Search results for "Inheritance"

showing 10 items of 160 documents

VACTERL with hydrocephalus: A further case with probable autosomal recessive inheritance

1994

Hand deformityGeneticsFatal outcomeAutosomal recessive inheritancebusiness.industrymedicinemedicine.diseasebusinessGenetics (clinical)HydrocephalusAmerican Journal of Medical Genetics
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Comparison of healthy behavior in Ukrainian and Polish students of physical education

2021

Introduction: This study aimed to examine the healthy behaviors in undergraduate students of Physical Education (PE) from Ukraine and Poland in comparison to the control sample of students of other faculties. Material and methods: The group of 564 university students (67% of males), ranging in age from 18 to 41 years (M = 22.05, SD = 2.49), was surveyed using a written form of the Health Behavior Inventory (HBI). The HBI includes the following four subscales: healthy habits, nutrition (HHN), preventive behavior (PB), positive adjustments (PA), and healthy practices (HP). Undergraduates' sample consisted of 25% Ukrainian students of PE faculty, 30% Polish PE students, and 45% Polish sample o…

Healthy behaviorHealth (social science)Poetrybusiness.industryUkrainianeducationPhysical Therapy Sports Therapy and RehabilitationDigital librarylanguage.human_languageCultural inheritanceEducationPhysical educationVisual artsPublishinglanguageOrthopedics and Sports MedicinePsychologybusinessPhysical Activity Review
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Ancient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence

2016

The chromosome bands 15q24.1-15q24.3 contain a complex region with numerous segmental duplications that predispose to regional microduplications and microdeletions, both of which have been linked to intellectual disability, speech delay and autistic features. The region may also harbour common inversion polymorphisms whose functional and phenotypic manifestations are unknown. Using single nucleotide polymorphism (SNP) data, we detected four large contiguous haplotype-genotypes at 15q24 with Mendelian inheritance in 2,562 trios, African origin, high population stratification and reduced recombination rates. Although the haplotype-genotypes have been most likely generated by decreased or abse…

HeredityAutism Spectrum DisorderIntelligenceSocial SciencesChromosome DisordersMAN2C1 geneFamiliesMicePsychologylcsh:ScienceChildChildrenIn Situ HybridizationCognitive ImpairmentIntelligence Testseducation.field_of_studyIntelligence quotientBrainGenomicsNeurologyChromosome DeletionHumanGenotypeEvolutionSingle-nucleotide polymorphismFluorescenceEvolution Molecular03 medical and health sciencesalpha-MannosidaseIntellectual DisabilityMannosidasesGeneticsChromosome 15q24 2HumansPolymorphismeducationChromosome Aberrationslcsh:RHaplotypePair 15PongoBiology and Life SciencesComputational BiologyMolecularmedicine.diseaseIntellectual Disability/genetics030104 developmental biologyNeurodevelopmental DisordersDevelopmental PsychologyAfricalcsh:QPopulation GroupingsGene expressionEthiopiaAutismePopulation GeneticsNeuroscience0301 basic medicineAutismlcsh:MedicineGene ExpressionHomozygosityGeographical LocationsCohort StudiesChromosome Disorders/geneticsIntellectual disabilityMedicine and Health SciencesIn Situ Hybridization FluorescenceSegmental duplicationMannosidases/geneticsGeneticsMultidisciplinaryGenomeCognitive NeurologyHomozygoteSingle NucleotidePhenotypesymbolsInfantsResearch ArticleCognitive NeurosciencePopulationInfants -- DesenvolupamentBiologyPolymorphism Single NucleotideChromosomessymbols.namesakeDevelopmental NeurosciencemedicineAnimalsBrain/metabolismCromosomes humans -- AnomaliesAlleleChromosomes Human Pair 15Evolutionary BiologyPopulation BiologyGenome HumanChromosome 15qIntelligence/geneticsGenome AnalysisGenomic LibrariesExpressió gènicaMacaca mulattaRatsHaplotypesAge GroupsPeople and PlacesMendelian inheritanceCognitive Science
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MASPEGHI 2004 Mechanisms for Speialization, Generalization and Inheritance

2005

Rapport de Recherche Projet OCL, N° I3S/RR-2004-15-FR; International audience; MASPEGHI 2004 is the third edition of the MASPEGHI workshop. This year the organizers of both the ECOOP 2002 Inheritance Workshop and MASPEGHI 2003 came together to enlarge the scope of the workshop and to address new challenges. We succeeded in gathering a diverse group of researchers and practitioners interested in mechanisms for managing specialization and generalization of programming language components. The workshop contained a series of presentations with discussions as well as group work, and the interplay between the more than 22 highly skilled and inspiring people from many different communities gave ri…

Highly skilledScope (project management)Computer sciencebusiness.industryMultiple inheritance020207 software engineering02 engineering and technologyInheritance (object-oriented programming)020204 information systemsGeneralization (learning)Specialization (functional)0202 electrical engineering electronic engineering information engineeringEngineering ethics[INFO]Computer Science [cs]Artificial intelligenceGroup workbusiness
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Family Assets and Financial Misfortunes of the Castellví Family during the 17th Century

