Search results for "high resolution melting"

showing 4 items of 4 documents

Marked Neurospora crassa strains for competition experiments and Bayesian methods for fitness estimates

2019

AbstractThe filamentous fungusNeurospora crassa, a model microbial eukaryote, has a life cycle with many features that make it suitable for studying experimental evolution. However, it has lacked a general tool for estimating relative fitness of different strains in competition experiments. To remedy this need, we constructedN. crassastrains that contain a modifiedcsr-1locus and developed an assay for detecting the proportion of the marked strain using a post PCR high resolution melting assay. DNA extraction from spore samples can be performed on 96-well plates, followed by a PCR step, which allows many samples to be processed with ease. Furthermore, we suggest a Bayesian approach for estim…

0106 biological sciencesGenetics0303 health sciencesMating typeExperimental evolutionbiologyevoluutiobiologiaCrassaLocus (genetics)QH426-470biology.organism_classification010603 evolutionary biology01 natural sciencesDNA extractionhigh resolution meltingNeurospora crassacompetitive fitness03 medical and health sciencesGeneticsfungiexperimental evolutionAllelesienetGene030304 developmental biology
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Exploring evolutionary responses to increasing temperature in an environmental opportunistic pathogen

2017

bakteeritauditluonnonvalintafylogeniahigh resolution melting curvelämmönsietoympäristötekijätvirulenssievoluutioselectionkalatauditgenotyyppibakteeritvirulencethermal performance curveFlavobacterium columnaretaudinaiheuttajatsekvenssianalyysilämpötilamulti-locus sequence analysis
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Original data and analysis scripts for article: Marked Neurospora crassa strains for competition experiments and Bayesian methods for fitness estimat…

2019

fungiexperimental evolutionhigh resolution meltingcompetitive fitness
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A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report

2012

Abstract Background Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total inactivation of a lysosomal hydrolase, the enzyme α-galactosidase A (GLA). This inactivation is responsible for the storage of undegraded glycosphingolipids in the lysosomes with subsequent cellular and microvascular dysfunction. The incidence of disease is estimated at 1:40,000 in the general population, although neonatal screening initiatives have found an unexpectedly high prevalence of genetic alterations, up to 1:3,100, in newborns in Italy, and have identified a surprisingly high frequency of newborn males with genetic alterations (about 1:1,500) in Taiwan. Case presentation We des…

lcsh:Diseases of the circulatory (Cardiovascular) systemPathologyα-galactosidase AAnderson-Fabry mutationBiopsyDNA Mutational AnalysisCase Reportmedicine.disease_causeGlobotriaosylceramide0302 clinical medicineSettore BIO/13 - Biologia ApplicataPromoter Regions Genetic0303 health sciencesMutationeducation.field_of_studymedicine.diagnostic_testbiologyMetabolic disorderMagnetic Resonance Imaging3. Good healthPhenotypeCardiovascular DiseasesDisease ProgressionFemaleKidney DiseasesRenal biopsyCardiology and Cardiovascular MedicineAdultmedicine.medical_specialtyPopulation03 medical and health sciencesPredictive Value of TestsBiopsymedicineHumansHigh resolution meltingGenetic Predisposition to Diseaseeducation030304 developmental biologyFabry diseaseAlpha-galactosidasebusiness.industrymedicine.diseaseFabry diseaseIntronslcsh:RC666-701alpha-GalactosidaseMutationGLAbiology.proteinbusiness030217 neurology & neurosurgeryKidney disease
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