(Q24338476)

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IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ

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scholarly article

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IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ (English)

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Interleukin 1 receptor accessory protein like 1

1 reference

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Protein tyrosine phosphatase, receptor type, D

1 reference

GOA release 2020-03-11

SH3 and multiple ankyrin repeat domains 1

1 reference

GOA release 2020-03-11

Leucine rich repeat containing 4B

1 reference

GOA release 2020-03-11

Interleukin-1 receptor accessory protein-like 1

1 reference

GOA release 2020-03-11

Yoichiro Iwakura

7

object named as

Yoichiro Iwakura

author given names

Yoichiro

author last names

Iwakura

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

6

object named as

Ryo Taguchi

author given names

Ryo

author last names

Taguchi

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

author name string

Tomoyuki Yoshida

1

author given names

Tomoyuki

author last names

Yoshida

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

Misato Yasumura

2

author given names

Misato

author last names

Yasumura

1 reference

Europe PubMed Central

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15 May 2020

Takeshi Uemura

3

author given names

Takeshi

author last names

Uemura

1 reference

Europe PubMed Central

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15 May 2020

Sung-Jin Lee

4

author given names

Sung-Jin

author last names

Lee

1 reference

Europe PubMed Central

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15 May 2020

Moonjin Ra

5

author given names

Moonjin

author last names

Ra

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

Masayoshi Mishina

8

author given names

Masayoshi

author last names

Mishina

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

language of work or name

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publication date

21 September 2011

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Journal of Neuroscience

1 reference

Europe PubMed Central

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15 May 2020

31

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

13485-13499

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

38

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC6623287/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of autism: a review.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Shank family of scaffold proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired learning with enhanced hippocampal long-term potentiation in PTPdelta-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and characterization of two members of a novel class of the interleukin-1 receptor (IL-1R) family. Delineation of a new class of IL-1R-related proteins based on signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of dendritic spine morphology and synaptic function by Shank and Homer

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monogenic causes of X-linked mental retardation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The interleukin-1 receptor/Toll-like receptor superfamily: signal transduction during inflammation and host defense

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subtype switching of vesicular glutamate transporters at parallel fibre-Purkinje cell synapses in developing mouse cerebellum

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crystal structure of the Toll/interleukin-1 receptor domain of human IL-1RAPL.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct interaction of GluRdelta2 with Shank scaffold proteins in cerebellar Purkinje cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct roles of calcineurin-nuclear factor of activated T-cells and protein kinase A-cAMP response element-binding protein signaling in presynaptic differentiation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Remodeling of synaptic structures in the motor cortex following spinal cord injury.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression and distribution of JNK/SAPK-associated scaffold protein JSAP1 in developing and adult mouse brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation: many genes for a complex disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics and pathophysiology of mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein tyrosine phosphatases: from genes, to function, to disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dynamic aspects of CNS synapse formation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of neurexin 1 associated with autism spectrum disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

XLMR genes: update 2007.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A regular pattern of Ig super-motifs defines segmental flexibility as the elastic mechanism of the titin chain

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zebrafish orthologue of mental retardation protein IL1RAPL1 regulates presynaptic differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroligins and neurexins link synaptic function to cognitive disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The amino-terminal domain of glutamate receptor delta2 triggers presynaptic differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trans-synaptic adhesion between NGL-3 and LAR regulates the formation of excitatory synapses

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic advances in autism: heterogeneity and convergence on shared pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of synaptic vesicle accumulation and axon terminal remodeling during synapse formation by distinct Ca signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A postsynaptic signaling pathway that may account for the cognitive defect due to IL1RAPL1 mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trans-synaptic adhesions between netrin-G ligand-3 (NGL-3) and receptor tyrosine phosphatases LAR, protein-tyrosine phosphatase delta (PTPdelta), and PTPsigma via specific domains regulate excitatory synapse formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postsynaptic TrkC and presynaptic PTPσ function as a bidirectional excitatory synaptic organizing complex.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein tyrosine phosphatase σ regulates the synapse number of zebrafish olfactory sensory neurons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA expression cloning of the IL-1 receptor, a member of the immunoglobulin superfamily

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of the human transmembrane protein-tyrosine phosphatase delta. Evidence for tissue-specific expression of alternative human transmembrane protein-tyrosine phosphatase delta isoforms

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental regulation of gene expression for the MPTP delta isoforms in the central nervous system and the immune system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21940441

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.2136-11.2011

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

release_khyrbqcrkbahtit4i62mlf5kma

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6623287&resulttype=core&format=json

15 May 2020

ResearchGate publication ID

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