(Q36100981)

12 August 2017

Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD. (English)

1 reference

12 August 2017

Silvère M van der Maarel

object named as

Silvère M van der Maarel

9

0 references

Baziel van Engelen

5

object named as

Baziel G M van Engelen

1 reference

12 August 2017

8

Rabi Tawil

1 reference

12 August 2017

Judit Balog

1

1 reference

12 August 2017

Peter E Thijssen

2

1 reference

12 August 2017

Jessica C de Greef

3

1 reference

12 August 2017

Bharati Shah

4

1 reference

12 August 2017

Kyoko Yokomori

6

1 reference

12 August 2017

Stephen J Tapscott

7

1 reference

12 August 2017

1 June 2012

1 reference

12 August 2017

1 reference

12 August 2017

7

1 reference

12 August 2017

6

1 reference

12 August 2017

579-584

1 reference

Mapping and analysis of chromatin state dynamics in nine human cell types

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Clinical features of facioscapulohumeral muscular dystrophy 2.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Protocol for the fast chromatin immunoprecipitation (ChIP) method

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3398987

Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22522912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22522912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

CD8(+) T cells in facioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRI

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22522912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4161/EPI.20001

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

22522912

1 reference