Search results for "Placenta"

showing 10 items of 153 documents

The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot…

2020

Introduction. Evaluation of the first trimester uterine artery flow can predict the development of obstetrical complications. A genotype, making women prone to microthrombi. constitutes the main known susceptibility factor for anomalous development of placenta. Our aim was to study whether polymorphisms of 10 genes leading to blood clotting abnormalities are related to abnormal uterine artery blood flow in the first trimester, and may predict placenta-related diseases. Material and methods. In primary analyses we included 19 singleton pregnancies with abnormal blood flow in the uterine arteries during the first trimester of gestation, and 24 matched control with normal flow patterns. All pa…

Clinical BiochemistryPhysiology030204 cardiovascular system & hematologyArticlePreeclampsiaCorrelation03 medical and health sciences0302 clinical medicinegenetic polymorphismsPlacentamedicine.arteryGenotypemedicineUterine arterylcsh:R5-920030219 obstetrics & reproductive medicineabnormal uterine artery flowbiologybusiness.industryBlood flowmedicine.diseasemedicine.anatomical_structureMethylenetetrahydrofolate reductasebiology.proteinGestationHuman medicinebusinesslcsh:Medicine (General)Diagnostics
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Human fetal adrenal hydroxysteroid sulphotransferase: cDNA cloning, stable expression in V79 cells and functional characterisation of the expressed e…

1995

Dehydroepiandrosterone sulphate (DHEAS) is a major adrenal secretory product, particularly in the fetus where it serves as a substrate for oestrogen biosynthesis by the placenta. The enzyme in the adrenal responsible for synthesising DHEAS, hydroxysteroid sulphotransferase (HST), is therefore essential for human development. We have isolated a full-length cDNA clone, encoding human fetal adrenal HST, and constructed a stable cell line expressing it by transfection into V79 Chinese hamster lung fibroblast cells. This cDNA was essentially identical to that isolated from adult human liver, where the role of HST is less well understood. This recombinant cell line allowed determination of the su…

DNA ComplementaryMolecular Sequence DataGene ExpressionDehydroepiandrosteroneBiologyAndrosteroneTransfectionBiochemistryCell LineSubstrate Specificitychemistry.chemical_compoundCricetulusEndocrinologyCricetinaeComplementary DNAPlacentaAdrenal GlandsmedicineAnimalsHumansAmino Acid SequenceCloning MolecularLungMolecular Biologychemistry.chemical_classificationAndrosteroneBase SequenceSulfatesDehydroepiandrosteroneTransfectionRecombinant ProteinsEnzymemedicine.anatomical_structurechemistryBiochemistryCell culturePregnenolonePregnenoloneSulfotransferaseshormones hormone substitutes and hormone antagonistsmedicine.drugMolecular and Cellular Endocrinology
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Very early prenatal diagnosis of Cockayne’s syndrome by coelocentesis

2022

Cockayne’s syndrome (CS) is a rare autosomal recessive multisystem disease characterised by early severe progression of symptoms. This study reports the feasibility of earlier prenatal diagnosis of CS by coelocentesis at 8 weeks of gestation respect to amniocentesis or villocentesis. Three couples at risk for CS asked to perform prenatal diagnosis by coelocentesis. Coelomic fluid was aspired from coelomic cavity in four singleton pregnancy at 8 weeks of gestation and 40 foetal cells were recovered by micromanipulator. Maternal DNA contamination was evaluated by quantitative fluorescent PCR (QF-PCR) and target regions of foetal DNA containing parental mutations of ERCC6 gene were amplified a…

ERCC6Sex FactorsPregnancyPlacentaPrenatal diagnosisHumansObstetrics and GynecologyFemaleCelocentesis Cockayne’s syndrome Coelomic fluid CSBDNAPolymerase Chain ReactionFoetal cell
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Is the PGM1 locus subject to selection?

1973

The placental phosphoglucomutase phenotypes controlled by the first locus of 235 German and 119 non-German samples were determined. Both in the pooled material and in the sample containing German subjects only there was a significant deviation from the expected Hardy-Weinberg equilibrium. A segregation analysis of 1174 families also revealed significant deviations in the phenotypes of the children, though the mating frequencies were as expected. The distribution of the children's phenotypes deviated significantly from Hardy-Weinberg equilibrium though this was not found in the parent samples. The results are discussed.

