Search results for "Phenotype"

showing 10 items of 1875 documents

No association between Helicobacter pylori genotypes and antibiotic resistance phenotypes within families.

2002

Background. Triple therapy combining a proton pump inhibitor with two antibiotics, e.g. clarythromycin (CLR), metronidazole (MTZ) or amoxicillin (AMX), represents the standard in Helicobacter pylori eradication regimens. Resistance to antimicrobial agents, particularly MTZ (up to 56% in Western countries) and CLR (up to 15% in southern Europe), is frequently observed and may be associated with treatment failure [1]. Recently, several studies indicated that individual H. pylori colonies from a single anatomic site may not always yield identical genotypes, or the identical patterns of susceptibility to antibiotics [2–5]. Representative for every single patient we analyzed 27 H. pylori antrum …

Genotypemedicine.drug_classAntibioticsDrug resistanceMicrobial Sensitivity TestsPolymerase Chain ReactionMicrobiologyHelicobacter InfectionsAntibiotic resistanceDrug Resistance BacterialmedicineHelicobacterbiologyHelicobacter pyloriGastroenterologyGeneral MedicineAmoxicillinHelicobacter pyloribiology.organism_classificationAntimicrobialAnti-Bacterial AgentsElectrophoresis Gel Pulsed-FieldMetronidazoleInfectious DiseasesPhenotypePolymorphism Restriction Fragment Lengthmedicine.drugHelicobacter
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Variable mycorrhizal benefits on the reproductive output ofGeranium sylvaticum, with special emphasis on the intermediate phenotype

2012

In several gynodioecious species, intermediate sex between female and hermaphrodite has been reported, but few studies have investigated fitness parameters of this intermediate phenotype. Here, we examined the interactions between plant sex and arbuscular mycorrhizal (AM) fungal species affecting the reproductive output of Geranium sylvaticum, a sexually polymorphic plant species with frequent intermediate sexes between females and hermaphrodites, using a common garden experiment. Flowering phenology, AM colonisation levels and several plant vegetative and reproductive parameters, including seed and pollen production, were measured. Differences among sexes were detected in flowering, fruit …

GeraniumStamenFlowersPlant ScienceGynodioecymedicine.disease_causeSymbiosisHermaphroditeMycorrhizaePollenBotanymedicineHermaphroditic OrganismsSymbiosisEcology Evolution Behavior and SystematicsMutualism (biology)biologyReproductionta1183fungiFungifood and beveragesGeneral Medicinebiology.organism_classificationColonisationPhenotypeFruitSeedsGeranium sylvaticumPollenta1181Plant Biology
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Effects of the common PNPLA3 p.I148 M polymorphism on the fatty liver phenotypes in German patients: results from the FLAG “real life” cohort

2019

GermanGeneticsFatty liverCohortlanguagemedicineBiologymedicine.diseasePhenotypelanguage.human_languageZeitschrift für Gastroenterologie
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Genetic influences on adult body mass index followed over 29 years and their effects on late-life mobility: a study of twin sisters.

2009

Background: The rise in body mass index (BMI) during adulthood increases the risk for metabolic disorders, functional limitations and disability in old age. This twin study examined prospectively whether genetic and environmental influences on women’s BMI also account for mobility 29 years later. Methods: The sample consisted of 103 monozygotic and 114 dizygotic pairs of twin sisters reared together. Body mass index was initially evaluated in 1975, when the women were aged 42.6±3.4 years, and was followed-up in 1981, 1990, 2001 and 2004. Mobility was evaluated using the standardised 6-minute walking test in 2001, when the women were aged 68.6±3.2 years, and followed-up 3 years later. An inv…

GerontologyAdultAgingTWINS/GENETICSEpidemiologyAdult Women030209 endocrinology & metabolismMotor ActivityWeight GainGenetic determinismBody Mass Index03 medical and health sciences0302 clinical medicineRisk FactorsmedicineGeneticsTwins DizygoticHumansGenetic Predisposition to Disease030212 general & internal medicineObesityMobility LimitationFinlandAged2. Zero hungerMobilitybusiness.industrySiblingsPublic Health Environmental and Occupational HealthGenetic VariationTwins Monozygoticmedicine.diseaseTwin studyObesityMiddle agePhenotypeMobility LimitationLongitudinalHealth educationFemalemedicine.symptomGENETIC EPIDEMbusinessBody mass indexWeight gainOBESITY EPIDISABILITY SIFollow-Up StudiesJournal of epidemiology and community health
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Cohort profile: the cardiovascular risk in Young Finns Study.

