Functional genetic analysis of mutations implicated in a human speech and language disorder (Q34567203)

3 August 2017

title

Functional genetic analysis of mutations implicated in a human speech and language disorder (English)

1 reference

3 August 2017

1 reference

9

1 reference

3 August 2017

Sonja C Vernes

1

0 references

Louise E Bird

object named as

Louise E Bird

7

0 references

Fanny M Elahi

object named as

Fanny M Elahi

3

0 references

Kay Davies

8

object named as

Kay E Davies

1 reference

3 August 2017

2

Jérôme Nicod

1 reference

3 August 2017

Julie A Coventry

4

1 reference

3 August 2017

Niamh Kenny

5

1 reference

3 August 2017

Anne-Marie Coupe

6

1 reference

3 August 2017

language of work or name

1 reference

19 September 2006

1 reference

3 August 2017

published in

Human Molecular Genetics

1 reference

3 August 2017

volume

15

1 reference

3 August 2017

issue

21

1 reference

3 August 2017

page(s)

3154-3167

1 reference

Genetic and environmental risks for specific language impairment in children

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Deciphering the genetic basis of speech and language disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

A forkhead-domain gene is mutated in a severe speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

FOXP2 in focus: what can genes tell us about speech and language?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Language fMRI abnormalities associated with FOXP2 gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Forkhead transcription factors: key players in development and metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Fox's in development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

FoxP2 expression in avian vocal learners and non-learners

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Molecular cloning and developmental expression of foxP2 in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

The eloquent ape: genes, brains and the evolution of language

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

An evolutionary perspective on FoxP2: strictly for the birds?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Structure of the forkhead domain of FOXP2 bound to DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

FOXP2: novel exons, splice variants, and CAG repeat length stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

The ins and outs of FoxO shuttling: mechanisms of FoxO translocation and transcriptional regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Inhibition of nuclear import by protein kinase B (Akt) regulates the subcellular distribution and activity of the forkhead transcription factor AFX.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Phosphorylation of serine 256 suppresses transactivation by FKHR (FOXO1) by multiple mechanisms. Direct and indirect effects on nuclear/cytoplasmic shuttling and DNA binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Inhibition of proteasomal activity causes inclusion formation in neuronal and non-neuronal cells overexpressing Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Hassles with taking out the garbage: aggravating aggresomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Aggresomes, inclusion bodies and protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Aggresomes formed by alpha-synuclein and synphilin-1 are cytoprotective

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

MRI analysis of an inherited speech and language disorder: structural brain abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Dynamic DNA contacts observed in the NMR structure of winged helix protein-DNA complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

The interaction of DNA with the DNA-binding domain encoded by the Drosophila gene fork head.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Five years on the wings of fork head

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Tissue-dependent isoforms of mammalian Fox-1 homologs are associated with tissue-specific splicing activities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Microtubule disruption inhibits autophagosome-lysosome fusion: implications for studying the roles of aggresomes in polyglutamine diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL392

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL392

1 reference

3 August 2017

1 reference