Search results for "HIF"

showing 10 items of 1515 documents

Cognitive behavioral therapy for shift workers with chronic insomnia

2012

Abstract Objective Shift work is a challenge in the screening and treatment of chronic insomnia. The aim of this study was to examine the implementation and effectiveness of a cognitive behavioral group intervention for insomnia (CBT-I) among shift workers with chronic insomnia. We also studied whether insomnia symptoms and intervention effects differed on work days and days off. Methods The study design was a non-randomized group intervention, including a waiting period prior to CBT-I as a control condition. A total of 19 media workers who worked irregular hours and had non-organic insomnia with features of psychological insomnia completed the study. We followed up with the results for a p…

AdultMalemedicine.medical_specialtymedicine.medical_treatmentOccupational safety and healthShift work03 medical and health sciences0302 clinical medicineQuality of lifeSleep Initiation and Maintenance DisordersSurveys and QuestionnairesWork Schedule Tolerancemental disordersInsomniamedicineHumans030212 general & internal medicineCognitive Behavioral Therapybusiness.industryActigraphyGeneral MedicineActigraphy3. Good healthCognitive behavioral therapyQuality of LifePhysical therapyFemaleSleep diarySleep onset latencymedicine.symptombusiness030217 neurology & neurosurgeryClinical psychologySleep Medicine
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Solid variant of mammary "adenoid cystic carcinoma with basaloid features" merging with "small cell carcinoma"

2005

We describe a rare case of a solid variant of a mammary adenoid cystic carcinoma with basaloid features (sbACC) and its coexistence with a "small cell" carcinoma (SCC), identified and confirmed by histological and immunohistochemical observations: the absence of glandular structures and PAS-positive globules, positivity for neuroendocrine markers (NSE, synaptophysin and chromogranin), and negativity for 34betaE12 and SMA actin were the aspects suggesting the presence of SCC. Furthermore, positivity for CD10 was found both in sbA CC and in SCC, supporting the hypothesis that the two components share the same histogenetic myoepithelial origin and represent an example of dedifferentiation alon…

AdultPathologymedicine.medical_specialtyAdenoid cystic carcinoma2734Breast NeoplasmsBiologyHistogenesisSettore MED/08 - Anatomia PatologicaMastectomy SegmentalSmall-cell carcinomaPathology and Forensic MedicineNeoplasms Multiple PrimaryBiomarkers TumormedicineCarcinomaHumansBreastCarcinoma Small CellneoplasmsSmall cell carcinomaMyoepithelial cellChromogranin ABasaloid adenoid cystic carcinomaCell BiologyPeriodic Acid-Schiff Reactionmedicine.diseaseCarcinoma Adenoid CysticImmunohistochemistrystomatognathic diseasesSettore MED/18 - Chirurgia GeneraleCarcinoma Basal CellChemotherapy AdjuvantAxillaSynaptophysinbiology.proteinLymph Node ExcisionImmunohistochemistryFemaleBasaloid adenoid cystic carcinoma; Breast; Small cell carcinoma; Adult; Axilla; Biomarkers Tumor; Breast Neoplasms; Carcinoma Adenoid Cystic; Carcinoma Basal Cell; Carcinoma Small Cell; Chemotherapy Adjuvant; Female; Humans; Immunohistochemistry; Lymph Node Excision; Mastectomy Segmental; Neoplasms Multiple Primary; Periodic Acid-Schiff Reaction; 2734Breast NeoplasmHuman
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A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily

2005

Summary Background  Lipoid proteinosis (LP), also known as Urbach–Wiethe disease, is a rare autosomal recessive disorder characterized by a hoarse voice, warty skin infiltration and scarring. Mutations within the extracellular matrix protein 1 (ECM1) gene cause LP. Objectives  We report the molecular analysis of the ECM1 gene in a Sicilian patient with LP in order to extend the mutation spectrum of this genodermatosis. Methods  We studied a 32-year-old female born from consanguineous parents who was diagnosed at the age of 11 years as having LP. She has a clinical phenotype corresponding to Urbach–Wiethe disease characterized by papules/nodules, indurated plaques and sometimes ulcerated les…

