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Journal of Hematology & Oncology|April 29, 2024
Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort studySvenja Kastellan, Reinhard Kalb, Bia Sajjad, et al.
Nucleic Acids Research|November 25, 2003
A novel approach to describe a U1 snRNA binding siteMarcel Freund, Corinna Asang, Susanne Kammler, et al.
Nature Communications|March 11, 2023
Hypomorphic Brca2 and Rad51c double mutant mice display Fanconi anemia, cancer and polygenic replication stressKarl-Heinz Tomaszowski, Sunetra Roy, Carolina Guerrero, et al.
American Journal of Human Genetics|September 28, 2010
Correct mRNA processing at a mutant TT splice donor in FANCC ameliorates the clinical phenotype in patients and is enhanced by delivery of suppressor U1 snRNAsLinda Hartmann, Kornelia Neveling, Stephanie Borkens, et al.
Pediatric Nephrology (Berlin, Germany)|April 14, 2018
Patterns and frequency of renal abnormalities in Fanconi anaemia: implications for long-term managementVijaya Sathyanarayana, Beth Lee, Neville B Wright, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 6, 2006
A severe form of human combined immunodeficiency due to mutations in DNA ligase IVAnselm Enders, Paul Fisch, Klaus Schwarz, et al.
Plos One|January 28, 2014
Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancerSandra Kohlhase, Natalia V Bogdanova, Peter Schürmann, et al.
The Journal of Biological Chemistry|September 21, 2004
A role for the Fanconi anemia C protein in maintaining the DNA damage-induced G2 checkpointBrian W Freie, Samantha L M Ciccone, Xiaxin Li, et al.
The Journal of Cell Biology|April 10, 2023
RFWD3 promotes ZRANB3 recruitment to regulate the remodeling of stalled replication forksChandler E Moore, Selin E Yalcindag, Hanna Czeladko, et al.
Molecular Cell|June 3, 2017
RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous RecombinationShojiro Inano, Koichi Sato, Yoko Katsuki, et al.
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