Search results for "IDIFO"

showing 9 items of 9 documents

Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report.

2005

A newborn with an unusual association of hepatic mesenchymal hamartoma and mesenchymal stem villous hyperplasia of the placenta is presented. At birth, the large hepatic mass caused severe respiratory distress necessitating early surgical intervention. This report on the association of hepatic mesenchymal hamartoma and mesenchymal stem villous hyperplasia of the placenta strongly suggests a common pathogenetic origin of the 2 lesions.

Adultcongenital hereditary and neonatal diseases and abnormalitiesPathologymedicine.medical_specialtyHepatic massHamartomaPlacentaUltrasonography PrenatalDiagnosis DifferentialMesodermPostoperative ComplicationsPregnancyPlacentamedicineEdemaHepatectomyHumansRespiratory Distress Syndrome NewbornHyperplasiaRespiratory distressbusiness.industryLiver DiseasesMesenchymal stem cellInfant NewbornGeneral MedicineHydatidiform MoleHyperplasiamedicine.diseaseJaundice Obstructivemedicine.anatomical_structureHepatic Mesenchymal Hamartomaembryonic structuresPediatrics Perinatology and Child HealthUterine NeoplasmsSurgeryFemaleChorionic VillibusinessJournal of pediatric surgery
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Integrative taxonomy of crustacean y-larvae (Thecostraca: Facetotecta) using laboratory-rearing and molecular analyses of single specimens, with the …

2022

AbstractFacetotecta, the taxon established for ‘y-larvae’, is the last major crustacean group for which the adult stage remains unknown. With only 14 described nominal species, all in the genus Hansenocaris, their incompletely known life cycle, small size and dearth of molecular data have hampered assessments of their true species diversity. Based on field studies during which > 11 000 y-larvae were sampled, a new integrative approach for studying the taxonomy of y-larvae is outlined. It focuses on last-stage nauplii and y-cyprids and includes methods for rearing lecithotrophic y-larvae for documenting the morphology of specimens with live photomicroscopy and scanning electron micros…

ArthropodaDemodicidaeArachnidaAnimaliaAnimal Science and ZoologyBiologia marinaTrombidiformesBiodiversityEcology Evolution Behavior and SystematicsTaxonomy
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2002

by Mohamed Elbandya), Tomofumi Miyamotob), Cle¬ment Delaudec), and Marie-Aleth Lacaille-Dubois*a) a) Laboratoire de Pharmacognosie, Unite¬ de Mole¬cules d×Inte¬re√ t Biologique (UMIB JE 2244), Faculte¬ de Pharmacie, Universite¬ de Bourgogne, 7 Bd Jeanne d×Arc, BP 87900, F-21079 Dijon Cedex b) Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan c) Centre de Recherche Phytochimique, Universite¬ de Lieige, Institut de Chimie-B6, Sart Tilman B-4000-Lieige I

Inorganic ChemistryStereochemistryChemistryMuraltia ononidifoliaOrganic ChemistryDrug DiscoveryPhysical and Theoretical ChemistryBiochemistryCatalysisMedicagenic acidHelvetica Chimica Acta
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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting…

2020

Abstract Background PADI6 is a component of the subcortical maternal complex, a group of proteins that is abundantly expressed in the oocyte cytoplasm, but is required for the correct development of early embryo. Maternal-effect variants of the subcortical maternal complex proteins are associated with heterogeneous diseases, including female infertility, hydatidiform mole, and imprinting disorders with multi-locus imprinting disturbance. While the involvement of PADI6 in infertility is well demonstrated, its role in imprinting disorders is less well established. Results We have identified by whole-exome sequencing analysis four cases of Beckwith-Wiedemann syndrome with multi-locus imprintin…

MaleBeckwith-Wiedemann SyndromeGenomic imprintingMulti-locus imprinting disturbanceBeckwith–Wiedemann syndromeWhole Exome SequencingProtein-Arginine Deiminase Type 60302 clinical medicinePregnancyImprinting (psychology)ChildGenetics (clinical)Genetics0303 health sciencesDNA methylationPADI6Beckwith-Wiedemann syndrome; DNA methylation; Genomic imprinting; Infertility; Maternal-effect variants; Multi-locus imprinting disturbance; PADI6; Subcortical maternal complex; Adolescent; Adult; Beckwith-Wiedemann Syndrome; Child Preschool; DNA Methylation; Female; Genomic Imprinting; Heterozygote; Humans; Hydatidiform Mole; Infant; Infertility Female; Male; Maternal Inheritance; Mutation; Oocytes; Pedigree; Phenotype; Pregnancy; Protein-Arginine Deiminase Type 6; Siblings; Whole Exome SequencingFemale infertilityMaternal effectHydatidiform MolePedigreePhenotypeChild Preschool030220 oncology & carcinogenesisDNA methylationFemaleMaternal InheritanceInfertility FemaleAdultHeterozygoteAdolescentSubcortical maternal complexBiology03 medical and health sciencesExome SequencingGeneticsmedicineHumansMaternal-effect variantsPreschoolMolecular BiologyLoss function030304 developmental biologyMaternal-effect variantResearchSiblingsInfantmedicine.diseaseHuman geneticsInfertilityMutationOocytesGenomic imprintingDevelopmental BiologyClinical Epigenetics
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Specific expression patterns of epithelial to mesenchymal transition factors in gestational molar disease.

