334 results on '"Sidoti, Antonina"'
Search Results
2. The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis
3. From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases
4. Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration
5. Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells
6. N-retinylidene-N-retinylethanolamine adduct induces expression of chronic inflammation cytokines in retinal pigment epithelium cells
7. 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
8. Exploring Trimethylaminuria: Genetics and Molecular Mechanisms, Epidemiology, and Emerging Therapeutic Strategies.
9. Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells
10. Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners
11. An Innovative Gene Prioritization Pipeline for DNA-Sequencing Analyses
12. Innovations in Data Visualization for Straightforward Interpretation of Nucleic Acid Omics Outcomes
13. Variant Calling on RNA Sequencing Data: State of Art and Future Perspectives
14. New Integrated Mitochondrial DNA Bioinformatics Pipeline to Improve Quality Assessment of Putative Pathogenic Variants from NGS Experiments
15. Subject Index
16. New Integrated Differential Expression Approach for RNA-Seq Data Analysis
17. Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies
18. Relevance of CCM gene polymorphisms for clinical management of sporadic cerebral cavernous malformations
19. Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis
20. GLO1 gene polymorphisms and their association with retinitis pigmentosa: a case–control study in a Sicilian population
21. How Many Alzheimer–Perusini’s Atypical Forms Do We Still Have to Discover?
22. Evaluation of Qualitative Outcomes after Surgical Intervention on Patients Affected by Arteriovenous Malformations
23. The microtubule-associated molecular pathways may be genetically disrupted in patients with Bipolar Disorder. Insights from the molecular cascades
24. Retraction Note: Non-coding RNAome of RPE cells under oxidative stress suggests unknown regulative aspects of Retinitis pigmentosa etiopathogenesis
25. Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations
26. RETRACTED ARTICLE: Non-coding RNAome of RPE cells under oxidative stress suggests unknown regulative aspects of Retinitis pigmentosa etiopathogenesis
27. The impact of modifier genes on cone-rod dystrophy heterogeneity: An explorative familial pilot study and a hypothesis on neurotransmission impairment
28. Deciphering impact of single nucleotide polymorphisms on cotranscriptional modification in CCM gene mRNAs
29. Evaluation of the role of MAPK1 and CREB1 polymorphisms on treatment resistance, response and remission in mood disorder patients
30. miRNAexpression profile of retinal pigment epithelial cells under oxidative stress conditions
31. Pharmacogenetics of antidepressant drugs: An update
32. Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations
33. Epitranscriptome Analysis of Oxidative Stressed Retinal Epithelial Cells Depicted a Possible RNA Editing Landscape of Retinal Degeneration
34. Evidences of PIEZO1 involvement in cerebral cavernous malformation pathogenesis
35. The molecular interaction between the glutamatergic, noradrenergic, dopaminergic and serotoninergic systems informs a detailed genetic perspective on depressive phenotypes
36. Editome landscape of CCM-derived endothelial cells
37. Investigating the role of imprinted genes in pediatric sporadic brain arteriovenous malformations
38. Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes
39. The Combination of New Missense Mutation with [A(TA)7TAA] Dinucleotide Repeat in UGT1A1 Gene Promoter Causes Gilbertʼs Syndrome
40. Absence of mutations at SERPINI1 gene in a cohort of patients with Cerebral Cavernous Malformations
41. Oxidative Stress and the Neurovascular Unit
42. Impairments of Photoreceptor Outer Segments Renewal and Phototransduction Due to a Peripherin Rare Haplotype Variant: Insights from Molecular Modeling
43. Gut-Brain Axis Cross-Talk and Limbic Disorders as Biological Basis of Secondary TMAU
44. Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation
45. New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?
46. Advances in Bioinformatics, Biostatistics and Omics Sciences
47. Antiretroviral treatment leading to secondary trimethylaminuria: Genetic associations and successful management with riboflavin
48. Expression of Pro-Angiogenic Markers Is Enhanced by Blue Light in Human RPE Cells
49. Possible A2E Mutagenic Effects on RPE Mitochondrial DNA from Innovative RNA-Seq Bioinformatics Pipeline
50. Germline Mutation Enrichment in Pathways Controlling Endothelial Cell Homeostasis in Patients with Brain Arteriovenous Malformation: Implication for Molecular Diagnosis
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