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Heterochromatin dysregulation in human diseases.

Heterochromatin dysregulation in human diseases.

http://www.wikidata.org/entity/Q37723199

about

Discovering chromatin motifs using FAIRE sequencing and the human diploid genome Histones: at the crossroads of peptide and protein chemistry.Histone H3 N-terminal acetylation sites especially K14 are important for rDNA silencing and aging.Statistical Enrichment of Epigenetic States Around Triplet Repeats that Can Undergo Expansions.A two-state activation mechanism controls the histone methyltransferase Suv39h1.Histone modifications and exercise adaptations.Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application.Suv4-20h2 mediates chromatin compaction and is important for cohesin recruitment to heterochromatin.The Hedgehog-GLI pathway in embryonic development and cancer: implications for pulmonary oncology therapy.The complex roles of histone demethylases in vivo.C3G shows regulated nucleocytoplasmic exchange and represses histone modifications associated with euchromatin Histone chaperone Spt16p is required for heterochromatin mediated silencing in budding yeast.PORP vs. TORP: a meta-analysis.

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Heterochromatin dysregulation in human diseases.

http://www.wikidata.org/entity/Q37723199

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on April 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Heterochromatin dysregulation in human diseases.

@en

Heterochromatin dysregulation in human diseases.

@nl

type

label

Heterochromatin dysregulation in human diseases.

@en

Heterochromatin dysregulation in human diseases.

@nl

prefLabel

Heterochromatin dysregulation in human diseases.

@en

Heterochromatin dysregulation in human diseases.

@nl

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JAPPLPHYSIOL.00053.2010

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Journal of Applied Physiology

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Heterochromatin dysregulation in human diseases.

@en

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Gunnar Schotta

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Matthias Hahn

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Silvia Dambacher

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P2860

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

UBE3A/E6-AP mutations cause Angelman syndrome

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

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

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

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

Genomic imprinting disorders in humans: a mini-review

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

HDAC inhibitors correct frataxin deficiency in a Friedreich ataxia mouse model

High-resolution profiling of histone methylations in the human genome

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232-242

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scholarly article

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10.1152/JAPPLPHYSIOL.00053.2010

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1

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109

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2010-04-01T00:00:00Z

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42833656

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20360431

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