Search results for " DNA"

showing 10 items of 2475 documents

Sintesi di Nuovi Derivati del Sistema Triciclico Pirazolo[3,4-d][1,2,3]triazolo[1,5-a]pirimidinico DNA interattivi

2008

Pirazolo[34-d][123]triazolo[15-a]pirimidine DNASettore CHIM/08 - Chimica Farmaceutica
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Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mec…

2014

Genomic imprinting is a form of epigenetic regulation that results in the expression of either the maternally or paternally inherited allele of a subset of genes (Ramowitz and Bartolomei 2011). This imprinted expression of transcripts is crucial for normal mammalian development. In humans, loss-of-imprinting of specific loci results in a number of diseases exemplified by the reciprocal growth phenotypes of the Beckwith-Wiedemann and Silver-Russell syndromes, and the behavioral disorders Angelman and Prader-Willi syndromes (Kagami et al. 2008; Buiting 2010; Choufani et al. 2010; Eggermann 2010; Kelsey 2010; Mackay and Temple 2010). In addition, aberrant imprinting also contributes to multige…

PlacentaADNGene ExpressionBiologyMethylationGenomic ImprintingPregnancyGerm cellsGeneticsmedicineHumansEpigeneticsRNA-Directed DNA MethylationAllelesEmbryonic Stem CellsGenetics (clinical)GeneticsGenome HumanResearchDNAGenomicsDNA Methylationmedicine.diseaseUniparental disomyCèl·lules germinalsGenòmicaGerm CellsDifferentially methylated regionsDNA methylationIllumina Methylation AssayCpG IslandsFemaleMetilacióGenomic imprintingReprogrammingGenome Research
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Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)–Re-evaluation of chromosome aberration rates in early spontaneous…

2001

Comparative genomic hybridisation (CGH) represents an alternative molecular-cytogenetic technique capable of detecting chromosomal imbalances by reverse fluorescence in situ hybridisation. As the technique uses genomic DNA for assessment it does not rely on metaphase chromosomes in the test material and thus circumvents technical problems associated with tissue culturing. In the present study, we applied CGH to identify chromosome anomalies in 60 spontaneous abortions of the first trimester, that had failed to grow in culture. In 57 out of 60 cases CGH analyses were successful. The overall aneuploidy rate detected was 72%. Trisomy was the predominant chromosome anomaly accounting for 68.0% …

PlacentaAneuploidyGestational AgeAbortionBiologyChromosome aberrationPregnancyGeneticsmedicineHumansMetaphaseCells CulturedGenetics (clinical)Chromosome AberrationsGeneticsNucleic Acid HybridizationChromosomeKaryotypemedicine.diseaseAbortion SpontaneousPregnancy Trimester Firstgenomic DNAKaryotypingCytogenetic AnalysisFemaleTrisomyMaternal AgeEuropean Journal of Human Genetics
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Fast, non-toxic, and inexpensive n-butanol preparation of recombinant plasmids

2000

Various commercial and non-commercial plasmid preparation protocols are currently available. However, the kits are expensive and many of the protocols contain toxic chemicals. Here we present a novel, optimized and, therefore, very advantageous plasmid preparation protocol using n-butanol. The preparation can be performed quickly and no toxic chemicals are used, at overall costs of about one cent per plasmid preparation.Atualmente vários protocolos comerciais e não comerciais para preparação de plasmídeos estão disponíveis. Contudo, os kits são caros e muitos dos protocolos contêm substâncias químicas tóxicas. Apresentamos neste trabalho um novo, otimizado e portanto muito vantajoso protoco…

Plasmid preparationlcsh:QH426-470Biologylaw.inventionMicrobiologylcsh:Geneticschemistry.chemical_compoundPlasmidBiochemistrychemistrylawn-ButanolGeneticsRecombinant DNAMolecular BiologyGenetics and Molecular Biology
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Insect Cells for Heterologous Production of Recombinant Proteins

2010

Heterologous gene expression has become an indispensable and powerful tool for the production and subsequent functional analysis of proteins that are difficult to purify from their natural sources. Furthermore, it is the method of choice for the production of variants by introducing site-specific mutations into the DNA encoding the protein of interest. However, many systems are biased by disadvantages. The inability of bacteria to confer important post-translational modifications often results in functional failure of the recombinant protein. In addition, disulfide bonds are not formed properly in bacterial systems. Mammalian cells on the other hand modify properly, but they generally provi…

PlasmidBiochemistryChemistrylawRecombinant DNAProtein biosynthesisHeterologousSf9TransfectionHeterologous expressionlaw.inventionSf21
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Genetic polymorphism and taxonomic infrastructure of the Pleurotus eryngii species-complex as determined by RAPD analysis, isozyme profiles and ecomo…

