Search results for "Sang"

showing 10 items of 428 documents

Data from: Plant – herbivorous beetle networks: molecular characterization of trophic ecology within a threatened steppic environment

2015

DNA barcoding facilitates many evolutionary and ecological studies, including the examination of the dietary diversity of herbivores. In this study, we present a survey of ecological associations between herbivorous beetles and host plants from seriously threatened European steppic grasslands. We determined host plants for the majority (65%) of steppic leaf beetles (55 species) and weevils (59) known from central Europe using two barcodes (trnL and rbcL) and two sequencing strategies (Sanger for mono/oligophagous species and Illumina for polyphagous taxa). To better understand the ecological associations between steppic beetles and their host plants, we tested the hypothesis that leaf beetl…

Larinus obtususOtiorhynchus fulloCassida lineolaWildlife ManagementDibolia schillingiiSitona languidusBruchela rufipesPseudoprotapion elegantulumArgoptochus quadrisignatusAphthona czwalinaiCassida panzeriLongitarsus tabidusCryptocephalus fulvusAphthona cyparissiaeMecinus pascuorumCryptocephalus pygmaeusLife Sciencesfood and beveragesGaleruca pomonaeExapion elongatulumAphthona lacertosaZacladus geraniiGonioctena olivaceaMedicineTychius medicaginisPodagrica fuscicornisOmias globulusTychius crassirostrisSitona inopsCryptocephalus flavipesSphaeroderma testaceumPaophilus afflatusCryptocephalus violaceusAphthona pygmaeaMogulones javetiiLongitarsus exsoletusSibinia subellipticaCryptocephalus quadriguttatusLarinus turbinatusCentricnemus leucogrammusPhilopedon plagiatumRhinusa tetraChrysomelidaefungiLuperus xanthopodaGaleruca tanacetiCleopomiarus graminisCryptocephalus bilineatusSpecies InteractionsEntomoscelis adonidisCryptocephalus bameuliStenocarus ruficornisParafourcartia squamulataHemitrichapion pavidumCleopomiarus distinctusCryptocephalus vittatusLachnaia sexpunctataTychius aureolusSitona lateralisLabidostomis humeralisSmicronyx jungermanniaeEusomus ovulumSitona waterhouseimedicine and health careTychius sharpiPolydrusus inustusCurculionidaeCryptocephalus chrysopusPhyllotreta nodicornisCalomicrus circumfususLarinus sturnusCionus clairvilleiPolydrusus confluensStrophosoma faberCrioceris quinquepunctataTrichosirocalus troglodytesAphthona beckeriSmaragdina auritaSmaragdina affinisPachybrachis hippophaesTychius schneideriCyanapion plataleaHypera fuscocinereaLongitarsus quadriguttatusSitona striatellusPhrydiuchus tauCassida pannonicaLabidostomis longimanaHypocassida subferrugineaCycloderes pilosulusPseudoprotapion ergenenseCryptocephalus virensAphthona euphorbiaePhyllobius brevisSitona longulusChrysochus asclepiadeusPachybrachis tesselatusCrioceris quatuordecimpunctataTrichosirocalus barnevilleiPachybrachis fimbriolatusChrysolina cerealisPseudorchestes ermischiOmias puberulusThamiocolus signatusMesotrichapion punctirostreDiet AnalysisCoptocephala unifasciataSibinia tibialisPsylliodes cucullataMogulones geographicusCassida margaritaceaAphthona ovataSitona humeralisAphthona venustulaSquamapion elongatulumGonioctena fornicataSibinia vittataDibolia cryptocephalaPseudoperapion brevirostreCheilotoma musciformisCoevolutionNeocrepidodera ferrugineaChrysolina sanguinolenta
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Vascular labeling of the head and neck vessels : technique, advantages and limitations

2017

Background Vascular staining techniques have been used to describe the vascular structures of several anatomic areas. However, few reports have described this procedure in the head and neck region. This paper describes a head and neck vascular labeling procedure, and describes some of the technical complications that may occur. Material and methods Fifteen specimen cadaver heads were prepared. After drying the vascular system, the internal carotid arteries were ligated and a solution with latex and a gelling agent was injected into the internal carotid arteries and external jugular veins. Two different colors were employed to differentiate arteries from veins. A total of 60ml latex was inje…

Lingual arteryArtèries caròtidesInvestigació mèdicaDissection (medical)Odontologia03 medical and health sciences0302 clinical medicineBlood vesselsMedicine researchCadavermedicine.arterymedicineAnatomia humana030223 otorhinolaryngologyHead and neckGeneral DentistryVasos sanguinisPlexusbusiness.industryResearchColl030206 dentistryAnatomymedicine.disease:CIENCIAS MÉDICAS [UNESCO]Capmedicine.anatomical_structureExternal JugularDentistryHuman anatomyUNESCO::CIENCIAS MÉDICAScardiovascular systemOral SurgeryCadaveric spasmbusinessHeadCarotid arteryNeckBlood vessel
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Effects of asymmetric dimethylarginine on renal arteries in portal hypertension and cirrhosis

