Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. - Wikidata - wikimedia - TriplyDB

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

http://www.wikidata.org/entity/Q34341154

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The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.A developmental and genetic classification for malformations of cortical development: update 2012 Neurogenomics of speech and language disorders: the road ahead Androgen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalization Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers The evolutionary history of genes involved in spoken and written language: beyond FOXP2.Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders Recent Advances in the Genetics of Vocal Learning Globularity and language-readiness: generating new predictions by expanding the set of genes of interest ASD-relevant Animal Models of the Foxp Family of Transcription Factors Polymicrogyria: a common and heterogeneous malformation of cortical development.Over-expression of either MECP2_e1 or MECP2_e2 in neuronally differentiated cells results in different patterns of gene expression Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism.Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex.Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.SRPX2 promotes cell migration and invasion via FAK dependent pathway in pancreatic cancer.Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development Genome-wide analysis identifies a role for common copy number variants in specific language impairment Insights into the Neural and Genetic Basis of Vocal Communication.Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk.Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c.The conundrums of understanding genetic risks for autism spectrum disorders Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.Insights into the genetic foundations of human communication.Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System.CNTNAP2 is a direct FoxP2 target in vitro and in vivo in zebra finches: complex regulation by age and activity.The Key Regulator for Language and Speech Development, FOXP2, is a Novel Substrate for SUMOylation.MicroRNA screening identifies a link between NOVA1 expression and a low level of IKAP in familial dysautonomia.From where to what: a neuroanatomically based evolutionary model of the emergence of speech in humans Decoding the molecular evolution of human cognition using comparative genomics.Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene.The untold stories of the speech gene, the FOXP2 cancer gene.Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

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P2860

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

http://www.wikidata.org/entity/Q34341154

description

2010 nî lūn-bûn

@nan

2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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type

label

Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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prefLabel

Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Human Molecular Genetics

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Molecular networks implicated ...... ulates the SRPX2/uPAR complex.

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Annick Massacrier

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Edouard Hirsch

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Jennifer Cillario

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Magali Ponsole-Lenfant

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Manal Khalife

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Nadine Bruneau

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Pierre Szepetowski

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P2860

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.

Two candidate downstream target genes for E2A-HLF

Molecular evolution of FOXP2, a gene involved in speech and language

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

A functional genetic link between distinct developmental language disorders

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

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

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4848-4860

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10.1093/HMG/DDQ415

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24

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19

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Gabrielle Rudolf

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2010-09-21T00:00:00Z

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46393005

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2989892

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