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Cell|April 6, 2010
53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaksSamuel F Bunting, Elsa Callén, Nancy Wong, et al.Molecular Cell|February 2, 2019
BRCA1 Haploinsufficiency Is Masked by RNF168-Mediated Chromatin UbiquitylationDali Zong, Salomé Adam, Yifan Wang, et al.Cell|January 29, 2013
Identification of early replicating fragile sites that contribute to genome instabilityJacqueline H Barlow, Robert B Faryabi, Elsa Callén, et al.Molecular Cell|May 4, 2020
BRCA1 Mutational Complementation Induces Synthetic ViabilityJoseph Nacson, Daniela Di Marcantonio, Yifan Wang, et al.Blood|November 4, 2004
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from SpainElsa Callén, José A Casado, Marc D Tischkowitz, et al.Journal of Medical Genetics|January 11, 2011
Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impactMaria Castella, Roser Pujol, Elsa Callén, et al.Journal of Medical Genetics|November 16, 2006
A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research NetworkJosé Antonio Casado, Elsa Callén, Ariana Jacome, et al.Blood|January 29, 2011
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutationsMaria Castella, Roser Pujol, Elsa Callén, et al.Pageof 2