Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis

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Main Authors: Luca Dalle Carbonare, Arianna Minoia, Alberto Gandini, Francesca Cristiana Piritore, Cristina Patuzzo, Lucrezia Ceretti, Anna Vareschi, Antonino Aparo, Mattia Cominacini, Giovanni Malerba, Maria Grazia Romanelli, Joao Pessoa, Daniele Guardavaccaro, Franco Antoniazzi, Maria Teresa Valenti
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2025-07-01
Series:Genes and Diseases
Online Access:http://www.sciencedirect.com/science/article/pii/S2352304224002460
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author Luca Dalle Carbonare
Arianna Minoia
Alberto Gandini
Francesca Cristiana Piritore
Cristina Patuzzo
Lucrezia Ceretti
Anna Vareschi
Antonino Aparo
Mattia Cominacini
Giovanni Malerba
Maria Grazia Romanelli
Joao Pessoa
Daniele Guardavaccaro
Franco Antoniazzi
Maria Teresa Valenti
author_facet Luca Dalle Carbonare
Arianna Minoia
Alberto Gandini
Francesca Cristiana Piritore
Cristina Patuzzo
Lucrezia Ceretti
Anna Vareschi
Antonino Aparo
Mattia Cominacini
Giovanni Malerba
Maria Grazia Romanelli
Joao Pessoa
Daniele Guardavaccaro
Franco Antoniazzi
Maria Teresa Valenti
author_sort Luca Dalle Carbonare
collection DOAJ
format Article
id doaj-art-85ed25ef8c87476fbea9685ac00dc9cf
institution DOAJ
issn 2352-3042
language English
publishDate 2025-07-01
publisher KeAi Communications Co., Ltd.
record_format Article
series Genes and Diseases
spelling doaj-art-85ed25ef8c87476fbea9685ac00dc9cf2025-08-20T03:10:58ZengKeAi Communications Co., Ltd.Genes and Diseases2352-30422025-07-0112410144910.1016/j.gendis.2024.101449Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasisLuca Dalle Carbonare0Arianna Minoia1Alberto Gandini2Francesca Cristiana Piritore3Cristina Patuzzo4Lucrezia Ceretti5Anna Vareschi6Antonino Aparo7Mattia Cominacini8Giovanni Malerba9Maria Grazia Romanelli10Joao Pessoa11Daniele Guardavaccaro12Franco Antoniazzi13Maria Teresa Valenti14Department of Engineering for the Innovation Medicine, University of Verona, Verona 37100, ItalyDepartment of Engineering for the Innovation Medicine, University of Verona, Verona 37100, ItalyDepartment of Surgery, Dentistry, Pediatrics and Gynecology, University of Verona, Verona 37100, ItalyDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona 37100, ItalyDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona 37100, ItalyDepartment of Surgery, Dentistry, Pediatrics and Gynecology, University of Verona, Verona 37100, ItalyDepartment of Engineering for the Innovation Medicine, University of Verona, Verona 37100, ItalyResearch Center LURM (Interdepartmental Laboratory of Medical Research), University of Verona, Verona 37100, ItalyDepartment of Engineering for the Innovation Medicine, University of Verona, Verona 37100, ItalyDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona 37100, ItalyDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona 37100, ItalyDepartment of Medical Sciences and Institute of Biomedicine-iBiMED, University of Aveiro, Aveiro 3810-193, PortugalDepartment of Biotechnology, University of Verona, Verona 37134, ItalyDepartment of Surgery, Dentistry, Pediatrics and Gynecology, University of Verona, Verona 37100, ItalyDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona 37100, Italy; Corresponding author.http://www.sciencedirect.com/science/article/pii/S2352304224002460
spellingShingle Luca Dalle Carbonare
Arianna Minoia
Alberto Gandini
Francesca Cristiana Piritore
Cristina Patuzzo
Lucrezia Ceretti
Anna Vareschi
Antonino Aparo
Mattia Cominacini
Giovanni Malerba
Maria Grazia Romanelli
Joao Pessoa
Daniele Guardavaccaro
Franco Antoniazzi
Maria Teresa Valenti
Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
Genes and Diseases
title Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
title_full Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
title_fullStr Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
title_full_unstemmed Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
title_short Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
title_sort unraveling runx2 mutation in a cleidocranial dysplasia patient molecular insights into osteogenesis and proteostasis
url http://www.sciencedirect.com/science/article/pii/S2352304224002460
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