Matches in SemOpenAlex for { <https://semopenalex.org/work/W1966897722> ?p ?o ?g. }
- W1966897722 endingPage "63" @default.
- W1966897722 startingPage "57" @default.
- W1966897722 abstract "Abstract Protein p53 is the tumor suppressor involved in cell cycle control and apoptosis. There are several polymorphisms reported for p53 which can affect important regions involved in protein tumor suppressor activity. Amongst the polymorphisms described, R213R and 13949 g→a are rarely studied, with an estimate frequency not yet available for the Brazilian population. The purpose of this study was to investigate the genotype and allele frequencies and associations of these polymorphisms in a group of patients with altered esophageal tissue from South Brazil and compare with the frequency observed for a control population. A total of 35 patients for R213R and 45 for 13494 g→a polymorphisms analysis with gastroesophageal reflux disease (GERD) symptoms diagnosed by upper digestive endoscopy and confirmed by biopsy were studied. For both groups, 100 controls were used for comparison. Loss of heterozygosity (LOH) was also analyzed for a selected group of patients where normal and affected tissue was available. There was one patient with Barrett’s Esophagus (BE) showing LOH for R213R out of two heterozygous samples analyzed and two patients (esophagitis and BE) for 13494 g→a polymorphism. We also aimed to build a haplotype for both polymorphisms collectively analyzed with R27P polymorphism, previously reported by our group. There were no significant differences in allele and genotype distribution between patients and controls. Although using esophagitis, intestinal metaplasia of the cardia and BE samples, all non-neoplastic lesions, we can conclude that these sites do not represent genetic susceptibility markers for the development and early progression of GERD to BE and esophageal cancer. Additional studies are required in order to investigate other determiners of early premalignant lesions known to predispose to esophageal cancer." @default.
- W1966897722 created "2016-06-24" @default.
- W1966897722 creator A5023714420 @default.
- W1966897722 creator A5030631021 @default.
- W1966897722 creator A5047973621 @default.
- W1966897722 creator A5083975743 @default.
- W1966897722 date "2007-05-25" @default.
- W1966897722 modified "2023-10-18" @default.
- W1966897722 title "Analysis of R213R and 13494 g→a polymorphisms of the p53 gene in individuals with esophagitis, intestinal metaplasia of the cardia and Barrett’s Esophagus compared with a control group" @default.
- W1966897722 cites W126395858 @default.
- W1966897722 cites W1618742753 @default.
- W1966897722 cites W1844813598 @default.
- W1966897722 cites W1963866649 @default.
- W1966897722 cites W1985757925 @default.
- W1966897722 cites W1992917167 @default.
- W1966897722 cites W2018256508 @default.
- W1966897722 cites W2023603800 @default.
- W1966897722 cites W2027878192 @default.
- W1966897722 cites W2032052263 @default.
- W1966897722 cites W2047277742 @default.
- W1966897722 cites W2060639749 @default.
- W1966897722 cites W2062339695 @default.
- W1966897722 cites W2065795446 @default.
- W1966897722 cites W2065813095 @default.
- W1966897722 cites W2072345559 @default.
- W1966897722 cites W2073297648 @default.
- W1966897722 cites W2089507123 @default.
- W1966897722 cites W2094117733 @default.
- W1966897722 cites W2108942254 @default.
- W1966897722 cites W2111110115 @default.
- W1966897722 cites W2118094114 @default.
- W1966897722 cites W2122280377 @default.
- W1966897722 cites W2126997278 @default.
- W1966897722 cites W2150840727 @default.
- W1966897722 cites W2157712861 @default.
- W1966897722 cites W2170405327 @default.
- W1966897722 cites W2181443855 @default.
- W1966897722 cites W2184831674 @default.
- W1966897722 cites W2334572072 @default.
- W1966897722 cites W2402960337 @default.
- W1966897722 cites W2413247660 @default.
- W1966897722 cites W2415856308 @default.
- W1966897722 cites W2428105606 @default.
- W1966897722 doi "https://doi.org/10.1007/s11568-007-9007-4" @default.
- W1966897722 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2276888" @default.
- W1966897722 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18923929" @default.
- W1966897722 hasPublicationYear "2007" @default.
- W1966897722 type Work @default.
- W1966897722 sameAs 1966897722 @default.
- W1966897722 citedByCount "7" @default.
- W1966897722 countsByYear W19668977222013 @default.
- W1966897722 countsByYear W19668977222014 @default.
- W1966897722 countsByYear W19668977222018 @default.
- W1966897722 countsByYear W19668977222021 @default.
- W1966897722 crossrefType "journal-article" @default.
- W1966897722 hasAuthorship W1966897722A5023714420 @default.
- W1966897722 hasAuthorship W1966897722A5030631021 @default.
- W1966897722 hasAuthorship W1966897722A5047973621 @default.
- W1966897722 hasAuthorship W1966897722A5083975743 @default.
- W1966897722 hasBestOaLocation W19668977221 @default.
- W1966897722 hasConcept C104317684 @default.
- W1966897722 hasConcept C121608353 @default.
- W1966897722 hasConcept C126322002 @default.
- W1966897722 hasConcept C135763542 @default.
- W1966897722 hasConcept C143589142 @default.
- W1966897722 hasConcept C180754005 @default.
- W1966897722 hasConcept C197754878 @default.
- W1966897722 hasConcept C2775894508 @default.
- W1966897722 hasConcept C2776497702 @default.
- W1966897722 hasConcept C2777014526 @default.
- W1966897722 hasConcept C2777819096 @default.
- W1966897722 hasConcept C2778589982 @default.
- W1966897722 hasConcept C2779134260 @default.
- W1966897722 hasConcept C2779357193 @default.
- W1966897722 hasConcept C2779920096 @default.
- W1966897722 hasConcept C2780323790 @default.
- W1966897722 hasConcept C2781182431 @default.
- W1966897722 hasConcept C2908647359 @default.
- W1966897722 hasConcept C2909576783 @default.
- W1966897722 hasConcept C37463918 @default.
- W1966897722 hasConcept C43270747 @default.
- W1966897722 hasConcept C54355233 @default.
- W1966897722 hasConcept C71924100 @default.
- W1966897722 hasConcept C86803240 @default.
- W1966897722 hasConcept C90924648 @default.
- W1966897722 hasConcept C99454951 @default.
- W1966897722 hasConceptScore W1966897722C104317684 @default.
- W1966897722 hasConceptScore W1966897722C121608353 @default.
- W1966897722 hasConceptScore W1966897722C126322002 @default.
- W1966897722 hasConceptScore W1966897722C135763542 @default.
- W1966897722 hasConceptScore W1966897722C143589142 @default.
- W1966897722 hasConceptScore W1966897722C180754005 @default.
- W1966897722 hasConceptScore W1966897722C197754878 @default.
- W1966897722 hasConceptScore W1966897722C2775894508 @default.
- W1966897722 hasConceptScore W1966897722C2776497702 @default.
- W1966897722 hasConceptScore W1966897722C2777014526 @default.
- W1966897722 hasConceptScore W1966897722C2777819096 @default.
- W1966897722 hasConceptScore W1966897722C2778589982 @default.