Search results for "Heterogeneity."

showing 10 items of 388 documents

Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability.

2020

PurposeMarfanoid habitus (MH) combined with intellectual disability (ID) (MHID) is a clinically and genetically heterogeneous presentation. The combination of array CGH and targeted sequencing of genes responsible for Marfan or Lujan–Fryns syndrome explain no more than 20% of subjects.MethodsTo further decipher the genetic basis of MHID, we performed exome sequencing on a combination of trio-based (33 subjects) or single probands (31 subjects), of which 61 were sporadic.ResultsWe identified eight genes with de novo variants (DNVs) in at least two unrelated individuals (ARID1B, ATP1A1, DLG4, EHMT1, NFIX, NSD1, NUP205 and ZEB2). Using simulation models, we showed that five genes (DLG4, NFIX, …

ProbandMale[SDV]Life Sciences [q-bio]intellectual deficiencyMESH: NFI Transcription Factorschromatin remodelingMarfan SyndromeCraniofacial AbnormalitiesMESH: ChildIntellectual disabilityMESH: Craniofacial AbnormalitiesMESH: Mental Retardation X-LinkedExomeChildde novo variantsGenetics (clinical)Exome sequencingGeneticsMESH: ExomeMESH: Middle AgedbiologyMESH: Genetic Predisposition to DiseaseMiddle AgedNFIXMESH: Young AdultFemaleAdultMESH: MutationAdolescentChromatin remodelingMESH: Intellectual DisabilityMESH: Marfan SyndromeEHMT1Young AdultMESH: Whole Exome SequencingIntellectual DisabilityExome SequencingGeneticsmedicineHumansGenetic Predisposition to Diseasemarfanoid habitusGeneMESH: Neurodevelopmental DisordersMESH: AdolescentMESH: HumansGenetic heterogeneityMESH: Chromatin Assembly and DisassemblyMESH: Histone-Lysine N-MethyltransferaseMESH: AdultHistone-Lysine N-Methyltransferasemedicine.diseaseChromatin Assembly and DisassemblyMESH: MaleNFI Transcription FactorsNeurodevelopmental DisordersMutationbiology.proteinMental Retardation X-LinkedMESH: FemaleJournal of medical genetics
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The democratization process: An empirical appraisal of the role of political protest

2020

Abstract This paper analyses the role of peaceful and violent protest in the democratization process. We interpret the democratization process as a sequence of phases so as to allow citizens' and elites' preferences for democracy to vary according to the particular phase that a country is experiencing. By doing so we jointly model the probability of protest and of moving through different phases of democracy taking into account time-constant and time-varying unobserved heterogeneity. In particular, we develop a multivariate finite mixture model that introduces a latent variable to capture unobservable factors. On a sample of 171 countries from 1971 to 2010, we provide evidence that protest …

Economics and EconometricsDemocratization processProcess (engineering)media_common.quotation_subject05 social sciencesSample (statistics)Latent variableUnobservableDemocracy0506 political scienceDemocratic consolidationPoliticsPeaceful and violent protestUnobserved heterogeneityPolitical sciencePolitical economy0502 economics and businessPolitical Science and International Relations050602 political science & public administrationDemocratization050207 economicsmedia_commonEuropean Journal of Political Economy
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Geochemical constraints on basalt petrogenesis in the Strait of Sicily Rift Zone (Italy): Insights into the importance of short lengthscale mantle he…

2020

Igneous activity from the late Miocene to historic time (most recently 1891 CE) in the Strait of Sicily has created two volcanic islands (Pantelleria and Linosa) and several seamounts. These volcanoes are dominated by transitional (ol + hy-normative) to alkaline (ne-normative) basaltic lavas and scoriae; volcanic felsic rocks (peralkaline trachyte-rhyolite) crop out only on Pantelleria. Although most likely erupted through continental crust, basalts demonstrate no evidence of crustal contamination and are geochemically similar to oceanic island basalts (OIB). Despite their isotopic similarities, there are considerable compositional differences with respect to major and trace element geochem…

