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Mirko Luoni

6PUBLICATIONS

51CO-AUTHORS

Haematological tumoursNeurogeneticsMedical molecular engineering of nucleic acids and proteinsTransgenesisVision science

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Publications (6)

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|Apr 23, 2026

MeCP2 gene dosage-dependent neurodevelopmentally restricted defects arise by aberrant activation of cell fate-determining bivalent genes.

|Feb 27, 2026

NEDAMSS syndrome-related truncating and missense mutations are associated with aberrant liquid-liquid phase separation of IRF2BPL.

Marco Dell'Oca, Stefania Boggio Bozzo, Serena Vaglietti

|Jul 05, 2023

Genome-wide screening in pluripotent cells identifies Mtf1 as a suppressor of mutant huntingtin toxicity.

Giorgia Maria Ferlazzo, Anna Maria Gambetta, Sonia Amato

|Feb 15, 2023

Intrathymic AAV delivery results in therapeutic site-specific integration at TCR loci in mice.

Andrea Calabria, Carlo Cipriani, Giulio Spinozzi

|Jan 16, 2023

MCT1-dependent energetic failure and neuroinflammation underlie optic nerve degeneration in Wolfram syndrome mice.

Greta Rossi, Gabriele Ordazzo, Niccolò N Vanni

|Mar 25, 2020

Whole brain delivery of an instability-prone <i>Mecp2</i> transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome.

Mirko Luoni, Serena Giannelli, Marzia Tina Indrigo

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Frequent Collaborators

4 joint publications

Vania Broccoli

3 joint publications

Serena Giannelli

1 joint publications

Piera Calamita

1 joint publications

Benjamin Deverman

1 joint publications

Gabriele Ordazzo

1 joint publications

Edoardo Bellini

1 joint publications

Sharon Muggeo

1 joint publications

Andrea Calabria

1 joint publications

Carlo Cipriani

1 joint publications

Laura Rudilosso

Frequent Collaborators

4 joint publications

Vania Broccoli

3 joint publications

Serena Giannelli

1 joint publications

Piera Calamita

1 joint publications

Benjamin Deverman

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