Search results for "MIP"

showing 10 items of 623 documents

Low fruit set in a dioecious tree: pollination ecology of Commiphora harveyi in South Africa

2005

Dioecious plant species differ in floral morphology and rewards between females and males. Pistillate flowers on female plants often lack pollen and can be less attractive to pollinators, which can have consequences for the visitation rates of the sexes. We studied the pollination ecology of the dioecious tree Commiphora harveyi in a coastal scarp forest in eastern South Africa. Floral display, visiting insect species, visitation rate and natural fruit set were recorded. Additionally, we pollinated flowers by hand to determine experimental fruit set. We found that male trees had more and larger flowers per inflorescence than female trees. Both sexes produced nectar in low amounts. During 20…

PollinationbiologyDioecyfungifood and beveragesmedicine.disease_causebiology.organism_classificationInflorescencePollinatorPollenBotanymedicineNectarCommiphoraBurseraceaeEcology Evolution Behavior and SystematicsJournal of Tropical Ecology
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Using semi-permeable membrane devices as passive samplers

2007

Abstract We discuss the present state of, and future developments in, using semi-permeable membrane devices (SPMDs) for environmental monitoring of organic pollutants. SPMDs allow the determination of time-weighted average concentrations of bioavailable pollutants in the sampled media, reducing significantly the costs of analysis compared with active samplers. We summarize developments in SPMDs, including simplified devices and devices modified by incorporating solvents other than triolein, and applications. We review contaminants (e.g., organotin compounds, polycyclic musk, triclosan, petroleum biomarkers, nitrated PAHs, polychlorinated naphthalenes and a wide range of pesticides sampled i…

PollutantChemistryAir pollutionContaminationPesticidemedicine.disease_causeAnalytical ChemistryClean-upTriclosanchemistry.chemical_compoundEnvironmental chemistryEnvironmental monitoringmedicineSemipermeable membraneSpectroscopyTrAC Trends in Analytical Chemistry
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New perspectives in the use of semipermeable membrane devices as passive samplers.

2007

This review shows the state of the art, from 2000 to nowadays, of the use of semipermeable membrane devices (SPMDs) for monitoring persistent organic pollutants in both, air and aquatic environments. Since their first use in 1990, SPMDs have been employed for many environmental purposes, like air and water pollution monitoring. We have focussed the study in three subjects: (i) novel compounds accumulated by SPMDs, (ii) modifications of SPMDs to improve their specific uptake properties and (iii) alternatives in sample pre-treatment for the determination of pollutants accumulated in SPMDs.

PollutantSemipermeable membrane devicesChemistryAquatic environmentEnvironmental chemistryAir pollutionmedicineSemipermeable membranemedicine.disease_causeWater pollutionAnalytical ChemistryTalanta
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Dual removal and selective recovery of phosphate and an organophosphorus pesticide from water by a Zr-based metal-organic framework

2021

The authors express their thanks for the financial support provided by the Marie Sklodowska-Curie Individual Fellowships (H2020-MSCA-IF-2019-EF-ST-888972-PSustMOF, F.J.C.; H2020-MSCA-IF-2016-GF-749359-EnanSET, N.M.P.) within the European Union H2020 programme and EU FEDER. MINECO (CTQ2017-84692-R, PID2020-113608RB-I00, PEJ2018-004022-A), Universidad de Granada (Plan Propio de Investigacion and Programa Operativo FEDER Andalucia 2014-2020: B-FQM-364-UGR18), Junta de Andalucia (P18-RT-612) and 2020 Post-doctoral Junior Leadere-Retaining Fellowship, la Caixa Foundation (ID 100010434 and fellowship code LCF/BQ/PR20/11770014, N.M.P.) are also acknowledged for funding. Funding for open access cha…

Polymers and PlasticsHydrogenInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionDesorptionWater decontaminationMaterials ChemistryPhosphorus circular economyEutrophication021001 nanoscience & nanotechnologyPhosphateOrganophosphates6. Clean water0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry13. Climate actionPyreneCarbonateMetal-organic framework0210 nano-technologyFenamiphosMaterials Today Chemistry
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Comparison between mercury intrusion porosimetry and nuclear magnetic resonance relaxometry to study the pore size distribution of limestones treated…

