Search results for "nuclei"

showing 10 items of 1273 documents

Complete cDNA sequence coding for the MHC class II RT1.B alpha chain of the Lewis rat.

1989

Macromolecular SubstancesGenes MHC Class IIMolecular Sequence Datachemistry.chemical_compoundComplementary DNAGeneticsAnimalsBase sequenceAmino Acid SequenceCodonPeptide sequenceSequence (medicine)GeneticsMHC class IIbiologyBase SequenceNucleic acid sequenceHistocompatibility Antigens Class IIDNAIsotypeMolecular biologyRatschemistryRats Inbred Lewbiology.proteinDNANucleic acids research
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Transient structural ordering of the RNA-binding domain of carnation mottle virus p7 movement protein modulates nucleic acid binding.

2005

Plant viral movement proteins bind to RNA and participate in the intra- and intercellular movement of the RNAs from plant viruses. However, the role and magnitude of the conformational changes associated with the formation of RNA-protein complexes are not yet defined. Here we describe studies on the relevance of a preexisting nascent alpha-helix at the C terminus of the RNA-binding domain of p7, a movement protein from carnation mottle virus, to RNA binding. Synthetic peptide analogues and single amino acid mutation at the RNA-binding domain of recombinant p7 protein were used to correlate the transient structural order in aqueous solution with RNA-binding potential.

Magnetic Resonance SpectroscopyMolecular Sequence DataBiochemistryViral ProteinsPlant virusAmino Acid SequenceBinding siteMovement proteinMolecular BiologyBinding SitesbiologyC-terminusOrganic ChemistryRNARNA-Binding Proteinsbiology.organism_classificationRecombinant ProteinsProtein Structure TertiarySpectrometry FluorescenceBiochemistryCarnation mottle virusMutationNucleic acidMolecular MedicineRNAPeptidesBinding domainChembiochem : a European journal of chemical biology
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Simultaneous pituitary–gonadal recrudescence in two Corsican populations of male blue tits with asynchronous breeding dates

2006

Animal populations living in geographically variable environments respond to different selection pressures. The adaptive character of the responses to environmental information determines the degree of synchrony of the breeding period with local optimal conditions. An example is provided by two populations of Mediterranean blue tits (Parus caeruleus) in Corsica, breeding in different habitats, with a 1-month difference in the onset of egg laying. This difference in the onset of lay is supposed to be adaptive because, although chicks from both populations are raised mostly on caterpillars, the timing of the appearance of caterpillars is earlier for populations of tits associated with deciduo…

Male0106 biological sciencesMediterranean climateLH01 natural sciencesGonadotropin-Releasing HormoneSongbirdsBehavioral Neuroscience0302 clinical medicineEndocrinologyTestisTestosteroneTestesComputingMilieux_MISCELLANEOUSmedia_commonGonadotropineducation.field_of_studyEcologyReproductionOrgan SizeAdaptation PhysiologicalDeciduousHabitatPituitary GlandFemaleSeasonsReproductionParus caeruleus[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]media_common.quotation_subjectPopulationPopulationHypothalamusEnvironmentBiologyAnimal Population Groups010603 evolutionary biology03 medical and health sciencesSex FactorsBirdAnimals[ SDV.OT ] Life Sciences [q-bio]/Other [q-bio.OT]AdaptationeducationAnalysis of Variance[SDV.OT] Life Sciences [q-bio]/Other [q-bio.OT]Endocrine and Autonomic SystemsOvarySong control nucleiLuteinizing HormoneEvergreenCanto[SDE.ES]Environmental Sciences/Environmental and SocietySeasonVocalization AnimalAdaptation[SDE.BE]Environmental Sciences/Biodiversity and Ecology030217 neurology & neurosurgery
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Early impairment of epigenetic pattern in neurodegeneration: Additional mechanisms behind pyrethroid toxicity

