Search results for "Inheritance"

showing 10 items of 160 documents

ICOOLPS 2010 and MASPEGHI 2010.

2012

International audience; At ECOOP 2010 in Maribor, Slovenia, the two workshops MASPEGHI (MechAnisms for SPEcialization, Generalization and inHerItance) and ICOOOLPS (Implementation, Compilation, Optimization of Object-Oriented Languages, Programs and Systems) were combined because both were rather small and shared common concerns, their topic areas being strongly related. Six papers had been accepted to MASPEGHI, but only five were presented because the authors of one paper could not attend the conference and workshop. Three papers had been accepted to ICOOOLPS, and all were also presented. The workshop authors were later asked to submit extended versions of their papers for possible publica…

Optimization050208 financeInheritance[INFO.INFO-PL]Computer Science [cs]/Programming Languages [cs.PL]GeneralizationComputer sciencemedia_common.quotation_subject05 social sciencesGeneralizationCompilationInheritance (object-oriented programming)[INFO.INFO-CR]Computer Science [cs]/Cryptography and Security [cs.CR]Work (electrical)Implementation0502 economics and businessSpecialization (logic)Special sectionMathematics educationQuality (business)050207 economicsTopic areasSoftwaremedia_commonSpecialization
researchProduct

Le limitazioni al regime di circolazione e valorizzazione delle azioni e quote, profili civilistici

2022

Il presente contributo propone l'analisi di alcuni strumenti giuridici offerti dall’autonomia privata in ambito societario, in modo da permettere all’imprenditore – in tutte le ipotesi in cui quest’ultimo intenda determinare, prima della sua morte, la successione dell’azienda di famiglia – di pianificare in modo efficace il passaggio generazionale, avvantaggiando o sfavorendo, a seconda dei casi, il trasferimento delle partecipazioni societarie, con il proposito di disinnescare i rischi di disgregazione dell’unità dell’impresa e di conflitti tra i membri della famiglia. This contribution proposes the analysis of some legal instruments offered by private autonomy in the corporate sphere, in …

Passaggio generazionale Clausole di circolazione e valorizzazione delle azioni e quote Patti successori Azienda ImpresaSettore IUS/01 - Diritto PrivatoGenerational handover circulation clauses and valorisation of shares and quotas inheritance agreements company enterprise
researchProduct

Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

2001

BACKGROUNDHirschsprung disease (HSCR) is a frequent congenital disorder with an incidence of 1 in 5000 live births, characterised by the absence of parasympathetic intramural ganglion cells in the hindgut resulting in intestinal obstruction in neonates and severe constipation in infants and adults. Intestinal neuronal dysplasia (IND) shares clinical features with HSCR but the submucosal parasympathetic plexus is affected. IND has been proposed as one of the most frequent causes of chronic constipation and is often associated with HSCR.METHODSWe examined 29 patients diagnosed with sporadic HSCR, 20 patients with IND, and 12 patients with mixed HSCR/IND for mutations in the coding regions of …

Pathologymedicine.medical_specialtyGlial Cell Line-Derived Neurotrophic Factor ReceptorsHirschsprung diseaseMUTATION ANALYSISNerve Tissue ProteinsTYROSINE KINASEEDNRBArticleExonGermline mutationProto-Oncogene ProteinsNEUROTROPHIC FACTOR GDNFmedicineGlial cell line-derived neurotrophic factorDrosophila ProteinsHumansGlial Cell Line-Derived Neurotrophic FactorNerve Growth FactorsAlleleintestinal neuronal dysplasiaAllelesPolymorphism Single-Stranded ConformationalIntestinal neuronal dysplasiabiologyReceptors EndothelinSHAH-WAARDENBURG SYNDROMEProto-Oncogene Proteins c-retENDOTHELIN-B-RECEPTORMULTIGENIC INHERITANCEGastroenterologyReceptor Protein-Tyrosine KinasesSequence Analysis DNAGERMLINE MUTATIONSbiochemical phenomena metabolism and nutritionPROTOONCOGENEmedicine.diseasePHENOTYPIC-EXPRESSIONGDNFPedigreeProto-Oncogene Proteins c-retDysplasiaCase-Control StudiesMutationbiology.proteinLIGANDRETCongenital disorderEDN3
researchProduct

Differential Gene Expression of Medullary Thyroid Carcinoma Reveals Specific Markers Associated with Genetic Conditions

2013

Maliszewska, Agnieszka et al.

Pathologymedicine.medical_specialtyendocrine system diseasesInheritance PatternsMultiple endocrine neoplasia type 2ApoptosisBiologyGermlinePathology and Forensic MedicineThyroid carcinomaAntigens CDCell Line TumormedicineBiomarkers TumorGene silencingCluster AnalysisHumansGenetic Predisposition to DiseaseAC133 AntigenGene SilencingThyroid NeoplasmsRNA Small InterferingGlycoproteinsRegulation of gene expressionTissue microarrayReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingWnt signaling pathwaymedicine.diseaseImmunohistochemistryCarcinoma NeuroendocrineGene expression profilingGene Expression Regulation NeoplasticGene Knockdown TechniquesCancer researchPeptides
researchProduct

