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UnknownInteraction and Subcellular Association of PRRT1/SynDIG4 With AMPA Receptors.
Not available
S-EPMC8365426 | biostudies-literature
UnknownSynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function.
Not available
S-EPMC5856126 | biostudies-literature
ProteomicsInteractomes of GluA1 and GluA3 subunit containing AMPARs reveal distinct protein composition
The AMPA glutamate receptor (AMPAR) is the major type of synaptic excitatory ionotropic receptor in the brain. The most abundant AMPAR subtypes in the hippocampus are GluA1/2 and GluA2/3 heterotetramers. Each subtype contributes differentially to mechanisms of synaptic plasticity, which may be in pa...
ORGANISM(S): Mus musculus (Mouse) 
2022-12-12 | PXD031603 | Pride
Proteomics Prrt1 Glua1/2 Tarp- γ8 Subcomplexes Ampar Glua2/3 Ms-dap 
UnknownGene expression in salivary glands: effects of diet and mouse chromosome 17 locus regulating macronutrient intake.
Not available
S-EPMC4393215 | biostudies-literature
UnknownIdentification and Validation of Circadian Rhythm-Related Genes Involved in Intervertebral Disc Degeneration and Analysis of Immune Cell Infiltration via Machine Learning.
Not available
S-EPMC11994230 | biostudies-literature
UnknownDissecting the pathogenic effects of smoking in blood DNA methylation on allergic diseases.
Not available
S-EPMC11617736 | biostudies-literature
UnknownNovel Genes Involved in Hypertrophic Cardiomyopathy: Data of Transcriptome and Methylome Profiling.
Not available
S-EPMC9739701 | biostudies-literature
Methylation profilingHypertrophic cardiomyopathy: data of transcriptome profiling and epigenome-wide DNA methylation analysis
Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease, and its pathogenesis is still being intensively studied to explain the reasons of significant genetic and phenotypic heterogeneity of the disease. To search for possible HCM modifier genes involved in the HCM development w...
ORGANISM(S): Homo sapiens 
2022-12-14 | GSE207095 | GEO
TranscriptomicsHypertrophic cardiomyopathy: data of transcriptome profiling and epigenome-wide DNA methylation analysis
Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease, and its pathogenesis is still being intensively studied to explain the reasons of significant genetic and phenotypic heterogeneity of the disease. To search for possible HCM modifier genes involved in the HCM development w...
ORGANISM(S): Homo sapiens 
2022-06-30 | GSE206978 | GEO
UnknownExpression and Interaction Proteomics of GluA1- and GluA3-Subunit-Containing AMPARs Reveal Distinct Protein Composition.
Not available
S-EPMC9688267 | biostudies-literature
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