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http://purl.uniprot.org/citations/37940970http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37940970http://www.w3.org/2000/01/rdf-schema#comment"The GPCR HCAR1 is known to be the sole receptor for lactate, which modulates its metabolic effects. Despite its significant role in many processes, mice deficient in HCAR1 exhibit no visible phenotype and are healthy and fertile. We performed transcriptomic analysis on HCAR1 deficient cells, in combination with lactate, to explore pathophysiologically altered processes. Processes such as immune regulation, various cancers, and neurodegenerative diseases were significantly enriched for HCAR1 transcriptomic signature. However, the most affected process of all was autism spectrum disorder. We performed behavioral tests on HCAR1 KO mice and observed that these mice manifest autistic-like behavior. Our data opens new avenues for research on HCAR1 and lactate effect at a pathological level. Video Abstract."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.org/dc/terms/identifier"doi:10.1186/s12964-023-01188-z"xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/author"Chemtob S."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/author"Joyal J.S."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/author"Cagnone G."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/author"Mohammad Nezhady M.A."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/name"Cell Commun Signal"xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/pages"196"xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/title"Lack of HCAR1, the lactate GPCR, signaling promotes autistic-like behavior."xsd:string
http://purl.uniprot.org/citations/37940970http://purl.uniprot.org/core/volume"21"xsd:string
http://purl.uniprot.org/citations/37940970http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/37940970
http://purl.uniprot.org/citations/37940970http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/37940970
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http://purl.uniprot.org/uniprot/#_A0A4Y1JWM1-mappedCitation-37940970http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37940970
http://purl.uniprot.org/uniprot/#_B9UM22-mappedCitation-37940970http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37940970
http://purl.uniprot.org/uniprot/#_Q8C131-mappedCitation-37940970http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37940970
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http://purl.uniprot.org/uniprot/A0A4Y1JWM1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/37940970
http://purl.uniprot.org/uniprot/Q8C131http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/37940970
http://purl.uniprot.org/uniprot/E9PZR8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/37940970