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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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2020 | 1 |
2022 | 3 |
2024 | 0 |
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Page 1
Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 gene.
Stem Cell Res. 2022 Dec;65:102971. doi: 10.1016/j.scr.2022.102971. Epub 2022 Nov 14.
Stem Cell Res. 2022.
PMID: 36403546
Free article.
The Readthrough Isoform AQP4ex Is Constitutively Phosphorylated in the Perivascular Astrocyte Endfeet of Human Brain.
Pati R, Palazzo C, Valente O, Abbrescia P, Messina R, Surdo NC, Lefkimmiatis K, Signorelli F, Nicchia GP, Frigeri A.
Pati R, et al. Among authors: valente o.
Biomolecules. 2022 Apr 25;12(5):633. doi: 10.3390/biom12050633.
Biomolecules. 2022.
PMID: 35625560
Free PMC article.
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Alteration of the translational readthrough isoform AQP4ex induces redistribution and downregulation of AQP4 in human glioblastoma.
Valente O, Messina R, Ingravallo G, Bellitti E, Zimatore DS, de Gennaro L, Abbrescia P, Pati R, Palazzo C, Nicchia GP, Trojano M, Signorelli F, Frigeri A.
Valente O, et al.
Cell Mol Life Sci. 2022 Feb 20;79(3):140. doi: 10.1007/s00018-021-04123-y.
Cell Mol Life Sci. 2022.
PMID: 35187599
Free PMC article.
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Tissue Distribution of the Readthrough Isoform of AQP4 Reveals a Dual Role of AQP4ex Limited to CNS.
Palazzo C, Abbrescia P, Valente O, Nicchia GP, Banitalebi S, Amiry-Moghaddam M, Trojano M, Frigeri A.
Palazzo C, et al. Among authors: valente o.
Int J Mol Sci. 2020 Feb 24;21(4):1531. doi: 10.3390/ijms21041531.
Int J Mol Sci. 2020.
PMID: 32102323
Free PMC article.
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