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List of works by Rosalia D'Angelo

A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens

scientific article

Age dependent switching role of cyclin D1 in breast cancer.

scientific article published in January 2012

Ageing, hormonal behaviour and cyclin D1 in ductal breast carcinomas

scientific article published on 19 April 2005

CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: a case-control study

scientific article published on 28 February 2012

CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study

scientific article

Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.

scientific article

Distribution of the mutated delta 32 allele of the CCR5 gene in a Sicilian population.

scientific article published on June 2005

Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells

scientific article published on 20 November 2020

FMO3 allelic variants in Sicilian and Sardinian populations: Trimethylaminuria and absence of fish-like body odor ⬇️

scientific article published on December 21, 2012

First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation.

scientific article published on 22 June 2016

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report

scientific article

GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case-control study in a Sicilian population

scientific article published on 11 August 2018

Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis

scientific article published on 17 June 2020

Identification of a novel CCM2 gene mutation in an Italian family with multiple cerebral cavernous malformations and epilepsy: a causative mutation?

scientific article published on 19 September 2012

New Omics-Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?

scientific article published on 23 December 2020

New evaluation methods of read mapping by 17 aligners on simulated and empirical NGS data: an updated comparison of DNA- and RNA-Seq data from Illumina and Ion Torrent technologies

scientific article published on 16 June 2021

Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline

scientific article published on 20 November 2020

Possible protective role of the ABCA4 gene c.1268A>G missense variant in Stargardt disease and syndromic retinitis pigmentosa in a Sicilian family: Preliminary data.

scientific article

RETRACTED ARTICLE: Non-coding RNAome of RPE cells under oxidative stress suggests unknown regulative aspects of Retinitis pigmentosa etiopathogenesis

retracted scholarly article

Reduced intraplatelet magnesium concentrations in elderly patients with non-insulin dependent diabetes mellitus (NIDDM)

scientific article published on 01 November 1997

Regulation of flavin-containing mono-oxygenase (Fmo3) gene expression by steroids in mice and humans.

scientific article

Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations.

scientific article published on 29 June 2017

Retraction Note: Non-coding RNAome of RPE cells under oxidative stress suggests unknown regulative aspects of Retinitis pigmentosa etiopathogenesis

scientific article published on 25 September 2019

Role of oxidative stress in Retinitis pigmentosa: new involved pathways by an RNA-Seq analysis

scientific article published on 28 December 2018

Sarcoglycan subcomplex expression in normal human smooth muscle

scientific article

Sporadic cerebral cavernous malformations: report of further mutations of CCM genes in 40 Italian patients

scientific article

Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis?

scientific article published in February 2018

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

scientific article published on 20 December 2016

Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis

scientific article published on 06 December 2018

miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions.

scientific article published on 2 January 2018

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