AdultPathologymedicine.medical_specialtySettore MED/09 - Medicina InternaBiopsyMolecular Sequence DataNonsense mutationDermatologyBiologyUrbach–Wiethe diseasemedicine.disease_causePolymerase Chain ReactionFrameshift mutationExtracellular matrix protein 1ExonmedicineHumanseducationSicilyGeneExtracellular Matrix Proteinseducation.field_of_studyMutationBase SequenceGenodermatosisSkin Diseases Geneticmedicine.diseasePedigreeECM1 gene lipoid proteinosis mutationSettore MED/03 - Genetica MedicaCodon NonsenseLipoid Proteinosis of Urbach and WietheSettore MED/26 - NeurologiaFemaleBritish Journal of Dermatology
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Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent

2006

Familial hypercholesterolemia (FH) is an autosomal dominant inherited disease caused by mutations in the gene coding for the low density lipoprotein receptor (LDL-R). It is characterized by a high concentration of low density lipoprotein (LDL), which frequently gives rise to premature coronary artery disease. We studied the probands of five FH Sicilian families with 'definite' FH and one proband of Paraguayan descent with homozygous FH who has been treated with an effective living-donor liver transplantation. In order to seek the molecular defect in these six families, we used direct sequencing to define the molecular defects of the LDL-R gene responsible for the disease. We described three…

AdultProbandhypercholesterolemia LDL receptor gene mutation analysis direct sequencing splicing living-donor transplantationSettore MED/09 - Medicina InternaDNA Mutational AnalysisDirect sequencingHypercholesterolemiaFamilial hypercholesterolemiaBiologyGene mutationSplicingmedicine.disease_causeFrameshift mutationHyperlipoproteinemia Type IIExonGeneticsmedicineHumansMissense mutationRNA MessengerChildSicilyCells CulturedLiving-donor transplantationLDL receptor geneGeneticsMutationIntronExonsGeneral MedicineMiddle Agedmedicine.diseaseLipidsMolecular biologyPedigreeDirect sequencing; Hypercholesterolemia; LDL receptor gene; Living-donor transplantation; Mutation analysis; SplicingMutation analysisReceptors LDLParaguayChild PreschoolMutationBiological Assay
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Similar contributions of BRCA1 and BRCA2 germline mutations to early-onset breast cancer in Germany.

2003

This study was undertaken to investigate the prevalence of BRCA1 and BRCA2 germline mutations in 91 German patients unselected for family history, who were diagnosed with breast cancer before the age of 41 years. Clinical information and blood samples were obtained from all patients. A comprehensive BRCA1 and BRCA2 mutational analysis was performed using the protein truncation assay and single-strand conformational polymorphism analysis followed by DNA sequencing of variant signals detected by these assays. Five different deleterious germline mutations including four frameshift mutations and one missense mutation were identified, three in BRCA1 (3.3%) and two mutations (2.2%) in BRCA2. Both…

Adultendocrine system diseasesDNA Mutational AnalysisGenes BRCA2Genes BRCA1Mutation MissenseBreast NeoplasmsDiseaseBiologyGenetic determinismDNA sequencingFrameshift mutationGermline mutationBreast cancerGermanyGeneticsmedicineMissense mutationHumansGenetic TestingFamily historyskin and connective tissue diseasesFrameshift MutationGenetics (clinical)Germ-Line MutationGeneticsmedicine.diseaseFemaleEuropean journal of human genetics : EJHG
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Synthesis, characterization of diorganotin(IV) complexes of N-(2-hydroxyarylidene)aminoacetic acid and antitumour screening in vivo in ehrlich ascite…

2001

Some new diorganotin(IV) complexes have been prepared by reacting potassium N-(2-hydroxyarylidene)aminoacetate with R2SnCl2(R = Me,nBu,Ph). The complexes have been characterized by 1H,13C,119Sn NMR, IR and 119mSn Mössbauer spectroscopic techniques in combination with elemental analysis. In the solid state, the complexes possess penta- and hexa-coordinated tin centres. The hexa-coordinated tin complexes were found to dissociate in solution, giving rise to penta-coordinated species as revealed by 119Sn NMR spectroscopy. Antitumour screening in vivo of the complexes L4snPh2,L4SnPh2· Ph3SnCl and L4SntBU2·t Bu2SnCl2 (L4 = N-(2-hydroxyacetophenone)aminoacetate) is also reported. Copyright © 2001 …

