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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. 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.
Proteomic analysis of the effect of hemin in breast cancer.
Coló GP, Schweitzer K, Oresti GM, Alonso EG, Chávez LF, Mascaró M, Giorgi G, Curino AC, Facchinetti MM. Coló GP, et al. Among authors: mascaro m. Sci Rep. 2023 Jun 21;13(1):10091. doi: 10.1038/s41598-023-35125-4. Sci Rep. 2023. PMID: 37344532 Free PMC article.
Regions of homozygosity confer a worse prognostic impact in myelodysplastic syndrome with normal karyotype.
Mallo M, Tuechler H, Arenillas L, Raynaud S, Cluzeau T, Shih LY, Tung-Liang C, Ganster C, Shirneshan K, Haase D, Mascaró M, Palomo L, Cervera J, Such E, Trim N, Jeffries S, Ridgway E, Marconi G, Martinelli G, Solé F. Mallo M, et al. Among authors: mascaro m. EJHaem. 2023 Feb 7;4(2):446-449. doi: 10.1002/jha2.651. eCollection 2023 May. EJHaem. 2023. PMID: 37206269 Free PMC article.
90 results