ElectrophoresisErythrocytesDenmarkPlacentaLocus (genetics)BiologyGermanPregnancyPGM1GeneticsHumansMetabolic diseaseSelection GeneticMolecular BiologyGenetics (clinical)GeneticsPolymorphism GeneticGermany WestBlood Protein Electrophoresislanguage.human_languageGenetics PopulationPhenotypeEnglandGenesPhosphoglucomutaselanguagePhosphoglucomutaseFemaleHumangenetik
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Fetal presentation of Morquio disease type A.

1992

A fetus with mucopolysaccharidosis type IV A (Morquio type A) is described. The family had one affected child exhibiting symptoms of classical Morquio A disease, and late in the subsequent pregnancy prenatal diagnosis was requested. At 23 weeks' gestation, moderate ascites was detected by detailed ultrasound scan and keratan sulphate was found in the amniotic fluid. The pregnancy was terminated by prostaglandin induction and the diagnosis of mucopolysaccharidosis type IV A was confirmed by demonstration of a deficiency of N-acetylgalactosamine-6-sulphate (GalNac-6-S) sulphatase in cultured amniotic cells and in post-mortem fibroblast cultures. The activities of beta-galactosidase and arylsu…

ElectrophoresisMalemedicine.medical_specialtyAmniotic fluidPlacentaMucopolysaccharidosis type IVNeuraminidasePrenatal diagnosisConsanguinityPregnancyHydrops fetalisInternal medicineLysosomal storage diseaseMedicineHumansChildGenetics (clinical)GlycosaminoglycansUltrasonographyFetusPregnancybusiness.industryObstetrics and GynecologyAscitesMucopolysaccharidosis IVmedicine.diseaseAmniotic Fluidbeta-GalactosidaseEndocrinologyKeratan SulfatePregnancy Trimester SecondMucopolysaccharidosis IVAmniocentesisFemaleSulfatasesbusinessPrenatal diagnosis
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Prenatal exposure to mixtures of xenoestrogens and repetitive element DNA methylation changes in human placenta

2014

BACKGROUND: Prenatal exposure to endocrine disrupting compounds (EDCs) has previously shown to alter epigenetic marks. OBJECTIVES: In this work we explore whether prenatal exposure to mixtures of xenoestrogens has the potential to alter the placenta epigenome, by studying DNA methylation in retrotransposons as a surrogate of global DNA methylation. METHODS: The biomarker total effective xenoestrogen burden (TEXB) was measured in 192 placentas from participants in the longitudinal INMA Project. DNA methylation was quantitatively assessed by bisulfite pyrosequencing on 10 different retrotransposons including 3 different long interspersed nuclear elements (LINEs), 4 short interspersed nuclear …

Embaràs -- ComplicacionsAdultMalemedicine.medical_specialtyPlacentaEndocrine Disruptors010501 environmental sciencesBiology01 natural sciencesStatistics NonparametricArticleRepetitive ElementCohort Studies03 medical and health sciencesSex FactorsPregnancyInternal medicinePlacentamedicineHumansEndocrine systemLongitudinal StudiesEpigeneticsPrenatal exposurelcsh:Environmental sciencesChromatography High Pressure Liquid030304 developmental biology0105 earth and related environmental sciencesGeneral Environmental Sciencelcsh:GE1-3500303 health sciencesEstrogensHuman placentaDNA Methylation3. Good healthPlacenta -- MetabolismeBiomarkerLong Interspersed Nucleotide ElementsEndocrinologymedicine.anatomical_structureMaternal ExposureSpainDNA methylationBody BurdenRegression AnalysisEnvironmental PollutantsFemaleMetilacióEnvironment International
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Developmental programming of adult haematopoiesis system

