(Q37723199)

22 August 2017

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title

Heterochromatin dysregulation in human diseases (English)

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22 August 2017

Matthias Hahn

1

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22 August 2017

Silvia Dambacher

series ordinal

2

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22 August 2017

Gunnar Schotta

series ordinal

3

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22 August 2017

language of work or name

English

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publication date

1 April 2010

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Journal of Applied Physiology

22 August 2017

published in

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22 August 2017

volume

109

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22 August 2017

issue

1

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22 August 2017

page(s)

232-242

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Whole chromosome instability caused by Bub1 insufficiency drives tumorigenesis through tumor suppressor gene loss of heterozygosity

22 August 2017

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The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure

21 January 2018

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Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation

21 January 2018

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Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

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Oncogene-induced senescence as an initial barrier in lymphoma development

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Genomic imprinting disorders in humans: a mini-review

21 January 2018

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 January 2018

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Genomic instability in mice lacking histone H2AX

21 January 2018

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Leukaemogenesis: more than mutant genes

21 January 2018

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

21 January 2018

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

21 January 2018

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Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations

21 January 2018

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Epigenetic silencing in Friedreich ataxia is associated with depletion of CTCF (CCCTC-binding factor) and antisense transcription

21 January 2018

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Epigenetic regulation of mammalian genomic imprinting

21 January 2018

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Clinical and genetic abnormalities in patients with Friedreich's ataxia

21 January 2018

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Su(var) genes regulate the balance between euchromatin and heterochromatin in Drosophila

21 January 2018

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Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

21 January 2018

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Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer

21 January 2018

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Inappropriate Gene Activation in FSHD

21 January 2018

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Role of the RB1 family in stabilizing histone methylation at constitutive heterochromatin

21 January 2018

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ATM signaling facilitates repair of DNA double-strand breaks associated with heterochromatin

21 January 2018

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Repeat-induced epigenetic changes in intron 1 of the frataxin gene and its consequences in Friedreich ataxia

21 January 2018

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Transcription and RNA interference in the formation of heterochromatin.

21 January 2018

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https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Promoter-associated RNA is required for RNA-directed transcriptional gene silencing in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Muscular dystrophy candidate gene FRG1 is critical for muscle development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Promoter targeted small RNAs induce long-term transcriptional gene silencing in human cells

21 January 2018

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Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Domains of heterochromatin protein 1 required for Drosophila melanogaster heterochromatin spreading

21 January 2018

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Genomic imprinting mechanisms in mammals.

21 January 2018

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Involvement of AGO1 and AGO2 in mammalian transcriptional silencing

21 January 2018

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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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain

21 January 2018

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Argonaute-1 directs siRNA-mediated transcriptional gene silencing in human cells

21 January 2018

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UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

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Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level

21 January 2018

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Evidence for histone eviction in trans upon induction of the yeast PHO5 promoter

21 January 2018

1 reference

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Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase

21 January 2018

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Chromatin remodeling in the noncoding repeat expansion diseases

21 January 2018

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Derepression of CLDN3 and CLDN4 during ovarian tumorigenesis is associated with loss of repressive histone modifications

21 January 2018

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Trilogies of histone lysine methylation as epigenetic landmarks of the eukaryotic genome

21 January 2018

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An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals

21 January 2018

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Reexpression of epigenetically silenced AML tumor suppressor genes by SUV39H1 inhibition

21 January 2018

1 reference

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Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

21 January 2018

1 reference

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Expandable DNA repeats and human disease.

21 January 2018

1 reference

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Genome-scale profiling of histone H3.3 replacement patterns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Epigenetic control of mammalian LINE-1 retrotransposon by retinoblastoma proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Bidirectional transcription directs both transcriptional gene activation and suppression in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Rb-mediated heterochromatin formation and silencing of E2F target genes during cellular senescence

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

The pathogenesis of Friedreich ataxia and the structure and function of frataxin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

PR-SET7 and SUV4-20H regulate H4 lysine-20 methylation at imprinting control regions in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

The imprinting mechanism of the Prader-Willi/Angelman regional control center

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Retrotransposon silencing and telomere integrity in somatic cells of Drosophila depends on the cytosine-5 methyltransferase DNMT2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

A functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Many paths to one goal? The proteins that recognize methylated DNA in eukaryotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Position-effect variegation and the genetic dissection of chromatin regulation in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

A silencing pathway to induce H3-K9 and H4-K20 trimethylation at constitutive heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

21 January 2018

Epigenetics in cancer

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Pharmacologic disruption of Polycomb-repressive complex 2-mediated gene repression selectively induces apoptosis in cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Facultative heterochromatin: is there a distinctive molecular signature?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Loss of DNA methylation and histone H4 lysine 20 trimethylation in human breast cancer cells is associated with aberrant expression of DNA methyltransferase 1, Suv4-20h2 histone methyltransferase and methyl-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Loss of histone H4K20 trimethylation occurs in preneoplasia and influences prognosis of non-small cell lung cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

FRG1P-mediated aggregation of proteins involved in pre-mRNA processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Regulation of higher-order chromatin structures by nucleosome-remodelling factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

DNA triplexes and Friedreich ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Angelman syndrome 2005: updated consensus for diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FJAPPLPHYSIOL.00053.2010

10.1152/JAPPLPHYSIOL.00053.2010

21 January 2018

Identifiers

DOI

1 reference

22 August 2017

1 reference