Search results for "length polymorphism"

showing 10 items of 177 documents

Genetic analysis of IDDM: The GAW5 multiplex family dataset

1989

In a collaborative effort by 12 centers from Europe and North America, data were assembled from 94 multiplex families with insulin-dependent diabetes mellitus (IDDM) for analysis of genetic and other factors of possible etiological importance. The dataset contains information on the following genetic markers: HLA-DR beta and -DQ beta restriction fragment length polymorphisms (RFLPs), three RFLPs detected with two probes that map 5' to the insulin gene, the serologically defined HLA loci, and the immunoglobulin allotypes. Data also were included for auto-antibodies to insulin and pancreatic islet cells as possible indicators of pathogenesis and for antibodies to certain viruses that have bee…

Geneticsendocrine system diseasesEpidemiologyImmunoglobulin AllotypesHuman leukocyte antigenBiologymedicine.diseaseGenetic analysisGenetic markerDiabetes mellitusmedicinebiology.proteinMultiplexRestriction fragment length polymorphismAntibodyGenetics (clinical)Genetic Epidemiology
researchProduct

Reliability of Restriction Enzyme Digestions of Genomic DNA for the Generation of DNA Fingerprints

1991

Since minisatellite DNA probes are used for the detection of hypervariable loci in eucaryotic genomes [1] the application of so called DNA fingerprints and DNA technology itself in paternity testing and forensic casework is critically discussed ([3]; Brinkmann et al., this volume). A particular problem is the possibility of obtaining partially digested genomic DNA in casework after treatment with restriction enzymes leading to inconclusive or even false results. This is even more important when multilocus DNA probes are used, since the total number of fragments in a given person is not known in advance. But also with single locus probes, where only two allelic fragments are usually detected…

Geneticsgenomic DNARestriction enzymeMinisatelliteRestriction mapDNA profilingGenomic libraryRestriction fragment length polymorphismBiologySequencing by ligation
researchProduct

No Association Between the Dopamine D2 Receptor Taq I A1 Allele and Earlier Age of Onset of Alcohol Dependence According to Different Specified Crite…

2001

BACKGROUND: The presence of the A1 allele of the dopamine D2 receptor TaqI restriction fragment length polymorphism has been reported to be associated with an earlier age of onset of alcohol dependence as a marker for severity. METHODS: We tested this hypothesis with special regard to the definition of the age of onset of alcoholism in 243 patients with alcohol dependence, according to DSM-IV criteria assessed by the standardized interview Munchner Composite International Diagnostic Interview (M-CIDI), consecutively admitted for detoxification. Additionally, the Addiction Severity Index (ASI) was performed. The TaqIA polymorphism was amplified by polymerase chain reaction (PCR), and the PCR…

Geneticsmedicine.medical_specialtyTaqIAlcohol dependenceMedicine (miscellaneous)Binge drinkingToxicologyPsychiatry and Mental healthchemistry.chemical_compoundchemistryPolymorphism (computer science)Internal medicinemedicineAlleleAge of onsetRestriction fragment length polymorphismPsychologyAllele frequencyAlcoholism: Clinical and Experimental Research
researchProduct

Role and importance of polymorphisms with respect to DNA methylation for the expression of CYP2E1 enzyme

2014

Different individuals possess slightly different genetic information and show genetically-determined differences in several enzyme activities due to genetic variability. Following an integrated approach, we studied the polymorphisms and methylation of sites contained in the 5' flanking region of the metabolizing enzyme CYP2E1 in correlation to its expression in both tumor and non-neoplastic liver cell lines, since to date little is known about the influence of these (epi)genetic elements in basal conditions and under induction by the specific inductor and a demethylating agent. In treated cells, reduced DNA methylation, assessed both at genomic and gene level, was not consistently associate…

Genotype5' Flanking RegionCell Survival5' flanking regionMinisatellite RepeatsBiologyGene Expression Regulation EnzymologicGenotypeGeneticsCYP2E1 gene polymorphismTumor Cells CulturedHumansGeneHepatocellular carcinoma cell lines; CYP2E1 gene polymorphisms; DNA methylation; 5-Azacytidine; Ethanol;GeneticsPolymorphism GeneticEthanolLiver cellHaplotype5-AzacytidineCytochrome P-450 CYP2E1General MedicineMethylationHep G2 CellsHepatocellular carcinoma cell lineDNA MethylationMolecular biologySettore BIO/18 - GeneticaDNA methylationAzacitidineRestriction fragment length polymorphismPolymorphism Restriction Fragment Length
researchProduct

High-resolution genotyping of Campylobacter strains isolated from poultry and humans with amplified fragment length polymorphism fingerprinting.

1999

ABSTRACT For epidemiological studies of Campylobacter infections, molecular typing methods that can differentiate campylobacters at the strain level are needed. In this study we used a recently developed genotyping method, amplified fragment length polymorphism (AFLP), which is based on selective amplification of restriction fragments of chromosomal DNA, for genetic typing of Campylobacter jejuni and Campylobacter coli strains derived from humans and poultry. We developed an automated AFLP fingerprinting method in which restriction endonucleases Hin dIII and Hha I were used in combination with one set of selective PCR primers. This method resulted in evenly distributed band patterns for amp…

GenotypeGenetics and Molecular BiologyCampylobacter coliDeoxyribonuclease HindIIImedicine.disease_causeApplied Microbiology and BiotechnologyCampylobacter jejuniPolymerase Chain ReactionPoultryMicrobiologyRestriction fragmentCampylobacter jejuniGenotypeCampylobacter InfectionsmedicineAnimalsDeoxyribonucleases Type II Site-SpecificGenotypingDNA PrimersGeneticsEcologybiologyCampylobacterfood and beveragesReproducibility of ResultsCampylobacterbiology.organism_classificationDNA FingerprintingBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldDNA profilingCampylobacter colibiology.proteinAmplified fragment length polymorphismFood ScienceBiotechnologyApplied and environmental microbiology
researchProduct

