Defective oxytocin function: a clue to understanding the cause of autism? - Wikidata - wikimedia - TriplyDB

Defective oxytocin function: a clue to understanding the cause of autism?

Defective oxytocin function: a clue to understanding the cause of autism?

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Epigenetics meets endocrinology.Antiaggressive activity of central oxytocin in male rats.All-trans retinoic acid upregulates reduced CD38 transcription in lymphoblastoid cell lines from Autism spectrum disorder Autism, oxytocin and interoception DNA methylation of specific CpG sites in the promoter region regulates the transcription of the mouse oxytocin receptor.Plasma Oxytocin in Children with Autism and Its Correlations with Behavioral Parameters in Children and Parents.Sensorimotor integration and psychopathology: motor control abnormalities related to psychiatric disorders.Working up autism: the practical role of medical genetics.Exposure to synthetic oxytocin during delivery and its effect on psychomotor development.Stranger Fear and Early Risk for Social Anxiety in Preschoolers with Fragile X Syndrome Contrasted to Autism Spectrum Disorder.

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Defective oxytocin function: a clue to understanding the cause of autism?

http://www.wikidata.org/entity/Q33511680

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2009 nî lūn-bûn

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2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Defective oxytocin function: a clue to understanding the cause of autism?

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Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Vaccines and autism: a tale of shifting hypotheses

The genetics of autistic disorders and its clinical relevance: a review of the literature

Advances in autism genetics: on the threshold of a new neurobiology

Neuroligins and neurexins link synaptic function to cognitive disease

Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Strong association of de novo copy number mutations with autism

Examination of association of genes in the serotonin system to autism

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