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International Journal of Molecular Medicine|August 8, 2002
Population-based screening for hereditary breast cancer in a region of North-Central ItalySilvia Casadei, Fabio Falcini, Carlo Naldoni, et al.Journal of Medical Genetics|October 16, 2020
CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genesTom Walsh, Silvia Casadei, Katherine M Munson, et al.JAMA Oncology|July 21, 2017
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish WomenTom Walsh, Jessica B Mandell, Barbara M Norquist, et al.Cancer Research|February 3, 2011
Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancerSilvia Casadei, Barbara M Norquist, Tom Walsh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2018
Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significanceGinger J Tsai, John Michael O Rañola, Christina Smith, et al.Breast Cancer Research and Treatment|December 20, 2007
Results of a population-based screening for hereditary breast cancer in a region of North-Central Italy: contribution of BRCA1/2 germ-line mutationsIan J Seymour, Silvia Casadei, Valentina Zampiga, et al.Proceedings of the National Academy of Sciences of the United States of America|May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.Proceedings of the National Academy of Sciences of the United States of America|July 10, 2010
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencingTom Walsh, Ming K Lee, Silvia Casadei, et al.Biorxiv : the Preprint Server for Biology|September 16, 2024
The proteomic landscape and temporal dynamics of mammalian gastruloid developmentRiddhiman K Garge, Valerie Lynch, Rose Fields, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposisBrian H Shirts, Stephen J Salipante, Silvia Casadei, et al.Pageof 5