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Year | Number of Results |
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2019 | 1 |
2022 | 2 |
2023 | 3 |
2024 | 2 |
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Page 1
A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure.
Br J Haematol. 2023 Dec;203(5):852-859. doi: 10.1111/bjh.19023. Epub 2023 Aug 23.
Br J Haematol. 2023.
PMID: 37610030
Emerging Roles of the TRIM E3 Ubiquitin Ligases MID1 and MID2 in Cytokinesis.
Zanchetta ME, Meroni G.
Zanchetta ME, et al.
Front Physiol. 2019 Mar 19;10:274. doi: 10.3389/fphys.2019.00274. eCollection 2019.
Front Physiol. 2019.
PMID: 30941058
Free PMC article.
Review.
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A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation.
Persico I, Fontana G, Faleschini M, Zanchetta ME, Ammeti D, Cappelli E, Corsolini F, Mosa C, Guarina A, Bogliolo M, Surrallés J, Dufour C, Farruggia P, Savoia A, Bottega R.
Persico I, et al. Among authors: zanchetta me.
Front Genet. 2023 Jul 20;14:1209138. doi: 10.3389/fgene.2023.1209138. eCollection 2023.
Front Genet. 2023.
PMID: 37547463
Free PMC article.
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The dual action of glioma-derived exosomes on neuronal activity: synchronization and disruption of synchrony.
Spelat R, Jihua N, Sánchez Triviño CA, Pifferi S, Pozzi D, Manzati M, Mortal S, Schiavo I, Spada F, Zanchetta ME, Ius T, Manini I, Rolle IG, Parisse P, Millán AP, Bianconi G, Cesca F, Giugliano M, Menini A, Cesselli D, Skrap M, Torre V.
Spelat R, et al. Among authors: zanchetta me.
Cell Death Dis. 2022 Aug 13;13(8):705. doi: 10.1038/s41419-022-05144-6.
Cell Death Dis. 2022.
PMID: 35963860
Free PMC article.
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GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.
Barozzi S, Pecci A, Marinoni M, Fontana G, Zanchetta ME, Noris P, Savoia A, Faleschini M.
Barozzi S, et al. Among authors: zanchetta me.
Ann Hematol. 2023 Mar;102(3):677-679. doi: 10.1007/s00277-022-05079-0. Epub 2022 Dec 21.
Ann Hematol. 2023.
PMID: 36539614
No abstract available.
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A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs.
Mascaro M, D'Ambrosio L, Lazzari E, Almoguera B, Swafiri ST, Zanchetta ME, Meroni G.
Mascaro M, et al. Among authors: zanchetta me.
Biochim Biophys Acta Mol Basis Dis. 2024 Apr;1870(4):167126. doi: 10.1016/j.bbadis.2024.167126. Epub 2024 Mar 18.
Biochim Biophys Acta Mol Basis Dis. 2024.
PMID: 38508475
Free article.
No abstract available.
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ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype.
Zanchetta ME, Barozzi S, Isidori F, Marconi C, Farinasso L, Bottega R, Savoia A, Pecci A, Faleschini M.
Zanchetta ME, et al.
Br J Haematol. 2024 Apr 9. doi: 10.1111/bjh.19457. Online ahead of print.
Br J Haematol. 2024.
PMID: 38594875
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