Publications by authors named "Sebastian Fantini"

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Identification of pyrazolo-piperidinone derivatives targeting YAP-TEAD interface 3 as anticancer agents through integrated virtual screening and mass spectrometry proteomics.
Laura Scalvini, Lorenzo Tagliazucchi, Gian Marco Elisi, Dana Zappaterra, Maria Gaetana Moschella, Sebastian Fantini

Eur J Med Chem· December 2025

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Inhibition of ERK1/2 signaling prevents bone marrow fibrosis by reducing osteopontin plasma levels in a myelofibrosis mouse model.
Elisa Bianchi, Sebastiano Rontauroli, Lara Tavernari, Margherita Mirabile, Francesca Pedrazzi, Sebastian Fantini

Leukemia· May 2023

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The Response to Oxidative Damage Correlates with Driver Mutations and Clinical Outcome in Patients with Myelofibrosis.
Elena Genovese, Margherita Mirabile, Sebastiano Rontauroli, Stefano Sartini, Sebastian Fantini

Antioxidants (Basel)· January 2022

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Increased Plasma Levels of lncRNAs , and Correlate with Negative Prognostic Factors in Myelofibrosis.
Sebastian Fantini, Sebastiano Rontauroli, Stefano Sartini, Margherita Mirabile, Elisa Bianchi

Cancers (Basel)· September 2021

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Gene expression profile correlates with molecular and clinical features in patients with myelofibrosis.
Sebastiano Rontauroli, Sara Castellano, Paola Guglielmelli, Roberta Zini, Elisa Bianchi, Sebastian Fantini

Blood Adv· March 2021

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Mutated clones driving leukemic transformation are already detectable at the single-cell level in CD34-positive cells in the chronic phase of primary myelofibrosis.
Sandra Parenti, Sebastiano Rontauroli, Chiara Carretta, Selene Mallia, Elena Genovese, Sebastian Fantini

NPJ Precis Oncol· February 2021

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Promoter Methylation Leads to Decreased Expression and Deregulated NLRP3 Inflammasome Activation in Psoriatic Fibroblasts.
Matteo Bertesi, Sebastian Fantini, Claudia Alecci, Roberta Lotti, Andrea Martello

Front Med (Lausanne)· January 2021

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Genomic Analysis of Hematopoietic Stem Cell at the Single-Cell Level: Optimization of Cell Fixation and Whole Genome Amplification (WGA) Protocol.
Chiara Carretta, Selene Mallia, Elena Genovese, Sandra Parenti, Sebastiano Rontauroli, Sebastian Fantini

Int J Mol Sci· October 2020

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Wnt/CTNNB1 Signal Transduction Pathway Inhibits the Expression of ZFP36 in Squamous Cell Carcinoma, by Inducing Transcriptional Repressors SNAI1, SLUG and TWIST.
Emma D Zanfi, Sebastian Fantini, Roberta Lotti, Matteo Bertesi, Alessandra Marconi

Int J Mol Sci· August 2020

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Depletion of Trichoplein (TpMs) Causes Chromosome Mis-Segregation, DNA Damage and Chromosome Instability in Cancer Cells.
Angela Lauriola, Andrea Martello, Sebastian Fantini, Gaetano Marverti, Tommaso Zanocco-Marani

Cancers (Basel)· April 2020

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Physiological expression of miR-130a during differentiation of CD34 human hematopoietic stem cells results in the inhibition of monocyte differentiation.
Fabiana Mammoli, Sandra Parenti, Mariana Lomiento, Claudia Gemelli, Claudio Giacinto Atene, Sebastian Fantini

Exp Cell Res· September 2019

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KLF4 Mediates the Effect of 5-ASA on the β-Catenin Pathway in Colon Cancer Cells.
Sandra Parenti, Lucia Montorsi, Sebastian Fantini, Fabiana Mammoli, Claudia Gemelli

Cancer Prev Res (Phila)· August 2018

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HOX cluster-embedded micro-RNAs and cancer.
Sebastian Fantini, Valentina Salsi, Vincenzo Zappavigna

Biochim Biophys Acta Rev Cancer· April 2018

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The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients.
Sebastian Fantini, Valentina Salsi, Luca Reggiani, Antonino Maiorana, Vincenzo Zappavigna

Oncotarget· January 2017

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NUP98 fusion oncoproteins interact with the APC/C(Cdc20) as a pseudosubstrate and prevent mitotic checkpoint complex binding.
Valentina Salsi, Sebastian Fantini, Vincenzo Zappavigna

Cell Cycle· September 2016

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MicroRNA-196b is transcribed from an autonomous promoter and is directly regulated by Cdx2 and by posterior Hox proteins during embryogenesis.
Sebastian Fantini, Valentina Salsi, Antonio Vitobello, Filippo M Rijli, Vincenzo Zappavigna

Biochim Biophys Acta· August 2015

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NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint.
Valentina Salsi, Silvia Ferrari, Paolo Gorello, Sebastian Fantini, Francesca Chiavolelli

Cancer Res· February 2014

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An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning.
Nathalie Brison, Philippe Debeer, Sebastian Fantini, Christine Oley, Vincenzo Zappavigna

Hum Mol Genet· June 2012

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Electrochemical reduction of O2 in 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid containing Zn2+ cations: deposition of non-polar oriented ZnO nanocrystalline films.
Eneko Azaceta, Rebeca Marcilla, David Mecerreyes, Mariana Ungureanu, Apurba Dev, Sebastian Fantini

Phys Chem Chem Phys· August 2011

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Control of pelvic girdle development by genes of the Pbx family and Emx2.
Terence D Capellini, Karen Handschuh, Laura Quintana, Elisabetta Ferretti, Giuseppina Di Giacomo, Sebastian Fantini

Dev Dyn· May 2011

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Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.
Terence D Capellini, Giulia Vaccari, Elisabetta Ferretti, Sebastian Fantini, Mu He

Development· August 2010

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A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype.
Sebastian Fantini, Giulia Vaccari, Nathalie Brison, Philippe Debeer, Przemko Tylzanowski

Hum Mol Genet· March 2009

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