Detalhe da pesquisa
1.
Northern lights assay: a versatile method for comprehensive detection of DNA damage.
Nucleic Acids Res
; 46(20): e118, 2018 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30053193
2.
Dysfunctional telomeres in human BRCA2 mutated breast tumors and cell lines.
Mutat Res
; 729(1-2): 90-9, 2012 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22019625
3.
Cytogenetic polyclonality of breast carcinomas: association with clinico-pathological characteristics and outcome.
Genes Chromosomes Cancer
; 50(11): 930-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21910159
4.
BRCA2 Haploinsufficiency in Telomere Maintenance.
Genes (Basel)
; 13(1)2021 12 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35052422
5.
Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes.
Breast Cancer Res
; 11(4): R47, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19589159
6.
Aurora-A amplification associated with BRCA2 mutation in breast tumours.
Cancer Lett
; 248(1): 96-102, 2007 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-16860930
7.
Differentiation potential of a basal epithelial cell line established from human bronchial explant.
In Vitro Cell Dev Biol Anim
; 43(8-9): 283-9, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17876679
8.
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
Nat Commun
; 8: 14755, 2017 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28466842
9.
Effect of hypoxia and TP53 mutation status and cytogenetics of normal and malignant mammary epithelium.
Cancer Genet Cytogenet
; 165(2): 144-50, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16527608
10.
Human breast microvascular endothelial cells retain phenotypic traits in long-term finite life span culture.
In Vitro Cell Dev Biol Anim
; 42(10): 332-40, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17316068
11.
Establishment of three human breast epithelial cell lines derived from carriers of the 999del5 BRCA2 Icelandic founder mutation.
In Vitro Cell Dev Biol Anim
; 41(10): 337-42, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16448223
12.
A de novo 1.13 Mb microdeletion in 12q13.13 associated with congenital distal arthrogryposis, intellectual disability and mild dysmorphism.
Eur J Med Genet
; 55(6-7): 437-40, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22534424
13.
Selection for EGFR gene amplification in a breast epithelial cell line with basal-like phenotype and hereditary background.
In Vitro Cell Dev Biol Anim
; 47(2): 139-48, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21082277
14.
MYC amplification and TERT expression in breast tumor progression.
Cancer Genet Cytogenet
; 176(2): 93-9, 2007 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17656250
15.
Cytogenetic changes in nonmalignant breast tissue.
Genes Chromosomes Cancer
; 41(1): 47-55, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15236316