Alternative splicing of APOBEC3D generates functional diversity and its role as a DNA mutator
Author:
Funder
National Institutes of Health
American Cancer Society
Harvard Stem Cell Institute
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12185-020-02904-y.pdf
Reference37 articles.
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2. Henderson S, Fenton T. APOBEC3 genes: retroviral restriction factors to cancer drivers. Trends Mol Med. 2015;21:274–84.
3. Maul RW, Gearhart PJ. AID and somatic hypermutation. Adv Immunol. 2010;105:159–91.
4. Knisbacher BA, Gerber D, Levanon EY. DNA Editing by APOBECs: a genomic preserver and transformer. Trends Genet. 2016;32:16–28.
5. Xiao X, Yang H, Arutiunian V, Fang Y, Besse G, Morimoto C, et al. Structural determinants of APOBEC3B non-catalytic domain for molecular assembly and catalytic regulation. Nucleic Acids Res. 2017;45:7540.
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1. Cytidine deaminases APOBEC3C and APOBEC3D promote DNA replication stress resistance in pancreatic cancer cells;Nature Cancer;2024-03-06
2. APOBEC3 degradation is the primary function of HIV-1 Vif determining virion infectivity in the myeloid cell line THP-1;mBio;2023-08-09
3. APOBEC3 degradation is the primary function of HIV-1 Vif for virus replication in the myeloid cell line THP-1;2023-03-30
4. Comprehensive bioinformatics analyses of APOBECs family and identification of APOBEC3D as the unfavorable prognostic biomarker in clear cell renal cell carcinoma;Journal of Cancer;2021
5. APOBEC3s: history of an antiviral and mutagenic protein family;Virologie;2020-12
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