Detalhe da pesquisa
1.
Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process.
J Math Biol
; 72(1-2): 47-86, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25833184
2.
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
N Engl J Med
; 365(15): 1384-95, 2011 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21995386
3.
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.
Nat Genet
; 7(1): 103-7, 1994 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-8075631
4.
A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome.
Nat Genet
; 2(2): 132-4, 1992 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-1303262
5.
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.
Nat Genet
; 15(1): 103-5, 1997 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8988179
6.
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21.
Nat Genet
; 13(4): 461-3, 1996 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8696342
7.
Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene.
Nat Genet
; 11(4): 441-3, 1995 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-7493027
8.
Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
Nat Genet
; 12(3): 309-11, 1996 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-8589723
9.
BRCA2 mutations in primary breast and ovarian cancers.
Nat Genet
; 13(2): 238-40, 1996 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-8640235
10.
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation.
Nat Genet
; 11(4): 428-33, 1995 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-7493024
11.
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours.
Nat Genet
; 24(2): 197-200, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10655070
12.
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.
J Med Genet
; 47(5): 342-7, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19948536
13.
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition.
Br J Cancer
; 100(2): 370-5, 2009 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-19165201
14.
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.
Oncogene
; 26(50): 7158-62, 2007 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17525745
15.
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
Bioinformatics
; 23(13): 1689-91, 2007 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17485433
16.
Hereditary predisposition to breast cancer.
Curr Opin Genet Dev
; 6(1): 93-7, 1996 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-8791478
17.
A polymorphic stop codon in BRCA2.
Nat Genet
; 14(3): 253-4, 1996 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-8896551
18.
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
J Natl Cancer Inst
; 91(11): 943-9, 1999 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-10359546
19.
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations.
J Natl Cancer Inst
; 90(15): 1138-45, 1998 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-9701363
20.
Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction.
Cancer Res
; 49(22): 6324-7, 1989 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-2680062