2008

In Finland, coronary heart disease (CHD) incidence was very high in the 1960s and 1970s. In line with this high incidence, the Seven Countries Study showed that the level of serum cholesterol in Finns was also the highest among the investigated countries in the 1960s. Because several studies indicated that the atherosclerotic process starts early in life, and in accord with the World Health Organization Recommendation of 1978 which stated that studies assessing atherosclerosis precursors in children should be initiated, a program was launched in Finland in the late 1970s to study cardiovascular risk in the youth. The Cardiovascular Risk in Young Finns Study was designed as a collaborative e…

GerontologyAdultCarotid Artery DiseasesMalemedicine.medical_specialtyPediatricsAdolescentGenotypeEpidemiology030204 cardiovascular system & hematology03 medical and health sciencesYoung Adult0302 clinical medicineSeven Countries StudyRisk FactorsmedicineHumans030212 general & internal medicineYoung adultRisk factorChildLife StyleFinlandUltrasonographybusiness.industryPublic healthIncidence (epidemiology)Retrospective cohort studyGeneral Medicine3. Good healthCross-Sectional StudiesPhenotypeCardiovascular DiseasesChild PreschoolCohortFemalebusinessTunica IntimaCohort studyFollow-Up StudiesInternational journal of epidemiology
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Multidisciplinary management of Hunter syndrome.

2009

Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase. In the absence of sufficient enzyme activity, glycosaminoglycans accumulate in the lysosomes of many tissues and organs and contribute to the multisystem, progressive pathologies seen in Hunter syndrome. The nervous, cardiovascular, respiratory, and musculoskeletal systems can be involved in individuals with Hunter syndrome. Although the management of some clinical problems associated with the disease may seem routine, the management is typically complex and requires the physician to be aware of the special issues surrounding the patient with Hunter syndrome, and a multidiscipl…

GerontologyAdultMalemedicine.medical_specialtyAdolescentGenotypeIdursulfaseDiseaseIduronate SulfataseYoung AdultInternal medicineAnesthesiologymedicineHumansEnzyme Replacement TherapyCooperative BehaviorIntensive care medicineChildInfusions IntravenousMucopolysaccharidosis IIRandomized Controlled Trials as TopicPatient Care Teambusiness.industryHematopoietic Stem Cell TransplantationInfant NewbornInfantHunter syndromeEnzyme replacement therapymedicine.diseaseCombined Modality TherapyRecombinant ProteinsPulmonologyPhenotypeOtorhinolaryngologyChild PreschoolPediatrics Perinatology and Child HealthInterdisciplinary CommunicationNeurosurgerybusinessmedicine.drugPediatrics
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Genotypic and phenotypic aspects of longevity: results from a Sicilian survey and implication for the prevention and the treatment of age-related dis…

2019

Background:It is well known that long living individuals are a model of successful ageing and that the identification of both genetic variants and environmental factors that predispose to a long and healthy life is of tremendous interest for translational medicine.Methods:We present the preliminary findings obtained from an ongoing study on longevity conducted on a sample of Sicilian long-lived individuals.Results:We review the characteristics of longevity in Sicily, taking into account lifestyle, environment, genetics, hematochemical values, body composition and immunophenotype. In addition, we discuss the possible implications of our data for the prevention and/or treatment of age-related…

GerontologyAgingGenotypemedia_common.quotation_subjectSettore MED/42 - Igiene Generale E ApplicataAge-related diseases; Sicily; body composition; genetics; immunosenescence; longevity01 natural sciences03 medical and health scienceslongevityAge relatedSurveys and QuestionnairesDrug DiscoveryGenotypeMedicineHumansLife StyleSicily030304 developmental biologymedia_commonPharmacologyimmunosenescenceSettore MED/04 - Patologia Generale0303 health sciencesage-related diseasebody compositionbusiness.industryTranslational medicineLongevityImmunosenescencelanguage.human_language0104 chemical sciences010404 medicinal & biomolecular chemistryPhenotypeAgeinglanguageIdentification (biology)geneticbusinessSicilian
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Age and Gender-related Variations of Molecular and Phenotypic Parameters in A Cohort of Sicilian Population: from Young to Centenarians

