Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD). (Q33480945)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Keith D. Robertson

object named as

Keith D Robertson

9

0 references

Silvère M van der Maarel

object named as

Silvère M van der Maarel

17

0 references

13

object named as

Rune R Frants

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

12

object named as

Judit Balog

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Jessica C de Greef

2

object named as

Jessica C de Greef

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

author name string

Weihua Zeng

1

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Yen-Yun Chen

3

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Richard Chien

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Xiangduo Kong

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Heather C Gregson

6

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Sara T Winokur

7

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

April Pyle

8

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

John A Schmiesing

10

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Virginia E Kimonis

11

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Alexander R Ball

14

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Leslie F Lock

15

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Peter J Donovan

16

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Kyoko Yokomori

18

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

publication date

10 July 2009

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

e1000559

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

copyright license

Creative Commons Attribution 4.0 International

10 July 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Cohesins form chromosomal cis-interactions at the developmentally regulated IFNG locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Diverse roles of HP1 proteins in heterochromatin assembly and functions in fission yeast.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Architectural roles of multiple chromatin insulators at the human apolipoprotein gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Cohesins functionally associate with CTCF on mammalian chromosome arms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Cohesin mediates transcriptional insulation by CCCTC-binding factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

The epigenomics of cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Interchromosomal interactions and olfactory receptor choice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Condensin I interacts with the PARP-1-XRCC1 complex and functions in DNA single-strand break repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Histone H3 lysine 9 methyltransferase G9a is a transcriptional coactivator for nuclear receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Gfi1 coordinates epigenetic repression of p21Cip/WAF1 by recruitment of histone lysine methyltransferase G9a and histone deacetylase 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Histone H3 lysine 9 methylation and HP1gamma are associated with transcription elongation through mammalian chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Interchromosomal associations between alternatively expressed loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Genomic maps and comparative analysis of histone modifications in human and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Activating the PARP-1 sensor component of the groucho/ TLE1 corepressor complex mediates a CaMKinase IIdelta-dependent neurogenic gene activation pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

A Suv39h-dependent mechanism for silencing S-phase genes in differentiating but not in cycling cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Partitioning and plasticity of repressive histone methylation states in mammalian chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Chromosomal cohesin forms a ring

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Looping and interaction between hypersensitive sites in the active beta-globin locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Transvection effects in Drosophila

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Chromatin modification and epigenetic reprogramming in mammalian development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

A chromatin remodelling complex that loads cohesin onto human chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Inappropriate Gene Activation in FSHD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

The many faces of histone lysine methylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Recruitment of cohesin to heterochromatic regions by Swi6/HP1 in fission yeast

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Requirement of heterochromatin for cohesion at centromeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

A potential role for human cohesin in mitotic spindle aster assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Activation of beta-major globin gene transcription is associated with recruitment of NF-E2 to the beta-globin LCR and gene promoter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2700282

21 June 2018

Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Evidence for the existence of an HP1-mediated subcode within the histone code.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Evidence that homologous X-chromosome pairing requires transcription and Ctcf protein.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Effects of tethering HP1 to euchromatic regions of the Drosophila genome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Dynamic assembly of silent chromatin during thymocyte maturation

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Neurotrophins mediate human embryonic stem cell survival

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000559

21 January 2018

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19593370

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD

1 reference

https://pubmed.ncbi.nlm.nih.gov/19593370

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19593370

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19593370

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19593370

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1000559

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33480945&oldid=2248806208"