Nicoletta ZOPPI

Professor

University of Brescia

Italy

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Articles (6)

Year:

2023

Year:

2022

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (6)

Nicola Chiarelli

Assistant Professor in Medical Genetics

University of Brescia

ITALY

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Francesco ANGELUCCI

Full Professor of Biochemistry

University of L'Aquila

ITALY

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RODOLFO IPPOLITI

FULL PROFESSOR OF MOLECULAR BIOLOGY

University of L'Aquila

ITALY

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Marina Colombi

Full professor of Medical Genetics

University of Brescia

ITALY

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Ruggero De Paulis

Saint Camillus International University of Health Sciences

ITALY

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Francesco Brancati

Professor

University of L'Aquila

ITALY

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Nicoletta ZOPPI

Research Interests

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Articles (6)

Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome.

RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms

Matrix Metalloproteinases Inhibition by Doxycycline Rescues Extracellular Matrix Organization and Partly Reverts Myofibroblast Differentiation in Hypermobile Ehlers-Danlos Syndrome Dermal Fibroblasts: A Potential Therapeutic Target?

Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts

COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap

Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy

Collaborators (6)

Nicola Chiarelli

Francesco ANGELUCCI

RODOLFO IPPOLITI

Marina Colombi

Ruggero De Paulis

Francesco Brancati

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Nicoletta ZOPPI

Research Interests

Explore related searches

Contact this professor

Articles (6)

Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome.

RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms

Matrix Metalloproteinases Inhibition by Doxycycline Rescues Extracellular Matrix Organization and Partly Reverts Myofibroblast Differentiation in Hypermobile Ehlers-Danlos Syndrome Dermal Fibroblasts: A Potential Therapeutic Target?

Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts

COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap

Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A &gt; G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy

Collaborators (6)

Nicola Chiarelli

Francesco ANGELUCCI

RODOLFO IPPOLITI

Marina Colombi

Ruggero De Paulis

Francesco Brancati

Make your next move.

Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagy