Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
about
The genetics of attention deficit/hyperactivity disorder in adults, a reviewbeta-Arrestins bind and decrease cell-surface abundance of the Na+/H+ exchanger NHE5 isoformDock3 induces axonal outgrowth by stimulating membrane recruitment of the WAVE complexGenome-wide association scan of the time to onset of attention deficit hyperactivity disorderDedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilitiesIdentifying autism loci and genes by tracing recent shared ancestryMoving towards causality in attention-deficit hyperactivity disorder: overview of neural and genetic mechanismsUsing Sibling Designs to Understand Neurodevelopmental Disorders: From Genes and Environments to Prevention ProgrammingThe DOCK protein sponge binds to ELMO and functions in Drosophila embryonic CNS developmentFamily-based genome-wide association scan of attention-deficit/hyperactivity disorderThe atypical guanine nucleotide exchange factor Dock4 regulates neurite differentiation through modulation of Rac1 GTPase and actin dynamicsLoss of modifier of cell adhesion reveals a pathway leading to axonal degeneration.Chromosomal inversions between human and chimpanzee lineages caused by retrotransposonsMicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptomsAn inside job: how endosomal Na(+)/H(+) exchangers link to autism and neurological diseaseCharacterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.The emerging role of guanine nucleotide exchange factors in ALS and other neurodegenerative diseases.Neuronal activity-regulated gene transcription in synapse development and cognitive function.SLC9A9 mutations, gene expression, and protein-protein interactions in rat models of attention-deficit/hyperactivity disorder.Patterns of ancestry, signatures of natural selection, and genetic association with stature in Western African pygmies.Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay.X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction.Evolutionary origins of eukaryotic sodium/proton exchangers.Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148Differential expression of SLC9A9 and interacting molecules in the hippocampus of rat models for attention deficit/hyperactivity disorderGenome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.Genome-wide association studies in ADHD.Functional evaluation of autism-associated mutations in NHE9.Dock protein family in brain development and neurological disease.Molecular genetics of attention-deficit/hyperactivity disorder: an overviewSevere combined immunodeficiences: new and old scenarios.Genetics of attention-deficit/hyperactivity disorder: current findings and future directions.Na+/H+ exchangers.The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder.Traditional and emerging roles for the SLC9 Na+/H+ exchangers.The molecular genetic architecture of attention deficit hyperactivity disorder.Endosomal system genetics and autism spectrum disorders: A literature review.SLC9A9 Co-expression modules in autism-associated brain regions.Genome-wide linkage scan for athlete status in 700 British female DZ twin pairs.
P2860
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P2860
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Disruption of a novel member o ...... tivity disorder-like phenotype
@ast
Disruption of a novel member o ...... tivity disorder-like phenotype
@en
Disruption of a novel member o ...... tivity disorder-like phenotype
@nl
type
label
Disruption of a novel member o ...... tivity disorder-like phenotype
@ast
Disruption of a novel member o ...... tivity disorder-like phenotype
@en
Disruption of a novel member o ...... tivity disorder-like phenotype
@nl
prefLabel
Disruption of a novel member o ...... tivity disorder-like phenotype
@ast
Disruption of a novel member o ...... tivity disorder-like phenotype
@en
Disruption of a novel member o ...... tivity disorder-like phenotype
@nl
P2093
P2860
P356
P1476
Disruption of a novel member o ...... tivity disorder-like phenotype
@en
P2093
E Fitzpatrick
M Delatycki
M G de Silva
R Williamson
P2860
P304
P356
10.1136/JMG.40.10.733
P407
P577
2003-10-01T00:00:00Z