289 results on '"Rosati, Jessica"'
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2. Circadian profile, daytime activity, and the Parkinson's phenotype: A motion sensor pilot study with neurobiological underpinnings
3. 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)
4. Amniotic fluid stem cell‐derived extracellular vesicles educate type 2 conventional dendritic cells to rescue autoimmune disorders in a multiple sclerosis mouse model
5. Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome
6. Contributors
7. Induced pluripotent stem cells for modeling Smith–Magenis syndrome
8. List of contributors
9. Functional outcomes of copy number variations of Chrna7 gene
10. Metabolic Profile of Patients with Smith-Magenis Syndrome: An Observational Study with Literature Review
11. Adaptive multi-attribute diversity for recommender systems
12. DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient
13. Clinical Implications of Universal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing in Pregnancy
14. Preference Queries with Ceteris Paribus Semantics for Linked Data
15. Effects of the electromagnetic fields (EMFs) on cellular redox homeostasis
16. Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene
17. Corrigendum: Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview
18. Building a relatedness graph from Linked Open Data: A case study in the IT domain
19. Transplantation of clinical-grade human neural stem cells reduces neuroinflammation, prolongs survival and delays disease progression in the SOD1 rats
20. Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview
21. Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3
22. Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome
23. Glucose transportation in the brain and its impairment in Huntington disease: one more shade of the energetic metabolism failure?
24. Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases.
25. Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein
26. Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene
27. Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies
28. Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region
29. Skeletal Muscle Pathogenesis in Polyglutamine Diseases
30. Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene
31. Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein
32. Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene
33. Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients
34. Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients
35. Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation
36. N ε -lysine acetylation determines dissociation from GAP junctions and lateralization of connexin 43 in normal and dystrophic heart
37. Chapter 9 - Induced pluripotent stem cells for modeling Smith–Magenis syndrome
38. Chapter 12 - Functional outcomes of copy number variations of Chrna7 gene: current knowledge and new insight from induced pluripotent stem cells studies
39. HDAC2 Blockade by Nitric Oxide and Histone Deacetylase Inhibitors Reveals a Common Target in Duchenne Muscular Dystrophy Treatment
40. Partner testing of severe acute respiratory syndrome coronavirus 2–positive women presenting for delivery
41. I12 Deciphering the neuroprotective role of sigma1 receptor, an important function to overcome the symptoms of neurodegenerative disorders
42. Stem cells from human amniotic fluid exert immunoregulatory function via secreted indoleamine 2,3-dioxygenase1
43. Complex Energy Networks Optimization: Part I \u2014 Development and Validation of a Software for Optimal Load Allocation
44. Complex Energy Networks Optimization: Part II \u2013\u2014 Software Application to a Case Study
45. Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein
46. Definition of management criteria and design of complex electrical, thermal and cooling energy and fuel distribution networks
47. Influence of the Prosumer Allocation and Heat Production on a District Heating Network
48. Complex Energy Networks Optimization: Part II—Software Application to a Case Study
49. Complex Energy Networks Optimization: Part I—Development and Validation of a Software for Optimal Load Allocation
50. Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene
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