2014

La rama del linaje valenciano de los Castellví iniciada a principios del quinientos por el señor de Puchol protagonizó durante el siglo XVII un significativo proceso de acumulación patrimonial. En el origen del mismo se sitúan las adquisiciones realizadas por los sucesivos miembros que lo encabezaron, pero tan importante como ello resultó la estrategia matrimonial de los titulares del linaje, el reducido número de hijos y la reversión a la línea principal de legados de los miembros de la familia que no contrajeron matrimonio o fallecieron sin descendencia. En contrapartida, diversos factores se conjugaron para provocar un endeudamiento progresivo, especialmente acusado desde la década de 16…

Historia moderna y contemporáneaHistoryModern historymedia_common.quotation_subjectValencianlanguage.human_languageGenealogyGeographyHistòria modernalanguageInheritanceHumanitiesmedia_commonStudia Historica: Historia Moderna
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Derechos de la viuda en la Valencia foral

2001

This article is about the rights of widows over their deceased husbands’ goods. We can not forget that, because of regulations regarding the separation of properties, these women are in a defenceless situation if they lack their own property, having to depend in most cases on their husbands’ testament. The severity of the system has to be alleviated with dowries, in order that when their husbands die women without inheritance could have at least a certain security. They are in a situation of economic vulnerability, especially grave when their husbands die without property. In this case, the widow’s rights are important in order to ameliorate the economic suffering they experience in their j…

HistoryAño de lutomedia_common.quotation_subjectUniversal usufructVulnerabilitySocial SciencesUsufructo universalWidowhoodDowryDerechos de las indotadasRights of womenViudedad; Año de luto; Derechos de las indotadas; Usufructo universallcsh:Social Scienceslcsh:HHViudedadLawMourning yearWidowhood; Mourning year; Rights of women; Dowry; Universal usufructSociologyInheritancemedia_commonHispania : Revista española de historia
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La violència física i econòmica contra les dones a la Mallorca del segle XVII : una aproximació

2020

Resum: En aquesta primera aproximació a la Mallorca del segle XVII, es pot veure com les dones patien diferents tipus de violència. Per una banda, la física, que era exercida tant per part de desconeguts com per part dels marits dins de l’entorn conjugal. La fugida de la maltractada era la solució més habitual i, en moltes ocasions, la disputa acaba amb divorci. per altra banda, s’ha documentat l’existència d’una violència que es pot denominar econòmica i que es basa en l’exclusió de la dona de les seves pròpies possessions, cosa que conduïa a llargs litigis per a la restitució dotal o per a reclamar una herència. Generalment, aquesta violència es donava quan les dones quedaven soles i en s…

HistoryUNESCO::CIENCIAS DE LAS ARTES Y LAS LETRASLiterature and Literary TheoryPolitical sciencemedia_common.quotation_subject:CIENCIAS DE LAS ARTES Y LAS LETRAS [UNESCO]DowryInheritanceHumanitiesSocial vulnerabilityLanguage and Linguisticsmedia_common
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Monozygotic twins in history: enlightenment by mythology and ethnography

2020

Abstract Birth in mankind is planned in single. The birth of twins is a rare event, occurring in about 1% of pregnancies. This chapter presents different aspects of mythology, history and ethnography for the better understanding of the meaning of twins throughout times. Twins are and will always be a source of artistic inspiration, cultural inheritance and social (re)interpretation.

Historymedia_common.quotation_subjectInterpretation (philosophy)EthnographyEnlightenmentMythologyMeaning (existential)Artistic inspirationhumanitiesGenealogyCultural inheritancemedia_common
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Girl With Partial Turner Syndrome and Absence Epilepsy

2007

This report describes a 16-year-old girl with short stature (-5 standard deviations), normal puberty, panic attacks, absence epilepsy, some stigmata of Turner syndrome, and a Madelung deformity. Routine chromosomal analysis revealed a female karyotype with one abnormal chromosome X, with the suspicion of additional material on the short arm. With fluorescent in situ hybridization and array-multiplex amplifiable probe hybridization methodology, a complex aberration was detected, with a deletion of the distal part of Xp22.33 (including the short-stature homeobox gene) and a duplication of Xp22.32-p22.12 proximal to the deleted segment. The deletion in our patient involves the Xp22.33 region. …

Homeodomain ProteinsGeneticsAdolescentTurner SyndromeKaryotypeBiologymedicine.diseaseShort statureEpilepsy AbsenceShort Stature Homeobox ProteinDevelopmental NeuroscienceNeurologyShort Stature Homeobox ProteinPediatrics Perinatology and Child HealthGene duplicationTurner syndromemedicineOMIM : Online Mendelian Inheritance in ManHumansHomeoboxFemaleNeurology (clinical)medicine.symptomX chromosomePediatric Neurology
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Dissensus, death and division

2009

The modeling of switching systems describing networks where death and duplication processes occur is described. A dissensus protocol, complementary to consensus protocol, is introduced and the convergence or divergence of the agents' state evolution is studied. We discuss some properties of the topology reached by the network when different rules of duplication and inheritance are implemented.

Impulsive networksHybrid systemsComputer scienceDistributed computingconsnesus problemsSwitching systemsDivision (mathematics)biological modelDivergence (computer science)Consensus protocolsInheritance (object-oriented programming)Settore ING-INF/04 - Automaticaconsnesus problems biological model networksnetworksConvergence (routing)Settore MAT/09 - Ricerca OperativaProtocol (object-oriented programming)Biological models; Consensus protocols; Hybrid systems; Impul-sive networks; Switching systems;Biological models; Consensus protocols; Hybrid systems; Impulsive networks; Switching systemsBiological models2009 American Control Conference
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