Detalhe da pesquisa
1.
Structure-based classification predicts drug response in EGFR-mutant NSCLC.
Nature
; 597(7878): 732-737, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34526717
2.
Development of oxaalkyne and alkyne fatty acids as novel tracers to study fatty acid beta-oxidation pathways and intermediates.
J Lipid Res
; 63(4): 100188, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35247455
3.
Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counseling.
Breast Cancer Res Treat
; 185(1): 195-204, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-32918117
4.
Multigene assessment of genetic risk for women for two or more breast cancers.
Breast Cancer Res Treat
; 188(3): 759-768, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-33826040
5.
Mutation profile differences in younger and older patients with advanced breast cancer using circulating tumor DNA (ctDNA).
Breast Cancer Res Treat
; 185(3): 639-646, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-33219484
6.
Cell-Free Circulating Tumor DNA Improves Standard Genotyping of Non-Small-Cell Lung Cancer and Increases Detection of Targetable Alterations in a Selected Hispanic Cohort.
Oncology
; 99(8): 539-546, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33902046
7.
A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
Cancer
; 123(10): 1721-1730, 2017 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28085182
8.
Lynch Syndrome Patients with Limited Family History Identified in a Laboratory Setting: A Descriptive Study.
Oncology
; 89(4): 221-6, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26393997
9.
Hereditary cancer-associated mutations in women diagnosed with two primary cancers: an opportunity to identify hereditary cancer syndromes after the first cancer diagnosis.
Oncology
; 88(4): 226-33, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25503195
10.
Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories.
Oncology
; 89(5): 288-93, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-26315041
11.
Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer.
Cancer
; 120(7): 963-7, 2014 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24415441
12.
Identification of KRASG12C Mutations in Circulating Tumor DNA in Patients With Cancer.
JCO Precis Oncol
; 6: e2100547, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35862868
13.
Therapeutic Actionability of Circulating Cell-Free DNA Alterations in Carcinoma of Unknown Primary.
JCO Precis Oncol
; 52021.
Artigo
Inglês
| MEDLINE | ID: mdl-34778692
14.
Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing.
J Ovarian Res
; 14(1): 61, 2021 Apr 29.
Artigo
Inglês
| MEDLINE | ID: mdl-33926482
15.
The C. elegans Tousled-like kinase contributes to chromosome segregation as a substrate and regulator of the Aurora B kinase.
Curr Biol
; 15(10): 894-904, 2005 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-15916946
16.
How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay.
Genet Med
; 10(3): 181-6, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18344707
17.
ZEN-4/MKLP1 is required to polarize the foregut epithelium.
Curr Biol
; 14(11): 932-41, 2004 Jun 08.
Artigo
Inglês
| MEDLINE | ID: mdl-15182666
18.
The C. elegans Tousled-like kinase (TLK-1) has an essential role in transcription.
Curr Biol
; 13(22): 1921-9, 2003 Nov 11.
Artigo
Inglês
| MEDLINE | ID: mdl-14614817
19.
Validation of a molecular and pathological model for five-year mortality risk in patients with early stage lung adenocarcinoma.
J Thorac Oncol
; 10(1): 67-73, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25396679
20.
CYK-4/GAP provides a localized cue to initiate anteroposterior polarity upon fertilization.
Science
; 313(5791): 1298-301, 2006 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-16873611