Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults. - Wikidata - wikimedia - TriplyDB

Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults.

Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults.

http://www.wikidata.org/entity/Q37634526

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Dopaminergic and behavioral changes in a loss-of-imprinting model of Cdkn1c.In vivo structures of an intact type VI secretion system revealed by electron cryotomography.Developmental Epigenetics: Phenotype and the Flexible Epigenome Loss of Imprinting of Protects against Age and Diet-Induced Obesity

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P2860

Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults.

http://www.wikidata.org/entity/Q37634526

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2017

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

@en

Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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type

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Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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J.CELREP.2017.01.010

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Visualizing Changes in Cdkn1c ...... rint Mis-regulation in Adults.

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Alessandro Sardini

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Allifia Abbas

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Amanda G Fisher

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Amelie Feytout

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Gráinne McNamara

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James McGinty

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Ludovica Bruno

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Mathew Van de Pette

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Matthias Merkenschlager

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Wilson K To

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P2860

Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome.

A maternal-offspring coadaptation theory for the evolution of genomic imprinting

Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.

CDKN1C (p57) is a direct target of EZH2 and suppressed by multiple epigenetic mechanisms in breast cancer cells

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1090-1099

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scholarly article

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10.1016/J.CELREP.2017.01.010

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5

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Dominic J Withers

Anne C. Ferguson-Smith

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2017-01-01T00:00:00Z

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