Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
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Evaluation of Pax6 mutant rat as a model for autism.Paternal Aging Affects Behavior in Pax6 Mutant Mice: A Gene/Environment Interaction in Understanding Neurodevelopmental DisordersNew perspectives on rodent models of advanced paternal age: relevance to autism.Evolutionary approaches to autism- an overview and integration.Overstimulation of NMDA receptors impairs early brain development in vivo.Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia.Aniridia.Endosomal sorting of Notch receptors through COMMD9-dependent pathways modulates Notch signaling.Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGHAssessment of PAX6 alleles in 66 families with aniridia.Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome.Cellular localization and characterization of cytosolic binding partners for Gla domain-containing proteins PRRG4 and PRRG2.A de novo 11p13 Microduplication in a Patient with Some Features Invoking Silver-Russell Syndrome.LGR4/GPR48 inactivation leads to aniridia-genitourinary anomalies-mental retardation syndrome defects.The role of neurotrophic factors in autism.Autism spectrum disorders--a genetics review.BDNF-TrkB signalling in fear learning: from genetics to neural networks.Developmental psychopathology: the role of structural variation in the genome.Autism spectrum disorders: the quest for genetic syndromes.The developmental brain gene NPAS3 contains the largest number of accelerated regulatory sequences in the human genome.The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene.Sustained endocrine profiles of a girl with WAGR syndrome11p Microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: a case report.3D Electrospun scaffolds promote a cytotrophic phenotype of cultured primary astrocytes.Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4.
P2860
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P2860
Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
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 18 December 2008
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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
Characterization of 11p14-p12 ...... mental retardation and autism.
@en
Characterization of 11p14-p12 ...... mental retardation and autism.
@nl
type
label
Characterization of 11p14-p12 ...... mental retardation and autism.
@en
Characterization of 11p14-p12 ...... mental retardation and autism.
@nl
prefLabel
Characterization of 11p14-p12 ...... mental retardation and autism.
@en
Characterization of 11p14-p12 ...... mental retardation and autism.
@nl
P2093
P356
P1476
Characterization of 11p14-p12 ...... mental retardation and autism.
@en
P2093
P304
P356
10.1159/000172086
P577
2008-12-18T00:00:00Z