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• W2132900512 abstract "The gene encoding NOS-I (NOS1) displays a complex transcriptional regulation, with nine alternative first exons. Exon 1c and 1f are the most abundant forms in the brain. A functional single nucleotide polymorphism (SNP) in exon 1c and a polymorphism in exon 1f, consisting of a variable number of tandem repeats (VNTR) originating short (S) and long (L) alleles, were studied in 184 patients with Alzheimer's disease (AD) and 144 gender- and age-matched controls. No differences were found for the Ex1c G-84A. The Ex1f-VNTR S allele was significantly more common in AD (55% versus 44%, P=0.009, OR=1.52) as was the S/S genotype (28% versus 14%, P=0.008; OR=2.37). The S allele showed a highly significant interaction with the ApoE epsilon 4 allele (OR: 10.83). Therefore, short alleles of the NOS1 exon 1f-VNTR are likely to be susceptibility factors for AD, and interact with the epsilon 4 allele to markedly increase the AD risk." @default.
• W2132900512 created "2016-06-24" @default.
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• W2132900512 date "2008-09-01" @default.
• W2132900512 modified "2023-10-14" @default.
• W2132900512 title "Association of a NOS1 promoter repeat with Alzheimer's disease" @default.
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• W2132900512 doi "https://doi.org/10.1016/j.neurobiolaging.2007.03.003" @default.
• W2132900512 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17418914" @default.
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