A. Urciuolo

发表

Customized bioreactor enables the production of 3D diaphragmatic constructs influencing matrix remodeling and fibroblast overgrowth

A. Cani, M. Piccoli, P. de Coppi, 2022, npj Regenerative Medicine.

Intravital three-dimensional bioprinting

N. Elvassore, G. Giobbe, P. de Coppi, 2020, Nature Biomedical Engineering.

Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration

N. Maraldi, M. Sandri, E. Bertaggia, 2010, Nature Medicine.

Mitochondrial fission links ECM mechanotransduction to metabolic redox homeostasis and metastatic chemotherapy resistance

Charles T. Hindmarch, N. Elvassore, A. Rosato, 2022, Nature Cell Biology.

Cyclosporin A Promotes in vivo Myogenic Response in Collagen VI-Deficient Myopathic Mice

P. Braghetta, P. Bonaldo, F. Gattazzo, 2014, Front. Aging Neurosci..

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

P. Bonaldo, P. Sabatelli, L. Merlini, 2008, Neurology.

Critical Evaluation of the Use of Cell Cultures for Inclusion in Clinical Trials of Patients Affected by Collagen VI Myopathies

P. Bonaldo, P. Bernardi, A. Angelin, 2011, Journal of cellular physiology.

Differential and restricted expression of novel collagen VI chains in mouse.

M. Paulsson, P. Bonaldo, P. Sabatelli, 2011, Matrix biology : journal of the International Society for Matrix Biology.

3D ECM-rich environment sustains the identity of naive human iPSCs.

D. Cacchiarelli, N. Elvassore, C. Luni, 2022, Cell stem cell.

Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies

E. Bertini, E. Mercuri, A. Ferlini, 2010, BMC Medical Genetics.

Autosomal recessive Bethlem myopathy

E. Mercuri, A. Ferlini, S. Messina, 2009, Neurology.

Human Pluripotent Stem Cell-Derived Micropatterned Ectoderm Allows Cell Sorting of Meso-Endoderm Lineages

N. Elvassore, F. Michielin, O. Gagliano, 2022, Frontiers in Bioengineering and Biotechnology.

3D high-resolution two-photon crosslinked hydrogel structures for biological studies.

N. Elvassore, S. Giulitti, R. Liska, 2017, Acta biomaterialia.

Four-dimensional hydrogel-in-hydrogel bioprinting for the spatiotemporal control of organoid and organotypic cultures

N. Elvassore, H. Clevers, G. Giobbe, 2021 .

Identification and characterization of novel collagen VI non‐canonical splicing mutations causing ullrich congenital muscular dystrophy

E. Bertini, M. Pane, E. Mercuri, 2009, Human mutation.

Collagen VI regulates satellite cell self-renewal and muscle regeneration

Marco Quarta, Giulio Cossu, Giovanni Vozzi, 2013, Nature Communications.

Three Novel Collagen VI Chains with High Homology to the α3 Chain*

M. Paulsson, P. Bonaldo, M. Koch, 2008, Journal of Biological Chemistry.

Extracellular matrix: A dynamic microenvironment for stem cell niche

P. Bonaldo, F. Gattazzo, Paolo Bonaldo, 2014, Biochimica et biophysica acta.

Restrictive tissue in the area of perimembranous ventricular septal defect. Cross-sectional and Doppler echocardiographic study.

A. Parri, R. Boldrini, A. Urciuolo, 1990, European heart journal.

Congenital aneurysm of the interventricular muscular septum with rupture into the right ventricle in a child.

A. Calzolari, A. Urciuolo, A. Magherini, 1988, American heart journal.

Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet

M. Pellegrini, F. Sambataro, M. Pennuto, 2016, Acta Neuropathologica.

Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration

K. Patel, S. Eaton, P. de Coppi, 2018, Scientific Reports.

MYOD modified mRNA drives direct on-chip programming of human pluripotent stem cells into skeletal myocytes.

N. Elvassore, E. Serena, P. de Coppi, 2021, Biochemical and biophysical research communications.

Multi-stage bioengineering of a layered oesophagus with in vitro expanded muscle and epithelial adult progenitors

S. Eaton, N. Sebire, P. de Coppi, 2018, Nature Communications.

Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale

N. Elvassore, S. Zatti, E. Serena, 2020, PloS one.

Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-Terminal domain: a case report

E. Bertini, A. D’Amico, S. Petrini, 2013, BMC Medical Genetics.

Microfluidic reprogramming to pluripotency of human somatic cells

N. Elvassore, C. Luni, O. Gagliano, 2019, Nature Protocols.

Native extracellular matrix promotes human neuromuscular organoid morphogenesis and function

D. Cacchiarelli, N. Elvassore, C. Luni, 2023, bioRxiv.

Three-dimensional in vitro models of neuromuscular tissue

A. Urciuolo, P. Raffa, Maria Easler, 2021, Neural regeneration research.

Decellularized Skeletal Muscles Support the Generation of In Vitro Neuromuscular Tissue Models

N. Elvassore, P. de Coppi, M. Gerli, 2021, Applied Sciences.

Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies.

M. Paulsson, P. Bonaldo, A. Zamparelli, 2011, The Journal of investigative dermatology.

Quantifying mechanical forces during vertebrate morphogenesis

N. Elvassore, P. Pavan, S. Todros, 2022 .

Multi-stage bioengineering of a layered oesophagus with in vitro expanded muscle and epithelial adult progenitors

S. Eaton, N. Sebire, P. de Coppi, 2018, Nature Communications.

Decellularized Tissue for Muscle Regeneration

P. de Coppi, A. Urciuolo, 2018, International journal of molecular sciences.

Decellularized skeletal muscles display neurotrophic effects in three‐dimensional organotypic cultures

N. Elvassore, C. Luni, P. de Coppi, 2020, Stem cells translational medicine.

Decellularized scaffolds for neuronal regeneration

A. Urciuolo, P. Raffa, 2020, Journal of Translational Science.