Search results for "Typing"

showing 10 items of 1051 documents

Tick-borne bacteria in Ixodes ricinus collected in southern Norway evaluated by a commercial kit and established real-time PCR protocols

2015

Ticks are important vectors of human pathogens. The knowledge of disease causing agents harboured by ticks in Norway is limited. The focus of this study was (a) to detect the bacteria of medical importance in ticks collected from the vegetation at locations in the southern part of the country and (b) to evaluate a novel commercially available multiplex PCR based method by comparing results with conventional established real-time PCR protocols. Borrelia burgdorferi sensu lato was confirmed to be the most prevalent pathogen detected (31%) among one hundred individually analysed adult ticks. Borrelia miyamotoi, a spirochete associated with relapsing fever, was detected in one sample. Anaplasma…

Malerelapsing feverBorrelia miyamotoiReal-Time Polymerase Chain Reactionmedicine.disease_causeMicrobiologyMicrobiologyBorreliaparasitic diseasesmedicineAnimalsAnaplasmaBorrelia burgdorferiBacteriaIxodesbiologyNorwaybacterial infections and mycosesmedicine.diseasebiology.organism_classificationVirologyAnaplasma phagocytophilumBacterial Typing TechniquesSpotted feverInfectious DiseasesRickettsia helveticaInsect SciencebacteriaArachnid VectorsFemaleParasitologyTicks and Tick-borne Diseases
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Sex reversal from functional disomy of Xp: Prenatal and post-mortem findings.

2008

Translocations involving the short arms of the X and Y chromosomes are uncommon and are often associated with anomalies in gonadal development. Segmental duplications of the X chromosome interfere with the formation of the testis in patients with a 46,XY karyotype. The gene products located within the duplicated segment, when present in double dose, may affect on male sex development. We report on a fetus with karyotype 46,XY,der (14)t(X;14) (p10;p10)dn. Attached to chromosome 14 is the entire short arm of the X chromosome. Therefore, the fetus is affected with a disomy of Xp, resulting in complete male to female sex reversal, as well as other structural defects. To the best of our knowledg…

Malesex severalDisorders of Sex DevelopmentChromosomal translocationBiologysex reversal • Xp disomy • DAX1 gene • multiple congenital anomaliesTranslocation GeneticChromosome PaintingSettore MED/38 - Pediatria Generale E SpecialisticaPregnancyPrenatal DiagnosisGene duplicationGeneticsHumansAbnormalities MultipleGenetics (clinical)X chromosomeSex Chromosome AberrationsSegmental duplicationUltrasonographyGeneticsChromosome AberrationsChromosomes Human Pair 14FetusChromosomes Human XSex ChromosomesInfant NewbornChromosomeKaryotypeSex reversalChromosome BandingPhenotypeSettore MED/03 - Genetica MedicaKaryotypingTetralogy of FallotFemaledisomy XpDandy-Walker Syndrome
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A tool in support of oral implantology

2009

Il brevetto si riferisce ad un dispositivo che trova applicazione nella tecnica “flap-less” in chirurgia impiantare (inserimento di impianti senza esecuzione di lembo chirurgico), tecnica meno invasiva e traumatica per il paziente; esso consente di: - eseguire in modo diretto e preciso la rilevazione del profilo osseo esterno del sito impiantare - determinare l’angolazione ottimale dell’asse di foratura - guidare l’operazione di fresatura secondo l’asse prescelto Il dispositivo, grazie alla sua adattabilità e modularità è utilizzabile per eseguire siti implantari sia singoli che multipli ed è adattabile a tutte le variabili anatomiche che si possono presentare, è inoltre sterilizzabile e qu…

Mechanical designVirtual prototypingOral ImplantologySettore ING-IND/15 - Disegno E Metodi Dell'Ingegneria Industriale
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The G428A Nonsense Mutation in FUT2 Provides Strong but Not Absolute Protection against Symptomatic GII.4 Norovirus Infection

2009

In November 2004, 116 individuals in an elderly nursing home in El Grao de Castellón, Spain were symptomatically infected with genogroup II.4 (GII.4) norovirus. The global attack rate was 54.2%. Genotyping of 34 symptomatic individuals regarding the FUT2 gene revealed that one patient was, surprisingly, a non-secretor, hence indicating secretor-independent infection. Lewis genotyping revealed that Lewis-positive and negative individuals were susceptible to symptomatic norovirus infection indicating that Lewis status did not predict susceptibility. Saliva based ELISA assays were used to determine binding of the outbreak virus to saliva samples. Saliva from a secretor-negative individual boun…