2016

AIM. To evaluate the effects of asymmetric dimethylarginine (ADMA) in renal arteries from portal hypertensive and cirrhotic rats. METHODS. Rat renal arteries from Sham (n = 15), pre-hepatic portal hypertension (PPVL; n = 15) and bile duct ligation and excision-induced cirrhosis (BDL; n = 15) were precontracted with norepinephrine, and additional contractions were induced with ADMA (10-6-10-3 mol/L), an endogenous inhibitor of nitric oxide (NO) synthase. Concentration-response curves to acetylcholine (1 × 10-9-3 × 10-6 mol/L) were determined in precontracted renal artery segments with norepinephrine in the absence and in the presence of ADMA. Kidneys were collected to determine the protein e…

Liver CirrhosisMale0301 basic medicineAsymmetric dimethylarginineCirrhosisArginineKidneyurologic and male genital diseasesRats Sprague-DawleyNorepinephrinechemistry.chemical_compoundRenal ArteryVasoconstrictor AgentsEnzyme InhibitorsPortal hypertensionKidneyGastroenterologyGeneral MedicineBasic StudyDimethylarginine dimethylaminohydrolaseNG-Nitroarginine Methyl Estermedicine.anatomical_structureCirrhosisCardiologyPortal hypertensionmedicine.symptommedicine.medical_specialtyCirrosi hepàticaEndotheliumArginineNitric OxidePressió sanguíniaAmidohydrolases03 medical and health sciencesInternal medicinemedicine.arteryHypertension PortalmedicineAnimalsHumansEndotheliumRenal arterybusiness.industrymedicine.diseaseAcetylcholineRats030104 developmental biologychemistryVasoconstrictionNitric oxide inhibitorsNitric Oxide SynthaseAsymmetric dimethylargininebusinessVasoconstriction
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Bendamustin in association with Rituximab (BR) in the treatment of patients with relapsed/refractory lymphoid neoplasm. A GISL retrospective study

2009

Lymphoid neoplasms bendamustinSettore MED/15 - Malattie Del Sangue
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CHARACTERIZATION AND ROLE OF POSSIBLE BIOLOGICAL MARKERS IN SPLENIC MARGINAL ZONE LYMPHOMA

Lymphoma Splenic marginal zone lymphomaSettore MED/15 - Malattie Del Sangue
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Transfusion sanguine. Responsabilité

1996

International audience; (Riom 6 avr. 1995, JCP 1995.4.325)

MEDECINEETABLISSEMENT DE SANTEClinique[SHS.DROIT]Humanities and Social Sciences/Law[SHS.DROIT] Humanities and Social Sciences/LawSIDATransfusion sanguineResponsabilité
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Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform

2017

Neurofibromatosis type 1 (NF1) is caused by mutations of the NF1 gene and is one of the most common human autosomal dominant disorders. The patient shows different signs on the skin and other organs from early childhood. The best known are six or more café au lait spots, axillary or inguinal freckling, increased risk of developing benign nerve sheath tumours and plexiform neurofibromas. Mutation detection is complex, due to the large gene size, the large variety of mutations and the presence of pseudogenes. Using Ion Torrent PGM™ Platform, 73 mutations were identified in 79 NF1 Italian patients, 51% of which turned out to be novel mutations. Pathogenic status of each variant was classifi…

Male0301 basic medicineDNA Mutational Analysismedicine.disease_causeChildGenetics (clinical)Sanger sequencingGeneticsMutationNeurofibromin 1biologyMosaicismCafe-au-Lait SpotsNeurofibromatosis type 1; Legius's syndrome; Next generation sequencingGeneral MedicineMiddle AgedItalyChild PreschoolsymbolsMedical geneticsFemalemedicine.symptomHumanAdultmedicine.medical_specialtyNeurofibromatosis 1AdolescentPseudogeneDNA Mutational Analysi03 medical and health sciencessymbols.namesakeGeneticNext generation sequencingCafé au lait spotSkin AbnormalitieGeneticsmedicineHumansCafe-au-Lait SpotNeurofibromatosisLegius's syndromeInfantSequence Analysis DNAIon semiconductor sequencingmedicine.diseaseNeurofibromin 1030104 developmental biologyMutationSkin Abnormalitiesbiology.proteinNeurofibromatosis type 1European Journal of Medical Genetics
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A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disability

