Search results for "templates"

showing 10 items of 19 documents

Reflections about the authentic document in "post mortem" fecundation

2018

[EN] The legislation on assisted reproduction contemplates the ¿post mortem¿ fecundation. Nevertheless, the document for the presentation of the assent raises some doubts in relation with the principle of party autonomy and the new technologies of the information and communication (ICTs). In the present work one thinks about these questions and one tries to contribute some solution of application in the Spanish legal system.

:CIENCIAS JURÍDICAS [UNESCO]Documento indubitadoFecundación post mortemfecundación ?post mortem?Authentic documentthe document for the presentation of the assent raises some doubts in relation with the principle of party autonomy and the new technologies of the information and communication (ICTs). In the present work one thinks about these questions and one tries to contribute some solution of application in the Spanish legal system. Documento indubitadoDERECHO CIVILLegislaciónUNESCO::CIENCIAS JURÍDICAS2386-4567 22661 Actualidad jurídica iberoamericana 502169 2018 9 6653336 Reflexiones acerca del documento indubitado en la fecundación ?post mortem? Ramón Fernándezlegislación.post mortem fecundationFrancisca The legislation on assisted reproduction contemplates the ?post mortem? fecundation. Nevertheless
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Generics: Ada 95 vs. C++ vs. Java 1.5

2005

Adatemplatesgenericsgeneric programmingC++Java
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Aromatic N-oxide templates open inclusion and dimeric capsular assemblies with methylresorcinarene

2015

C2-2-methylresorcinarene forms host–guest complexes with pyridine N-oxide and quinoline N-oxide. In solution the NMR studies support the 1 : 1 host–guest complexes while in the solid state, the single crystal X-ray diffraction studies reveal dimeric capsule-like assemblies with 2 : 3 and 2 : 2 host–guest stoichiometry.

General Chemical EngineeringQuinolineOxideSolid-statemacromolecular substancesGeneral Chemistryaromatic N-oxide templatesCrystallographychemistry.chemical_compoundTemplatechemistryPyridineSingle crystalta116StoichiometryRSC Advances
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A new method for the mapping of 5' ends of RNAs.

2008

In this article, we describe a new procedure to map 5' ends of RNAs. The procedure consists in the use of specific RNase H digestion of a hybrid formed by the RNA and a complementary DNA oligonucleotide. Northern blot hybridization of the resulting RNA fragment allows an accurate measurement of its length. Although we generally use this procedure as a control of previously performed primer extension analyses, the absence of nonspecific bands, which often occur in primer extensions on RNA templates with extended secondary structures, suggests that our method may be preferable when these difficult templates are analyzed.

GeneticsbiologyOligonucleotideRibonuclease HBiophysicsRNACell BiologyComputational biologyTemplates GeneticRibosomal RNABlotting NorthernBiochemistryPrimer extensionSettore BIO/18 - GeneticaRNA RibosomalComplementary DNASea Urchinsbiology.proteinAnimalsRNANorthern blotPrimer (molecular biology)RNase HMolecular Biology5'End mappingribonuclease H rRNAAnalytical biochemistry
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Translation of hepatitis B virus (HBV) surface proteins from the HBV pregenome and precore RNAs in Semliki Forest virus-driven expression.

2004

Hepatitis B virus (HBV) pregenome RNA (pgRNA) serves as a translation template for the HBV core (HBc) protein and viral polymerase (Pol). HBV precore RNA (pcRNA) directs the synthesis of the precore (preC) protein, a precursor of the hepatitis B e antigen (HBeAg). pgRNA and pcRNA were expressed in the Semliki Forest virus (SFV) expression system. Besides the HBc and preC proteins, there was revealed the synthesis of all three forms of HBV surface (HBs) proteins: long (LHBs), middle (MHBs) and short (SHBs), the start codons of which are located more than 1000 nt downstream of the HBc and preC start codons. Moreover, other HBV templates, such as 3′-truncated pgRNA lacking 3′ direct repeat and…

