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