Search results for "eNos"

showing 10 items of 1576 documents

Differences In Methacholine- And Adenosine 5-Monophosphate-Induced Changes In Forced Vital Capacity Between Methacholine-Responsive Subjects With All…

2012

Adenosine monophosphatechemistry.chemical_compoundVital capacitychemistrybusiness.industryImmunologymedicineMethacholinemedicine.diseasebusinessmedicine.drugAsthmaC38. ADVANCES IN ASTHMA AND COPD SCREENING AND MONITORING
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The Effect of Natural Allergen Exposure on the Maximal Response Plateau to Adenosine 5′-monophosphate and on Exhaled Nitric Oxide of Alveolar and Bro…

2010

Adenosine monophosphatechemistry.chemical_compoundchemistryMaximal response plateauImmunologyExhaled nitric oxideImmunologyImmunology and AllergyALLERGEN EXPOSUREPollen AllergyJournal of Allergy and Clinical Immunology
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Label-Free Pyrophosphate Recognition with Functionalized Asymmetric Nanopores

2016

[EN] The label¿free detection of pyrophosphate (PPi) anions with a nanofluidic sensing device based on asymmetric nanopores is demonstrated. The pore surface is functionalized with zinc complexes based on two di(2¿picolyl)amine [bis(DPA)] moieties using carbodiimide coupling chemistry. The complexation of zinc (Zn2+) ion is achieved by exposing the modified pore to a solution of zinc chloride to form bis(Zn2+¿DPA) complexes. The chemical functionalization is demonstrated by recording the changes in the observed current¿voltage (I¿V) curves before and after pore modification. The bis(Zn2+¿DPA) complexes on the pore walls serve as recognition sites for pyrophosphate anion. The experimental re…

Adenosine monophosphatechemistry.chemical_elementNanotechnology02 engineering and technologyZincPicolinic acid010402 general chemistry01 natural sciencesPyrophosphateBiomaterialsNanoporeschemistry.chemical_compoundPolymer chemistryGeneral Materials ScienceAminesPicolinic AcidsStaining and LabelingGeneral Chemistry021001 nanoscience & nanotechnologyPhosphate0104 chemical sciencesDiphosphatesAdenosine diphosphatechemistryFISICA APLICADASurface modificationAmine gas treating0210 nano-technologyBiotechnologySmall
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Pharmacological analysis of intrinsic neural control of rat duodenum motility in vitro

1988

Adenosine monophosphatemedicine.medical_specialtyDuodenumMotilitychemistry.chemical_compoundAdenosine TriphosphateAdenine nucleotideInternal medicinemedicineAnimalsPharmacologyAdenine NucleotidesMuscle SmoothAdenosine MonophosphateElectric StimulationIn vitroRatsAdenosine DiphosphateAdenosine diphosphateEndocrinologymedicine.anatomical_structurechemistryDuodenummedicine.symptomGastrointestinal MotilityAdenosine triphosphateMuscle ContractionMuscle contractionPharmacological Research Communications
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Biokinetisches Verhalten und Stoffwechselwirkungen von Fructose bei hochdosierter Dauerinfusion an der Ratte

1976

The steady-state blood level of fructose during 24 hours intravenous infusion in response to different doses follows saturation kinetics. Even after toxic doses of 1.5 g/kg/h no depletion of liver adenine nucleotides can be observed after 24 hours. In the kidneys, however, ATP, ADP and total adenine nucleotides were decreased after a dose of 1.5 g/kg/h of fructose. The blood glucose increased continuously at infusion rates of 1.5 g/kg/h. Inorganic phosphate in the blood increased at doses of 1.0 and 1.5 g/kg/h. The weight of the kidneys increased, presumably through water uptake. Urinary secretion was drastically reduced at doses above 1.0 g/kg/h. An appreciable activity of ketohexokinase c…

Adenosine monophosphatemedicine.medical_specialtyKidneyUrinary systemMedicine (miscellaneous)FructoseBiochemistrychemistry.chemical_compoundAdenosine diphosphateEndocrinologymedicine.anatomical_structurechemistryAdenine nucleotideInternal medicineWater uptakemedicineAdenosine triphosphateFood ScienceZeitschrift für Ernährungswissenschaft
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m6A RNA methylation of major satellite repeat transcripts facilitates chromatin association and RNA:DNA hybrid formation in mouse heterochromatin

2021

Abstract Heterochromatin has essential functions in maintaining chromosome structure, in protecting genome integrity and in stabilizing gene expression programs. Heterochromatin is often nucleated by underlying DNA repeat sequences, such as major satellite repeats (MSR) and long interspersed nuclear elements (LINE). In order to establish heterochromatin, MSR and LINE elements need to be transcriptionally competent and generate non-coding repeat RNA that remain chromatin associated. We explored whether these heterochromatic RNA, similar to DNA and histones, may be methylated, particularly for 5-methylcytosine (5mC) or methyl-6-adenosine (m6A). Our analysis in mouse ES cells identifies only b…

AdenosineAcademicSubjects/SCI00010HeterochromatinRNA methylationMethylationMice03 medical and health scienceschemistry.chemical_compound0302 clinical medicineHeterochromatinGene expressionGeneticsAnimals030304 developmental biology0303 health sciencesbiologyMethyltransferase complexGene regulation Chromatin and EpigeneticsRNAMouse Embryonic Stem CellsDNAChromatinCell biologyHistonechemistryTandem Repeat Sequencesbiology.proteinRNA030217 neurology & neurosurgeryDNANucleic Acids Research
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Machine learning of reverse transcription signatures of variegated polymerases allows mapping and discrimination of methylated purines in limited tra…

