(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

0 references

0 references

James S Sutcliffe

3

0 references

Antonio M Persico

object named as

Antonio M Persico

4

0 references

author name string

Daniel B Campbell

1

1 reference

26 July 2017

Chun Li

2

1 reference

26 July 2017

Pat Levitt

5

1 reference

26 July 2017

publication date

1 June 2008

1 reference

26 July 2017

1 reference

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

1 reference

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

26 July 2017

cites work

1 reference

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Chemically diverse toxicants converge on Fyn and c-Cbl to disrupt precursor cell function

21 June 2018

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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

1 reference

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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

1 reference

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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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21 June 2018

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A haplotype map of the human genome

21 June 2018

1 reference

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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

1 reference

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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

1 reference

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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

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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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

1 reference

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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

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

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

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

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

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

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