A. Condorelli

发表

Non-coding landscapes of colorectal cancer.

M. Ragusa, Cristina Barbagallo, D. Barbagallo, 2015, World journal of gastroenterology.

Non-coding landscapes of colorectal cancer 2015 Advances in Colorectal Cancer

M. Ragusa, Cristina Barbagallo, D. Barbagallo, 2015 .

Dysregulated miR-671-5p / CDR1-AS / CDR1 / VSNL1 axis is involved in glioblastoma multiforme

R. Parenti, F. Cicirata, M. Ragusa, 2015, Oncotarget.

CEBPA exerts a specific and biologically important proapoptotic role in pancreatic β cells through its downstream network targets

S. Piro, A. Rabuazzo, F. Purrello, 2014, Molecular biology of the cell.

miR-296-3p, miR-298-5p and their downstream networks are causally involved in the higher resistance of mammalian pancreatic α cells to cytokine-induced apoptosis as compared to β cells

S. Piro, A. Monello, Loriana G. Mascali, 2013, BMC Genomics.

RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development

E. Dellambra, S. Bondanza, G. Camerino, 2022, Orphanet Journal of Rare Diseases.

Combination Treatment with Hydroxytyrosol and Vitamin E Improves NAFLD-Related Fibrosis

G. Svegliati-Baroni, M. Bianchi, A. Alisi, 2022, Nutrients.

First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses

S. Rossi, G. Zambruno, D. Castiglia, 2020, International journal of molecular sciences.

Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe

R. Boldrini, G. Zambruno, S. Giancristoforo, 2020, Pediatric dermatology.

Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review

G. Zambruno, D. Castiglia, M. Naim, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening

D. Castiglia, F. Mariotti, B. Didona, 2022, Frontiers in Immunology.

MicroRNA‐145‐5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts

M. Teson, G. Zambruno, F. Cianfarani, 2019, The British journal of dermatology.

Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study

A. Novelli, G. Zambruno, C. Quintarelli, 2022, Biomedicines.

A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops

D. Ponzin, M. Tartaglia, S. Rossi, 2021, Genes.

Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy

E. Dellambra, E. Candi, V. Cianfanelli, 2021, Human molecular genetics.

Notch-ing up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway

E. Candi, G. Zambruno, D. Castiglia, 2021, Journal of Biomedical Science.

A Postzygotic ATP2A2 Novel Mutation Identified by Next-generation Sequencing in Mosaic Darier Disease.

C. Pedicelli, L. Guerra, D. Castiglia, 2018, Acta dermato-venereologica.

Circulating miRNAs profiles in tourette syndrome: molecular data and clinical implications

M. Barchitta, A. Agodi, M. Ragusa, 2015, Molecular Brain.

miR-296-3p, miR-298-5p and their downstream networks are causally involved in the higher resistance of mammalian pancreatic α cells to cytokine-induced apoptosis as compared to β cells

S. Piro, Loriana G. Mascali, F. Purrello, 2013, BMC Genomics.

IgE Sensitization Profile in Patients with Netherton Syndrome

R. Paganelli, D. Castiglia, B. Didona, 2022, International Archives of Allergy and Immunology.

SARS-CoV-2 infection of thymus induces loss of function that correlates with disease severity

C. Agrati, V. Bordoni, S. Petrini, 2023, Journal of Allergy and Clinical Immunology.

Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor‐like motif 2 of the β3 short arm

G. Zambruno, F. Cianfarani, D. Castiglia, 2018, The British journal of dermatology.

Epidermolysis Bullosa-Associated Squamous Cell Carcinoma: From Pathogenesis to Therapeutic Perspectives

E. Dellambra, G. Zambruno, D. Castiglia, 2019, International journal of molecular sciences.

Phenotypic Features of Epidermolysis Bullosa Simplex due to KLHL24 Mutations in 3 Italian Cases.

R. Boldrini, M. Tartaglia, G. Scuvera, 2019, Acta Dermato-Venereologica.

Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations.

C. Pedicelli, L. Guerra, D. Castiglia, 2017, Acta dermato-venereologica.

miRNAs Plasma Profiles in Vascular Dementia: Biomolecular Data and Biomedical Implications

P. Bosco, R. Spada, M. Ragusa, 2016, Front. Cell. Neurosci..

Multiple Skin Squamous Cell Carcinomas in Junctional Epidermolysis Bullosa Due to Altered Laminin-332 Function

E. Dellambra, F. Ricci, F. Passarelli, 2020, International journal of molecular sciences.

Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review

S. Rossi, G. Zambruno, M. El Hachem, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization

S. Rossi, D. Martinelli, G. Zambruno, 2021, Genes.

Cross-Sectional Study on Autosomal Recessive Congenital Ichthyoses: Association of Genotype with Disease Severity, Phenotypic, and Ultrastructural Features in 74 Italian Patients

S. Giancristoforo, M. El Hachem, A. Diociaiuti, 2024, Dermatology.

Gamma-secretase inhibitors down-regulate the pro-fibrotic Notch signaling pathway in recessive dystrophic epidermolysis bullosa.

T. Odorisio, D. Castiglia, R. Rota, 2024, The Journal of investigative dermatology.