Nsun3-flox 基因敲除小鼠

1. de Muijnck, Cansu, Brink, Jacoline B Ten, de Haan, Hugoline G, Boon, Camiel J F, van Genderen, Maria M. 2024. Mutations in NSUN3, a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy. In Genes, 15, . doi:10.3390/genes15050530. https://pubmed.ncbi.nlm.nih.gov/38790159/

2. Murakami, Yoshitaka, Wei, Fan-Yan, Kawamura, Yoshimi, Tomizawa, Kazuhito, Chujo, Takeshi. 2023. NSUN3-mediated mitochondrial tRNA 5-formylcytidine modification is essential for embryonic development and respiratory complexes in mice. In Communications biology, 6, 307. doi:10.1038/s42003-023-04680-x. https://pubmed.ncbi.nlm.nih.gov/36949224/

3. Haag, Sara, Sloan, Katherine E, Ranjan, Namit, Höbartner, Claudia, Bohnsack, Markus T. 2016. NSUN3 and ABH1 modify the wobble position of mt-tRNAMet to expand codon recognition in mitochondrial translation. In The EMBO journal, 35, 2104-2119. doi:. https://pubmed.ncbi.nlm.nih.gov/27497299/

4. Paramasivam, Arumugam, Meena, Angamuthu K, Venkatapathi, Challa, Pitceathly, Robert D S, Thangaraj, Kumarasamy. 2020. Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures. In Journal of molecular neuroscience : MN, 70, 1962-1965. doi:10.1007/s12031-020-01595-8. https://pubmed.ncbi.nlm.nih.gov/32488845/

5. Hughes, Riley O, Davis, Hannah J, Nease, Leona A, Piskounova, Elena. 2024. Decoding the role of tRNA modifications in cancer progression. In Current opinion in genetics & development, 88, 102238. doi:10.1016/j.gde.2024.102238. https://pubmed.ncbi.nlm.nih.gov/39088870/