EIF1AX mutation in thyroid nodules: a histopathologic analysis of 56 cases in the context of institutional practices
Author:
Funder
National Institutes of Health/National Cancer Institute
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00428-024-03914-5.pdf
Reference44 articles.
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2. Hinnebusch AG (2014) The scanning mechanism of eukaryotic translation initiation. Annu Rev Biochem 83:779–812. https://doi.org/10.1146/annurev-biochem-060713-035802
3. Battiste JL, Pestova TV, Hellen CU, Wagner G (2000) The eIF1A solution structure reveals a large RNA-binding surface important for scanning function. Mol Cell 5:109–19. https://doi.org/10.1016/s1097-2765(00)80407-4
4. Krishnamoorthy GP, Davidson NR, Leach SD, Zhao Z, Lowe SW, Lee G et al (2019) EIF1AX and RAS Mutations Cooperate to Drive Thyroid Tumorigenesis through ATF4 and c-MYC. Cancer Discov 9:264–281. https://doi.org/10.1158/2159-8290.CD-18-0606
5. Topf MC, Wang ZX, Furlong K, Miller JL, Tuluc M, Pribitkin EA (2018) EIF1AX Mutation in a Patient with Hürthle Cell Carcinoma. Endocr Pathol 29:27–29. https://doi.org/10.1007/s12022-017-9501-8
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