@prefix pubblicazioni: . @prefix unitaDiPersonaleInterno: . @prefix prodotto: . unitaDiPersonaleInterno:MATRICOLA8423 pubblicazioni:autoreCNRDi prodotto:ID4802 . @prefix prodottidellaricerca: . @prefix istituto: . istituto:CDS059 prodottidellaricerca:prodotto prodotto:ID4802 . @prefix modulo: . modulo:ID2692 prodottidellaricerca:prodotto prodotto:ID4802 . @prefix rdf: . @prefix retescientifica: . prodotto:ID4802 rdf:type retescientifica:ProdottoDellaRicerca , prodotto:TIPO1101 . @prefix rdfs: . prodotto:ID4802 rdfs:label "Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease (Articolo in rivista)"@en . @prefix xsd: . prodotto:ID4802 pubblicazioni:anno "2008-01-01T00:00:00+01:00"^^xsd:gYear ; pubblicazioni:doi "10.1159/000118634"^^xsd:string . @prefix skos: . prodotto:ID4802 skos:altLabel "
Seripa D.a; Matera M.G.a; Franceschi M.a; Bizzarro A.c; Paris F.a; Cascavilla L.a; Rinaldi M.d; Panza F.g; Solfrizzi V.g; Daniele A.c; Masullo C.c; Dallapiccola B.b,e,f; Pilotto A.a (2008)
Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease
in Dementia and geriatric cognitive disorders
"^^rdf:HTML ; pubblicazioni:autori "Seripa D.a; Matera M.G.a; Franceschi M.a; Bizzarro A.c; Paris F.a; Cascavilla L.a; Rinaldi M.d; Panza F.g; Solfrizzi V.g; Daniele A.c; Masullo C.c; Dallapiccola B.b,e,f; Pilotto A.a"^^xsd:string ; pubblicazioni:paginaInizio "287"^^xsd:string ; pubblicazioni:paginaFine "292"^^xsd:string ; pubblicazioni:altreInformazioni "Author Keywords: Alzheimer's disease; glutamate receptor; ionotropic; N-methyl-D-aspartate 2B; N-methyl-D-aspartate; single-nucleotide polymorphism\nKeyWords Plus: APOLIPOPROTEIN-E GENOTYPES; ENZYME GENE POLYMORPHISMS; LONG-TERM POTENTIATION; NMDA RECEPTOR; ASSOCIATION ANALYSIS; VASCULAR DEMENTIA; MECHANISMS; PHOSPHORYLATION; SCHIZOPHRENIA; VARIANTS \nPublisher: KARGER, ALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND\nWeb of Science Category: Geriatrics & Gerontology; Clinical Neurology; Psychiatry\nSubject Category: Geriatrics & Gerontology; Neurosciences & Neurology; Psychiatry\nIDS Number: 271GS\nISSN: 1420-8008"^^xsd:string ; pubblicazioni:numeroVolume "25"^^xsd:string . @prefix ns11: . prodotto:ID4802 pubblicazioni:rivista ns11:ID192607 ; pubblicazioni:note "Epub 2008 Feb 26"^^xsd:string ; pubblicazioni:numeroFascicolo "3"^^xsd:string ; skos:note "ISI Web of Science (WOS)"^^xsd:string ; pubblicazioni:affiliazioni "a Geriatric Unit & Gerontology-Geriatrics Research Laboratory, Department of Medical Sciences;\nb IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo;\nc Institute of Neurology, Catholic University School of Medicine;\nd Institute of Neurobiology and Molecular Medicine, CNR-ARTOV;\ne CSS-Mendel Institute; and\nf Department of Experimental Medicine & Pathology, University `La Sapienza\u00B4, Rome; and\ng Department of Geriatrics, Center for Aging Brain, Memory Unit, University of Bari, Bari, Italy"^^xsd:string ; pubblicazioni:titolo "Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease"^^xsd:string ; prodottidellaricerca:abstract "Background: The glutamatergic neurotransmitter systems play a crucial role in memory formation and information processing. Alterations in this system contribute to the manifestation of symptoms in Alzheimer's disease (AD). Glutamate transmits signals via the N-methyl-D-aspartate receptors (NMDARs). Aims: The potential involvement of polymorphisms in the GRIN2B gene, encoding subunit 2B of the NMDA receptor, in the risk for AD was evaluated. Methods: We investigated the 3 single-nucleotide polymorphisms (SNPs) rs1019385, rs1806201 and rs890, i. e. the G(-200) -> T transversion in the 5'UTR, the A(2664) -> G transition in exon 13 and the G(5072) -> T transition in the 3'UTR of the GRIN2B gene, in 222 Caucasian AD patients and 170 healthy Caucasian age-matched controls. Results: No differences were found in the overall distribution of the single-nucleotide polymorphism genotypes between AD patients and healthy controls, even when the analysis was adjusted for sex, age and APOE. As expected from genotype frequencies, no differences were found in the distribution of the estimated allele and haplotype frequencies between AD patients and healthy controls. Conclusion: In this study no significant association between polymorphisms in the GRIN2B gene and AD was observed. Further investigations of polymorphisms in the gene encoding the NMDA receptor 2B subunit in AD patients with different genetic setting are needed to clarify their role in the pathogenesis of AD."@en ; prodottidellaricerca:prodottoDi modulo:ID2692 , istituto:CDS059 ; pubblicazioni:autoreCNR unitaDiPersonaleInterno:MATRICOLA8423 . @prefix parolechiave: . prodotto:ID4802 parolechiave:insiemeDiParoleChiave . ns11:ID192607 pubblicazioni:rivistaDi prodotto:ID4802 . parolechiave:insiemeDiParoleChiaveDi prodotto:ID4802 .