Francesca Sciandra (F Sciandra)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 10

Top Venues

Consiglio Nazionale delle Ricerche Istituto di Chimica del Riconoscimento Molecolare Unita Organizzativa di Supporto di Roma

Università degli Studi di Roma La Sapienza (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Consiglio Nazionale delle Ricerche Istituto di Chimica del Riconoscimento Molecolare Unita Organizzativa di Supporto di Roma Oct 03 2011

Italy

researcher

Università Cattolica del Sacro Cuore, Facoltà di Medicina e Chirurgia

Italy

Contract Professor

Fondazione Telethon

Italy

Post-doctoral Fellowship

Education History

Università degli Studi di Roma La Sapienza Oct 01 2000 - Mar 01 2004

Italy

PHD :: Biochemistry

Universität Basel Department Biozentrum Sep 01 2002 - May 01 2003

Switzerland

PHD

Università degli Studi di Roma La Sapienza - Mar 21 2000

Italy

BSC

Publications

Rui Lois Tan, Francesca Sciandra, Wolfgang Hübner, Manuela Bozzi, Jens Reimann, Susanne Schoch, Andrea Brancaccio, Sandra Blaess
The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization. Disease models & mechanisms 17 (6) (2024)
Rui Lois Tan, Francesca Sciandra, Wolfgang Hübner, Manuela Bozzi, Jens Reimann, Susanne Schoch, Andrea Brancaccio, Sandra Blaess
Missense mutation (C667F) in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization. Disease models & mechanisms (2024)
Rui Lois Tan, Francesca Sciandra, Wolfgang Hübner, Manuela Bozzi, Jens Reimann, Susanne Schoch, Andrea Brancaccio, Sandra Blaess
The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization. Disease models & mechanisms 17 (6) (2024)
Rui Lois Tan, Francesca Sciandra, Wolfgang Hübner, Manuela Bozzi, Jens Reimann, Susanne Schoch, Andrea Brancaccio, Sandra Blaess
The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization. Disease models & mechanisms 17 (6) (2024)
G Friggeri, I Moretti, Francesco Amato, Andrea Giacomo Marrani, Francesca Sciandra, Stella Garcia Colombarolli, Alberto Vitali, S Viscuso, A Augello, Lishan Cui, Giordano Perini, Marco De Spirito, Massimiliano Papi, Valentina Palmieri
Multifunctional scaffolds for biomedical applications: Crafting versatile solutions with polycaprolactone enriched by graphene oxide. APL bioengineering 8 (1) (2024)
G Friggeri, I Moretti, Francesco Amato, Andrea Giacomo Marrani, Francesca Sciandra, Stella Garcia Colombarolli, Alberto Vitali, S Viscuso, A Augello, Lishan Cui, Giordano Perini, Marco De Spirito, Massimiliano Papi, Valentina Palmieri
Multifunctional scaffolds for biomedical applications: Crafting versatile solutions with polycaprolactone enriched by graphene oxide. APL bioengineering 8 (1) (2024)
Rui Lois Tan, Francesca Sciandra, Wolfgang Hübner, Manuela Bozzi, Jens Reimann, Susanne Schoch, Andrea Brancaccio, Sandra Blaess
The missense mutation C667F in murine β-dystroglycan causes embryonic lethality, myopathy and blood-brain barrier destabilization. Disease models & mechanisms 17 (6) (2024)
Francesca Sciandra, Patrizia Bottoni, Marinella De Leo, Alessandra Braca, Andrea Brancaccio, Manuela Bozzi
Verbascoside Elicits Its Beneficial Effects by Enhancing Mitochondrial Spare Respiratory Capacity and the Nrf2/HO-1 Mediated Antioxidant System in a Murine Skeletal Muscle Cell Line. International journal of molecular sciences 24 (20) (2023)
Francesca Sciandra, Bianca Maria Scicchitano, Giulia Signorino, Maria Giulia Bigotti, Barbara Tavazzi, Francesca Lombardi, Manuela Bozzi, Gigliola Sica, Bruno Giardina, Sandra Blaess, Andrea Brancaccio
Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene. BMC research notes 10 (1) (2017)
Giulia Signorino, Sonia Covaceuszach, Manuela Bozzi, Wolfgang Hübner, Viola Mönkemöller, Petr V Konarev, Alberto Cassetta, Andrea Brancaccio, Francesca Sciandra
A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein. Human mutation 39 (2) (2017)

Francesca Sciandra.css-eqlu8i{font-size:small;padding-left:4px;} (F Sciandra)

Publication Activity (10 Years)

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Francesca Sciandra (F Sciandra)