2020

AbstractReverse transcription (RT) of RNA templates containing RNA modifications leads to synthesis of cDNA containing information on the modification in the form of misincorporation, arrest, or nucleotide skipping events. A compilation of such events from multiple cDNAs represents an RT-signature that is typical for a given modification, but, as we show here, depends also on the reverse transcriptase enzyme. A comparison of 13 different enzymes revealed a range of RT-signatures, with individual enzymes exhibiting average arrest rates between 20 and 75%, as well as average misincorporation rates between 30 and 75% in the read-through cDNA. Using RT-signatures from individual enzymes to trai…

AdenosineAcademicSubjects/SCI00010Machine learningcomputer.software_genre[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyMethylationMachine Learning03 medical and health sciences0302 clinical medicineComplementary DNA[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]GeneticsMolecular BiologyPolymerase030304 developmental biologychemistry.chemical_classification0303 health sciencesOligoribonucleotidesGuanosinebiologybusiness.industryRNA-Directed DNA PolymeraseRNARNA-Directed DNA Polymerase[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyReverse TranscriptionMethylationReverse transcriptaseEnzymechemistryTransfer RNAbiology.protein[SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Artificial intelligenceTranscriptomebusinesscomputer030217 neurology & neurosurgery
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The 18S ribosomal RNA m 6 A methyltransferase Mettl5 is required for normal walking behavior in Drosophila

2020

RNA modifications have recently emerged as an important layer of gene regulation. N6-methyladenosine (m6A) is the most prominent modification on eukaryotic messenger RNA and has also been found on noncoding RNA, including ribosomal and small nuclear RNA. Recently, several m6A methyltransferases were identified, uncovering the specificity of m6A deposition by structurally distinct enzymes. In order to discover additional m6A enzymes, we performed an RNAi screen to deplete annotated orthologs of human methyltransferase-like proteins (METTLs) in Drosophila cells and identified CG9666, the ortholog of human METTL5. We show that CG9666 is required for specific deposition of m6A on 18S ribosomal …

AdenosineBiochimiem 6 AMettl5WalkingBiologyBiochemistryRibosome18S ribosomal RNA03 medical and health sciences0302 clinical medicineGene expressionRNA Ribosomal 18SGeneticsAnimalsHumansRNA methyltransferase[SDV.BDD]Life Sciences [q-bio]/Development BiologyMolecular Biology030304 developmental biologyBehavior0303 health sciencesMessenger RNAbehaviorBiologie moléculaireRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyMethyltransferasesm6ARibosomal RNANon-coding RNARibosome[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biomolecules [q-bio.BM]3. Good healthCell biologyribosomeRNA RibosomalDrosophilaBiologie030217 neurology & neurosurgerySmall nuclear RNAReportsEMBO reports
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CD73-generated extracellular adenosine in chronic lymphocytic leukemia creates local conditions counteracting drug-induced cell death

2011

Abstract Extracellular adenosine (ADO), generated from ATP or ADP through the concerted action of the ectoenzymes CD39 and CD73, elicits autocrine and paracrine effects mediated by type 1 purinergic receptors. We have tested whether the expression of CD39 and CD73 by chronic lymphocytic leukemia (CLL) cells activates an adenosinergic axis affecting growth and survival. By immunohistochemistry, CD39 is widely expressed in CLL lymph nodes, whereas CD73 is restricted to proliferation centers. CD73 expression is highest on Ki-67+ CLL cells, adjacent to T lymphocytes, and is further localized to perivascular areas. CD39+/CD73+ CLL cells generate ADO from ADP in a time- and concentration-dependen…

AdenosineCellular differentiationChronic lymphocytic leukemia5'-Nucleotidase; Adenosine; Adenosine Diphosphate; Adenosine Triphosphate; Antigens CD; Antineoplastic Agents Phytogenic; Apyrase; Autocrine Communication; Cell Death; Cell Differentiation; Cell Movement; Cell Survival; Etoposide; Extracellular Space; GPI-Linked Proteins; Humans; Leukemia Lymphocytic Chronic B-Cell; Paracrine Communication; Receptor Adenosine A2A; Tumor Cells Cultured; Biochemistry; Immunology; Hematology; Cell BiologyMICROENVIRONMENTCD38BiochemistryACTIVATIONAdenosine TriphosphateCell MovementPhytogenichemic and lymphatic diseasesTumor Cells CulturedChronic5'-NucleotidaseEtoposideLeukemiaCulturedCell DeathTUMOR-GROWTHApyrasePurinergic receptorCell DifferentiationHematologyLymphocyticCDTumor CellsCell biologyAdenosine DiphosphateAutocrine CommunicationLeukemiaReceptorIMMUNE SUPPRESSIONReceptor Adenosine A2ACell SurvivalImmunologyAntineoplastic AgentsAdenosinergicBiologyGPI-Linked ProteinsDAMAGE-INDUCED APOPTOSISAdenosine A2AParacrine signallingAntigens CDParacrine CommunicationmedicineHumansAntigensAutocrine signallingImmunobiologyB-CellCell BiologyDAMAGE-INDUCED APOPTOSIS; T-CELLS; IMMUNE SUPPRESSION; ZAP-70 EXPRESSION; TUMOR-GROWTH; RECEPTOR; CD73; ACTIVATION; CD38; MICROENVIRONMENTmedicine.diseaseAntineoplastic Agents PhytogenicLeukemia Lymphocytic Chronic B-CellSettore MED/15 - MALATTIE DEL SANGUET-CELLSCD73Extracellular SpaceZAP-70 EXPRESSIONCD38Blood
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A1 receptor-mediated modulatory effects of adenosine on the contractility in mouse ileum: characterization of signal transduction pathway

2008

AdenosineMouse ileumMechanical activityAdenosine A1 receptorSettore BIO/09 - FisiologiaP1 purinoceptorPotassium channels
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