Genetic and epigenetic dysregulation of imprinted genes in the brain. - Wikidata - awgldk - TriplyDB

Genetic and epigenetic dysregulation of imprinted genes in the brain.

Genetic and epigenetic dysregulation of imprinted genes in the brain.

http://www.wikidata.org/entity/Q37961799

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DNA modifications: function and applications in normal and disease States DNA Methylation of Regulatory Regions of Imprinted Genes at Birth and Its Relation to Infant Temperament.Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease Roles of imprinted genes in neural stem cells.The Role of Epigenetic Change in Autism Spectrum Disorders.The abundance of cis-acting loci leading to differential allele expression in F1 mice and their relationship to loci harboring genes affecting complex traits.Novel polymorphisms within the Dlk1-Dio3 imprinted locus in rat: a putative genetic basis for strain-specific allelic gene expression.Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease.Atypical aging in Down syndrome.The epigenetics of stroke recovery and rehabilitation: from polycomb to histone deacetylases.Modeling neurodevelopmental disorders using human pluripotent stem cells.

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Genetic and epigenetic dysregulation of imprinted genes in the brain.

http://www.wikidata.org/entity/Q37961799

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article científic

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article scientifique

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Genetic and epigenetic dysregulation of imprinted genes in the brain.

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Genetic and epigenetic dysregulation of imprinted genes in the brain.

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Genetic and epigenetic dysregulation of imprinted genes in the brain.

@en

Genetic and epigenetic dysregulation of imprinted genes in the brain.

@nl

prefLabel

Genetic and epigenetic dysregulation of imprinted genes in the brain.

@en

Genetic and epigenetic dysregulation of imprinted genes in the brain.

@nl

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Genetic and epigenetic dysregulation of imprinted genes in the brain.

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Kristin D Kernohan

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Nathalie G Bérubé

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P2860

Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation

BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources.

The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

Parental imprinting of the mouse H19 gene

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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743-763

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scholarly article

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10.2217/EPI.10.61

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6

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2

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2010-12-01T00:00:00Z

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22122080

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