YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.

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YY1 Is a Structural Regulator of Enhancer-Promoter Loops.Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene.

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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YY1 Haploinsufficiency Causes ...... nal and Chromatin Dysfunction.

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YY1 Haploinsufficiency Causes ...... nal and Chromatin Dysfunction.

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YY1 Haploinsufficiency Causes ...... nal and Chromatin Dysfunction.

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P1476

YY1 Haploinsufficiency Causes ...... nal and Chromatin Dysfunction.

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P2093

Anne Ronan

http://www.w3.org/2001/XMLSchema#string

Anneke T Vulto-van Silfhout

http://www.w3.org/2001/XMLSchema#string

Arie van Haeringen

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Asbjørg Stray-Pedersen

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Bert B A de Vries

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Bregje W M van Bon

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Charlotte Brasch-Andersen

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Christeen Ramane J Pedurupillay

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Christian Gilissen

http://www.w3.org/2001/XMLSchema#string

Christian P Schaaf

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P2860

The histone H3 lysine 27-specific demethylase Jmjd3 is required for neural commitment

MAnorm: a robust model for quantitative comparison of ChIP-Seq data sets

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

A YY1-INO80 complex regulates genomic stability through homologous recombination-based repair

Transcriptional repression by YY1, a human GLI-Krüppel-related protein, and relief of repression by adenovirus E1A protein

Isolation of a candidate repressor/activator, NF-E1 (YY-1, delta), that binds to the immunoglobulin kappa 3' enhancer and the immunoglobulin heavy-chain mu E1 site

The polycomb group protein EED interacts with YY1, and both proteins induce neural tissue in Xenopus embryos

Improved side-chain torsion potentials for the Amber ff99SB protein force field

Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities

Severe expressive-language delay related to duplication of the Williams-Beuren locus.

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907-925

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scholarly article

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10.1016/J.AJHG.2017.05.006

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English

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100

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2017-06-01T00:00:00Z

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28575647

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P921

disability

haploinsufficiency

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5473733

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.

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P2860

P2860

YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.

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