BasaltContinental-OIBStrait of Sicily Rift ZoneFelsicAlkali Basalt010504 meteorology & atmospheric sciencesContinental crustAlkali basaltKeywords: Strait of Sicily Rift Zone Continental-OIB Alkali basalt Mantle melting Mantle heterogeneitySettore GEO/07 - Petrologia E PetrografiaPartial meltingGeochemistryGeologyCrust010502 geochemistry & geophysics01 natural sciencesMantle (geology)Geochemistry and PetrologyAsthenosphereMantle HeterogeneityMantle MeltingGeology0105 earth and related environmental sciencesChemical Geology
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Fine‐grain beta diversity of Palaearctic grassland vegetation

2021

QUESTIONS: Which environmental factors influence fine-grain beta diversity of vegetation and do they vary among taxonomic groups? LOCATION: Palaearctic biogeographic realm. METHODS: We extracted 4,654 nested-plot series with at least four different grain sizes between 0.0001 m² and 1,024 m² from the GrassPlot database, covering a wide range of different grassland and other open habitat types. We derived extensive environmental and structural information for these series. For each series and four taxonomic groups (vascular plants, bryophytes, lichens, all), we calculated the slope parameter (z-value) of the power law species–area relationship (SAR), as a beta diversity measure. We tested whe…

0106 biological sciencesCzechAgriculture and Food SciencesFine grainelevation333.7: Landflächen NaturerholungsgebietehabitatPlant ScienceMaster planFine-grain beta diversity01 natural sciencesScale dependenceevolutionaryRICHNESSvascular plantsHABITATMacroecologyComputingMilieux_MISCELLANEOUSmedia_commonMean occupancyProductivity2. Zero hungerdisturbance0303 health sciencesEcologySettore BIO/02 - Botanica SistematicaEnvironmental researchPalaearctic grasslanddifferentiationenvironmental heterogeneityspecies-area relationship (SAR)gradientDIFFERENTIATION580: Pflanzen (Botanik)disturbance; elevation; fine-grain beta diversity; heterogeneity; land use; macroecology; mean occupancy; Palaearctic grassland; productivity; scale dependence; species–area relationship (SAR); z-valuescale dependencelanguagemacroecologyproductivitymedia_common.quotation_subjectmean occupancyLibrary scienceSpecies–area relationship (SAR)Environmental drivers Grasslands Lichens Mosses Species-area relationship SAR Vascular Plands010603 evolutionary biologySpecies-area curve03 medical and health sciencesspecies–area relationship (SAR)ExcellencePolitical scienceGRADIENTSlovak030304 developmental biologyspatial scalefine-grain beta diversityBiology and Life Sciencesland useDisturbance15. Life on landZ-valuelanguage.human_languageENVIRONMENTAL HETEROGENEITYEarth and Environmental Sciencesz-valueElevationLand useEVOLUTIONARYSPATIAL SCALESPECIES-AREA RELATIONSHIPSVASCULAR PLANTS[SDE.BE]Environmental Sciences/Biodiversity and EcologyheterogeneityHeterogeneityrichness
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Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and bra…

2016

The 13 subtypes of oral-facial-digital syndrome (OFDS) belong to the heterogeneous group of ciliopathies. Disease-causing genes encode for centrosomal proteins, components of the transition zone or proteins implicated in ciliary signaling. A unique consanguineous family presenting with an unclassified OFDS with skeletal dysplasia and brachymesophalangia was explored. Homozygosity mapping and exome sequencing led to the identification of a homozygous mutation in IFT57, which encodes a protein implicated in ciliary transport. The mutation caused splicing anomalies with reduced expression of the wild-type transcript and protein. Both anterograde ciliary transport and sonic hedgehog signaling w…

0301 basic medicineGeneticsSanger sequencingGenetic heterogeneityBiologyDisease gene identificationmedicine.diseaseCiliopathies3. Good health03 medical and health sciencesCiliopathysymbols.namesake030104 developmental biologyGeneticsmedicinesymbolsExomeGenetics (clinical)Exome sequencingEllis–van Creveld syndromeClinical Genetics
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Next-generation sequencing confirms the implication ofSLC24A1in autosomal-recessive congenital stationary night blindness

