Detalhe da pesquisa
1.
Identification of a novel large EPCAM-MSH2 duplication, concurrently with LOHs in chromosome 20 and X, in a family with Lynch syndrome.
Int J Colorectal Dis
; 34(11): 1999-2002, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31655866
2.
First evidence of a large CHEK2 duplication involved in cancer predisposition in an Italian family with hereditary breast cancer.
BMC Cancer
; 14: 478, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24986639
3.
Circulating hsa-miR-5096 predicts 18F-FDG PET/CT positivity and modulates somatostatin receptor 2 expression: a novel miR-based assay for pancreatic neuroendocrine tumors.
Front Oncol
; 13: 1136331, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37287922
4.
Prevalence of a BRCA2 Pathogenic Variant in Hereditary-Breast-and-Ovarian-Cancer-Syndrome Families with Increased Risk of Pancreatic Cancer in a Restricted Italian Area.
Cancers (Basel)
; 15(7)2023 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046793
5.
Comparative Analysis of Free-Circulating and Vesicle-Associated Plasma microRNAs of Healthy Controls and Early-Stage Lung Cancer Patients.
Pharmaceutics
; 14(10)2022 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36297464
6.
Dissecting Molecular Heterogeneity of Circulating Tumor Cells (CTCs) from Metastatic Breast Cancer Patients through Copy Number Aberration (CNA) and Single Nucleotide Variant (SNV) Single Cell Analysis.
Cancers (Basel)
; 14(16)2022 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36010918
7.
Irradiation causes senescence, ATP release, and P2X7 receptor isoform switch in glioblastoma.
Cell Death Dis
; 13(1): 80, 2022 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35075119
8.
Lineage-specific mechanisms and drivers of breast cancer chemoresistance revealed by 3D biomimetic culture.
Mol Oncol
; 16(4): 921-939, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34109737
9.
Case Report: Analysis of Circulating Tumor Cells in a Triple Negative Spindle-Cell Metaplastic Breast Cancer Patient.
Front Med (Lausanne)
; 8: 689895, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34249978
10.
Estrogen and Androgen Receptor Inhibitors: Unexpected Allies in the Fight Against COVID-19.
Cell Transplant
; 30: 963689721991477, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33522308
11.
Integrated genomic-metabolic classification of acute myeloid leukemia defines a subgroup with NPM1 and cohesin/DNA damage mutations.
Leukemia
; 35(10): 2813-2826, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34193978
12.
ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients.
Cell Transplant
; 29: 963689720968749, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33108902
13.
Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients.
Diagnostics (Basel)
; 10(5)2020 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32365798
14.
From cfDNA to Sequencing: Workflows and Potentials.
Methods Mol Biol
; 1909: 119-125, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30580427
15.
Multigene Panel Testing Increases the Number of Loci Associated with Gastric Cancer Predisposition.
Cancers (Basel)
; 11(9)2019 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31514334
16.
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
Oncotarget
; 8(29): 47064-47075, 2017 Jul 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28423363
17.
Combined Inhibition of CDK4/6 and PI3K/AKT/mTOR Pathways Induces a Synergistic Anti-Tumor Effect in Malignant Pleural Mesothelioma Cells.
Neoplasia
; 19(8): 637-648, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28704762
18.
Preclinical evidence of multiple mechanisms underlying trastuzumab resistance in gastric cancer.
Oncotarget
; 7(14): 18424-39, 2016 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26919099
19.
Morphological and genetic heterogeneity in multifocal lung adenocarcinoma: The case of a never-smoker woman.
Lung Cancer
; 96: 52-5, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27133750
20.
Multiple primary tumors in a family with Li-Fraumeni syndrome with a TP53 germline mutation identified by next-generation sequencing.
Int J Biol Markers
; 31(4): e461-e465, 2016 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-27516001