Colocalisation of predicted exonic splicing enhancers in BRCA2 with reported sequence variants.

Colocalisation of predicted exonic splicing enhancers in BRCA2 with reported sequence variants.

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http://www.wikidata.org/entity/Q52582443
New sequence variants in BRCA1 and BRCA2 genes detected by high-resolution melting analysis in an elderly healthy female population in Croatia.Analysis of 30 putative BRCA1 splicing mutations in hereditary breast and ovarian cancer families identifies exonic splice site mutations that escape in silico prediction.Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2 transcripts.Prediction and assessment of splicing alterations: implications for clinical testing.Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay.Functional analysis of a large set of BRCA2 exon 7 variants highlights the predictive value of hexamer scores in detecting alterations of exonic splicing regulatory elements.Identification of Eight Spliceogenic Variants in BRCA2 Exon 16 by Minigene Assays.
P2860

Colocalisation of predicted exonic splicing enhancers in BRCA2 with reported sequence variants.

Item
http://www.wikidata.org/entity/Q52582443
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Colocalisation of predicted ex ...... th reported sequence variants.
@en
Colocalisation of predicted ex ...... th reported sequence variants.
@nl
type
label
Colocalisation of predicted ex ...... th reported sequence variants.
@en
Colocalisation of predicted ex ...... th reported sequence variants.
@nl
prefLabel
Colocalisation of predicted ex ...... th reported sequence variants.
@en
Colocalisation of predicted ex ...... th reported sequence variants.
@nl
P1433
P1476
P2093
P2888
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Colocalisation of predicted ex ...... th reported sequence variants.
@en
P2093
P2888
P304
P31
P356
P407
P433
P478
P50
P577
P698