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Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD.
Strafella C, Caputo V, Bortolani S, Torchia E, Megalizzi D, Trastulli G, Monforte M, Colantoni L, Caltagirone C, Ricci E, Tasca G, Cascella R, Giardina E. Strafella C, et al. Among authors: caltagirone c. Front Genet. 2023 Aug 22;14:1235589. doi: 10.3389/fgene.2023.1235589. eCollection 2023. Front Genet. 2023. PMID: 37674478 Free PMC article.
Primary and Recall Immune Responses to SARS-CoV-2 in Breakthrough Infection.
D'Orso S, Pirronello M, Verdiani A, Rossini A, Guerrera G, Picozza M, Sambucci M, Misiti A, De Marco L, Salvia A, Caltagirone C, Giardina E, Battistini L, Borsellino G. D'Orso S, et al. Among authors: caltagirone c. Vaccines (Basel). 2023 Nov 9;11(11):1705. doi: 10.3390/vaccines11111705. Vaccines (Basel). 2023. PMID: 38006037 Free PMC article.
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families.
Strafella C, Colantoni L, Megalizzi D, Trastulli G, Piorgo EP, Primiano G, Sancricca C, Ricci G, Siciliano G, Caltagirone C, Filosto M, Tasca G, Ricci E, Cascella R, Giardina E. Strafella C, et al. Among authors: caltagirone c. Clin Genet. 2024 Mar;105(3):335-339. doi: 10.1111/cge.14466. Epub 2023 Dec 2. Clin Genet. 2024. PMID: 38041579
985 results