Lista de obras - Angelo G Condorelli - Dominio Público Uruguay

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Circulating miRNAs profiles in Tourette syndrome: molecular data and clinical implications.

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2020

Infantile bullous pemphigoid following vaccination

scientific article published on 01 October 2018

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.

artículo científico publicado en 2017

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

scientific article published on 20 February 2020

Non-coding landscapes of colorectal cancer

artículo científico publicado en 2015

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

article

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

artículo científico publicado en 2022

miR-145-5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts

scientific article published on 20 October 2019

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

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Lista de obras de Angelo G Condorelli

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

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

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

Circulating miRNAs profiles in Tourette syndrome: molecular data and clinical implications.

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

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

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

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

Infantile bullous pemphigoid following vaccination

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.

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

Non-coding landscapes of colorectal cancer

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

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

miR-145-5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts

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

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