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The Journal of Biological Chemistry|July 16, 2011
ATM protein-dependent phosphorylation of Rad50 protein regulates DNA repair and cell cycle controlMagtouf Gatei, Burkhard Jakob, Philip Chen, et al.Genes & Development|December 6, 2015
FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathwayKenichiro Matsuzaki, Valerie Borel, Carrie A Adelman, et al.The EMBO Journal|March 31, 2007
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathwayChen Ling, Masamichi Ishiai, Abdullah Mahmood Ali, et al.Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|November 8, 2003
Fanconi's anemia and clinical radiosensitivity report on two adult patients with locally advanced solid tumors treated by radiotherapyMichael Bremer, Detlev Schindler, Michaela Gross, et al.Cell Reports|August 19, 2014
BRCA1 is a histone-H2A-specific ubiquitin ligaseReinhard Kalb, Donna L Mallery, Conor Larkin, et al.Nature Genetics|January 4, 2007
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerSarah Reid, Detlev Schindler, Helmut Hanenberg, et al.Plos One|May 11, 2017
Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiationAnna Maierhofer, Julia Flunkert, Marcus Dittrich, et al.The Journal of Clinical Investigation|July 11, 2017
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemiaKerstin Knies, Shojiro Inano, María J Ramírez, et al.Plos One|January 4, 2013
Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challengesKerstin Knies, Beatrice Schuster, Najim Ameziane, et al.Molecular Genetics & Genomic Medicine|August 5, 2020
Severe reaction to radiotherapy provoked by hypomorphic germline mutations in ATM (ataxia-telangiectasia mutated gene)Reza Asadollahi, Christian Britschgi, Pascal Joset, et al.Pageof 13