2019

Abstract Pore-space properties, such as pore-size distribution and connected porosity, are relevant factors in the evaluation of the performance of a consolidation treatment. In this study, two different techniques – Mercury Intrusion Porosimetry (MIP) and Nuclear Magnetic Resonance Relaxometry (NMRR) – were adopted to study the compatibility and the efficacy of a new consolidation product for limestones. This work aims at comparing and combining data obtained by MIP and NMRR; to confirm the relationship between the quantitative results of MIP and the qualitative ones of NMRR, a calibration which leads to correlate T2 distribution and pore size distribution has been applied. Experimental re…

Pore sizeRelaxometryMaterials scienceConsolidation (soil)Applied Mathematics020208 electrical & electronic engineering010401 analytical chemistry02 engineering and technologyCondensed Matter Physics01 natural sciences0104 chemical sciencesMIP; NMR relaxometry; Porosity; Stone conservation;MIPNuclear magnetic resonanceStone conservation0202 electrical engineering electronic engineering information engineeringNMR relaxometryElectrical and Electronic EngineeringPorosityMercury intrusion porosimetryInstrumentationPorositySettore CHIM/12 - Chimica dell'Ambiente e dei Beni Culturali
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No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures

2005

A missense mutation in the gene encoding the alpha(2) Subunit of the Na+,K+ ATPase pump (ATP1A2) was found in a family with both familial hemiplegic migraine (FHM) and Benign Familial Infantile Seizures (BFIC). As it is still unclear whether ATP1A2 is responsible for pure BFIC syndromes, we checked mutations of the ATP1A2 gene in probands of 12 Italian multiplex families with pure BFIC, who were negative for mutations in the SCN2A gene. We screened the ATP1A2 gene by denaturing high performance liquid chromatography (D-HPLC) and direct sequencing of DNA fragments showing an aberrant elution pattern. We found one exonic variant and five intronic variants, none leading to significant amino ac…

ProbandBenign NeonatalMigraine DisordersMutation MissenseBenign familial infantile convulsionsBiologymedicine.disease_causeDenaturing high performance liquid chromatographyBenign familial infantile convulsions; Epilepsy; Familial hemiplegic migraine; Genetics; Epilepsy Benign Neonatal; Exons; Family Health; Humans; Infant; Introns; Italy; Migraine Disorders; Sodium-Potassium-Exchanging ATPase; Mutation MissenseExonATP1A2GeneticsmedicineHumansMissense mutationGeneFamilial hemiplegic migraineFamilial hemiplegic migraineFamily HealthGeneticsMutationEpilepsyGeneral NeuroscienceInfantExonsmedicine.diseaseEpilepsy Benign NeonatalIntronsItalyMutationBenign familial infantile convulsionMissenseSodium-Potassium-Exchanging ATPaseNeuroscience Letters
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Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.

2006

Summary: Purpose: Benign familial infantile seizures (BFIS) is a genetically heterogeneous condition characterized by partial seizures, onset age from 3 to 9 months, and favorable outcome. BFIS loci were identified on chromosomes 19q12-13.1 and 16p12-q12, allelic to infantile convulsions and choreathetosis. The identification of SCN2A mutations in families with only infantile seizures indicated that BFNIS and BFIS may show overlapping clinical features. Infantile seizures also were in a family with familial hemiplegic migraine and mutations in the ATP1A2 gene. We have examined the heterogeneous genetics of BFIS by means of linkage analysis. Methods: Sixteen families were examined. Probands …

ProbandMaleGenetic LinkagePenetranceEpilepsyModelsgeneticsTomographyFamilial hemiplegic migraineGeneticsNeurologic ExaminationBrainChromosome MappingElectroencephalographyPenetranceMagnetic Resonance Imagingstatistics /&/ numerical dataPedigreeX-Ray ComputedNeurologyFemaleHumanmedicine.medical_specialtyBenign NeonatalBrain; pathology/radiography Chromosome Mapping Chromosomes; Human; Pair 16; genetics Chromosomes; Pair 19; genetics Electroencephalography; statistics /&/ numerical data Epilepsy; Benign Neonatal; diagnosis/genetics Family Female Genetic Heterogeneity Genetic Linkage Haplotypes Humans Magnetic Resonance Imaging Male Models; Genetic Mutation; genetics Neurologic Examination Pedigree Penetrance Tomography; X-Ray Computedpathology/radiographyChromosomesGenetic HeterogeneityGeneticGenetic linkageFebrile seizureGenetic modelmedicineHumansFamilyPsychiatryEpilepsyModels GeneticPair 19Genetic heterogeneitybusiness.industryPair 16medicine.diseaseEpilepsy Benign NeonatalHaplotypesMutationNeurology (clinical)Tomography X-Ray ComputedbusinessChromosomes Human Pair 19Chromosomes Human Pair 16diagnosis/genetics
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ATP1A2 mutations in 11 families with familial hemiplegic migraine.

