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Genes|January 20, 2019
Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair DisordersMaria Marín, María José Ramírez, Miriam Aza Carmona, et al.
Nucleic Acids Research|March 23, 2011
The FANC pathway is activated by adenovirus infection and promotes viral replication-dependent recombinationGioia Cherubini, Valeria Naim, Paola Caruso, et al.
Blood|May 22, 2012
On the role of FAN1 in Fanconi anemiaJuan P Trujillo, Leonardo B Mina, Roser Pujol, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemiaMassimo Bogliolo, Dominique Bluteau, James Lespinasse, et al.
The EMBO Journal|February 17, 2007
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stabilityMassimo Bogliolo, Alex Lyakhovich, Elsa Callén, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 16, 2018
From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemiaCsilla Krausz, Antoni Riera-Escamilla, Chiara Chianese, et al.
Frontiers in Genetics|August 7, 2023
A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutationIlaria Persico, Giorgia Fontana, Michela Faleschini, et al.
Frontiers in Genetics|March 8, 2021
FANCA Gene Mutations in North African Fanconi Anemia PatientsAbir Ben Haj Ali, Olfa Messaoud, Sahar Elouej, et al.
Cell Stem Cell|September 24, 2019
NHEJ-Mediated Repair of CRISPR-Cas9-Induced DNA Breaks Efficiently Corrects Mutations in HSPCs from Patients with Fanconi AnemiaFrancisco José Román-Rodríguez, Laura Ugalde, Lara Álvarez, et al.
NPJ Breast Cancer|September 10, 2021
Clinical consequences of BRCA2 hypomorphismLaia Castells-Roca, Sara Gutiérrez-Enríquez, Sandra Bonache, et al.
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