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本文引用的文献

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POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Am J Hum Genet. 2023 May 4;110(5):809-825. doi: 10.1016/j.ajhg.2023.03.014. Epub 2023 Apr 18.
2
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.
Nature. 2023 Feb;614(7948):564-571. doi: 10.1038/s41586-022-05682-1. Epub 2023 Feb 8.
3
Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development.
Proc Natl Acad Sci U S A. 2022 Aug 2;119(31):e2116974119. doi: 10.1073/pnas.2116974119. Epub 2022 Jul 26.
4
Nucleolin loss of function leads to aberrant Fibroblast Growth Factor signaling and craniofacial anomalies.
Development. 2022 Jun 15;149(12). doi: 10.1242/dev.200349. Epub 2022 Jun 28.
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Ribosome-associated quality-control mechanisms from bacteria to humans.
Mol Cell. 2022 Apr 21;82(8):1451-1466. doi: 10.1016/j.molcel.2022.03.038.
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Ribosomal protein L5 facilitates rDNA-bundled condensate and nucleolar assembly.
Life Sci Alliance. 2022 Mar 23;5(7). doi: 10.26508/lsa.202101045. Print 2022 Jul.
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The Ribosomal Protein L5 Functions During Anterior Development Through Apoptotic Pathways.
Front Cell Dev Biol. 2022 Feb 22;10:777121. doi: 10.3389/fcell.2022.777121. eCollection 2022.
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Surface tension and super-stoichiometric surface enrichment in two-component biomolecular condensates.
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A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis.
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