Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene (Q21563391)

9

Silvère M

van der Maarel

1 reference

2 September 2022

Michael Kyba

4

Michael

Kyba

1 reference

2 September 2022

7

Rabi

Tawil

Rabi Tawil

1 reference

2 September 2022

Lauren Snider

1

Lauren

Snider

1 reference

2 September 2022

Linda N Geng

2

Linda N

Geng

1 reference

2 September 2022

Richard J L F Lemmers

3

Richard J L F

Lemmers

1 reference

2 September 2022

Carol B Ware

5

Carol B

Ware

1 reference

2 September 2022

Angelique M Nelson

6

Angelique M

Nelson

1 reference

2 September 2022

Galina N Filippova

8

Galina N

Filippova

1 reference

2 September 2022

Stephen J Tapscott

10

Stephen J

Creative Commons Attribution 4.0 International

Tapscott

1 reference

2 September 2022

language of work or name

English

0 references

publication date

October 2010

0 references

published in

PLOS Genetics

0 references

volume

6

0 references

page(s)

e1001181

0 references

issue

10

0 references

copyright license

start time

28 October 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageQuant

object named as

ImageQuant TL

2 references

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2965761/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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

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

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

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

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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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Facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1001181

1 reference

1014852

1014852

1 reference

1 reference

1 reference