2016

Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous retinal disorder which represents rod photoreceptor dysfunction or signal transmission defect from photoreceptors to adjacent bipolar cells. Patients displaying photoreceptor dysfunction show a Riggs-electroretinogram (ERG) while patients with a signal transmission defect show a Schubert–Bornschein ERG. The latter group is subdivided into complete or incomplete (ic) CSNB. Only few CSNB cases with Riggs-ERG and only one family with a disease-causing variant in SLC24A1 have been reported. Whole-exome sequencing (WES) in a previously diagnosed icCSNB patient identified a homozygous nonsense variant in SL…

0301 basic medicineCongenital stationary night blindnessGeneticsRetinal Disordergenetic structuresmedicine.diagnostic_testGenetic heterogeneityBiologyCompound heterozygosityeye diseases03 medical and health sciences030104 developmental biology0302 clinical medicine030221 ophthalmology & optometryGeneticsmedicineMissense mutationsense organsExomeErgGenetics (clinical)ElectroretinographyClinical Genetics
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Somatic copy number alterations are associated with EGFR amplification and shortened survival in patients with primary glioblastoma.

2019

Glioblastoma (GBM) is the most common malignant primary tumor of the central nervous system. With no effective therapy, the prognosis for patients is terrible poor. It is highly heterogeneous and EGFR amplification is its most frequent molecular alteration. In this light, we aimed to examine the genetic heterogeneity of GBM and to correlate it with the clinical characteristics of the patients. For that purpose, we analyzed the status of EGFR and the somatic copy number alterations (CNAs) of a set of tumor suppressor genes and oncogenes. Thus, we found GBMs with high level of EGFR amplification, low level and with no EGFR amplification. Highly amplified tumors showed histological features of…

0301 basic medicineMaleCancer ResearchBiopsyL-amp GB EGFR-low amplified glioblastomamedicine.disease_causewt wildtypeMYBPC3 myosin-binding protein C0302 clinical medicineHIC1 hypermethylated in cancer 1Gene duplicationIn Situ Hybridization FluorescenceIDH2 isocitrate dehydrogenase 2MutationRB-pat RB signaling pathwayEGFRvIII epidermal growth factor receptor variant number IIIPAH phenylalanine hydroxylaseGBM glioblastoma IDH-wildtype (glioblastoma multiforme primary glioblastoma).ANOVA ANalysis Of VArianceN-amp GB EGFR-no amplified glioblastomaMiddle AgedCDKN2A cyclin-dependent kinase inhibitor 2Alcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogensPrognosisPrimary tumorImmunohistochemistryH-amp GB EGFR-high amplified glioblastomaErbB ReceptorsTKR-pat tyrosine-kinase receptors signaling pathway030220 oncology & carcinogenesisDisease ProgressionCDK6 cyclin-dependent kinase 6CDH1 Cadherin 1FemaleCREM cAMP response element modulatorIHC immunohistochemistryAdultOriginal articleDNA Copy Number VariationsCDKN1B cyclin-dependent kinase inhibitor 1BBiologyRARB retinoic acid receptor betaCNS central nervous systemlcsh:RC254-282IDH1 isocitrate dehydrogenase 1BCL2 B-cell cll/ lymphoma 2CNAs copy number algerationsWHO World Health Organization03 medical and health sciencesYoung Adultp53-pat p53 signaling pathwaymedicineBiomarkers TumorTMA tissue microarrayPTENHumansProtein kinase BPI3K/AKT/mTOR pathwaySurvival analysisAgedGenetic heterogeneityGene AmplificationGFAP glial fibrillary acidic proteinMLPA multiplex ligation-dependent probe amplificationmedicine.diseaseFISH fluorescence in situ hibridizationSurvival AnalysisCDKN2B cyclin-dependent kinase inhibitor 2BPTEN phosphatase and tensin homologEGFR epidermal growth factor receptorCNV-load load of copy number variations030104 developmental biologyMutationPARK2 parkinCancer researchbiology.proteinTCGA The Cancer Genome AtlasLARGE1 acetylglucosaminyltransferase-like protein 1GlioblastomaCHD7 Chromodomain Helicase DNA Binding Protein 7DAPI 4′6-diamidino-2-phenylindoleNeoplasia (New York, N.Y.)
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Genetic heterogeneity in the VP7 of group C rotaviruses.