2021

People are living longer, but lifespan increase does not coincide with a boost in health-span. Thus, improving the quality of life of older people is a priority. Centenarians reach extreme longevity in a relatively good health status, escaping or delaying fatal or strongly invalidating diseases. Therefore, studying processes involved in longevity is important to explain the biological mechanisms of health and well-being, since knowledge born from this approach can provide valuable information on how to slow aging. We performed the present study in a well characterized very homogeneous sample of 173 people from Western Sicily, to update existing literature on some phenotypic aspects of aging…

Gerontologyphenotypemedia_common.quotation_subjectPopulationDiseasecentenarianOrginal ArticlePathology and Forensic MedicineAge and genderlongevitygenderMedicineYoung adulteducationmedia_commonSettore MED/04 - Patologia Generaleeducation.field_of_studybusiness.industryagingLongevityCell BiologyAnthropometryinflammationCohortNeurology (clinical)Geriatrics and GerontologyCentenarianbusinessAging and disease
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Evolutionary morphology in shape and size of haptoral anchors in 14 Ligophorus spp. (Monogenea: Dactylogyridae).

2017

The search for phylogenetic signal in morphological traits using geometric morphometrics represents a powerful approach to estimate the relative weights of convergence and shared evolutionary history in shaping organismal form. We assessed phylogenetic signal in the form of ventral and dorsal haptoral anchors of 14 species of Ligophorus occurring on grey mullets (Osteichthyes: Mugilidae) from the Mediterranean, the Black Sea and the Sea of Azov. The phylogenetic relationships among these species were mapped onto the morphospaces of shape and size of dorsal and ventral anchors and two different tests were applied to establish whether the spatial positions in the morphospace were dictated by …

Gills0106 biological sciences0301 basic medicinelcsh:MedicineMorphology (biology)Animal Phylogenetics01 natural sciencesEcologia marinaMathematical and Statistical Techniqueslcsh:SciencePhylogenyData ManagementPrincipal Component AnalysisMultidisciplinarybiologyPhylogenetic treePhylogenetic AnalysisPeixosBiological EvolutionSmegmamorphaPhylogeneticsPhenotypePhysical SciencesStatistics (Mathematics)MonogeneaResearch ArticleComputer and Information SciencesEvolutionary ProcessesParàsitsImaging TechniquesZoologyResearch and Analysis Methods010603 evolutionary biologyHost SpecificityHost-Parasite Interactions03 medical and health sciencesSpecies SpecificityPhylogeneticsAnimalsEvolutionary SystematicsParasite EvolutionStatistical MethodsTaxonomyMorphometricsEvolutionary BiologyEvolutionary Developmental BiologyMorphometrylcsh:RBiology and Life Sciencesbiology.organism_classificationDactylogyridae030104 developmental biologyPlatyhelminthsMultivariate AnalysisEvolutionary developmental biologyParasitologylcsh:QAllometryZoologyMathematicsDevelopmental BiologyPLoS ONE
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Co-factors, Microbes, and Immunogenetics in Celiac Disease to Guide Novel Approaches for Diagnosis and Treatment.

2021

Celiac disease (CeD) is a frequent immune-mediated disease that affects not only the small intestine but also many extraintestinal sites. The role of gluten proteins as dietary triggers, HLA-DQ2 or -DQ8 as major necessary genetic predisposition, and tissue transglutaminase (TG2) as mechanistically involved autoantigen, are unique features of CeD. Recent research implicates many cofactors working in synergism with these key triggers, including the intestinal microbiota and their metabolites, nongluten dietary triggers, intestinal barrier defects, novel immune cell phenotypes, and mediators and cytokines. In addition, apart from HLA-DQ2 and -DQ8, multiple and complex predisposing genetic fact…

GlutensTissue transglutaminaseHuman leukocyte antigenDiseaseGut floraImmunologic Testsmedicine.disease_causeBioinformaticsAutoimmunityImmune systemPredictive Value of TestsRisk FactorsGenetic predispositionMedicineAnimalsHumansGenetic Predisposition to DiseaseImmunogenetic PhenomenaIrritable bowel syndromeHepatologybiologyBacteriabusiness.industryfungiGastroenterologynutritional and metabolic diseasesmedicine.diseasebiology.organism_classificationPrognosisGastrointestinal MicrobiomeIntestinesCeliac DiseaseDisease Models AnimalPhenotypeHost-Pathogen Interactionsbiology.proteinbusinessGastroenterology
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