Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD (Q21563357)

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28 February 2020

title

Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD (English)

1 reference

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9

Paul Knopp

Paul

Knopp

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28 February 2020

6

Zizhen Yao

Zizhen

Yao

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28 February 2020

10

Peter S Zammit

Peter S

Zammit

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Silvère M van der Maarel

17

object named as

Silvère M van der Maarel

Silvère M

van der Maarel

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7

Lisa

Maves

Lisa Maves

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14

Rune R

Frants

Rune R Frants

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28 February 2020

13

George W

Padberg

George W Padberg

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12

Baziel G M

van Engelen

Baziel G M van Engelen

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15

Rabi

Tawil

Rabi Tawil

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Yvonne D Krom

1

Yvonne D

Krom

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Peter E Thijssen

2

Peter E

Thijssen

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Janet M Young

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Janet M

Young

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Bianca den Hamer

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Bianca

den Hamer

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28 February 2020

Judit Balog

5

Judit

Balog

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Lauren Snider

8

Lauren

Snider

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28 February 2020

Tonnie Rijkers

11

Tonnie

Rijkers

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28 February 2020

Stephen J Tapscott

16

Stephen J

Tapscott

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language of work or name

English

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publication date

4 April 2013

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28 February 2020

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28 February 2020

volume

9

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issue

4

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28 February 2020

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e1003415

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Creative Commons Attribution 4.0 International

28 February 2020

copyright license

start time

4 April 2013

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April 2022 Public Data File from Crossref

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cites work

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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

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12 September 2017

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12 September 2017

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FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy

12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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Inappropriate Gene Activation in FSHD

12 September 2017

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

12 September 2017

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Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q

12 September 2017

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An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

30 May 2018

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The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

30 May 2018

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21 January 2018

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21 January 2018

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Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD

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7 January 2021

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Identifiers

DOI

10.1371/JOURNAL.PGEN.1003415

2 references

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28 February 2020

1 reference

2 references

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28 February 2020

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