2015

Introduction The epithelial to mesenchymal transition, a well-known and re-emerging model in pathology, has not been completely investigated in the field of gestational pathology. This study aims at improving the comprehension of this process in molar disease, even looking for new possible immunohistochemical markers. Materials and methods We have analysed the immunohistochemical expression of Twist1 and Snai2, two of the most important transcription factors involved in epithelial to mesenchymal transition, in formalin-fixed paraffin-embedded samples of 23 spontaneous abortive pregnancies, 22 molar pregnancies (10 partial and 12 complete) and 7 term placentas. Results Twist1 and Snai2 were …

MolarPathologymedicine.medical_specialtyStromal cellEpithelial-Mesenchymal TransitionBiologyPregnancymedicineHumansEpithelial–mesenchymal transitionTwistClaudinComplete mole; EMT; Molar disease; Snai2; Twist; Twist1; Obstetrics and Gynecology; Reproductive Medicine; Developmental BiologyCadherinTwist-Related Protein 1EMTObstetrics and GynecologyTrophoblastNuclear ProteinsHydatidiform MoleImmunohistochemistryComplete mole; EMT; Molar disease; Snai2; Twist; Twist1Complete moleSNAI2Molar diseasemedicine.anatomical_structureReproductive MedicineSnai2Case-Control StudiesImmunohistochemistryFemaleSnail Family Transcription FactorsBiomarkersTwist1Developmental BiologyTranscription FactorsPlacenta
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Obstetrics outcomes after complete and partial molar pregnancy: Review of the literature and meta-analysis.

2021

The hydatidiform mole is a rare gynecological disease rising from the trophoblastic. Post-molar pregnancies have an extremely variable course, varying from repeated abortions, stillbirths, preterm births, live births, or recurring in further molar pregnancies. Literature on obstetric outcomes following molar pregnancy is poor, often including monocentric studies, and with data collected from national databases. This review and meta-analysis aim to analyze the obstetric outcomes after conservative management of complete (CHM) and partial (PHM) molar pregnancies. The meta-analysis was performed following the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) and the preferred repo…

Molarmedicine.medical_specialtyMiscarriage03 medical and health sciences0302 clinical medicineMolar pregnancyPregnancyEpidemiologymedicineHumans030212 general & internal medicinePregnancy030219 obstetrics & reproductive medicineObstetricsbusiness.industryInfant NewbornObstetrics and GynecologyHydatidiform Molemedicine.diseaseConfidence intervalObstetricsSystematic reviewReproductive MedicineMeta-analysisUterine NeoplasmsPremature BirthFemaleNeoplasm Recurrence LocalbusinessEuropean journal of obstetrics, gynecology, and reproductive biology
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Il modulo "Meccanica Statistica e Struttura della Materia"

2010

Settore FIS/08 - Didattica E Storia Della FisicaMeccanica statisticaFormazione insegnantiIDIFO
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Foldameerien isäntä-vieraskemia

2017

Tutkielman kirjallisessa osassa tarkastellaan foldameerejä isäntä-vieraskemian näkökulmasta. Foldameerit voivat sitoa rakenteeseensa erilaisia vierasmolekyylejä, jolloin muodostuu isäntä-vieraskomplekseja. Kirjallisuudesta valittiin tarkasteluun mielenkiintoisimpia anioneja, kationeja ja neutraaleja vierasmolekyylejä sitovia foldameereja ja perehdyttiin niiden vuorovaikutuksiin. Lisäksi tarkasteltiin vierasmolekyylin sitoutumisen aikaansaamia muutoksia foldameerien konformaatiossa. Kokeellisen osan tarkoituksena oli syntetisoida pitkä, 11 aromaattista rengasta sisältävä aryyliamidifoldameeri käyttäen hyväksi pääasiassa peptidikytkentäreaktioita. Koska synteesi osoittautui erittäin haasteell…

anionitaryyliamidifoldameerikationitfoldameeritpeptidikytkentä
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Quill mites (Acari: Syringophilidae) from Aegithalos caudatus (Passeriformes: Aegithalidae)

2004

Three species of syringophilid mites (Acari: Syringophilidae) were collected from quills of Aegithalos caudatus (Passeriformes: Aegithalidae) in Poland, Picobia caudati sp. n. from body feathers, Dissonus scirpaceus Skoracki, 1999 from rectrices, and Syringophilopsis aegithali Bochkov et al., 2001 from secondaries.

food.ingredientArthropodaZoologyTrombidiformesfoodArachnidaAnimaliaAcariSyringophilidaeEcology Evolution Behavior and SystematicsTaxonomyDissonidaeSiphonostomatoidabiologyEcologyAegithalidaeAegithalos caudatusBiodiversitybiology.organism_classificationFlight featherSyringophilopsisFeathervisual_artvisual_art.visual_art_mediumAnimal Science and ZoologySyringophilidaeMaxillopoda
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