http://www.cnr.it/ontology/cnr/individuo/prodotto/ID11737
Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease. (Articolo in rivista)
- Type
- Label
- Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease. (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s00702-009-0276-z (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Scacchi R; Gambina G; Moretto G; Corbo RM. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.scopus.com/inward/record.url?eid=2-s2.0-69549084437&partnerID=40&md5=750243725914811bc626c82d0972a2bf (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CORBO Rosa Maria, Department of Biology and Biotechnology, Sapienza University, Rome, Italy
SCACCHI Renato, CNR Institute of Molecular Biology and Pathology, Rome, Italy (literal)
- Titolo
- Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease. (literal)
- Abstract
- An important pathological aspect of Alzheimer's
disease (AD) is the apoptosis of neuronal and glial
cells. Two members of the same protein family that regulates
many genes involved in apoptosis are P53 and the
heterologue P73. One single nucleotide polymorphism
(SNP) in the gene encoding P53 (Arg72Pro, RS1042522),
one dinucleotide polymorphism (G4C14-to-A4T14, RS
2273953, RS1801173) in the gene encoding P73, and two
further SNPs in the same gene (-386 G/A, RS3765728;
exon 5 T/C, RS1801174) were studied to determine whether
DNA variations could influence the occurrence of the
disease in a sample of Italian subjects with the sporadic
late-onset form of AD. We observed that carrying the Pro/
Pro genotype of P53 Arg72Pro was a risk factor with
respect to the Pro/Arg ? Arg/Arg genotypes [Odds Ratio
(OR) = 2.02; 95% Confidence Interval (CI) 1.02-4.00;
p = 0.047]. Furthermore, carrying the G/G genotype of the
P73 -386 G/A was a risk factor with respect to the G/
A ? A/A genotypes (OR = 4.27; 95% CI 1.00-18.65;
p = 0.047). A significant result was also obtained for P73
G4C14-to-A4T14. Among the patients, the homozygotes
for the AT allele of this SNP had developed AD symptoms
5 years earlier than other genotypes (ANOVA p = 0.017).
Though the results of particular polymorphisms analyses
were not higly significant after correction for multiple
comparisons, present data suggest that variation at the two
genes may have a role in AD occurrence. (literal)
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