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Search for publications relevant for "non-homologous end-joining"
non-homologous end-joining
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publication
Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired De Novo via Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining
2021 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism
2008 |
Second Faculty of Medicine
publication
The BRCA1 alternative splicing variant Delta 14-15 with an in-frame deletion of part of the regulatory serine-containing domain (SCD) impairs the DNA repair capacity in MCF-7 cells
2012 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly
2018 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Chromatin Remodeler Smarca5 Is Required for Cancer-Related Processes of Primary Cell Fitness and Immortalization
2022 |
First Faculty of Medicine, Faculty of Science
publication
Expression of human BRCA1 Delta 17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response
2013 |
First Faculty of Medicine, Third Faculty of Medicine
publication
DNA Repair and Ovarian Carcinogenesis: Impact on Risk, Prognosis and Therapy Outcome
2020 |
First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Ornithine carbamoyltransferase deficiency: molecular characterization of 29 families
2013 |
First Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
2012 |
First Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
2012 |
Second Faculty of Medicine
publication
Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
Publication without faculty affiliation
publication
Small molecule inhibitors of DNA-PK for tumor sensitization to anticancer therapy
2017 |
Faculty of Medicine in Hradec Králové
publication
Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q
2008 |
Second Faculty of Medicine
publication
Double-strand break repair and colorectal cancer: gene variants within 3 ' UTRs and microRNAs binding as modulators of cancer risk and clinical outcome
2016 |
First Faculty of Medicine