Search results for "Forming"

showing 10 items of 1719 documents

Coexpression of extracellular matrix glycoproteins undulin and tenascin in human autosomal dominant polycystic kidney disease.

1993

Autosomal dominant polycystic kidney disease (ADPKD) is the most common entity of cystic diseases of the kidney leading to end-stage renal insufficiency. Changes in extracellular matrix (ECM) are regarded to be an important pathogenic factor connected with the genes assumed to be responsible for human ADPKD. In order to assess the biological significance of altered expression and deposition of ECM glycoproteins for human ADPKD at molecular levels fresh-frozen tissue from ADPKD kidneys, fetal kidneys and normal adult kidneys were comparatively tested by immunohistochemistry for the presence of multifunctional ECM glycoproteins undulin, tenascin and fibronectin, interstitial collagen types I,…

Pathologymedicine.medical_specialtyCell Adhesion Molecules NeuronalAutosomal dominant polycystic kidney diseaseTenascinGene ExpressionKidneyExtracellular matrixFetusLamininTransforming Growth Factor betamedicineHumansRNA MessengerCells CulturedGlycoproteinsBasement membraneKidneyExtracellular Matrix Proteinsbiologyurogenital systemTenascinmedicine.diseasePolycystic Kidney Autosomal DominantImmunohistochemistryEpitheliumCell biologyFibronectinsFibronectinmedicine.anatomical_structurebiology.proteinCollagenLamininNephron
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Dupuytren's contracture: an update of biomolecular aspects and therapeutic perspectives.

2005

The so-called fibrogenic cytokines, able to induce the growth of fibroblasts and their differentiation into myofibroblasts and to stimulate their production of extracellular matrix, are involved in the genesis of Dupuytren’s contracture. Although many studies have been made of biomolecular aspects of palmar fibromatosis, practical applications from them are still far from imminent because of the real difficulty of blocking their action in vivo, even in a chronic, progressive lesion such as Dupuytren’s disease. Consequently, surgical excision of the palmar fascia still remains the treatment of choice.

Pathologymedicine.medical_specialtyGENETIC SUSCEPTIBILITYFIBRONECTINBioinformaticsDISEASEExtracellular matrixTransforming Growth Factor betamedicineFIBROSISHumansGenetic Predisposition to DiseaseDupuytren's contracturePlatelet-Derived Growth FactorTransplantationEpidermal Growth Factorbusiness.industryGROWTH-FACTOR-BETANONOPERATIVE TREATMENTSTEROIDSFibromatosisGranulocyte-Macrophage Colony-Stimulating FactorTissue Inhibitor of MetalloproteinasesFasciaASSOCIATIONmedicine.diseaseHandCOLLAGENFasciotomyFibronectinsbody regionsDupuytren Contracturemedicine.anatomical_structureMetalloproteasesSurgeryContracturemedicine.symptombusinessPalmar fasciaMyofibroblastMATRIXPalmar FibromatosisJournal of hand surgery (Edinburgh, Scotland)
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Pathobiology of Hodgkin Lymphoma

2010

Despite its well-known histological and clinical features, Hodgkin's lymphoma (HL) has recently been the object of intense research activity, leading to a better understanding of its phenotype, molecular characteristics, histogenesis, and possible mechanisms of lymphomagenesis. There is complete consensus on the B-cell derivation of the tumor in most cases, and on the relevance of Epstein-Barr virus infection and defective cytokinesis in at least a proportion of patients. The REAL/WHO classification recognizes a basic distinction between lymphocyte predominance HL (LP-HL) and classic HL (cHL), reflecting the differences in clinical presentation and behavior, morphology, phenotype, and molec…

Pathologymedicine.medical_specialtybusiness.industryMixed cellularityLymphocyteHematologyReview ArticleHistogenesismedicine.diseasePhenotypeVirusLymphomaPathobiologymedicine.anatomical_structurehemic and lymphatic diseasesmedicineHodgkin lymphomaDiseases of the blood and blood-forming organsRC633-647.5businessWho classificationHodgkin lymphoma; microenvironment.Hodgkin lymphomamicroenvironment.Advances in Hematology
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Transfer of the active form of transforming growth factor-beta 1 gene to newborn rat lung induces changes consistent with bronchopulmonary dysplasia.

2003

Bronchopulmonary dysplasia is a chronic lung disease of premature human infancy that shows pathological features comprising varying sized areas of interstitial fibrosis in association with distorted large alveolar spaces. We have previously shown that transfer of active transforming growth factor (TGF)-beta 1 (AdTGF beta 1(223/225)) genes by adenovirus vector to embryonic lungs results in inhibition of branching morphogenesis and primitive peripheral lung development, whereas transfer to adult lungs results in progressive interstitial fibrosis. Herein we show that transfer of TGF-beta1 to newborn rat pups results in patchy areas of interstitial fibrosis developing throughout a period of 28 …

Pathologymedicine.medical_specialtymedicine.medical_treatmentPulmonary FibrosisPathology and Forensic MedicineRats Sprague-DawleyTransforming Growth Factor beta1FibrosisTransforming Growth Factor betaPulmonary fibrosismedicineAnimalsHumansLungBronchopulmonary DysplasiaLungbiologyRespiratory diseaseGene Transfer TechniquesInfant NewbornTransforming growth factor betarespiratory systemmedicine.diseaseRatsDisease Models AnimalCytokinemedicine.anatomical_structureBronchopulmonary dysplasiaAnimals Newbornbiology.proteinAnimal ModelTransforming growth factorThe American journal of pathology
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Splenomegaly Impacts Prognosis in Essential Thrombocythemia and Polycythemia Vera: A Single Center Study

