about
Unravelling the role of sphingolipids in cystic fibrosis lung diseaseDocking of molecules identified in bioactive medicinal plants extracts into the p50 NF-kappaB transcription factor: correlation with inhibition of NF-kappaB/DNA interactions and inhibitory effects on IL-8 gene expressionVirtual screening against p50 NF-kappaB transcription factor for the identification of inhibitors of the NF-kappaB-DNA interaction and expression of NF-kappaB upregulated genes.Virtual screening against nuclear factor κB (NF-κB) of a focus library: Identification of bioactive furocoumarin derivatives inhibiting NF-κB dependent biological functions involved in cystic fibrosis.Regulation of expression of O6-methylguanine-DNA methyltransferase and the treatment of glioblastoma (Review).Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.GBA2-encoded β-glucosidase activity is involved in the inflammatory response to Pseudomonas aeruginosa.Tracking the immunopathological response to Pseudomonas aeruginosa during respiratory infections.miRNA array screening reveals cooperative MGMT-regulation between miR-181d-5p and miR-409-3p in glioblastoma.MicroRNA miR-93-5p regulates expression of IL-8 and VEGF in neuroblastoma SK-N-AS cells.High levels of apoptosis are induced in human glioma cell lines by co-administration of peptide nucleic acids targeting miR-221 and miR-222.Regulation of IL-8 gene expression in gliomas by microRNA miR-93.Antibacterial and anti-inflammatory activity of a temporin B peptide analogue on an in vitro model of cystic fibrosis.Trimethylangelicin promotes the functional rescue of mutant F508del CFTR protein in cystic fibrosis airway cells.Pseudomonas aeruginosa reduces the expression of CFTR via post-translational modification of NHERF1.Uptake by human glioma cell lines and biological effects of a peptide-nucleic acids targeting miR-221.Expression of microRNA-93 and Interleukin-8 during Pseudomonas aeruginosa-mediated induction of proinflammatory responses.Effects of decoy molecules targeting NF-kappaB transcription factors in Cystic fibrosis IB3-1 cells: recruitment of NF-kappaB to the IL-8 gene promoter and transcription of the IL-8 gene.Modulators of sphingolipid metabolism reduce lung inflammation.Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells.Heparan sulfate glycosaminoglycans are receptors sufficient to mediate the initial binding of adenovirus types 2 and 5.Trimethylangelicin reduces IL-8 transcription and potentiates CFTR function.Late generation lentiviral vectors: evaluation of inflammatory potential in human airway epithelial cells.Increased cytosolic calcium in cystic fibrosis neutrophils effect on stimulus-secretion coupling.Anti-inflammatory effect of miglustat in bronchial epithelial cells.Chemical conjugation of DeltaF508-CFTR corrector deoxyspergualin to transporter human serum albumin enhances its ability to rescue Cl- channel functions.Induction of IL-6 gene expression in a CF bronchial epithelial cell line by Pseudomonas aeruginosa is dependent on transcription factors belonging to the Sp1 superfamily.A His-155 to Tyr polymorphism confers gain-of-function to the human P2X7 receptor of human leukemic lymphocytes.Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis.The vacuolating toxin of Helicobacter pylori mimicks the CFTR-mediated chloride conductance.Activation of NF-kB mediates ICAM-1 induction in respiratory cells exposed to an adenovirus-derived vector.Alternative antibiotics for the treatment of Pseudomonas infections in cystic fibrosis.ICAM-1 induction in respiratory cells exposed to a replication-deficient recombinant adenovirus in vitro and in vivo.Changes in neutral amino acid efflux and membrane potential associated with the expression of CFTR protein.Use of a membrane potential-sensitive probe to assess biological expression of the cystic fibrosis transmembrane conductance regulator.Protein kinase C activates chloride conductance in C127 cells stably expressing the cystic fibrosis gene.The sensitivity of cystic fibrosis cells to diphtheria toxin.Effect of modulation of protein kinase C on the cAMP-dependent chloride conductance in T84 cells.Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.cAMP dependent chloride conductance is not different in cystic fibrosis fibroblasts.
