Detalles de la búsqueda
1.
Sequential screening for lung cancer in a high-risk group: randomised controlled trial: LungSEARCH: a randomised controlled trial of Surveillance using sputum and imaging for the EARly detection of lung Cancer in a High-risk group.
Eur Respir J
; 54(4)2019 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31537697
2.
Stratifying tumour subtypes based on copy number alteration profiles using next-generation sequence data.
Bioinformatics
; 31(16): 2713-20, 2015 Aug 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25847006
3.
The clonal relationships between pre-cancer and cancer revealed by ultra-deep sequencing.
J Pathol
; 237(3): 296-306, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26096211
4.
Using common variants to indicate cancer genes.
Int J Cancer
; 136(1): 241-5, 2015 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24798945
5.
A novel genomic signature reclassifies an oral cancer subtype.
Int J Cancer
; 137(10): 2364-73, 2015 Nov 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26014678
6.
Clinical and genomic analysis of a randomised phase II study evaluating anastrozole and fulvestrant in postmenopausal patients treated for large operable or locally advanced hormone-receptor-positive breast cancer.
Br J Cancer
; 113(4): 585-94, 2015 Aug 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-26171933
7.
Estimating optimal window size for analysis of low-coverage next-generation sequence data.
Bioinformatics
; 30(13): 1823-9, 2014 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24603986
8.
Investigation of p16(INK4a) as a prognostic biomarker in oral epithelial dysplasia.
J Oral Pathol Med
; 43(4): 245-9, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24372672
9.
Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription.
Genes Chromosomes Cancer
; 52(4): 402-9, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23341332
10.
Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution.
Hum Mutat
; 34(10): 1432-8, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23766071
11.
Correcting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data.
Bioinformatics
; 28(1): 40-7, 2012 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-22039209
12.
A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma.
Genomics
; 99(1): 18-24, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22050995
13.
Genomic evidence of pre-invasive clonal expansion, dispersal and progression in bronchial dysplasia.
J Pathol
; 224(2): 153-9, 2011 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-21506132
14.
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens.
Nucleic Acids Res
; 38(14): e151, 2010 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-20525786
15.
Progressive 3q amplification consistently targets SOX2 in preinvasive squamous lung cancer.
Am J Respir Crit Care Med
; 182(1): 83-91, 2010 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-20299530
16.
The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons.
Dev Biol
; 313(2): 648-58, 2008 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18054781
17.
The genomic road to invasion-examining the similarities and differences in the genomes of associated oral pre-cancer and cancer samples.
Genome Med
; 9(1): 53, 2017 06 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28592326
18.
Targeted disruption of the 3p12 gene, Dutt1/Robo1, predisposes mice to lung adenocarcinomas and lymphomas with methylation of the gene promoter.
Cancer Res
; 64(18): 6432-7, 2004 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-15374951
19.
Past and future impact of next-generation sequencing in head and neck cancer.
Head Neck
; 38 Suppl 1: E2395-402, 2016 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-25900457
20.
Cre-loxP chromosome engineering of a targeted deletion in the mouse corresponding to the 3p21.3 region of homozygous loss in human tumours.
Oncogene
; 21(29): 4521-9, 2002 Jul 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-12085230