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Atlas of Genetics and Cytogenetics in Oncology and Haematology|July 6, 2019
XRCC2 (X-ray repair cross complementing 2)Paul R Andreassen, Helmut HanenbergAtlas of Genetics and Cytogenetics in Oncology and Haematology|August 16, 2019
PALB2 (partner and localizer of BRCA2)Helmut Hanenberg, Paul R AndreassenGenes|August 6, 2021
Understanding BRCA2 Function as a Tumor Suppressor Based on Domain-Specific Activities in DNA Damage ResponsesPaul R Andreassen, Joonbae Seo, Constanze Wiek, et al.Nucleic Acids Research|May 15, 2016
FANCJ is essential to maintain microsatellite structure genome-wide during replication stressJoanna Barthelemy, Helmut Hanenberg, Michael LeffakCurrent Gene Therapy|January 10, 2017
Stem Cell Genetic Therapy for Fanconi Anemia - A New HopeHelmut Hanenberg, Katharina Roellecke, Constanze WiekJournal of Medical Genetics|May 22, 2016
Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia geneJung-Young Park, Elizabeth L Virts, Anna Jankowska, et al.Human Molecular Genetics|July 29, 2022
Identification of new RAD51D-regulating microRNAs that also emerge as potent inhibitors of the Fanconi anemia/homologous recombination pathwaysNina Hater, Katharina M Iwaniuk, Carina Leifeld, et al.Nucleic Acids Research|February 5, 2019
Deficiency of the Fanconi anemia E2 ubiqitin conjugase UBE2T only partially abrogates Alu-mediated recombination in a new model of homology dependent recombinationTodd W Lewis, Joanna R Barthelemy, Elizabeth L Virts, et al.Molecular and Cellular Neurosciences|November 24, 2004
Peripheral myelin protein 22 kDa and protein zero: domain specific trans-interactionsBirgit Hasse, Frank Bosse, Helmut Hanenberg, et al.Human Molecular Genetics|February 1, 2023
A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutationsIvana Radulovic, Michael M Schündeln, Lisa Müller, et al.Pageof 22