AldiminesynthesisStereochemistryMossbauer spectroscopyInfrared spectroscopyAntitumour activityanimal cellantineoplastic activitydissociationChemical synthesisMedicinal chemistryEhrlich ascites tumor cellEhrlich ascites carcinomaInorganic Chemistryin vivo studychemistry.chemical_compoundAcetic acidOrganotinmalecomplex formationorganotin compoundcontrolled studyCarboxylateinfrared spectroscopyEhrlich ascites carcinoma cellmouseglycine derivativenuclear magnetic resonance spectroscopychemistry.chemical_classificationSchiff basenonhumananimal modelarticleGeneral ChemistryNuclear magnetic resonance spectroscopysolid stateNMRAmino acidchemistryreaction analysiSettore CHIM/03 - Chimica Generale E InorganicaIRSchiff baseschemical analysi
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Nonlocalization Properties of Time Operators Transformations

2014

It is presented a general approach to the problem of extension of time operators and the associated Lambda transformations on singular measures. It is also shown that Lambda transformations defined on function spaces having the Urysohn property are non localized. Particular attention has been devoted to time and Lambda operators associated with the Walsh-Paley system and to a characterization of their domain and non locality.

AlgebraPure mathematicsProperty (philosophy)Physics and Astronomy (miscellaneous)Function spaceGeneral MathematicsExtension (predicate logic)Characterization (mathematics)Operator theoryLambdaShift operatorDomain (mathematical analysis)MathematicsInternational Journal of Theoretical Physics
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Elliptic convolution operators on non-quasianalytic classes

2001

For those nonquasianalytic classes in which an extension of the classical Borel's theorem holds we show that every elliptic convolution operator is the composition of a translation and an invertible ultradifferential operator. This answers a question asked by Chou in: La transformation de Fourier complexe et l'equation de convolution, LNM 325, Berlin-Heidelberg-New York (1973).

AlgebraSemi-elliptic operatorsymbols.namesakeOperator (computer programming)Fourier transformGeneral MathematicssymbolsConvolution theoremConvolution powerShift operatorCircular convolutionConvolutionMathematicsArchiv der Mathematik
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Waveguiding properties of a photonic crystal fiber with a solid core surrounded by four large air holes

2009

The polarization-dependent guiding properties of a hexagonal-lattice photonic crystal fiber with a solid-core surrounded by four large air holes are investigated. The appearance of a polarization dependent cutoff frequency, together with several parameters as the birefringence, the modal effective area, the group velocity dispersion and the polarization dependent loss are analyzed. A collection of fibers with different structural parameters were fabricated and characterized. An effective anti-guide structure from at least 450 nm to 1750 nm, a polarizing fiber with a polarization dependent loss of 16 dB/m at 1550 nm, and an endlessly singlemode polarization-maintaining fiber with group biref…

All-silica fiberMaterials scienceOptical fiberPhysics::OpticsPolarization-maintaining optical fiberSensitivity and SpecificityGraded-index fiberlaw.inventionDouble-clad fiberOpticslawScattering RadiationDispersion-shifted fiberComputer SimulationOptical FibersPhotonsbusiness.industryReproducibility of ResultsEquipment DesignMicrostructured optical fiberModels TheoreticalÒpticaAtomic and Molecular Physics and OpticsEquipment Failure AnalysisComputer-Aided DesignOptoelectronicsCristallsCrystallizationbusinessPhotonic-crystal fiber
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Sensitivity optimization with cladding-etched long period fiber gratings at the dispersion turning point

2016

This work presents a refractive index sensor based on a long period fiber grating (LPFG) made in a reduced cladding fiber whose low order cladding modes have the turning point at large wavelengths. The combination of these parameters results in an improved sensitivity of 8734 nm/refractive index unit (RIU) for the LP0,3 mode in the 1400-1650 wavelength range. This value is similar to that obtained with thin-film coated LPFGs, which permits to avoid the coating deposition step. The numerical simulations are in agreement with the experimental results. This work was supported in part by the Spanish Ministry of Education and Science-FEDER TEC2013-43679-R. J.L. Cruz also acknowledges financial s…

All-silica fiberMaterials sciencebusiness.industry010401 analytical chemistryFiber optics sensorsLong-period fiber gratingCladding (fiber optics)01 natural sciencesGraded-index fiberAtomic and Molecular Physics and Optics0104 chemical sciencesFibers single-mode010309 opticsOpticsDouble-clad fiberNormalized frequency (fiber optics)Fiber Bragg grating0103 physical sciencesFiber Bragg gratingsDispersion-shifted fiberbusinessOptics Express
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