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Michela Faleschini
Michela Faleschini
Exome sequencing
Protein tyrosine phosphatase
Gene silencing
Loss function
Molecular biology
2
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25
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A new form of inherited thrombocytopenia caused by loss-of-function mutations in PTPRJ
2019
Blood
Caterina Marconi
Christian A. Di Buduo
Kellie LeVine
Serena Barozzi
Michela Faleschini
Valeria Bozzi
Flavia Palombo
Spencer U McKinstry
Giuseppe Lassandro
Paola Giordano
Patrizia Noris
Carlo L. Balduini
Anna Savoia
Alessandra Balduini
Tommaso Pippucci
Marco Seri
Nicholas Katsanis
Alessandro Pecci
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Citations (25)
Role of the mutations identified in the 5’UTR of ANKRD26 responsible for an inherited form of thrombocytopenia
2013
Chiara Gnan
Laura Arnoldo
Daniela De Rocco
Martina Cusan
Riccardo Sgarra
Michela Faleschini
Guidalberto Manfioletti
Anna Savoia
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