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International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|October 13, 2009
Family history of cancer rather than p53 status predicts efficacy of pegylated liposomal doxorubicin and oxaliplatin in relapsed ovarian cancerMaria Ornella Nicoletto, Roberta Bertorelle, Lucia Borgato, et al.
Frontiers in Digital Health|March 13, 2026
From raw data to actionable insights: preprocessing real-world data for machine learning in diabetes careMarco Montagna, Aleksandar Svilenov Rabadzhiev, Alberto Traverso, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 1, 2008
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast ItalySandro Malacrida, Simona Agata, Monia Callegaro, et al.
Journal of the National Cancer Institute|February 16, 2006
Association between MDM2-SNP309 and age at colorectal cancer diagnosis according to p53 mutation statusChiara Menin, Maria Chiara Scaini, Gian Luca De Salvo, et al.
Human Mutation|March 25, 2014
CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessmentMaria Chiara Scaini, Giovanni Minervini, Lisa Elefanti, et al.
European Journal of Human Genetics : EJHG|September 2, 2004
Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutationsFabio Marroni, Paolo Aretini, Emma D'Andrea, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 6, 2009
Altered tumor formation and evolutionary selection of genetic variants in the human MDM4 oncogeneGurinder Singh Atwal, Tomas Kirchhoff, Elisabeth E Bond, et al.
European Journal of Cancer (Oxford, England : 1990)|June 9, 2006
Establishment and characterization of xenografts and cancer cell cultures derived from BRCA1 -/- epithelial ovarian cancersStefano Indraccolo, Veronica Tisato, Simona Agata, et al.
Mutation Research|August 29, 2009
Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutationMaria Chiara Scaini, Elisabetta Rossi, Paula Lobao Antunes de Siqueira Torres, et al.
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