Matches in UGent Biblio for { <https://biblio.ugent.be/publication/1169919#aggregation> ?p ?o. }
Showing items 1 to 47 of
47
with 100 items per page.
- aggregation classification "A1".
- aggregation creator B256262.
- aggregation creator B256263.
- aggregation creator B256264.
- aggregation creator B256265.
- aggregation creator B256266.
- aggregation creator B256267.
- aggregation creator B256268.
- aggregation creator B256269.
- aggregation creator B256270.
- aggregation creator B256271.
- aggregation creator B256272.
- aggregation creator B256273.
- aggregation creator B256274.
- aggregation creator B256275.
- aggregation creator B256276.
- aggregation creator person.
- aggregation date "2009".
- aggregation format "application/pdf".
- aggregation hasFormat 1169919.bibtex.
- aggregation hasFormat 1169919.csv.
- aggregation hasFormat 1169919.dc.
- aggregation hasFormat 1169919.didl.
- aggregation hasFormat 1169919.doc.
- aggregation hasFormat 1169919.json.
- aggregation hasFormat 1169919.mets.
- aggregation hasFormat 1169919.mods.
- aggregation hasFormat 1169919.rdf.
- aggregation hasFormat 1169919.ris.
- aggregation hasFormat 1169919.txt.
- aggregation hasFormat 1169919.xls.
- aggregation hasFormat 1169919.yaml.
- aggregation isPartOf urn:issn:1059-7794.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Medicine and Health Sciences".
- aggregation title "Functional redundancy of Exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A > G (p.I2285V) variant".
- aggregation abstract "Variants of unknown significance (VUS) in BRCA1 and BRCA2 are common, and present significant challenges for genetic counseling. We observed that BRCA2: c.6853A>G (p.I2285V) (Breast Cancer Information Core [BIC] name: 7081A > G; http://research.nhgri.nih.gov/bic/) co-occurs in trans with the founder mutation c.5946delT (p.S1982RfsX22) (BIC name: 6174deIT), supporting the published classification of p.I2285V as a neutral variant. However, we also noted that when compared with wild,type BRCA2, p.I2285V resulted in increased exclusion of exon 12. Functional assay using allelic complementation in Brca2-null mouse embryonic stern cells revealed that p.I2285V, an allele with exon 12 deleted and wild-type BRCA2 were all phenotypically indistinguishable, as measured by sensitivity to DNA-damaging agents, effect on irradiation-induced Rad51. foci formation, homologous recombination, and overall genontic integrity. An allele frequency study showed the p.I2285V variant was identified in 15 out of 722 (2.1%) Ashkenazi Jewish cases and 10 out of 475 (2.1%) ethnically,matched controls (odds ratio, 0.99; 95% confidence interval: 0.44-2.21; P = 0.97). Thus the p.I2285V variant is not associated with an increased risk for breast cancer. Taken together, our clinical and functional studies strongly suggest that exon 12 is functionally redundant and therefore missense variants in this exon are likely to be neutral. Such comprehensive functional studies will be important adjuncts to genetic studies of variants. Hum Mutat 30:1543-1550, 2009. Published 2009 Wiley-Liss, Inc.".
- aggregation authorList BK530820.
- aggregation endPage "1550".
- aggregation issue "11".
- aggregation startPage "1543".
- aggregation volume "30".
- aggregation aggregates 1169946.
- aggregation isDescribedBy 1169919.
- aggregation similarTo humu.21101.
- aggregation similarTo LU-1169919.