feb 20;68(8):578-82.

PMID:
17229919
16.

The Heterochromatin Protein 1 family.

Lomberk G, Wallrath L, Urrutia R.

Genome Biol. 2006;7(7):228. Review.

17.

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.

Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.

Neurology. 2007 Feb 20;68(8):569-77.

PMID:
17151338
18.

FRG1P-mediated aggregation of proteins involved in pre-mRNA processing.

van Koningsbruggen S, Straasheijm KR, Sterrenburg E, de Graaf N, Dauwerse HG, Frants RR, van der Maarel SM.

Chromosoma. 2007 Feb;116(1):53-64.

PMID:
17103222
19.

Nuclear envelope transmembrane proteins (NETs) that are up-regulated during myogenesis.

Chen IH, Huber M, Guan T, Bubeck A, Gerace L.

BMC Cell Biol. 2006 Oct 24;7:38.

20.

Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes.

Celegato B, Capitanio D, Pescatori M, Romualdi C, Pacchioni B, Cagnin S, Viganò A, Colantoni L, Begum S, Ricci E, Wait R, Lanfranchi G, Gelfi C.

Proteomics. 2006 Oct;6(19):5303-21.

PMID:
17013991
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