HBV RNA encapsidation signal epsilonHepatitis B virusvirusesGene ExpressionLeaky scanningDNA-Directed DNA Polymerasemedicine.disease_causeSemliki Forest virusVirus ReplicationCell LineViral Envelope ProteinsVirologymedicineAnimalsHepatitis B e AntigensRNA MessengerCloning MolecularProtein PrecursorsHepatitis B virusHepatitis B Surface Antigensbiologyvirus diseasesRNA virusTemplates Geneticbiology.organism_classificationVirologyMolecular biologyHepatitis B Core AntigensImmunohistochemistrySemliki forest virusdigestive system diseasesGenetic translationHBeAgHepadnaviridaeProtein BiosynthesisRNA ViralThe Journal of general virology
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A method for rapid generation of competitive standard molecules for RT-PCR avoiding the problem of competitor/probe cross-reactions.

1995

The analysis of gene expression is a widespread issue in a growing number of fields such as molecular genetics, immunology, and medical diagnostics. The ideal method for mRNA detection should be fast, inexpensive, sensitive, and reliable. Well-elaborated standard methods such as Northern hybridization, Sl-mapping, and RNAse protection are useful and recommended, but only reverse transcription PCR (RT-PCR) gives the highest possible sensitivity required. For many issues it is necessary not only to detect a distinct mRNA but to compare changes in mRNA levels. The use of RT-PCR for such semiquantitative and quantitative approaches resolves problems attributable to the intrinsic property of PCR…

KeratinocytesDNA ComplementaryTime FactorsMolecular Sequence DataBiologyBinding CompetitivePolymerase Chain Reactionlaw.inventionCell Linechemistry.chemical_compoundMicelawGene expressionGeneticsAnimalsRNA MessengerCloning MolecularGenetics (clinical)Polymerase chain reactionDNA PrimersGel electrophoresisBase SequenceRNA-Directed DNA PolymeraseTemplates GeneticMolecular biologyActinsReverse transcription polymerase chain reactionLeukemia Virus MurineReal-time polymerase chain reactionchemistryBiochemistryYield (chemistry)Nitric Oxide SynthaseEthidium bromideArtifactsDNAPCR methods and applications
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Reiterative transcription initiation from galP2 promoter of Escherichia coli

2000

The expression of gal operon in Escherichia coli is driven by two promoters, P1 and P2 separated by 5 bp. The transcription initiated from the P2 generates a large amount of abortive transcripts to produce a comparable amount of full-length transcript as P1 in vitro. In this study, we investigated the source of the abortive transcripts by employing a quantitative potassium permanganate footprinting method that determines the extent of open promoter complex formation. The extents of open promoter complex formation at the two gal promoters were about the same during the given reaction time while the amount of transcription initiation determined by in vitro transcription assay showed a conside…

Models MolecularCyclic AMP Receptor ProteinTranscription GeneticDNA FootprintingBiophysicsRNA polymerase IIBiochemistryAbortive initiationchemistry.chemical_compoundPotassium PermanganateStructural BiologyRNA polymeraseEscherichia coliGeneticsPromoter Regions GeneticbiologyGeneral transcription factorPromoterDNA-Directed RNA PolymerasesTemplates GeneticMolecular biologyKineticschemistrybiology.proteinRNATranscription factor II FTranscription factor II DCarrier ProteinsTranscription factor II BBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression
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Visible Photoluminescence of Variable-Length Zinc Oxide Nanorods Embedded in Porous Anodic Alumina Template for Biosensor Applications

