Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Journal of Experimental & Clinical Cancer Research : CR|August 23, 2013
External Quality Assessment (EQA) program for the preanalytical and analytical immunohistochemical determination of HER2 in breast cancer: an experience on a regional scaleIrene Terrenato, Vincenzo Arena, Sara Pizzamiglio, et al.
Human Mutation|July 4, 2012
Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target siteBrooke L Brewster, Francesca Rossiello, Juliet D French, et al.
Cancers|February 12, 2021
Analysis of Italian <i>BRCA1/2</i> Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern ItalyGisella Figlioli, Arcangela De Nicolo, Irene Catucci, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 17, 2024
Neoadjuvant Chemotherapy in High-Grade Myxoid Liposarcoma: Results of the Expanded Cohort of a Randomized Trial From Italian (ISG), Spanish (GEIS), French (FSG), and Polish Sarcoma Groups (PSG)Alessandro Gronchi, Emanuela Palmerini, Vittorio Quagliuolo, et al.
JAMA Network Open|November 6, 2025
Histopathological Response After Neoadjuvant Chemotherapy for High-Risk Soft-Tissue Sarcomas: A Secondary Analysis of a Randomized Clinical TrialSandro Pasquali, Paola Collini, Cleofe Romagosa, et al.
Journal of the National Cancer Institute|July 5, 2022
Predictive Role of CD36 Expression in HER2-Positive Breast Cancer Patients Receiving Neoadjuvant TrastuzumabFrancesca Ligorio, Serena Di Cosimo, Paolo Verderio, et al.
Virchows Archiv : an International Journal of Pathology|August 3, 2014
Evaluation of colon cancer histomorphology: a comparison between formalin and PAXgene tissue fixation by an international ring trialSibylle Gündisch, Julia Slotta-Huspenina, Paolo Verderio, et al.
Human Molecular Genetics|July 2, 2015
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factorPaolo Peterlongo, Irene Catucci, Mara Colombo, et al.
Pageof 7