2019

Abstract Permethrin is a synthetic pyrethroid extensively used as anti-woodworm agent and for indoor and outdoor pest control. The main route of human exposure is through fruit, vegetable and milk intake. Low dosage exposure to permethrin during neonatal brain development (from postnatal day 6 to postnatal day 21) leads to dopamine decrease in rat striatum nucleus, oxidative stress and behavioural changes linked to the development of Parkinson's like neurodegeneration later in life. The aim of this study was to evaluate the expression of genes involved in the dopaminergic pathway and epigenetic regulatory mechanisms in adolescent rats treated with permethrin during neonatal brain developmen…

Male0301 basic medicineAgingDopamineStriatumPharmacologyBiologyBiochemistryEpigenesis GeneticMECP203 medical and health sciences0302 clinical medicineEndocrinologyDopamineNuclear Receptor Subfamily 4 Group A Member 2parasitic diseasesGeneticsmedicineAnimalsEpigeneticsRats WistarPromoter Regions GeneticDNA Modification MethylasesMolecular BiologyPermethrinOrphan receptorDopaminergicNeurodegenerationNeurodegenerative DiseasesCell BiologyDNA Methylationmedicine.diseaseCorpus StriatumRatsMolecular Docking Simulation030104 developmental biologyAnimals Newbornalpha-SynucleinProtein Multimerization030217 neurology & neurosurgeryPermethrinmedicine.drugExperimental Gerontology
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Functional Plasticity after Unilateral Vestibular Midbrain Infarction in Human Positron Emission Tomography.

2016

The aim of the study was to uncover mechanisms of central compensation of vestibular function at brainstem, cerebellar, and cortical levels in patients with acute unilateral midbrain infarctions presenting with an acute vestibular tone imbalance. Eight out of 17 patients with unilateral midbrain infarctions were selected on the basis of signs of a vestibular tone imbalance, e.g., graviceptive (tilts of perceived verticality) and oculomotor dysfunction (skew deviation, ocular torsion) in F18-fluordeoxyglucose (FDG)-PET at two time points: A) in the acute stage, and B) after recovery 6 months later. Lesion-behavior mapping analyses with MRI verified the exact structural lesion sites. Group su…

Male0301 basic medicineBrain Stem Infarctionslcsh:MedicinePathology and Laboratory MedicineMidbrainDiagnostic Radiology0302 clinical medicineThalamusMesencephalonCortex (anatomy)Medicine and Health SciencesMedicinelcsh:ScienceTomographyPostural BalanceVestibular systemNeuronal PlasticityMultidisciplinaryRadiology and ImagingBrainAnatomyFrontal eye fieldsMagnetic Resonance Imagingmedicine.anatomical_structureVestibular DiseasesInfarctionThalamic NucleiFemaleBrainstemAnatomyBrainstemResearch ArticleImaging TechniquesThalamusNeuroimagingResearch and Analysis Methods03 medical and health sciencesSigns and SymptomsDiagnostic MedicineOcular SystemHumansSkew deviationAgedbusiness.industrylcsh:RBiology and Life SciencesVestibular cortex030104 developmental biologyVisual cortexCase-Control StudiesPositron-Emission TomographyLesionsEyeslcsh:QbusinessHeadNeurosciencePositron Emission Tomography030217 neurology & neurosurgeryNeurosciencePLoS ONE
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Mitochondrial genetic haplogroups and cardiovascular diseases: Data from the Osteoarthritis Initiative

2019

Background Some case-control studies reported that mitochondrial haplogroups could be associated with the onset of cardiovascular diseases (CVD), but the literature regarding this topic is limited. We aimed to investigate whether any mitochondrial haplogroup carried a higher or lower risk of CVD in a large cohort of North American people affected by knee osteoarthritis or at high risk for this condition. Materials and methods A longitudinal cohort study including individuals from the Osteoarthritis Initiative was done. Haplogroups were assigned through a combination of sequencing and PCR-RFLP techniques. All the mitochondrial haplogroups have been named following this nomenclature: HV, JT, …

