FRA2A is a CGG repeat expansion associated with silencing of AFF3 - Wikidata - awgldk - TriplyDB

FRA2A is a CGG repeat expansion associated with silencing of AFF3

FRA2A is a CGG repeat expansion associated with silencing of AFF3

http://www.wikidata.org/entity/Q35156954

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Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex.Combined transcriptome studies identify AFF3 as a mediator of the oncogenic effects of β-catenin in adrenocortical carcinoma.Evidence for chromosome fragility at the frataxin locus in Friedreich ataxia.A sequence variant associating with educational attainment also affects childhood cognition RNA biology of disease-associated microsatellite repeat expansions.Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.

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FRA2A is a CGG repeat expansion associated with silencing of AFF3

http://www.wikidata.org/entity/Q35156954

description

2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2014 թվականի ապրիլին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

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2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@ast

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@en

type

label

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@ast

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@en

prefLabel

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@ast

FRA2A is a CGG repeat expansion associated with silencing of AFF3

@en

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JOURNAL.PGEN.1004242

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FRA2A is a CGG repeat expansion associated with silencing of AFF3

@en

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Chandra Sekhar Reddy Chilamakuri

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

Edwin Reyniers

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

Eric Haan

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

Evelyn Douglas

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

Geoffrey Thompson

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

Harris Morrison

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

Hemant Bengani

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

Jacqueline Rainger

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

Liesbeth Rooms

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

Sofie Metsu

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

P2860

AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23)

Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4

LAF-4 encodes a lymphoid nuclear protein with transactivation potential that is homologous to AF-4, the gene fused to MLL in t(4;11) leukemias

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1

Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

A new paradigm for West syndrome based on molecular and cell biology

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Fragile sites and human disease

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e1004242

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scholarly article

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10.1371/JOURNAL.PGEN.1004242

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4

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10

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Martin S. Taylor

David R. FitzPatrick

Geert Vandeweyer

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2014-04-24T00:00:00Z

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261882080

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24763282

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3998887

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