Loss-of-function of zebrafish cdt1 causes retarded body growth and underdeveloped gonads resembling human Meier-Gorlin syndrome
Author:
Publisher
Zhejiang University Press
Subject
General Pharmacology, Toxicology and Pharmaceutics,General Veterinary,General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1631/jzus.B2300195.pdf
Reference15 articles.
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2. Bicknell LS, Walker S, Klingseisen A, et al., 2011. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarf-ism resembling Meier-Gorlin syndrome. Nat Genet, 43(4): 350–355. https://doi.org/10.1038/ng.776
3. de Munnik SA, Hoefsloot EH, Roukema J, et al., 2015. Meier-Gorlin syndrome. Orphanet J Rare Dis, 10:114. https://doi.org/10.1186/s13023-015-0322-x
4. Hofmann JF, Beach D, 1994. cdt1 is an essential target of the Cdc10/Sct1 transcription factor: requirement for DNA replication and inhibition of mitosis. EMBO J, 13(2): 425–434. https://doi.org/10.1002/j.1460-2075.1994.tb06277.x
5. Kanellou A, Giakoumakis NN, Panagopoulos A, et al., 2020. The licensing factor Cdt1 links cell cycle progression to the DNA damage response. Anticancer Res, 40(5):2449–2456. https://doi.org/10.21873/anticanres.14214
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