2005

Abstract Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. The disease is caused by mutations of at least three genes among which two have been identified, CACNA1A and ATP1A2. Very few mutations have been identified so far in ATP1A2. We screened the coding sequence of ATP1A2 in 26 unrelated FHM probands in whom CACNA1A screening was negative. A total of eight different mutations were identified in 11 of the probands (41%), including six missense mutations, one small deletion leading to a frameshift, and one in frame deletion. All were novel mutations. Two mutations were recurrent, in three and two families, respectively. Genotyping of 94 relatives of th…

ProbandMaleMigraine with AuraMolecular Sequence DataMutation MissenseBiologymedicine.disease_causeFrameshift mutationATP1A2GeneticsmedicineMissense mutationAnimalsHumansAmino Acid SequenceGenotypingGenetics (clinical)Familial hemiplegic migraineGeneticsFamily HealthMutationPolymorphism GeneticSequence Homology Amino AcidExonsmedicine.diseaseMigraine with auraPedigreeMutationFemalemedicine.symptomSodium-Potassium-Exchanging ATPase
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Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy

2020

An Italian family with familial hemiplegic migraine (FHM) with the absence of mutations in the known genes associated with this disorder, namely ATP1A2, ATP1A3, CACNA1A, and SCN1A, has recently been reported. Soon afterward, whole exome sequencing allowed the identification of the carrier status of a heterozygous ATP1A4 mutation c.1798 C >T, in four affected members of this family. Here we compare the clinical symptoms of the affected family members with those from the other FHM families linked to mutations in the known genes associated with this disorder. A further two-year follow-up, including clinical response to carbamazepine administered to the proband and the maternal grandmother due …

ProbandPediatricsmedicine.medical_specialtyATP1A4 genefamilial hemiplegic migraine; ATP1A4 gene; carbamazepine; clinical symptomsCase Reportmedicine.disease_causelcsh:RC321-57103 medical and health sciences0302 clinical medicineATP1A2ATP1A3medicine<i>ATP1A4</i> genefamilial hemiplegic migrainelcsh:Neurosciences. Biological psychiatry. NeuropsychiatryExome sequencingFamilial hemiplegic migraine030304 developmental biologyclinical symptoms0303 health sciencesMutationbusiness.industryGeneral NeuroscienceCarbamazepinemedicine.diseaseMigrainecarbamazepinebusiness030217 neurology & neurosurgerymedicine.drugBrain Sciences
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Iatrogenic acute aortic dissection type A: insight from the German Registry for Acute Aortic Dissection Type A (GERAADA)†

2013

OBJECTIVES: Previous investigators have reported a grave prognosis for iatrogenic acute aortic dissection (iAADA), but such studies are limited by their small sample sizes. The purpose of the current study was to analyse the clinical characteristics, current management and surgical outcomes in a large number of iAADA patients identified through a multicentre registry. METHODS: Between July 2006 and June 2010, 50 centres participated in the German Registry for Acute Aortic Dissection Type A (GERAADA). Of the 2137 patients included, 100 (5%) had iAADA. We compared the clinical features and 30-day outcomes of patients with iatrogenic and spontaneous acute aortic dissection type A (sAADA). RESU…

Pulmonary and Respiratory MedicineAortic dissectionmedicine.medical_specialtyAortabusiness.industryGeneral Medicinemedicine.diseaseAortic surgeryNew onsetSurgeryHemiparesisCardiac tamponademedicine.arterymedicineSurgeryIn patientComposite graftmedicine.symptomCardiology and Cardiovascular MedicinebusinessEuropean Journal of Cardio-Thoracic Surgery
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