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The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis
30/30 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 30 checked references that resolve
resolves10.1038/ng1136
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
resolves10.1038/ng1933
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
resolves10.1016/j.ajhg.2007.09.017
Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders
resolves10.1016/j.bbrc.2008.10.107
Mutations in the gene encoding CADM1 are associated with autism spectrum disorder
resolves10.1007/s00018-006-6061-3
The neuroligin and neurexin families: from structure to function at the synapse
resolves10.1074/jbc.272.41.26032
Binding Properties of Neuroligin 1 and Neurexin 1β Reveal Function as Heterophilic Cell Adhesion Molecules
resolves10.1371/journal.pone.0051155
Mutation in Parkinson Disease-Associated, G-Protein-Coupled Receptor 37 (GPR37/PaelR) Is Related to Autism Spectrum Disorder
resolves10.1007/s00439-011-0975-z
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
resolves10.1093/hmg/ddr208
Identification and functional characterization of rare mutations of the neuroligin-2 gene ( NLGN2 ) associated with schizophrenia
resolves10.1016/j.schres.2005.11.003
Screening for Neuroligin 4 (NLGN4) truncating and transmembrane domain mutations in schizophrenia
resolves10.1073/pnas.0906232107
De novo mutations in the gene encoding the synaptic scaffolding protein
<i>SHANK3</i>
in patients ascertained for schizophrenia
resolves10.1016/j.chc.2008.06.010
Developing Drugs for Core Social and Communication Impairment in Autism
resolves10.1016/S0167-4781(00)00182-2
The brain-specific G-protein coupled receptor GPR85 with identical protein sequence in man and mouse maps to human chromosome 7q31
resolves10.1006/geno.1997.4900
Cloning of GPR37, a Gene Located on Chromosome 7 Encoding a Putative G-Protein-Coupled Peptide Receptor, from a Human Frontal Brain EST Library
resolves10.1073/pnas.0710717105
The evolutionarily conserved G protein-coupled receptor SREB2/GPR85 influences brain size, behavior, and vulnerability to schizophrenia
resolves10.1006/bbrc.2000.2829
An Evolutionarily Conserved G-Protein Coupled Receptor Family, SREB, Expressed in the Central Nervous System
resolves10.1016/S0169-328X(99)00092-3
Molecular cloning and characterization of two putative G protein-coupled receptors which are highly expressed in the central nervous system
resolves10.1038/cddis.2010.23
Autism spectrum disorder is related to endoplasmic reticulum stress induced by mutations in the synaptic cell adhesion molecule, CADM1
resolves10.1006/bbrc.1995.1117
c-jun Inhibited the Alternative Splicing of Neuron-Specific Amyloid Precursor Protein, but Stimulated the Non-neuron Type One in P19 EC Cells
resolves10.1111/jnc.12022
A complex of synaptic adhesion molecule <scp>CADM</scp>1, a molecule related to autism spectrum disorder, with <scp>MUPP</scp>1 in the cerebellum
resolves10.1006/bbrc.1998.8815
Detection of Activated Caspase-3 by a Cleavage Site-Directed Antiserum during Naturally Occurring DRG Neurons Apoptosis
resolves10.1016/j.braindev.2004.08.003
Mutation analysis of methyl-CpG binding protein family genes in autistic patients
resolves10.1038/13810
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
resolves10.1007/s10803-006-0179-x
Studying the Emergence of Autism Spectrum Disorders in High-risk Infants: Methodological and Practical Issues
resolves10.1083/jcb.200207050
Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells
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