804 results on '"Cereda, Cristina"'
Search Results
2. ALDOC- and ENO2- driven glucose metabolism sustains 3D tumor spheroids growth regardless of nutrient environmental conditions: a multi-omics analysis
3. Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome
4. Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots
5. Long-term cytokine profile in multisystem inflammatory disease among children
6. Effective lowering of α-synuclein expression by targeting G-quadruplex structures within the SNCA gene
7. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease
8. Space research to explore novel biochemical insights on Earth
9. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
10. Breast cancer patient-derived organoids for the investigation of patient-specific tumour evolution
11. Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
12. Stroke and stroke-like episodes: recurrent manifestations in GLUT1 Deficiency SyndromeSara Olivottoa
13. Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype
14. Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
15. Extracellular vesicles secreted by cumulus cells contain microRNAs that are potential regulatory factors of mouse oocyte developmental competence
16. Role of epigenetics and alterations in RNA metabolism in leukodystrophies
17. Functional Study of SNCA p.V15A Variant: Further Linking α‐Synuclein and Glucocerebrosidase
18. Inflammation and cell-to-cell communication, two related aspects in frailty
19. Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
20. Fast quantification of extracellular vesicles levels in early breast cancer patients by Single Molecule Detection Array (SiMoA)
21. Functional analysis and transcriptome profile of meninges and skin fibroblasts from human‐aged donors.
22. BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes
23. A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset
24. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
25. Activated Human Adipose Tissue Transplantation Promotes Sensorimotor Recovery after Acute Spinal Cord Contusion in Rats
26. Detection of SARS-CoV-2 genome and whole transcriptome sequencing in frontal cortex of COVID-19 patients
27. Ruxolitinib in Aicardi-Goutières syndrome
28. Raman spectroscopy reveals biochemical differences in plasma derived extracellular vesicles from sporadic Amyotrophic Lateral Sclerosis patients
29. Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency
30. Prevalence and prognostic value of Delirium as the initial presentation of COVID-19 in the elderly with dementia: An Italian retrospective study
31. Hydroxychloroquine modulates immunological pathways activated by RNA:DNA hybrids in Aicardi–Goutières syndrome patients carrying RNASEH2 mutations
32. cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing
33. Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
34. Study of lncRNAs in Pediatric Neurological Diseases: Methods, Analysis of the State-of-Art and Possible Therapeutic Implications
35. Leveraging Non-negative Matrix Tri-Factorization and Knowledge-Based Embeddings for Drug Repurposing: an Application to Parkinson's Disease
36. Fifteen Years of Iodine Prophylaxis in Italy: Results of a Nationwide Surveillance (Period 2015-2019)
37. 3D photopolymerized microstructured scaffolds influence nuclear deformation, nucleo/cytoskeletal protein organization, and gene regulation in mesenchymal stem cells
38. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
39. RNA Metabolism and Therapeutics in Amyotrophic Lateral Sclerosis
40. From Neuronal Differentiation of iPSCs to 3D Neural Organoids: Modeling of Neurodegenerative Diseases
41. Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
42. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
43. A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS)
44. The role of clinical and neuroimaging features in the diagnosis of CADASIL
45. Air pollution as a contributor to the inflammatory activity of multiple sclerosis
46. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis
47. Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
48. Redox Imbalance in Neurological Disorders in Adults and Children
49. Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study
50. Menkes disease complicated by concurrent ACY1 deficiency: A case report
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