2001

The Pleurotus eryngii species-complex includes populations of choice edible mushrooms, growing in the greater Mediterranean area in close association with different genera of plants of the family Apiaceae. Their distinct host-specialization served as the principal criterion for the discrimination of several taxa; however, the genetic relationships among the various P. eryngii ecotypes remain ambiguous. In the present study, 46 Pleurotus strains with a wide range of geographical origins were isolated from Eryngium spp., Ferula communis, Cachrys ferulacea, Thapsia garganica and Elaeoselinum asclepium subsp. asclepium, and were subjected to isozyme and random amplified polymorphic DNA-PCR (RAP…

Pleurotus nebrodensisGenetic MarkersPleurotuseducation.field_of_studyGenetic diversityPolymorphism GeneticbiologyPopulationbiology.organism_classificationPleurotusMicrobiologyBiological EvolutionPolymerase Chain ReactionRAPDRandom Amplified Polymorphic DNA TechniqueIsoenzymesSpecies SpecificityEryngiumBotanyFerula communisPleurotus eryngiieducationPhylogenyApiaceaeMicrobiology (Reading, England)
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Titolo: SU UN CASO DI RICONOSCIMENTO MEDIANTE DETERMINAZIONE INDIRETTA DEL DNA

2005

Abstracts di comunicazioni o Posters presentati a Congressi Nazionali

Polimorfismi del DNA
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Pollution exposure and high DNA fragmentation index in human sperms: a case-control study

2016

Study question: Could pollution exposure play a key role on sperm quality, in terms of DNA fragmentation index (DFI)? Summary answer: Patients exposed to high level of pollution show an higher percentage of sperm DNA fragmentation index in contrast with patient from control group. What is known already: Taranto area is characterized by a number of steel factories and petrochemical industries. Data about the detrimental effects of environmental pollution are alarming. Pollution coming from the industrial plants causes health and fertility risks, mainly due to the exposure to several pollutant (PM10, heavy metals, etc). Toxic substances can affect DNA directly or indirectly, through oxidative…

Pollution DNA Fragmentaztion Sperm.Settore BIO/06 - Anatomia Comparata E Citologia
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ISOLATION OF RAT CDNA CLONES CODING FOR THE AUTOANTIGEN SS-B/LA - DETECTION OF SPECIES-SPECIFIC VARIATIONS

1993

Clones of cDNA coding for the autoantigen La (or SS-B) were isolated from a library made from rat liver. A comparison of the rat La cDNA (encoding from nt 38 to 1281 for rat La protein) with the sequences known for human and bovine La protein resulted in the identification of species-specific inserts. The inserts seem to be the result of multiplication of flanking sequences during evolution. In addition to these variations, we observed that rat La cDNAs exhibit non-canonical polyadenylation sites. Finally, a databank search resulted in the identification of a DNA sequence originally termed as TAG or TSG20X (GenBank accession No. X61893) which represents the C terminus of mouse La/SS-B prote…

PolyadenylationMolecular Sequence DataAutoantigensSingle-stranded binding proteinSpecies SpecificityComplementary DNASequence Homology Nucleic AcidGeneticsAnimalsHumansGenomic libraryAmino Acid SequenceCloning MolecularRibonucleoproteinGeneticsbiologyBase SequenceC-terminusNucleic acid sequenceGenetic VariationGeneral MedicineDNAMolecular biologyIntronsRatsRibonucleoproteinsGenBankbiology.protein
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Noncanonical RNAs from transcripts of the Drosophila muscleblind gene.

2006

It has become increasingly evident that eukaryotic cells produce RNA molecules from coding genes with constitutions other than those of typically spliced mRNA transcripts. Here we describe new cDNAs from the Drosophila melanogaster muscleblind (mbl ) locus that identify two such atypical RNA molecules: RNAs containing an incomplete exon 2 tandem repetition (mblE2E2#) or having exons with a different order compared to the corresponding genomic DNA (mblE2E3#E2#; exon scrambling). The existence of exon duplications and rearrangements in the genomic locus that might explain such cDNAs was ruled out by genomic Southern blotting and in silico analysis of the Drosophila genome sequence. The incomp…

PolyadenylationMolecular Sequence DataBiologyExonRapid amplification of cDNA endsComplementary DNAGeneticsAnimalsDrosophila ProteinsAmino Acid SequenceRNA MessengerMolecular BiologyGeneGenetics (clinical)DNA PrimersGeneticsBase SequenceReverse Transcriptase Polymerase Chain ReactionRNANuclear ProteinsExonsgenomic DNARNA splicingDrosophilaPoly ABiotechnologyThe Journal of heredity
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