Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder (Q33429117)

26 July 2017

title

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder (English)

1 reference

26 July 2017

main subject

autism spectrum disorder

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0 references

James S Sutcliffe

3

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Antonio M Persico

object named as

Antonio M Persico

4

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author name string

Daniel B Campbell

1

1 reference

26 July 2017

Chun Li

2

1 reference

26 July 2017

Pat Levitt

5

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26 July 2017

publication date

1 June 2008

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26 July 2017

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26 July 2017

volume

1

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26 July 2017

issue

3

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26 July 2017

page(s)

159-168

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Non-replication and inconsistency in the genome-wide association setting

26 July 2017

cites work

1 reference

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21 June 2018

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Autism spectrum disorders: developmental disconnection syndromes

21 June 2018

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A genetic variant that disrupts MET transcription is associated with autism

21 June 2018

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21 June 2018

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Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

21 June 2018

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Regulation and clinical significance of urokinase-receptor (u-PAR), an invasion-related molecule

21 June 2018

1 reference

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Autism and environmental genomics

21 June 2018

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A haplotype map of the human genome

21 June 2018

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Domain 2 of the urokinase receptor contains an integrin-interacting epitope with intrinsic signaling activity: generation of a new integrin inhibitor

21 June 2018

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Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

21 June 2018

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Dysregulated innate immune responses in young children with autism spectrum disorders: their relationship to gastrointestinal symptoms and dietary intervention

21 June 2018

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Regulation of neocortical interneuron development and the implications for neurodevelopmental disorders.

21 June 2018

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Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

21 June 2018

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Transgenic mice demonstrate novel promoter regions for tissue-specific expression of the urokinase receptor gene

21 June 2018

1 reference

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Intestinal pathophysiology in autism.

21 June 2018

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Hepatocyte growth factor/scatter factor is a motogen for interneurons migrating from the ventral to dorsal telencephalon

21 June 2018

1 reference

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Urokinase-type plasminogen activator receptor (CD87) is a ligand for integrins and mediates cell-cell interaction.

21 June 2018

1 reference

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Urokinase-type plasminogen activator receptors associate with beta1 and beta3 integrins of fibrosarcoma cells: dependence on extracellular matrix components.

21 June 2018

1 reference

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Structure-function analysis of hepatocyte growth factor: identification of variants that lack mitogenic activity yet retain high affinity receptor binding

21 June 2018

1 reference

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Disruption of cerebral cortex MET signaling in autism spectrum disorder.

21 June 2018

1 reference

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Spurious genetic associations

31 October 2018

1 reference

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Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

31 October 2018

1 reference

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Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

Frequency of gastrointestinal symptoms in children with autistic spectrum disorders and association with family history of autoimmune disease

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

Disruption of interneuron development

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

Region- and age-specific deficits in gamma-aminobutyric acidergic neuron development in the telencephalon of the uPAR(-/-) mouse

31 October 2018

1 reference

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Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

The family based association test method: strategies for studying general genotype--phenotype associations.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678909

31 October 2018

Identifiers

DOI

10.1002/AUR.27

1 reference

26 July 2017

1 reference

26 July 2017

1 reference