P50
Q28068094-9D343A60-52F4-41B6-B5A8-AA24A5927FBBQ33366140-402E138E-EECC-476C-8703-A5D69EFA200EQ33508859-13593EA8-D5B1-4FBF-BFD2-AE3C194EEA94Q33729936-A38A5321-40CB-4D95-B6D5-094455D09426Q34478948-E4592C71-7957-47AE-9EB8-16865286FABAQ35044633-2B54E6C3-35B0-49B4-9705-5A4C35C3781DQ35228672-2A760404-2160-4FB2-B5C5-448DB46FE53BQ38522938-068C1023-9EC4-4589-A232-D132ADC18FD8Q38779883-7CF28D17-AE0A-4A2F-AAAA-56A63C66E89EQ38785524-8D341355-B494-4DCF-8D60-CBAEDD1350D3Q38808735-420AEB3D-4A63-4CA1-94AE-0F6B300BBF3CQ38829417-3B8D3ED6-80D2-4BB5-A4EC-696F23C9C799Q38958442-3FFCD3F7-6001-417B-9BBE-7965B91C86F1Q38996193-1C4B6D81-C004-4663-9431-FC4DCFEC9EE5Q39018546-5F559166-CCDF-43B7-A471-1B58088906A6Q39018554-4ED42F79-01A9-468C-88EC-D04A6334A28FQ39033925-1FA759C3-AEC8-4DE9-AC28-1D7C6F2F6D96Q39318131-C42963A8-DDE3-463E-A9E6-2A1EA22DADAAQ39527379-6BECEBA5-7CD9-4C8C-A9BE-4C97F12E17F4Q39575146-3EA5E334-F164-4DDD-AAB7-2BBB1104B6F9Q39607095-9A6B8DDF-8246-41C7-97DB-B7AB90BDF3C1Q39621248-EC7B1E63-2964-4F72-AB9F-60DA926231F1Q39850427-BEF4056B-0EB0-4082-B77A-45FB8FABE0FCQ39858267-65FCBC5B-B884-4E02-A9DA-C52A0A5CFF80Q39936174-A5C9353A-4566-4AE6-9012-229C3EF420E9Q39976627-3D56FFCA-410A-4E42-86F2-C23B18539E4AQ40139648-44B805FB-2799-47CC-AC66-D95B83ED5566Q40406120-745C39F6-C52A-4D11-A878-87ADCF3DCB23Q40476858-7BDBFE89-CD38-4742-9ABE-82DEBD2B4A31Q40686303-7D9E1FD2-B75F-4131-84E0-2B82D2CAD41FQ40778609-BAFC2B10-D88B-4208-B10B-9B93876223AAQ40835273-409AA99B-7A16-4546-9DBB-9E22587A0DE5Q41052038-EE5576A8-0EEB-4666-AB88-979004323D50Q41193043-083D8F3A-DD0B-4A36-BEF9-67C8C38EDF06Q41286252-5856478F-4E7A-423B-8302-97D55A19087FQ41553081-375F4E5A-9A46-45B5-BE02-7F2958C48C20Q41570852-1213E316-372F-4C2F-B914-97DB760A1C6BQ41598989-6F1BA529-2415-4481-B282-4F4A68C6AD0CQ41665365-AF0489A9-471F-4382-82C3-D21DDDBBEC3BQ41752890-FB0C72D0-B907-4912-8EEA-CF68084FA95A
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Giulio Cabrini
@ast
Giulio Cabrini
@en
Giulio Cabrini
@es
Giulio Cabrini
@nl
Giulio Cabrini
@sl
type
label
Giulio Cabrini
@ast
Giulio Cabrini
@en
Giulio Cabrini
@es
Giulio Cabrini
@nl
Giulio Cabrini
@sl
prefLabel
Giulio Cabrini
@ast
Giulio Cabrini
@en
Giulio Cabrini
@es
Giulio Cabrini
@nl
Giulio Cabrini
@sl
P1053
K-4761-2016
P106
P21
P2798
P31
P3829
P496
0000-0003-2720-0742