Medicin och hälsovetenskapSalivaGenotypevirusesNonsense mutationPublic Health and Epidemiology/Infectious Diseaseslcsh:MedicineEnzyme-Linked Immunosorbent AssayBiologymedicine.disease_causeMedical and Health SciencesVirusABO Blood-Group SystemDisease OutbreaksLewis Blood Group Antigensfluids and secretionsVirologyGenotypemedicineHumansSalivalcsh:ScienceGenotypingPhylogenyCaliciviridae InfectionsMultidisciplinaryReverse Transcriptase Polymerase Chain ReactionNoroviruslcsh:Rvirus diseasesOutbreakFucosyltransferasesVirologyBiochemistry/Molecular EvolutionCodon NonsenseSpainViral evolutionNoroviruslcsh:QResearch ArticlePLoS ONE
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Predictive Role of the p16 Immunostaining Pattern in Atypical Cervical Biopsies with Less Common High Risk HPV Genotypes

2021

P16 immunostaining is considered a useful surrogate of transcriptionally active high-risk (hr) HPV infection. Only strong and widespread “block-like” immunoreactivity is considered specific, whereas weak/focal p16 positive immunostaining is considered not specific, and follow-up and HPV molecular detection is not indicated. The aim of the study was to evaluate the presence of HPV DNA and Ki67 immunostaining in 40 cervical atypical biopsies (CALs) with mild and focal histological features suggestive of HPV infection—20 cases with weak/focal p16 positive immunoreactivity and 20 cases negative for p16 expression. In 16/20 weak/focal p16 positive CALs (80%), the INNO-LiPA HPV genotyping detecte…

Medicine (General)Pathologymedicine.medical_specialtyhigh-risk HPVbusiness.industryClinical BiochemistryHPV infectionp16medicine.diseaseArticleP16 NegativeR5-920High risk hpvimmunohistochemistryGenotypeImmunohistochemistryMedicineHigh‐risk HPVStage (cooking)businessKi67GenotypingImmunostainingDiagnostics
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Chromosomal location polymorphism of major rDNA sites in two Mediterranean populations of the killifih Aphanius fasciatus (Pisces: Cyprinodontidae)

2005

The chromosomes of the Mediterranean killifish, Aphanius fasciatus from two populations, the Lagoon of Venice (LV, 15 specimens) and the Lagoon ‘Stagnone di Marsala’ (Sicily) (SM, 48 specimens), have been investigated using conventional Ag-staining and fluorescent in situ hybridization (FISH) with 18S rDNA probe. The two methods revealed variation in the number of major rDNA sites ranging from 8 to 14 (LV) and from 1 to 4 (SM) per individual. The fact that each individual possessed its own number of sites implies that observed variation was structural. Moreover, overlapping of silver staining and FISH patterns demonstrated that all ribosomal genes were transcriptionally active in each speci…

Mediterranean climateMaleSilverAphanius fasciatuAphaniusGeneral Physics and AstronomyZoologyrDNABiologyDNA RibosomalChromosomesKaryotype polymorphismMediterranean seaStructural BiologyPolymorphism (computer science)FundulidaeNucleolus Organizer RegionAnimalsGeneral Materials Science18s rdnaKillifishIn Situ Hybridization FluorescenceGeneticsPolymorphism GeneticStaining and LabelingCell BiologyRibosomal RNAbiology.organism_classificationGenetics PopulationItalyKaryotypingMediterranean seaFemaleIn situ hybridizationMediterranean killifish
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Involvement of the long arm of chromosome 9 in medulloblastoma in an adult.

1997

Abstract Medulloblastoma is the most common primitive neuroectodermal tumor (PNET) in children, but is very rare in adults. An isochromosome for the long arms of 17, i(17q), is found in about 30% of pediatric cases. Cytogenetic studies in adults are very scarce; only six cases have been described cytogenetically: three cases had normal karyotype, two were studied partially, and another presented only two clonal structural anomalies: del(9)(q12) and del(11)(q22). We studied the chromosomes from medulloblastoma in a 27-year-old woman and found one hypotetraploid stemline with clonal alterations. In the structural anomalies, chromosomes 3, 9, 12, and i(17q) were involved. Chromosome 9 presente…

MedulloblastomaAdultCancer Researchmedicine.medical_specialtyPathologyAdult MedulloblastomaIsochromosomeCytogeneticsChromosome 9KaryotypeAnatomyBiologymedicine.diseasePrimitive neuroectodermal tumorKaryotypingGeneticsmedicineHumansHistopathologyFemaleChromosome DeletionCerebellar NeoplasmsChromosomes Human Pair 9Molecular BiologyMedulloblastomaCancer genetics and cytogenetics
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Characterization of Human γδ T Lymphocytes Infiltrating Primary Malignant Melanomas

2012

T lymphocytes are often induced naturally in melanoma patients and infiltrate tumors. Given that gamma delta T cells mediate antigen-specific killing of tumor cells, we studied the representation and the in vitro cytokine production and cytotoxic activity of tumor infiltrating gamma delta T cells from 74 patients with primary melanoma. We found that gamma delta T cells represent the major lymphocyte population infiltrating melanoma, and both V delta 1(+) and V delta 2(+) cells are involved. The majority of melanoma-infiltrating gamma delta cells showed effector memory and terminally-differentiated phenotypes and, accordingly, polyclonal gamma delta T cell lines obtained from tumor-infiltrat…

