Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
about
A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genomeTagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancerBRIP1 (BACH1) variants and familial breast cancer risk: a case-control study.Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutationsA rare FANCA gene variation as a breast cancer susceptibility allele in an Iranian population.Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome.Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell linesG-quadruplex nucleic acids and human diseaseFanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes.Hereditary breast cancer and the BRCA1-associated FANCJ/BACH1/BRIP1.Fanconi anaemia genes and susceptibility to cancer.Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review.Inherited and acquired alterations in development of breast cancer.BRIP1 overexpression is correlated with clinical features and survival outcome of luminal breast cancer subtypes.Mutation analysis of BRIP1 in male breast cancer cases: a population-based study in Central Italy.Sequential immunotherapy in a patient with primary refractory Hodgkin lymphoma and novel mutations.The evolution of cancer risk assessment in the era of next generation sequencing
P2860
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P2860
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
@nl
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@ast
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@en
type
label
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
@nl
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@ast
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@en
prefLabel
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
@nl
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@ast
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@en
P2093
P2860
P50
P356
P1476
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.
@en
P2093
Aaron G Lewis
Anna Marsh
Geoffrey J Lindeman
Gulietta M Pupo
James Flanagan
Jane E Visvader
Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer
Melissa A Brown
P2860
P2888
P304
P356
10.1186/BCR1336
P407
P577
2005-10-21T00:00:00Z
P5875
P6179
1026862561