2021

Zinc oxide (ZnO) and porous anodic aluminum oxide (PAAO) are technologically important materials, rich with features that are of interest in optical applications, for example, in light-emitting and sensing devices. Here, we present synthesis method of aligned ZnO nanorods (NR) with 40 nm diameter and variable length in 150 to 500 nm range obtained by atomic layer deposition (ALD) of ZnO in pores of continuously variable thickness PAAO. The relative intensity of yellow (1.99 eV), green (2.35 eV), and blue (2.82 eV) photoluminescence (PL) components originating from the different types of defects, varied with non-monotonic dependency on the composite film thickness with a Fabry–Pérot like mod…

PhotoluminescenceMaterials sciencemultilayerschemistry.chemical_element02 engineering and technologyZinc010402 general chemistry01 natural sciencesAtomic layer depositionhybrid materialsMaterials ChemistryPorosityporous anodic aluminabusiness.industryzinc oxideSurfaces and InterfacesEngineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyFluorescence0104 chemical sciencesSurfaces Coatings and Filmschemistryfluorescent biosensing:NATURAL SCIENCES [Research Subject Categories]self-organized templatesOptoelectronicsNanorodphotoluminescenceTA1-20400210 nano-technologybusinessHybrid materialBiosensorCoatings
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Bioinformatic flowchart and database to investigate the origins and diversity of Clan AA peptidases

2009

Abstract Background Clan AA of aspartic peptidases relates the family of pepsin monomers evolutionarily with all dimeric peptidases encoded by eukaryotic LTR retroelements. Recent findings describing various pools of single-domain nonviral host peptidases, in prokaryotes and eukaryotes, indicate that the diversity of clan AA is larger than previously thought. The ensuing approach to investigate this enzyme group is by studying its phylogeny. However, clan AA is a difficult case to study due to the low similarity and different rates of evolution. This work is an ongoing attempt to investigate the different clan AA families to understand the cause of their diversity. Results In this paper, we…

Protein familySequence analysisImmunologyProtein domainMolecular Sequence DataBiologycomputer.software_genreGeneral Biochemistry Genetics and Molecular BiologyProtein Structure SecondaryPhylogeneticsSequence Analysis ProteinSoftware DesignConsensus SequenceConsensus sequenceAspartic Acid EndopeptidasesClanAmino Acid SequenceDatabases ProteinPeptide sequencelcsh:QH301-705.5Ecology Evolution Behavior and SystematicsPhylogenyDatabaseAgricultural and Biological Sciences(all)Biochemistry Genetics and Molecular Biology(all)Applied MathematicsResearchComputational BiologyGenetic VariationGene AnnotationTemplates GeneticMarkov ChainsProtein Structure Tertiarylcsh:Biology (General)Modeling and SimulationGeneral Agricultural and Biological SciencescomputerBiology Direct
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The microsomal epoxide hydrolase has a single membrane signal anchor sequence which is dispensable for the catalytic activity of this protein

1994

The microsomal epoxide hydrolase (mEH) catalyses the hydrolysis of reactive epoxides which are formed by the action of cytochromes P-450 from xenobiotics. In addition it has been suggested that mEH might mediate the transport of bile acids. For the mEH it has been shown that it is co-translationally inserted into the endoplasmic reticulum. Here we demonstrate that the N-terminal 20 amino acid residues of this protein serve as its single membrane anchor signal sequence and that the function of this sequence can also be supplied by a cytochrome P-450 (CYP2B1) anchor signal sequence. The evidence supporting this conclusion is as follows: (i) the rat mEH and a CYP2B1-mEH fusion protein, in whic…

Signal peptideDNA ComplementaryCytochromeMolecular Sequence DataProtein Sorting SignalsBiochemistryCatalysisDogsMicrosomesAnimalsAmino Acid SequenceEpoxide hydrolasePancreasMolecular BiologyEpoxide HydrolasesBase SequenceCell-Free SystembiologyChemistryEndoplasmic reticulumCell MembraneTemplates GeneticCell BiologyFusion proteinRatsMembraneBiochemistryProtein BiosynthesisMicrosomal epoxide hydrolaseMicrosomebiology.proteinResearch ArticleBiochemical Journal
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