MelanomasCytotoxicity ImmunologicMaleRENAL-CELL CARCINOMA OVERCOMING IMMUNOLOGICAL-TOLERANCE METASTATIC MELANOMA TUMOR-CELLS PHASE-I MEVALONATE PATHWAY TARGETING CTLA-4 LYMPH-NODES IMMUNOTHERAPY CANCERAnatomy and PhysiologySkin NeoplasmsTUMOR-CELLSLymphocytemedicine.medical_treatmentT-LymphocytesSettore MED/19 - Chirurgia PlasticaTARGETING CTLA-4Interleukin 21T-Lymphocyte SubsetsImmune PhysiologyMETASTATIC MELANOMACytotoxic T cellIL-2 receptorSkin TumorsMelanomaOVERCOMING IMMUNOLOGICAL-TOLERANCEAged 80 and overMultidisciplinaryT CellsMelanomaMalignant MelanomaQRReceptors Antigen T-Cell gamma-deltaMiddle AgedCANCERPHASE-Imedicine.anatomical_structureCytokinePhenotypeOncologyCytokinesMedicineFemaleResearch ArticleTumor ImmunologyAdultScienceT cellImmune CellsImmunologyMalignant Skin NeoplasmsDermatologyBiologyImmunophenotypingImmune systemLymphocytes Tumor-InfiltratingmedicineHumansIMMUNOTHERAPYBiologyAgedNeoplasm StagingSettore MED/04 - Patologia GeneraleLYMPH-NODESCancers and NeoplasmsImmunologic Subspecialtiesmedicine.diseaseImmune SystemImmunologyOVERCOMING IMMUNOLOGICAL-TOLERANCE; METASTATIC MELANOMA; TUMOR-CELLS; PHASE-I; MEVALONATE PATHWAY; TARGETING CTLA-4; LYMPH-NODES; IMMUNOTHERAPY; CANCERClinical ImmunologyImmunologic MemoryMEVALONATE PATHWAYPLoS ONE
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Panton-Valentine leukocidin positive sequence type 80 methicillin-resistant Staphylococcus aureus carrying a staphylococcal cassette chromosome mec t…

2012

Methicillin-resistant Staphylococcus aureus (MRSA) is a major antimicrobial drug-resistant pathogen causing serious infections. It was first detected in healthcare settings, but in recent years it has also become disseminated in the community. Children and young adults are most susceptible to infection by community-acquired (CA) MRSA strains. In this study 25 MRSA isolates implicated in infections of neonates and children admitted to an Algiers hospital during an 18 month period were characterized by molecular methods including staphylococcal cassette chromosome (SCC) mec typing, PCR amplification of pvl genes, pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). F…

Methicillin-Resistant Staphylococcus aureusCross InfectionMolecular EpidemiologyAdolescentBacterial ToxinsExotoxinsInfantMicrobial Sensitivity TestsStaphylococcal InfectionsSettore MED/42 - Igiene Generale E ApplicataPolymerase Chain ReactionBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldCommunity-Acquired InfectionsMRSA PVL CA-MRSA ST80 neonates childrenLeukocidinsAlgeriaChild PreschoolHumansChildMultilocus Sequence TypingThe new microbiologica
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Polyclonal non multiresistant methicillin resistant Staphylococcus aureus isolates from clinical cases of infection occurring in Palermo, Italy, duri…

2012

Abstract Background The evolving epidemiology of methicillin resistant Staphylococcus aureus (MRSA) is characterized by the emergence of infections caused by non multiresistant MRSA carrying staphylococcal chromosomal cassette (SCC)mec IV or V in the healthcare settings. A molecular epidemiological analysis of non multiresistant MRSA isolates from four acute general hospitals was performed in Palermo, Italy, during a one year period. Methods For the purpose of the study, MRSA isolates were defined as non multiresistant when they were susceptible to at least three classes of non β-lactam antibiotics. Seventy-five isolates were submitted to antimicrobial susceptibility testing, multilocus seq…

Methicillin-Resistant Staphylococcus aureusMicrobiology (medical)medicine.medical_specialtylcsh:QR1-502Microbial Sensitivity TestsDrug resistanceTigecyclineBiologyStaphylococcal infectionsmedicine.disease_causelcsh:MicrobiologyMicrobiologylcsh:Infectious and parasitic diseasesMedical microbiologyDrug Resistance Multiple BacterialmedicineHumanslcsh:RC109-216Researchlcsh:RM1-950General MedicineStaphylococcal Infectionsbiochemical phenomena metabolism and nutritionmedicine.diseasebacterial infections and mycosesMethicillin-resistant Staphylococcus aureusVirologyAnti-Bacterial AgentsInfectious Diseaseslcsh:Therapeutics. PharmacologyItalyMultilocus sequence typingMethicillin ResistanceDaptomycinPanton–Valentine leukocidinSentinel SurveillanceMultilocus Sequence Typingmedicine.drugAnnals of Clinical Microbiology and Antimicrobials
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