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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2001 | 1 |
2018 | 1 |
2019 | 3 |
2020 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 100609
6 results
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Page 1
RNA-methyltransferase Nsun5 controls the maternal-to-zygotic transition by regulating maternal mRNA stability.
Clin Transl Med. 2022 Dec;12(12):e1137. doi: 10.1002/ctm2.1137.
Clin Transl Med. 2022.
PMID: 36495115
Free PMC article.
NSUN5 Facilitates Viral RNA Recognition by RIG-I Receptor.
Sun B, Zeng H, Liang J, Zhang L, Hu H, Wang Q, Meng W, Li C, Ye F, Wang C, Zhu J.
Sun B, et al.
J Immunol. 2020 Dec 15;205(12):3408-3418. doi: 10.4049/jimmunol.1901455. Epub 2020 Nov 11.
J Immunol. 2020.
PMID: 33177158
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Loss of the ribosomal RNA methyltransferase NSUN5 impairs global protein synthesis and normal growth.
Heissenberger C, Liendl L, Nagelreiter F, Gonskikh Y, Yang G, Stelzer EM, Krammer TL, Micutkova L, Vogt S, Kreil DP, Sekot G, Siena E, Poser I, Harreither E, Linder A, Ehret V, Helbich TH, Grillari-Voglauer R, Jansen-Dürr P, Koš M, Polacek N, Grillari J, Schosserer M.
Heissenberger C, et al.
Nucleic Acids Res. 2019 Dec 16;47(22):11807-11825. doi: 10.1093/nar/gkz1043.
Nucleic Acids Res. 2019.
PMID: 31722427
Free PMC article.
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Expression of the RNA methyltransferase Nsun5 is essential for developing cerebral cortex.
Chen P, Zhang T, Yuan Z, Shen B, Chen L.
Chen P, et al.
Mol Brain. 2019 Aug 28;12(1):74. doi: 10.1186/s13041-019-0496-6.
Mol Brain. 2019.
PMID: 31462248
Free PMC article.
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Cognitive deficits in mice lacking Nsun5, a cytosine-5 RNA methyltransferase, with impairment of oligodendrocyte precursor cells.
Zhang T, Chen P, Li W, Sha S, Wang Y, Yuan Z, Shen B, Chen L.
Zhang T, et al.
Glia. 2019 Apr;67(4):688-702. doi: 10.1002/glia.23565. Epub 2018 Nov 28.
Glia. 2019.
PMID: 30485550
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Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
Doll A, Grzeschik KH.
Doll A, et al.
Cytogenet Cell Genet. 2001;95(1-2):20-7. doi: 10.1159/000057012.
Cytogenet Cell Genet. 2001.
PMID: 11978965
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