IRIS
Rosati, Jessica Diana
 Distribuzione geografica
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Continente #
EU - Europa 10
Totale 10
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Nazione #
IT - Italia 10
Totale 10
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Città #
Rome 9
Bracciano 1
Totale 10
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A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15 9
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) 3
Reciprocal Interactions of Mitochondria and the Neuroimmunoendocrine System in Neurodegenerative Disorders: An Important Role for Melatonin Regulation 3
Circadian profile, daytime activity, and the Parkinson's phenotype: A motion sensor pilot study with neurobiological underpinnings 2
Amniotic fluid stem cell-derived extracellular vesicles educate type 2 conventional dendritic cells to rescue autoimmune disorders in a multiple sclerosis mouse model 1
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients 1
HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment 1
P300/CBP associated factor regulates nitroglycerin-dependent arterial relaxation by N(ε)-lysine acetylation of contractile proteins 1
Transplantation of clinical-grade human neural stem cells reduces neuroinflammation, prolongs survival and delays disease progression in the SOD1 rats 1
Stem cells from human amniotic fluid exert immunoregulatory function via secreted indoleamine 2,3-dioxygenase1 1
Functional outcomes of copy number variations of Chrna7 gene: current knowledge and new insight from induced pluripotent stem cells studies 1
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile huntington disease 1
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 1
Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome 1
Histone deacetylase inhibitors: keeping momentum for neuromuscular and cardiovascular diseases treatment 1
Non coding RNA and brain 1
A nitric oxide-dependent cross-talk between class I and III histone deacetylases accelerates skin repair 1
The histone deacetylase inhibitor suberoylanilide hydroxamic acid reduces cardiac arrhythmias in dystrophic mice 1
NO points to epigenetics in vascular development 1
Skeletal Muscle Pathogenesis in Polyglutamine Diseases 1
Differential expression and localization of calmodulin-dependent phosphodiesterase genes during ontogenesis of chick dorsal root ganglion 1
Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome 1
Deepening the understanding of CNVs on chromosome 15q11-13 by using hiPSCs: An overview 1
Detrimental effect of class-selective histone deacetylase inhibitors during tissue regeneration following hindlimb ischemia 1
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 1
Induced pluripotent stem cells for modeling Smith Magenis syndrome 1
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7 1
Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies 1
Metabolic Profile of Patients with Smith-Magenis Syndrome: An Observational Study with Literature Review 1
Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects 1
Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein 1
Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of dentato-rubral-pallidoluysian atrophy (DRPLA) 1
Investigating the Impact of the Parkinson's-Associated GBA1 E326K Mutation on β-Glucocerebrosidase Dimerization and Interactome Dynamics Through an In Silico Approach 1
Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850) 1
Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene 1
Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases 1
COVID-19 Specific Immune Markers Revealed by Single Cell Phenotypic Profiling 1
Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation 1
Nε-lysine acetylation determines dissociation from GAP junctions and lateralization of connexin 43 in normal and dystrophic heart 1
Nitric oxide modulates chromatin folding in human endothelial cells via protein phosphatase 2A activation and class II histone deacetylases nuclear shuttling 1
CircHTT(2,3,4,5,6) - co-evolving with the HTT CAG-repeat tract - modulates Huntington's disease phenotypes 1
Alpha-7 Nicotinic Receptors in Nervous System Disorders: From Function to Therapeutic Perspectives 1
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein 1
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage 1
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 1
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 1
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage juvenile onset huntington's disease 1
DP71 and SERCA2 alteration in human neurons of a Duchenne muscular dystrophy patient 1
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region 1
Smad-interacting protein-1 and microRNA 200 family define a nitric oxide-dependent molecular circuitry involved in embryonic stem cell mesendoderm differentiation 1
Glucose transportation in the brain and its impairment in Huntington disease: one more shade of the energetic metabolism failure? 1
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome 1
Nitric oxide deficiency determines global chromatin changes in Duchenne muscular dystrophy 1
Molecular recognition in helix-loop-helix and helix-loop-helix-leucine zipper domains. Design of repertoires and selection of high affinity ligands for natural proteins 1
Nitric oxide determines mesodermic differentiation of mouse embryonic stem cells by activating class IIa histone deacetylases: potential therapeutic implications in a mouse model of hindlimb ischemia 1
Totale 68
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all - tutte 271
article - articoli 0
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Totale 271
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/202568 0 0 0 0 23 43 2 0 0 0 0 0
Totale 68