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本文引用的文献
1
Meier-Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of Mutations and the Development of a Prenatal Test.
Int J Mol Sci. 2022 Aug 17;23(16):9234. doi: 10.3390/ijms23169234.
2
The Licensing Factor Cdt1 Links Cell Cycle Progression to the DNA Damage Response.
Anticancer Res. 2020 May;40(5):2449-2456. doi: 10.21873/anticanres.14214.
3
PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components.
Nature. 2019 Apr;568(7751):259-263. doi: 10.1038/s41586-019-1057-y. Epub 2019 Apr 3.
4
Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype.
Hum Mol Genet. 2017 Nov 1;26(21):4168-4180. doi: 10.1093/hmg/ddx305.
5
Regulation and Function of Cdt1; A Key Factor in Cell Proliferation and Genome Stability.
Genes (Basel). 2016 Dec 22;8(1):2. doi: 10.3390/genes8010002.
6
Meier-Gorlin syndrome.
Orphanet J Rare Dis. 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x.
7
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
Nat Genet. 2011 Feb 27;43(4):350-5. doi: 10.1038/ng.776.
8
Nonsense-mediated mRNA decay effectors are essential for zebrafish embryonic development and survival.
Mol Cell Biol. 2009 Jul;29(13):3517-28. doi: 10.1128/MCB.00177-09. Epub 2009 May 4.
9
A p53-dependent checkpoint pathway prevents rereplication.
Mol Cell. 2003 Apr;11(4):997-1008. doi: 10.1016/s1097-2765(03)00099-6.
10
Inhibition of eukaryotic DNA replication by geminin binding to Cdt1.
Science. 2000 Dec 22;290(5500):2309-12. doi: 10.1126/science.290.5500.2309.
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