2007

AbstractEvidence for a possible zoonotic role of group C rotaviruses (GCRVs) has been recently provided. To gain information on the genetic relationships between human and animal GCRVs, we sequenced the VP7 gene of 10 porcine strains detected during a large surveillance study from different outbreaks of gastroenteritis in piglets. Four GCRV strains were genetically related to the prototype GCRV porcine Cowden strain. A completely new VP7 genotype included 4 strains (344/04-7-like) that shared 92.5% to 97.0% aa identity to each other, but <83% to human GCRVs and <79% to other porcine and bovine GCRVs. A unique 4-aa insertion (SSSV or SSTI), within a variable region at the carboxy-terminus of…

RotavirusGenotypeSequence analysisSwinevirusesMolecular Sequence DataBiologymedicine.disease_causeEvolution MolecularZoonosisGenetic HeterogeneityPhylogeneticsRotavirusVirologyGenotypemedicineAnimalsHumansAmino Acid SequencePeptide sequenceAntigens ViralPhylogenyGeneticsSequence Homology Amino AcidGenetic heterogeneityStrain (biology)Zoonosisvirus diseasesmedicine.diseaseVirologyEnteritisPigsCapsid ProteinsGroup C rotavirusSequence AnalysisVirology
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Restless legs syndrome: Epidemiological and clinicogenetic study in a South Tyrolean population isolate.

2006

Genetic contributions to restless legs syndrome (RLS) have been consistently recognized from population and family studies. To determine the clinical and genetic features of RLS in a population isolate and explore linkage to three previously described susceptibility loci on chromosomes 12q, 14q, and 9p, respectively, an isolated population in the South Tyrolean Alps was identified and 530 adults participated in the study. Using a two-step strategy, 47 patients with idiopathic RLS were ascertained. The prevalence in the population was 8.9%. Twenty-eight patients (59.6%) had at least one affected first-degree relative and were classified as hereditary cases. In a single extended pedigree, lin…

AdultGenetic MarkersMalemedicine.medical_specialtyPopulationFamily studiesLocus heterogeneityGermanyRestless Legs SyndromeSurveys and Questionnairesmental disordersEpidemiologymedicineHumansRestless legs syndromeeducationLinkage (software)Geneticseducation.field_of_studyPolymorphism Geneticbusiness.industryChromosome MappingReproducibility of Resultsmedicine.diseaseSurgeryPedigreeNeurologyItalyHomogeneousSusceptibility locusFemaleNeurology (clinical)business
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Clinical heterogeneity in infantile galactosialidosis

1987

A new case of infantile galactosialidosis is presented. The condition was diagnosed when the patient was 4 months of age and she died at 20 months. She exhibited some of the symptoms of classical infantile galactosialidosis but no corneal clouding, cherry-red macular spot or limitation of joint mobility. Sonographic examination showed large kidneys and thickened cardiac septa, two symptoms as yet undescribed in this disorder. Urinary oligosaccharide analysis gave grossly pathological results and subsequent fibroblast enzyme analysis showed a deficiency of alpha-neuraminidase and beta-galactosidase. The patient's clinical features are compared with the few cases so far described in the liter…

Pathologymedicine.medical_specialtyUrinary systemNeuraminidaseOligosaccharidesLarge kidneysKidneyLactose IntoleranceJoint mobilityCorneal cloudingClinical heterogeneityHumansMedicinePathologicalUltrasonographybusiness.industryMyocardiumInfantFibroblastsbeta-Galactosidasemedicine.diseaseGalactosidasesPediatrics Perinatology and Child HealthFemalebusinessGalactosialidosisEuropean Journal of Pediatrics
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