The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis (Q24322902)

Discs large MAGUK scaffold protein 4

GOA release 2020-03-11

1 reference

Discs large MAGUK scaffold protein 3

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Eriko Fujita-Jimbo

1

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Yuko Tanabe

2

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Zhiling Yu

3

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Karin Kojima

4

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Masato Mori

5

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Hong Li

6

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Sadahiko Iwamoto

7

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Takanori Yamagata

8

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Mariko Y Momoi

9

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Takashi Momoi

Creative Commons Attribution 4.0 International

10

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language of work or name

English

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publication date

2015

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published in

Molecular Autism

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volume

6

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issue

1

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page(s)

17

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copyright license

start time

13 March 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

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

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Screening for Neuroligin 4 (NLGN4) truncating and transmembrane domain mutations in schizophrenia

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The G protein-coupled receptor repertoires of human and mouse

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Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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The neuroligin and neurexin families: from structure to function at the synapse

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PDZ domains - common players in the cell signaling

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Cloning of GPR37, a gene located on chromosome 7 encoding a putative G-protein-coupled peptide receptor, from a human frontal brain EST library

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Binding properties of neuroligin 1 and neurexin 1beta reveal function as heterophilic cell adhesion molecules

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Binding of neuroligins to PSD-95

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The brain-specific G-protein coupled receptor GPR85 with identical protein sequence in man and mouse maps to human chromosome 7q31

19 March 2017

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De novo mutations in schizophrenia implicate synaptic networks

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The genetic landscapes of autism spectrum disorders

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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder

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Detection of activated Caspase-3 by a cleavage site-directed antiserum during naturally occurring DRG neurons apoptosis

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c-jun inhibited the alternative splicing of neuron-specific amyloid precursor protein, but stimulated the non-neuron type one in P19 EC cells.

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Mutations in the gene encoding CADM1 are associated with autism spectrum disorder

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A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum

21 January 2018

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Studying the emergence of autism spectrum disorders in high-risk infants: methodological and practical issues

21 January 2018

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