564 results on '"Cereda, Cristina"'
Search Results
2. Bone Marrow Mesenchymal Stem Cells Expanded Inside the Nichoid Micro-Scaffold: a Focus on Anti-Inflammatory Response
3. Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome
4. Long-term cytokine profile in multisystem inflammatory disease among children
5. Effective lowering of α-synuclein expression by targeting G-quadruplex structures within the SNCA gene
6. Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots
7. Space research to explore novel biochemical insights on Earth
8. ALDOC- and ENO2- driven glucose metabolism sustains 3D tumor spheroids growth regardless of nutrient environmental conditions: a multi-omics analysis
9. Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype
10. Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
11. Fast quantification of extracellular vesicles levels in early breast cancer patients by Single Molecule Detection Array (SiMoA)
12. Inflammation and cell-to-cell communication, two related aspects in frailty
13. Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
14. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease
15. Functional analysis and transcriptome profile of meninges and skin fibroblasts from human‐aged donors.
16. BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes
17. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
18. A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset
19. Detection of SARS-CoV-2 genome and whole transcriptome sequencing in frontal cortex of COVID-19 patients
20. Ruxolitinib in Aicardi-Goutières syndrome
21. Raman spectroscopy reveals biochemical differences in plasma derived extracellular vesicles from sporadic Amyotrophic Lateral Sclerosis patients
22. Functional Study of SNCA p.V15A Variant: Further Linking α‐Synuclein and Glucocerebrosidase.
23. Extracellular vesicles secreted by cumulus cells contain microRNAs that are potential regulatory factors of mouse oocyte developmental competence.
24. Role of epigenetics and alterations in RNA metabolism in leukodystrophies.
25. Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency
26. Prevalence and prognostic value of Delirium as the initial presentation of COVID-19 in the elderly with dementia: An Italian retrospective study
27. cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing
28. Hydroxychloroquine modulates immunological pathways activated by RNA:DNA hybrids in Aicardi–Goutières syndrome patients carrying RNASEH2 mutations
29. Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
30. Activated Human Adipose Tissue Transplantation Promotes Sensorimotor Recovery after Acute Spinal Cord Contusion in Rats.
31. Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
32. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
33. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
34. A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS)
35. The role of clinical and neuroimaging features in the diagnosis of CADASIL
36. Air pollution as a contributor to the inflammatory activity of multiple sclerosis
37. Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
38. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis
39. Study of lncRNAs in Pediatric Neurological Diseases: Methods, Analysis of the State-of-Art and Possible Therapeutic Implications.
40. De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
41. The absence that makes the difference: choroidal abnormalities in Legius syndrome
42. A Novel Nonsense Angiogenin Mutation is Associated With Alzheimer Disease
43. 3D photopolymerized microstructured scaffolds influence nuclear deformation, nucleo/cytoskeletal protein organization, and gene regulation in mesenchymal stem cells.
44. Striving for a pragmatic contribution of biomarkers results to lifelong health care.
45. Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis
46. Sporadic and familial glut1ds Italian patients: A wide clinical variability
47. 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)
48. Individual risk prediction of high grade prostate cancer based on the combination between total prostate-specific antigen (PSA) and free to total PSA ratio.
49. Reference intervals for thyroid biomarkers to enhance the assessment of thyroid status in childhood and adolescence.
50. Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study.
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