Genetic diversity of Dioscorea dumetorum (Kunth) Pax using Amplified Fragment Length Polymorphisms (AFLP) and cpDNA

2010

We have utilized Amplified Fragment Length Polymorphisms (AFLP) in conjunction with chloroplast DNA (cpDNA) sequence data to study the genetic diversity in 53 accessions of Dioscorea dumetorum from six countries in West and Central Africa. Our results provide a comparison of the two marker systems with regards to their applicability to differentiate intraspecific genotypes and the grouping of the accessions based on localities of collection. A total of 1052 AFLP fragments (of which 94.1% were polymorphic) produced from twelve primer combinations indicate a relatively high level of polymorphism among the accessions. Three major genetic groups that do not strictly follow a geographic distribu…

GermplasmGenetic diversityfood and beveragesBiologyBiochemistryDNA sequencingChloroplast DNAGenetic markerparasitic diseasesBotanyGenetic variationGenotypeAmplified fragment length polymorphismEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
researchProduct

Assessment of genetic variation in SicilianHelichrysum(Asteraceae) and implication to germplasm conservation

2008

Some taxa of Sicilian Helichrysum related to sect. Stoeachadina have an uncertain systematic position; moreover, they are rare and endangered. In order to preserve these taxa in a genebank, a strategy to keep their genetic variation as high as possible is required. The high informative content of AFLP markers was used to assess genetic variations within and between populations and their relationships. The results show that all populations are genetically similar, even though there are two distinct groups: the first is the population referred to H. pendulum, and the second is represented by other populations belonging to several different specific and intraspecific taxa. The H. pendulum popu…

Germplasmeducation.field_of_studyPopulationEndangered speciesPlant ScienceBiologybiology.organism_classificationIntraspecific competitionTaxonAFLP genetic variation Sicilian Helichrysum Asteraceae germplasm conservation genebankEvolutionary biologyGenetic variationBotanyHelichrysumAmplified fragment length polymorphismeducationEcology Evolution Behavior and SystematicsPlant Biosystems - An International Journal Dealing with all Aspects of Plant Biology
researchProduct

Molecular community and population studies of arbuscular mycorrhizal fungi (Glomeromycota)

2014

The arbuscular mycorrhizal symbiosis, which appeared at the same time as land plants, 460 million years ago, is a mutualistic beneficial association between most land plants, including those cultivated, and arbuscular mycorrhizal fungi (AMF). AMF, from the Glomeromycota phylum, are widespread soil microorganisms needing a photosynthetic host to complete their life cycle (obligate symbionts). The great potential of plant mineral nutrition improvement and crop production increased during this symbiosis, make AMF an asset in the context of an increase in the demand of world food crop production. The control of that symbiosis by ecology engineering in order to improve ecosystem services, especi…

Gloméromycètes[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesHigh-throughput sequencingCultural practicesPopulationPopulationsCommunityPolymorphisme de longueur de fragments de restrictionSéquençage haut-débitSymbiose mycorhizienneRhizophagus irregularisArbuscular mycorrhizaPratiques culturalesGlomeromycotaRestriction fragment length polymorphismCommunauté
researchProduct

Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots.

2008

Item does not contain fulltext Mutations in NIPA1 cause hereditary spastic paraplegia type 6 (SPG6 HSP). Sequencing of the whole gene has revealed alterations of either of two nucleotides in eight of nine SPG6 HSP families reported to date. By analysing CpG methylation, we provide a mechanistic explanation for a mutational hotspot to underlie frequent alteration of one of these nucleotides. We also developed PCR RFLP assays to detect recurrent NIPA1 changes and screened 101 independent HSP patients, including 45 index patients of autosomal dominant HSP families. Our negative finding in this cohort for which several other causes of HSP had been excluded suggests NIPA1 alterations at mutation…

Hereditary spastic paraplegiaDNA Mutational AnalysisMolecular Sequence DataCohort StudiesDegenerative diseaseCognitive neurosciences [UMCN 3.2]Polymorphism (computer science)DNA Mutational AnalysismedicineHumansGenetic TestingGeneGeneticsbusiness.industrySpastic Paraplegia HereditaryMembrane ProteinsMethylationDNA Methylationmedicine.diseaseNeurologyDNA methylationNeurology (clinical)Restriction fragment length polymorphismbusinessFunctional Neurogenomics [DCN 2]Polymorphism Restriction Fragment LengthJournal of the Neurological Sciences
researchProduct

Population structure and mitochondrial DNA gene flow in Old World populations of Drosophila subobscura

1992

An extensive survey of mitochondrial DNA (mtDNA) restriction polymorphism in 156 isofemale lines from 29 different geographic populations of Drosophila subobscura distributed throughout the Old World was carried out. Ten restriction enzymes were used, five of which revealed restriction site polymorphism. Of the 31 restriction sites detected, 13 were found to be polymorphic. Comparisons with the mtDNA map of Drosophila yakuba indicate that the variable sites are mainly concentrated in protein genes, especially those corresponding to the NADH complex. A total of 13 different haplotypes were observed, two of which (haplotypes I and II) are quite frequent and widely distributed throughout the p…

HeterozygoteMitochondrial DNAPopulationPopulation geneticsDNA MitochondrialGene FrequencyGeneticsAnimalseducationAllelesGenetics (clinical)Geneticseducation.field_of_studybiologybiology.organism_classificationDrosophila subobscuraIsoenzymesRestriction Site PolymorphismRestriction siteGenetics PopulationHaplotypesDrosophilaFemaleRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthDrosophila yakubaHeredity
researchProduct