The odyssey of MeCP2 and parental imprinting - Test2 - elhamkhani - TriplyDB

The odyssey of MeCP2 and parental imprinting

The odyssey of MeCP2 and parental imprinting

http://www.wikidata.org/entity/Q24671994

about

Diet and the epigenetic (re)programming of phenotypic differences in behavior DNA modifications: function and applications in normal and disease States A role for MeCP2 in switching gene activity via chromatin unfolding and HP1γ displacement.Blood mercury concentrations in CHARGE Study children with and without autism.Chromatin modifiers, cognitive disorders, and imprinted genes.Evidence for alterations in stimulatory G proteins and oxytocin levels in children with autism.Genomic imprinting in the development and evolution of psychotic spectrum conditions.Roles of imprinted genes in neural stem cells.Noncoding RNAs in mental retardation Annual Research Review: Development of the cerebral cortex: implications for neurodevelopmental disorders Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations.The contribution of oxytocin and vasopressin to mammalian social behavior: potential role in autism spectrum disorder.Genetic and epigenetic dysregulation of imprinted genes in the brain.The contribution of epigenetics to understanding genetic factors in autism.Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.Sex-specific Behavioral Features of Rodent Models of Autism Spectrum Disorder

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P2860

The odyssey of MeCP2 and parental imprinting

http://www.wikidata.org/entity/Q24671994

description

2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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The odyssey of MeCP2 and parental imprinting

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Janine M LaSalle

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P2860

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

Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice

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

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

UBE3A/E6-AP mutations cause Angelman syndrome

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans.

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

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5-10

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scholarly article

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10.4161/EPI.2.1.3697

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1

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2

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2006-12-12T00:00:00Z

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5879745

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17965611

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1866173

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