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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2015 1
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2017 1
2018 2
2019 4
2020 3
2021 6
2022 4
2023 5
2024 2
2025 6
2026 0

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Cited In for PMID: 26515094

33 results

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Page 1
ISGylation: is our genome yearning for such a modification?
Chen Z, Li Z, Wang Y, Dushimova Z, Gulnara K, Takeda S, Zhou Z, Xu X. Chen Z, et al. Acta Biochim Biophys Sin (Shanghai). 2025 Feb 28;57(11):1743-1757. doi: 10.3724/abbs.2025028. Acta Biochim Biophys Sin (Shanghai). 2025. PMID: 40103488 Free PMC article. Review.
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations.
Borbaran Bravo N, Deordieva E, Doll L, ElGamacy M, Dannenmann B, Azevedo J, Iannuzzo A, Delafontaine S, Lehners M, Kolodziej M, Hernandez Alvarez B, Hellmuth AS, Ritter M, Findik B, Zakharova V, Bräuning S, Kandabarau S, Lengerke C, Feil R, Meyts I, Delon J, Templin M, Sturm M, Rieß O, Zeidler C, Welte K, Shcherbina A, Klimiankou M, Skokowa J. Borbaran Bravo N, et al. Blood. 2025 May 15;145(20):2317-2335. doi: 10.1182/blood.2023022576. Blood. 2025. PMID: 39642330 Free PMC article.
33 results