A C57BL/6J Fancg-KO Mouse Model Generated by CRISPR/Cas9 Partially Captures the Human Phenotype

Fanconi anemia (FA) develops due to a mutation in one of the FANC genes that are involved in the repair of interstrand crosslinks (ICLs). FANCG, a member of the FA core complex, is essential for ICL repair. Previous FANCG-deficient mouse models were generated with drug-based selection cassettes in m...

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Vydáno v:	International journal of molecular sciences Ročník 24; číslo 13; s. 11129
Hlavní autoři:	Shah, Ronak, van den Berk, Paul C. M., Pritchard, Colin E. J., Song, Ji-Ying, Kreft, Maaike, Pilzecker, Bas, Jacobs, Heinz
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Switzerland MDPI AG 01.07.2023 MDPI
Témata:	Ablation Analysis Anemia Animals Bone marrow Cisplatin - metabolism CRISPR CRISPR-Cas Systems Crosslinked polymers DNA-Binding Proteins - metabolism Fanconi Anemia - genetics Fanconi Anemia - metabolism Fanconi Anemia Complementation Group G Protein - genetics Fanconi's anemia Fibroblasts Fibroblasts - metabolism Genetic aspects Genotype & phenotype Humans Immunotherapy Infertility Life expectancy Metabolism Mice Mice, Inbred C57BL Mitomycin Phenotype Proteins Stem cells Thymus gland Netherlands Germany fanconi anemia (FA) cisplatin (CsPt) hematopoiesis Mitomycin C (MMC) CRISPR/Cas9 DNA damage response interstrand crosslink (ICL) genetically engineered mouse model (GEMM) FANCG
ISSN:	1422-0067, 1661-6596, 1422-0067
On-line přístup:	Získat plný text
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