2019

The Barker hypothesis of ‘foetal origin of adult diseases’ has led to emphasize the concept of ‘developmental programming’, based on the crucial role of epigenetic factors. Accordingly, it has been demonstrated that parental adversity (before conception and during pregnancy) and foetal factors (i.e., hypoxia, malnutrition and placental insufficiency) permanently modify the physiological systems of the progeny, predisposing them to premature ageing and chronic disease during adulthood. Thus, an altered functionality of the endocrine, immune, nervous and cardiovascular systems is observed in the progeny. However, it remains to be understood whether the haematopoietic system itself also repres…

Epigenomics0301 basic medicineAgingHaematopoietic systemPro-health interventionHematopoietic SystemAgeing-related diseasePsychological interventionPlacental insufficiencyBiochemistryFoetal programmingDevelopmental psychologyFetal Development03 medical and health sciences0302 clinical medicinePregnancymedicineSettore MED/05 - Patologia ClinicaAnimalsHumansEndocrine systemEpigeneticsMolecular BiologyPregnancySettore BIO/11business.industryEpigeneticmedicine.diseaseHaematopoiesisMalnutrition030104 developmental biologyNeurologyFemaleEpigeneticsbusinessDevelopmental programmingAgeing-related disease; Epigenetics; Foetal programming; Haematopoietic system; Pro-health intervention030217 neurology & neurosurgeryBiotechnologyAgeing Research Reviews
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Placental DNA methylation signatures of maternal smoking during pregnancy and potential impacts on fetal growth.

2021

We would like to thank all the families that participated in these studies for their generous contribution. Detailed acknowledgements and funding can be found in Sup plementary Material.

EpigenomicsMaternal smokingPlacentaGeneral Physics and AstronomyReproductive health and childbirthBioinformaticsLow Birth Weight and Health of the NewbornEpigenesis GeneticFetal DevelopmentPregnancyInfant MortalityFetal growth2.1 Biological and endogenous factorsAetiologyPediatricMultidisciplinaryQSmokingCord bloodDNA methylationEpigeneticsFemalemedicine.symptomScience1.1 Normal biological development and functioningInflammationFetus -- Trastorns del creixementBiologyGeneral Biochemistry Genetics and Molecular BiologyArticleGenetic HeterogeneityGeneticPretermUnderpinning researchTobaccomedicineGeneticsHumansEpigeneticsConditions Affecting the Embryonic and Fetal PeriodsNucleotide MotifsPregnancyHormone activitydNaMGeneral ChemistryEpigenomeDNA MethylationPerinatal Period - Conditions Originating in Perinatal Periodmedicine.diseaseEmbarassades -- Consum de tabacGood Health and Well BeingRisk factorsEpigenesis
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Morphological assessment of the umbilical cord with three-dimensional ultrasonography

2002

ABSTRACTThe long cylindrical cord covered by a layer of amnion that extends from the umbilicus of the fetus to the fetal surface of the placenta is known as the umbilical cord, or, in older medical textbooks, as funiculis umbilicalis. The two umbilical arteries extend as branches of the internal iliac arteries that emerge from the fetal body at the umbilicus, and run a helical course through the umbilical cord carrying venous blood to the placenta. In most normal placentas, the umbilical arteries anastomose within 2 cm of insertion into the placenta. The fetal umbilical vein emerges from the placenta and carries oxygenated blood to the fetus. The cord vessels are supported by a matrix of my…

FetusCordbusiness.industryUmbilicus (mollusc)Connective tissueAnatomyPlacenta cord bankingUmbilical cordUmbilical veinmedicine.anatomical_structurePlacentaembryonic structuresmedicinebusinessreproductive and urinary physiologyThe Ultrasound Review of Obstetrics and Gynecology
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Extraembryonic tissues as a source of stem cells.

2009

The placenta is a fetal organ, responsible for nutrient and gas exchange between the mother and fetus throughout pregnancy [1]. At day 6.5, gastrulation begins in the posterior region of the embryo...

FetusEndocrinology Diabetes and MetabolismPlacentaStem CellsObstetrics and GynecologyAmniotic stem cellsEmbryoBiologyAmniotic FluidCell biologyEndocrinologymedicine.anatomical_structurePregnancyAmniotic epithelial cellsPlacentaembryonic structuresmedicineHumansFemaleAmnionStem cellreproductive and urinary physiologyAdult stem cellStem cell transplantation for articular cartilage repairGynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
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