2019

Splenomegaly is one of the major clinical manifestations of primary myelofibrosis and is common also in other chronic Philadelphia-negative myeloproliferative neoplasms, causing symptoms and signs and affecting quality of life of patients diagnosed with these diseases. We aimed to study the impact that such alteration has on thrombotic risk and on the survival of patients with essential thrombocythemia and patients with Polycythemia Vera (PV). We studied the relationship between splenomegaly (and its grade), thrombosis and survival in 238 patients with et and 165 patients with PV followed at our center between January 1997 and May 2019.

Pediatricsmedicine.medical_specialtySingle CenterArticle03 medical and health sciences0302 clinical medicinePolycythemia veraQuality of lifehemic and lymphatic diseasesmedicineMyelofibrosisPolycythemia VeraThrombotic riskessential thrombocythemiaEssential thrombocythemiabusiness.industrylcsh:RC633-647.5Hematologylcsh:Diseases of the blood and blood-forming organsmedicine.diseaseThrombosis030220 oncology & carcinogenesisSplenomegalysplenomegaly; polycythemia vera; essential thrombocythemiabusiness030215 immunologyHematology Reports; Volume 11; Issue 4; Pages: 8281
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Nonsense-mediated decay mechanism is a possible modifying factor of clinical outcome in nonsense cd39 beta thalassemia genotype

2012

Nonsense-mediated mRNA decay (NMD) is a surveillance system to prevent the synthesis of non-functional proteins. In β-thalassemia, NMD may have a role in clinical outcome. An example of premature translation stop codons appearing for the first time is the β-globin cd39 mutation; when homozygous, this results in a severe phenotype. The aim of this study was to determine whether the homozygous nonsense cd39 may have a milder phenotype in comparison with IVS1,nt110/cd39 genotype. Genotypes have been identified from a cohort of 568 patients affected by β-thalassemia. These genotypes were compared with those found in 577 affected fetuses detected among 2292 prenatal diagnoses. The…

Pediatricsmedicine.medical_specialtymedia_common.quotation_subjectNonsense-mediated decayNonsenseBeta thalassemiaBiologynonsense-mediated mRNA decay; beta-thalassemia; clinical outcame; beta-globin gene mutationsmedicine.diseaseGastroenterologynonsense-mediated mRNA decay beta-thalassemia beta-globin gene mutationsnonsense-mediated mRNA decay beta-thalassemia clinical outcame beta-globin gene mutations.Internal medicineGenotypemedicineDiseases of the blood and blood-forming organsRC633-647.5media_commonThalassemia Reports
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Performing Arts

2012

Performing arts Cultural Economics Public PolicySettore SECS-P/01 - Economia Politica
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Study of forming mechanics of magnetic field–assisted single point incremental forming

2022

This paper describes the forming characteristics and mechanics of magnetic field–assisted single point incremental forming (M-SPIF) in which an Nd-Fe-B magnet ball tool is placed on top of a piece of sheet metal and is driven by an Nd-Fe-B magnet placed below the workpiece. To gain an understanding of the force mechanics that power M-SPIF, the tool motion and forming force were experimentally analyzed. In M-SPIF, the forming force is applied multi-directionally, and the resultant force direction is nearly colinear with the polarity of the permanent magnet ball tool. This suggests that the forming characteristics in M-SPIF may be controllable by controlling the magnetic polarity of the tool.

Permanent magnet toolStrategy and ManagementManagement Science and Operations ResearchSingle point increment formingIndustrial and Manufacturing EngineeringAluminum
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Gendered power relations in the digital age : an analysis of Japanese women’s media choice and use within a global context

2021

This study investigates the persistence of gendered choice and use of media, particularly in Japanese domestic settings. It shows how women’s significant presence in the digital media environment does not necessarily translate into substantial changes in gendered power dynamics in choosing and using particular media for certain purposes at home. This project’s authors, researchers from Argentina, Finland, Israel, Japan, and the US, analyzed interview data from Japan by drawing on the Foucauldian concept of micro-level power, which is categorized into three main types: personal authority, media affordances, and space-time constellations. Through this process, we interviewed 77 individuals, r…

Persistence (psychology)naisetVisual Arts and Performing Artsmediankäyttödomestic settings [media use]micro-level powerContext (language use)käyttömedia choiceDigital mediasukupuoliGender StudiesMedia useCross-national researchSociologystereotypiatjapanilaisetbusiness.industryCommunicationmediaPower relationsGender studiespatriarkaalisuusjoukkoviestimetcross-national researchsukupuoliroolitMedia choicemiehetbusinessvalta
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MacLean, Sally-Beth, gen. ed. REED Online. Database

2019

PhilosophyHistoryHistory and Philosophy of ScienceLiterature and Literary TheoryVisual Arts and Performing Artsmedia_common.quotation_subjectOnline databaseLibrary scienceArtMusicmedia_commonRenaissance and Reformation
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