(Q37582304)

21 August 2017

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title

Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4. (English)

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21 August 2017

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Brian P Chadwick

1

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21 August 2017

publication date

19 August 2009

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21 August 2017

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21 August 2017

volume

118

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21 August 2017

issue

6

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21 August 2017

page(s)

675-681

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Epigenetic mechanisms of facioscapulohumeral muscular dystrophy

21 August 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS00412-009-0233-5

So much "junk" DNA in our genome

21 January 2018

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12 December 2020

Facioscapulohumeral muscular dystrophy

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12 December 2020

Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy.

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12 December 2020

Variation in Xi chromatin organization and correlation of the H3K27me3 chromatin territories to transcribed sequences by microarray analysis

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12 December 2020

Transcription and RNA interference in the formation of heterochromatin.

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12 December 2020

Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers

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12 December 2020

Dicer independent small RNAs associate with telomeric heterochromatin.

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12 December 2020

Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

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12 December 2020

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

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12 December 2020

Sequence organization of the human genome

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12 December 2020

A novel GC-rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomes

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12 December 2020

Establishment of histone h3 methylation on the inactive X chromosome requires transient recruitment of Eed-Enx1 polycomb group complexes

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12 December 2020

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

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12 December 2020

The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy.

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12 December 2020

Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.

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12 December 2020

Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes

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12 December 2020

Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation

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12 December 2020

Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin

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12 December 2020

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

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12 December 2020

Ubiquitinated proteins including uH2A on the human and mouse inactive X chromosome: enrichment in gene rich bands.

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12 December 2020

Epigenetics in cancer

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12 December 2020

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues

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12 December 2020

Role of histone H3 lysine 27 methylation in X inactivation

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12 December 2020

Roles of the Clr4 methyltransferase complex in nucleation, spreading and maintenance of heterochromatin.

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12 December 2020

Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity

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12 December 2020

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

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12 December 2020

Selfish DNA: the ultimate parasite

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12 December 2020

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

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12 December 2020

The profile of repeat-associated histone lysine methylation states in the mouse epigenome

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12 December 2020

X chromosome dosage compensation: how mammals keep the balance

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12 December 2020

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

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12 December 2020

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

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12 December 2020

Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome

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12 December 2020

Heterochromatin revisited

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12 December 2020

Analysis of the largest tandemly repeated DNA families in the human genome

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12 December 2020

Genetics and epigenetics of the multifunctional protein CTCF.

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12 December 2020

Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome

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12 December 2020

RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

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12 December 2020

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

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12 December 2020

An overview of the GAGE cancer/testis antigen family with the inclusion of newly identified members

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12 December 2020

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1

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12 December 2020

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

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12 December 2020

Gene action in the X-chromosome of the mouse (Mus musculus L.)

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12 December 2020

CTCF, a candidate trans-acting factor for X-inactivation choice

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12 December 2020

Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome

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12 December 2020

A 5' element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila

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12 December 2020

Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome.

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12 December 2020

The binding sites for the chromatin insulator protein CTCF map to DNA methylation-free domains genome-wide

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12 December 2020

DXZ4 chromatin adopts an opposing conformation to that of the surrounding chromosome and acquires a novel inactive X-specific role involving CTCF and antisense transcripts

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12 December 2020

10.1007/S00412-009-0233-5

Identifiers

DOI

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21 August 2017

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