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Effects of the Rho GTPase-activating toxin CNF1 on fibroblasts derived from Rett syndrome patients: A pilot study.
Cittadini C, Germinario EAP, Maroccia Z, Cosentino L, Maselli V, Gambardella L, Giambenedetti M, Guidotti M, Travaglione S, Fallerini C, Renieri A, Marcillo DIE, Ricceri L, Fortini P, De Filippis B, Fiorentini C, Fabbri A. Cittadini C, et al. Among authors: fallerini c. J Cell Mol Med. 2023 May;27(10):1315-1326. doi: 10.1111/jcmm.17624. Epub 2023 Apr 20. J Cell Mol Med. 2023. PMID: 37078409 Free PMC article.
Low-level TP53 mutational load antecedes clonal expansion in chronic lymphocytic leukaemia.
Pinto AM, Papa FT, Frullanti E, Meloni I, Tita R, Caselli R, Fallerini C, Lopergolo D, Cetta F, Mencarelli MA, Bocchia M, Gozzetti A, Renieri A. Pinto AM, et al. Among authors: fallerini c. Br J Haematol. 2019 Feb;184(4):657-659. doi: 10.1111/bjh.15147. Epub 2018 Feb 20. Br J Haematol. 2019. PMID: 29460960 Free article. No abstract available.
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome.
Landucci E, Brindisi M, Bianciardi L, Catania LM, Daga S, Croci S, Frullanti E, Fallerini C, Butini S, Brogi S, Furini S, Melani R, Molinaro A, Lorenzetti FC, Imperatore V, Amabile S, Mariani J, Mari F, Ariani F, Pizzorusso T, Pinto AM, Vaccarino FM, Renieri A, Campiani G, Meloni I. Landucci E, et al. Among authors: fallerini c. Exp Cell Res. 2018 Jul 15;368(2):225-235. doi: 10.1016/j.yexcr.2018.05.001. Epub 2018 May 4. Exp Cell Res. 2018. PMID: 29730163 Free PMC article.
A pilot study of next generation sequencing-liquid biopsy on cell-free DNA as a novel non-invasive diagnostic tool for Klippel-Trenaunay syndrome.
Palmieri M, Pinto AM, di Blasio L, Currò A, Monica V, Sarno LD, Doddato G, Baldassarri M, Frullanti E, Giliberti A, Mussolin B, Fallerini C, Molinaro F, Vaghi M, Renieri A, Primo L. Palmieri M, et al. Among authors: fallerini c. Vascular. 2021 Feb;29(1):85-91. doi: 10.1177/1708538120936421. Epub 2020 Jun 26. Vascular. 2021. PMID: 32588787
MET somatic activating mutations are responsible for lymphovenous malformation and can be identified using cell-free DNA next generation sequencing liquid biopsy.
Palmieri M, Di Sarno L, Tommasi A, Currò A, Doddato G, Baldassarri M, Frullanti E, Giliberti A, Fallerini C, Arzini A, Pinto A, Vaghi M, Renieri A. Palmieri M, et al. Among authors: fallerini c. J Vasc Surg Venous Lymphat Disord. 2021 May;9(3):740-744. doi: 10.1016/j.jvsv.2020.07.015. Epub 2020 Aug 26. J Vasc Surg Venous Lymphat Disord. 2021. PMID: 32858245
RB1 Germline Variant Predisposing to a Rare Ovarian Germ Cell Tumor: A Case Report.
Gelli E, Fallerini C, Valentino F, Giliberti A, Castiglione F, Laschi L, Palmieri M, Fabbiani A, Tita R, Mencarelli MA, Renieri A, Ariani F. Gelli E, et al. Among authors: fallerini c. Front Oncol. 2020 Aug 21;10:1467. doi: 10.3389/fonc.2020.01467. eCollection 2020. Front Oncol. 2020. PMID: 32974172 Free PMC article.
X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases.
Mastrangelo A, Giani M, Groppali E, Castorina P, Soldà G, Robusto M, Fallerini C, Bruttini M, Renieri A, Montini G. Mastrangelo A, et al. Among authors: fallerini c. Front Med (Lausanne). 2020 Nov 23;7:580376. doi: 10.3389/fmed.2020.580376. eCollection 2020. Front Med (Lausanne). 2020. PMID: 33330536 Free PMC article.
74 results