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The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment

PloS one, 2022-12, Vol.17 (12), p.e0278857-e0278857

2022

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Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells

Biochimica et biophysica acta. Molecular basis of disease, 2020-12, Vol.1866 (12), p.165956-165956, Article 165956

2020

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ROLES OF SINGLE-NUCLEOTIDE POLYMORPHISMS IN HEALTHY SUBJECTS AND DISEASE

Euromediterranean biomedical journal, 2018-10, Vol.13 (27), p.118-119

Simona Alibrandi

2018

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

International journal of molecular sciences, 2020-12, Vol.22 (1), p.70

2020

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Oxidative Stress and the Neurovascular Unit

Life (Basel, Switzerland), 2021-07, Vol.11 (8), p.767

2021

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Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling

International journal of molecular sciences, 2021-03, Vol.22 (7), p.3484

2021

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ROLE OF CCR5 -2150 A>G AND Δ32 POLYMORPHISMS IN RHEUMATOID ARTHRITIS: A CASE-CONTROL STUDY IN A SICILIAN POPULATION

Euromediterranean biomedical journal, 2017-05, Vol.12 (15), p.69-72

Simona Alibrandi

2017

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The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment

PloS one, 2022-12, Vol.17 (12)

2022

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Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa

Antioxidants, 2020-04, Vol.9 (4), p.318

2020

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Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies

Antioxidants, 2020-04, Vol.9 (4), p.307

2020

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

Antioxidants, 2020-11, Vol.9 (11), p.1154

2020

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Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration

Antioxidants, 2022-09, Vol.11 (10), p.1967

2022

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Editome landscape of CCM-derived endothelial cells

RNA biology, 2022-12, Vol.19 (1), p.852-865

2022

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

Antioxidants, 2020-11, Vol.9 (11), p.1158

2020

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Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Molecules (Basel, Switzerland), 2021-11, Vol.26 (22), p.7045

2021

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Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer-Perusini's Disease and Retinal Dystrophies

Biomedicines, 2023-12, Vol.11 (12), p.3258

2023

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Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa

Antioxidants, 2020-05, Vol.9 (5), p.416

2020

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How Many Alzheimer-Perusini's Atypical Forms Do We Still Have to Discover?

Biomedicines, 2023-07, Vol.11 (7), p.2035

2023

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Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration

Heliyon, 2024-04, Vol.10 (8), p.e29828-e29828, Article e29828

2024

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Methylome analysis of endothelial cells suggests new insights on sporadic brain arteriovenous malformation

Heliyon, 2024-08, Vol.10 (15), p.e35126, Article e35126

2024

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The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis

Heliyon, 2024-07, Vol.10 (14), p.e34756, Article e34756

2024

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Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations

Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale, 2021-12, Vol.94 (2)

2021

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Gut-Brain Axis Cross-Talk and Limbic Disorders as Biological Basis of Secondary TMAU

Journal of personalized medicine, 2021-01, Vol.11 (2), p.87

2021

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N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells

Experimental eye research, 2021-08, Vol.209, Article 108641

2021

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Small nucleolar and small Cajal Body-specific RNAs expression profile of oxidative stressed and normal RPE cells suggests unknown regulative aspects of retinitis pigmentosa etiopathogenesis

Atti della Accademia peloritana dei pericolanti. Classe I di scienze fis., mat. e naturali, 2018-01, Vol.96 (S3), p.A7

2018

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The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment

Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells

ROLES OF SINGLE-NUCLEOTIDE POLYMORPHISMS IN HEALTHY SUBJECTS AND DISEASE

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

Oxidative Stress and the Neurovascular Unit

Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling

ROLE OF CCR5 -2150 A>G AND Δ32 POLYMORPHISMS IN RHEUMATOID ARTHRITIS: A CASE-CONTROL STUDY IN A SICILIAN POPULATION

The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment

Transcriptome Analyses of lncRNAs in A2E-Stressed Retinal Epithelial Cells Unveil Advanced Links between Metabolic Impairments Related to Oxidative Stress and Retinitis Pigmentosa

Effects of A2E-Induced Oxidative Stress on Retinal Epithelial Cells: New Insights on Differential Gene Response and Retinal Dystrophies

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

Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration

Editome landscape of CCM-derived endothelial cells

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

Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer-Perusini's Disease and Retinal Dystrophies

Discovery of GLO1 New Related Genes and Pathways by RNA-Seq on A2E-Stressed Retinal Epithelial Cells Could Improve Knowledge on Retinitis Pigmentosa

How Many Alzheimer-Perusini's Atypical Forms Do We Still Have to Discover?

Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration

Methylome analysis of endothelial cells suggests new insights on sporadic brain arteriovenous malformation

The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis

Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations

Gut-Brain Axis Cross-Talk and Limbic Disorders as Biological Basis of Secondary TMAU

N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells

Small nucleolar and small Cajal Body-specific RNAs expression profile of oxidative stressed and normal RPE cells suggests unknown regulative aspects of retinitis pigmentosa etiopathogenesis

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