Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
about
Assessment of SLX4 Mutations in Hereditary Breast Cancers.Alterations of DNA repair genes in the NCI-60 cell lines and their predictive value for anticancer drug activity.Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genesLow prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.A low-frequency haplotype spanning SLX4/FANCP constitutes a new risk locus for early-onset breast cancer (<60 years) and is associated with reduced DNA repair capacity.
P2860
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
description
2012 nî lūn-bûn
@nan
2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@ast
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@en
type
label
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@ast
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@en
prefLabel
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@ast
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases.
@en
P2093
P2860
P50
P1433
P1476
Sequencing analysis of SLX4/FANCP gene in Italian familial breast cancer cases
@en
P2093
Elisa Cattaneo
Filomena Ficarazzi
Frederique Mariette
Irene Catucci
Loris Bernard
Monica Barile
P2860
P304
P356
10.1371/JOURNAL.PONE.0031038
P407
P577
2012-02-23T00:00:00Z