Febrile seizure and related syndromes

2018

Abstract Febrile seizures (FS) are the result of particular sensitivity to fever in the developing brain, have a major genetic predisposition, and nearly always have a benign outcome. Febrile seizures are the most common for of seizures in childhood. They have been observed in 2–6% of children before the age of 5 years, but in some populations this figure increase to 15%. Febrile seizures could be the first manifestations of epilepsy. About 13% of epileptic patients have a history of febrile seizures, and 30% have had recurrent febrile seizures Their phenotypic characteristics allow, in the majority of cases, a classification of the seizure, an elaboration of a prognosis and to assume a spe…

Pediatricsmedicine.medical_specialtybusiness.industryGeneral Neurosciencemedicine.disease03 medical and health sciencesPsychiatry and Mental healthEpilepsy0302 clinical medicineDravet syndrome030225 pediatricsAnesthesiaFebrile seizureEpilepsy syndromesGenetic predispositionMedicineMultifactorial InheritanceNeurology (clinical)Risk factorbusiness030217 neurology & neurosurgeryMedical literatureNeurology, Psychiatry and Brain Research
researchProduct

Plants mentioned in the Islamic Scriptures (Holy Qur'ân and Ahadith): Traditional uses and medicinal importance in contemporary times.

2019

Abstract Ethnopharmacological relevance Over the past thousand years, Islamic physicians have collected cultural, philosophical, sociological and historical backgrounds for understanding diseases and medications. The Prophet Mohammed (Peace Be Upon Him (PBUH) said: “There is no disease that Allah has created, except that Allah also has created its cure.” Therefore, Islamic scholars are encouraged to explore and use both traditional and modern forms of medicine. Aim of the study (1) To identify some of the medicinal plants mentioned in the Holy Qur'ân and Ahadith textbooks of the period 700–1500 AD; (2) to compare them with presently used traditional medicines; (3) to evaluate their value ba…

PharmacologyValue (ethics)0303 health sciencesModern medicineHistoryPlants Medicinalmedia_common.quotation_subjectIslamIslam03 medical and health sciences0302 clinical medicineHistory of religions030220 oncology & carcinogenesisEthnobotanyDrug DiscoveryRelevance (law)Natural (music)AnimalsHumansMedicine TraditionalSocial scienceInheritance030304 developmental biologymedia_commonJournal of ethnopharmacology
researchProduct

Violence and the Peasant Elite in Lower Satakunta (1550–1680)

2016

“The lengthy quarrels over inheritance hint that these people had fiery tempers”, wrote Mauno Jokipii in his pioneering article on the history of the Lavila family—one of the prominent families of freeholders in Lower Satakunta.1 In our study on the women from that same family, Virpi Nissila and I have encountered about 100 court cases from the 1620 to the 1650s, in which six women from two generations have been present. The most prominent of them is Anna Martensdotter who appeared in court 28 times in the four years for which we have the court minutes still intact. These records tell of her offensive behaviour: neighbours complaining about her physical violence, insults, appropriations, an…

Political sciencemedia_common.quotation_subjectEliteOffensiveSocial environmentGender studiesInheritanceViolent crimeBrotherPeasantAdministration (probate law)media_common
researchProduct

Quantized Dissensus in switching networks with nodes death and duplication* *Research supported by MURST-PRIN “Robust Techniques for uncertain system…

2009

Abstract In this paper we discuss agents exchanging quantized flows to diverge one from the others according to a dissensus protocol. A Quantized Gossip algorithm is considered. Evolutions of the states during switching intervals and at switching instants and their property are described and analyzed. The modeling of switching systems describing networks where death and duplication processes occur is described. Some properties of the topology reached by the network when different rules of duplication and inheritance are implemented.

Property (philosophy)Gossip algorithmsDistributed computingHybrid systemGene duplicationInheritance (genetic algorithm)Topology (electrical circuits)TopologyProtocol (object-oriented programming)MathematicsIFAC Proceedings Volumes
researchProduct

On the genetics of psoriasis

1973

To elucidate the mode of inheritance in psoriasis, Falconer's model for estimating heritability which is under the assumption of multifactorial inheritance, was applied to the data of Hellgren (1967) from Sweden. The heritability estimates were based on both manifest and potential psoriasis since a clear separation of these two categories was impossible. These estimates were 64% for parents, 60% for siblings and 52% for all first degree relatives which included the children of psoriatic cases. For second degree relatives it was 48%. None of these differences are statistically significant. The results are discussed.

PsoriasisSeparation (statistics)Inheritance (genetic algorithm)medicineMultifactorial InheritanceDermatologyGeneral MedicineHeritabilityBiologyFirst-degree relativesmedicine.diseaseDemographyArchiv f�r Dermatologische Forschung
researchProduct

Retinoblastoma: History of His Identification, Characterization and Treatment

2015

The first description of a tumor resembling retinoblastoma (RB) was provided on 1597 by Pieter Pauw, who described a malignancy invading the orbit, the temporal region, and the cranium, filled with a "substance similar to brain tissue mixed with thick blood and like crushed stone". Since then, a number of retinal tumors were described and named until the 1922 when Verhoeff called these tumors RB, a term that the American Ophthalmological Society adopted in 1926. In 1971 Knudson focused on RB, and proposed his ‘two-hit’ theory of the molecular etiology of RB. In 1986, the RB1 gene was identified and the ‘two-hit’ theory of Knudson was validated. Successively, new studies in developing retina…

Retinoblastomabusiness.industrymedicineCancer researchRetinoblastoma pediatric cancer RB1 gene retinoblastoma inheritance retinoblastoma therapyRb1 geneIdentification (biology)medicine.diseasebusinessPediatric cancer
researchProduct