2017

Abstract The autosomal recessive form of primary microcephaly (MCPH) is a rare disorder characterized by head circumference of at least 3 standard deviation below the mean. The MCPH exhibits genetic heterogeneity with thirteen loci (MCPH1-MCPH13) identified, and associated with variable degree of intellectual disability. It has been reported that WDR62 is the second causative gene of autosomal recessive microcephaly (MCPH2) playing a significant role in spindle formation and the proliferation of neuronal progenitor cells. We report a clinical feature, electroclinical findings, and clinical course of a patient with a severe phenotype of MCPH2 including microcephaly, refractory infantile spas…

Male0301 basic medicineMicrocephalyAdolescentMutation MissenseIntellectual disabilityCell Cycle ProteinsNerve Tissue ProteinsGenetic analysisReceptors G-Protein-CoupledConsanguinity03 medical and health sciences0302 clinical medicineDevelopmental NeuroscienceSettore M-PSI/08 - Psicologia ClinicaIntellectual disabilityHumansMedicineMissense mutationGeneWDR62GeneticsMCPHEpilepsybusiness.industryGenetic heterogeneityInfantGeneral MedicineInfantile Spasmmedicine.diseaseSettore MED/39 - Neuropsichiatria InfantilePedigreePhenotype030104 developmental biologyGPR56MutationPediatrics Perinatology and Child HealthMicrocephalyInfantile spasmNeurology (clinical)businessSpasms Infantile030217 neurology & neurosurgeryBrain and Development
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Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis

2020

Amyotrophic lateral sclerosis (ALS) is a multifactorial disease characterized by the interplay of genetic and environmental factors. In the majority of cases, ALS is sporadic, whereas familial forms occur in less than 10% of patients. Herein, we present the results of molecular analyses performed in a large cohort of Italian ALS patients, focusing on novel and already described variations in ALS-linked genes. Our analysis revealed that more than 10% of tested patients carried a mutation in one of the major ALS genes, with C9orf72 hexanucleotide expansion being the most common mutation. In addition, our study confirmed a significant association between ALS patients carrying the ATNX-1 interm…

Male0301 basic medicineSanger sequencingAgingTime FactorsDiseaseCohort Studies03 medical and health sciencessymbols.namesake0302 clinical medicineRisk FactorsC9orf72HumansMedicineAmyotrophic lateral sclerosisRisk factorGenePathologicalAtaxin-1Genetic Association StudiesAmyotrophic lateral sclerosiSanger sequencingGeneticsDNA Repeat ExpansionC9orf72 ProteinMolecular analysibusiness.industryMolecular analysisGeneral NeuroscienceGenetic VariationAmyotrophic lateral sclerosismedicine.disease030104 developmental biologyItalyMutation (genetic algorithm)symbolsFemaleNeurology (clinical)Geriatrics and Gerontologybusiness030217 neurology & neurosurgeryDevelopmental BiologyNeurobiology of Aging
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Impact of Consuming Extra-Virgin Olive Oil or Nuts within a Mediterranean Diet on DNA Methylation in Peripheral White Blood Cells within the PREDIMED…

2017

DNA methylation could be reversible and mouldable by environmental factors, such as dietary exposures. The objective was to analyse whether an intervention with two Mediterranean diets, one rich in extra-virgin olive oil (MedDiet + EVOO) and the other one in nuts (MedDiet + nuts), was influencing the methylation status of peripheral white blood cells (PWBCs) genes. A subset of 36 representative individuals were selected within the PREvención con DIeta MEDiterránea (PREDIMED-Navarra) trial, with three intervention groups in high cardiovascular risk volunteers: MedDiet + EVOO, MedDiet + nuts, and a low-fat control group. Methylation was assessed at baseline and at five-year follow-up. Ingenui…

Male0301 basic medicineTime FactorsMediterranean diet; DNA methylation; nuts; olive oil; blood cellsMediterranean dietADNPhysiologyComorbidity030204 cardiovascular system & hematologyDiet MediterraneanEpigenesis Genetic0302 clinical medicineRisk FactorsLeukocytesNutsCooking (Dried foods)Aged 80 and overchemistry.chemical_classificationDNA methylationNutrition and DieteticsMethylationMiddle AgedOli d'olivaTreatment OutcomeCpG siteCardiovascular DiseasesDNA methylationFemaleDiet HealthyMetilaciólcsh:Nutrition. Foods and food supplyPolyunsaturated fatty acidBlood cellslcsh:TX341-641nutsBiologyMethylationArticle03 medical and health sciencesMediterranean cookingMediterranean dietDiabetes mellitusCuina mediterràniamedicineHumansEpigeneticsOlive OilAgedMetabolismDNAProtective Factorsmedicine.diseaseCuina (Fruita seca)030104 developmental biologychemistrySpainCèl·lules sanguíniesCpG Islandsblood cellsEnergy MetabolismOlive oilFood Science
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