Male0301 basic medicineHeredityKneesCardiovascular MedicineBiochemistryHaplogroup0302 clinical medicineMedicine and Health SciencesMedicineLongitudinal StudiesProspective StudiesProspective cohort studyMusculoskeletal SystemEnergy-Producing Organelleseducation.field_of_studyMultidisciplinaryQHazard ratioRMiddle AgedOsteoarthritis KneeMitochondrial DNAMitochondriaNucleic acidsGenetic MappingGenes MitochondrialCardiovascular DiseasesResearch Design030220 oncology & carcinogenesisLegsMedicineFemaleCellular Structures and OrganellesAnatomyPolymorphism Restriction Fragment LengthResearch ArticleRiskmedicine.medical_specialtyForms of DNASciencecardiovascuar diseases (CVD)PopulationBioenergeticsResearch and Analysis MethodsLower riskDNA Mitochondrial03 medical and health sciencesRheumatologyInternal medicineOsteoarthritisGeneticsHumansGenetic Predisposition to DiseaseeducationAgedProportional Hazards ModelsEvolutionary BiologyPopulation Biologybusiness.industryProportional hazards modelArthritismitochondrial haplogroupHaplotypeBiology and Life SciencesCell BiologyDNA030104 developmental biologyHaplotypesCase-Control StudiesBody LimbsHaplogroupsbusinessPopulation GeneticsFollow-Up StudiesHuman mitochondrial DNA haplogroupPLOS ONE
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Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency

2016

S-adenosylhomocysteine hydrolase (AHCY) deficiency is a rare autosomal recessive disorder in methionine metabolism caused by mutations in the AHCY gene. Main characteristics are psychomotor delay including delayed myelination and myopathy (hypotonia, absent tendon reflexes etc.) from birth, mostly associated with hypermethioninaemia, elevated serum creatine kinase levels and increased genome wide DNA methylation. The prime function of AHCY is to hydrolyse and efficiently remove S-adenosylhomocysteine, the by-product of transmethylation reactions and one of the most potent methyltransferase inhibitors. In this study, we set out to more specifically characterize DNA methylation changes in blo…

Male0301 basic medicineMethyltransferaselcsh:MedicineArtificial Gene Amplification and ExtensionGlycine N-MethyltransferaseBiochemistryPolymerase Chain Reactionlaw.inventionMethionine0302 clinical medicinelawAmino Acidslcsh:SciencePolymerase chain reactionGeneticsDNA methylationMammalian GenomicsMultidisciplinaryOrganic CompoundsGenomicsMethylationChromatinEnzymes3. Good healthNucleic acidsChemistryPhysical SciencesDNA methylationEpigeneticsFemaleDNA modificationChromatin modificationResearch ArticleChromosome biologyCell biologyAlu elementBiologyResearch and Analysis MethodsGenomic Imprinting03 medical and health sciencesAlu ElementsGeneticsSulfur Containing Amino AcidsHumansRepeated SequencesMolecular Biology TechniquesMolecular BiologyAmino Acid Metabolism Inborn ErrorsGeneBiology and life sciencesOrganic Chemistrylcsh:RChemical CompoundsInfant NewbornProteinsInfantDNAMethyltransferasesCreatineMolecular biologyLong Interspersed Nucleotide Elements030104 developmental biologyDifferentially methylated regionsAnimal GenomicsEnzymologyAHCY ; Hypermethylationlcsh:QGene expressionGenomic imprinting030217 neurology & neurosurgeryDevelopmental BiologyPLOS ONE
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Balancing selection maintains polymorphisms at neurogenetic loci in field experiments

2017

Most variation in behavior has a genetic basis, but the processes determining the level of diversity at behavioral loci are largely unknown for natural populations. Expression of arginine vasopressin receptor 1a (Avpr1a) and oxytocin receptor (Oxtr) in specific regions of the brain regulates diverse social and reproductive behaviors in mammals, including humans. That these genes have important fitness consequences and that natural populations contain extensive diversity at these loci implies the action of balancing selection. In Myodes glareolus, Avpr1a and Oxtr each contain a polymorphic microsatellite locus located in their 5′ regulatory region (the regulatory region-associated microsatel…

