about
POPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein traffickingGenetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype.Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report.Signal transduction pathways triggered by selective formylpeptide analogues in human neutrophils.Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathyEffects of synthetic peptides on the inflammatory response and their therapeutic potential.Study of synthetic peptides derived from the PKI55 protein, a protein kinase C modulator, in human neutrophils stimulated by the methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-OH.Merkel Cell Carcinomas Arising in Autoimmune Disease Affected Patients Treated with Biologic Drugs, Including Anti-TNF.Tracing Males From Different Continents by Genotyping JC Polyomavirus in DNA From Semen Samples.The cytoplasmic C-terminus of polycystin-1 increases cell proliferation in kidney epithelial cells through serum-activated and Ca(2+)-dependent pathway(s).Hypermethylation-Induced Inactivation of the IRF6 Gene as a Possible Early Event in Progression of Vulvar Squamous Cell Carcinoma Associated With Lichen Sclerosus.Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia.Gene expression changes in progression of cervical neoplasia revealed by microarray analysis of cervical neoplastic keratinocytes.Methylation loss at H19 imprinted gene correlates with methylenetetrahydrofolate reductase gene promoter hypermethylation in semen samples from infertile males.Biodistribution and molecular studies on orally administered nanoparticle-AON complexes encapsulated with alginate aiming at inducing dystrophin rescue in mdx mice.In vitro mitochondrial failure and oxidative stress mimic biochemical features of Alzheimer disease.Early and delayed glutamate effects in rat primary cortical neurons. Changes in the subcellular distribution of protein kinase C isoforms and in intracellular calcium concentration.Protein kinase C activity, translocation, and selective isoform subcellular redistribution in the rat cerebral cortex after in vitro ischemia.Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor.Mice genetic immunization with plasmid DNA encoding a secreted form of HSV-1 gB induces a protective immune response against herpes simplex virus type 1 infection.Monoclonal antibodies against HLA class I antigens inhibit human lymphocyte proliferation but do not affect mitogen dependent second messenger generation.Formylpeptides trigger selective molecular pathways that are required in the physiological functions of human neutrophils.Co-operation in cell transformation between BK virus and the human c-Harvey-ras oncogene.A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation.Differential inhibition of signaling pathways by two new imidazo-pyrazoles molecules in fMLF-OMe- and IL8-stimulated human neutrophil.Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor.Sodium azide induced neuronal damage in vitro: evidence for non-apoptotic cell death.Effects of chemical ischemia in cerebral cortex slices. Focus on nitric oxide.Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors.Adaptative value of a PKC-PKI55 feedback loop of inhibition that prevents the kinase's deregulation.Effects of chemical ischemia on cerebral cortex slices: focus on mitogen-activated protein kinase cascade.Differential activation of protein kinase C isoforms following chemical ischemia in rat cerebral cortex slices.Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.A Family with γ-Thalassemia and High Hb A2 Levels.Huntington's disease-like presentation in Spinocerebellar ataxia type 12.Methylenetetrahydrofolate reductase gene promoter hypermethylation in semen samples of infertile couples correlates with recurrent spontaneous abortion.Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.Paternal germline mosaicism in collagen VI related myopathies.ChemInform Abstract: N-Aryl-2-phenyl-2,3-dihydro-imidazo[1,2-b]pyrazole-1-carboxamides 7-Substituted Strongly Inhibiting both fMLP-OMe- and IL-8-Induced Human Neutrophil ChemotaxisN-Aryl-2-phenyl-2,3-dihydro-imidazo[1,2-b]pyrazole-1-carboxamides 7-substituted strongly inhibiting both fMLP-OMe- and IL-8-induced human neutrophil chemotaxis
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Rita Selvatici
@ast
Rita Selvatici
@en
Rita Selvatici
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Rita Selvatici
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Rita Selvatici
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type
label
Rita Selvatici
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Rita Selvatici
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Rita Selvatici
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Rita Selvatici
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Rita Selvatici
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prefLabel
Rita Selvatici
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Rita Selvatici
@en
Rita Selvatici
@es
Rita Selvatici
@nl
Rita Selvatici
@sl
P106
P1153
6701382960
P21
P31
P496
0000-0002-3099-0100