Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.
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Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing TechnologyNeuropathological Mechanisms of Seizures in Autism Spectrum DisorderMutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in MiceMutations in ARID2 are associated with intellectual disabilities.Intelligence, Functioning, and Related Factors in Children with Cerebral Palsy.Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity.Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in NeurodevelopmentObsessive-Compulsive Disorder and Autism Spectrum Disorders: Longitudinal and Offspring Risk.[Public health policies for the intellectually disabled in Brazil: an integrative review].Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.Integrative genomic analyses for identification and prioritization of long non-coding RNAs associated with autism.Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotoniaAltered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability.Emerging genotype-phenotype relationships in patients with large NF1 deletions.Insights into the genetic foundations of human communication.Comparison of two subtelomeric assays for the screening of chromosomal rearrangements: analysis of 383 patients, literature review and further recommendations.Annual Research Review: Understudied populations within the autism spectrum - current trends and future directions in neuroimaging research.Altered thalamocortical development in the SAP102 knockout model of intellectual disability.De novo POGZ mutations in sporadic autism disrupt the DNA-binding activity of POGZ.Gene Coexpression Networks in Human Brain Developmental Transcriptomes Implicate the Association of Long Noncoding RNAs with Intellectual Disability.Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in MiceDe novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function.Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome.Aging in Place in Every Community: Social Exclusion Experiences of Parents of Adult children With Autism Spectrum Disorder.CRL4 antagonizes SCFFbxo7-mediated turnover of cereblon and BK channel to regulate learning and memory.Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.Loss-of-function mutation in RUSC2 causes intellectual disability and secondary microcephaly.The association between familial ASD diagnosis, autism symptomatology and developmental functioning in young children.Cognitive disorders: Deep brain stimulation for Rett syndrome.Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases.Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability.The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders.Rho GTPases in Intellectual Disability: From Genetics to Therapeutic Opportunities.Synaptic dysfunction in neurodegenerative and neurodevelopmental diseases: an overview of induced pluripotent stem-cell-based disease models
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P2860
Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.
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年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年學術文章
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name
Intellectual disability and au ...... enes and molecular mechanisms.
@ast
Intellectual disability and au ...... enes and molecular mechanisms.
@en
Intellectual disability and au ...... enes and molecular mechanisms.
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type
label
Intellectual disability and au ...... enes and molecular mechanisms.
@ast
Intellectual disability and au ...... enes and molecular mechanisms.
@en
Intellectual disability and au ...... enes and molecular mechanisms.
@nl
prefLabel
Intellectual disability and au ...... enes and molecular mechanisms.
@ast
Intellectual disability and au ...... enes and molecular mechanisms.
@en
Intellectual disability and au ...... enes and molecular mechanisms.
@nl
P2860
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P1476
Intellectual disability and au ...... enes and molecular mechanisms.
@en
P2093
Anand K Srivastava
Charles E Schwartz
P2860
P304
P356
10.1016/J.NEUBIOREV.2014.02.015
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P577
2014-04-04T00:00:00Z