Male0301 basic medicineReceptors Vasopressindensity-dependent selectionAvpr1aLocus (genetics)Regulatory Sequences Nucleic AcidBiologyBalancing selection03 medical and health sciencesMyodes glareolusGenotypeAnimalsAlleleGeneticsGenetic diversityMultidisciplinaryReproductive successArvicolinaeta1184ReproductionOxtrBiological SciencesOxytocin receptor030104 developmental biologyGene Expression RegulationReceptors Oxytocinsexual conflictta1181MicrosatelliteFemaleGenetic FitnessMicrosatellite RepeatsProceedings of the National Academy of Sciences
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Normalization with Corresponding Naïve Tissue Minimizes Bias Caused by Commercial Reverse Transcription Kits on Quantitative Real-Time PCR Results

2016

Real-time reverse transcription polymerase chain reaction (PCR) is the gold standard for expression analysis. Designed to improve reproducibility and sensitivity, commercial kits are commonly used for the critical step of cDNA synthesis. The present study was designed to determine the impact of these kits. mRNA from mouse brains were pooled to create serial dilutions ranging from 0.0625 μg to 2 μg, which were transcribed into cDNA using four different commercial reverse-transcription kits. Next, we transcribed mRNA from brain tissue after acute brain injury and naïve mice into cDNA for qPCR. Depending on tested genes, some kits failed to show linear results in dilution series and revealed s…

Male0301 basic medicineSerial dilutionlcsh:MedicineGene ExpressioncDNA synthesisArtificial Gene Amplification and ExtensionBioinformaticsBiochemistryPolymerase Chain ReactionMice0302 clinical medicineBrain Injuries Traumaticlcsh:ScienceGenes EssentialMultidisciplinaryReverse Transcriptase Polymerase Chain ReactionMessenger RNAComplementary DNAHousekeeping geneNucleic acidsReverse transcription polymerase chain reactionResearch ArticleNormalization (statistics)DNA ComplementaryForms of DNANucleic acid synthesisBiologyReal-Time Polymerase Chain ReactionResearch and Analysis Methods03 medical and health sciencesExtraction techniquesComplementary DNAGeneticsAnimalsRNA MessengerChemical synthesisRNA synthesisMolecular Biology TechniquesMolecular BiologyGeneMessenger RNABiology and life scienceslcsh:RDNAReverse TranscriptionMolecular biologyRNA extractionReverse transcriptaseMice Inbred C57BLBiosynthetic techniques030104 developmental biologyRNAlcsh:Q030217 neurology & neurosurgeryPLOS ONE
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Clinical application of embryo aneuploidy testing by next-generation sequencing

2019

Abstract We review here the evolution in the field of embryo aneuploidy testing over the last 20 years, from the analysis of a subset of chromosomes by fluorescence in situ hybridisation to the transition toward a more comprehensive analysis of all 24 chromosomes. This current comprehensive aneuploidy testing most commonly employs next-generation sequencing (NGS). We present our experience in over 130 000 embryo biopsies using this technology. The incidence of aneuploidy was lower in trophectoderm biopsies compared to cleavage-stage biopsies. We also confirmed by NGS that embryo aneuploidy rates increased with increasing maternal age, mostly attributable to an increase in complex aneuploid …

Male0301 basic medicineTime FactorsNoninvasive Prenatal TestingAneuploidySingle Embryo TransferBiologyMiscarriageAndrology03 medical and health sciences0302 clinical medicinePregnancyRisk FactorsRecurrent miscarriagemedicineHumansGenetic TestingBlastocystPrecision MedicinePreimplantation DiagnosisGenetic testingPregnancy030219 obstetrics & reproductive medicinemedicine.diagnostic_testMosaicismHigh-Throughput Nucleotide SequencingCell BiologyGeneral MedicineAneuploidyEmbryo Transfermedicine.diseaseEmbryo transferBlastocyst030104 developmental biologymedicine.anatomical_structureReproductive MedicineCytogenetic AnalysisFemaleCell-Free Nucleic AcidsBiology of Reproduction
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