Search results for "Haplotype"

showing 10 items of 444 documents

DVWA gene polymorphisms and osteoarthritis

2015

Background: Osteoarthritis (OA) is a degenerative joints disorder influenced by genetic predisposition. We reported that rs11718863 DVWA SNP was represented in Sicilian with a more severe Kellgren and Lawrence (KL) radiographic grade, displaying its predictive role as OA marker progression. Here, we describe the DVWA SNPs: rs11718863, rs7639618, rs7651842, rs7639807 and rs17040821 probably able to induce protein functional changes. Findings: Sixty-one Sicilian patients with knee OA and 100 healthy subjects were enrolled. Clinical and radiographic evaluation was performed using AKSS scores and KL. Linkage Disequilibrium (LD) analyses were performed in order to verify whether the SNPs segrega…

MaleLinkage disequilibriumShort ReportSingle-nucleotide polymorphismOsteoarthritisCollagen Type VIBioinformaticsPolymorphism Single NucleotideGeneral Biochemistry Genetics and Molecular BiologyLinkage DisequilibriumWhite PeopleGene FrequencyOsteoarthritisHaplotypeGenetic predispositionDVWAMedicineSNPHumansGenetic Predisposition to DiseaseAlleleOsteoarthritis DVWA Single nucleotide polymorphisms Haplotypes KLAllele frequencySicilyAllelesAgedMedicine(all)Aged 80 and overBiochemistry Genetics and Molecular Biology(all)business.industryHaplotypeHomozygoteGeneral MedicineSingle nucleotide polymorphismsMiddle AgedOsteoarthritis Kneemedicine.diseaseSingle nucleotide polymorphismKLHaplotypesOsteoarthritiFemalebusinessPseudogenesBMC Research Notes
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Identifying Genetic Traces of Historical Expansions: Phoenician Footprints in the Mediterranean

2008

10 páginas, 1 figura, 4 páginas.-- et al.

MaleMediterranean climatePopulation DynamicsPopulationHomelandBiologyPolymorphism Single NucleotideHaplogroup03 medical and health sciencesMediterranean seaGene FrequencyReportEthnicityMediterranean SeaGeneticsHumansAnalytical strategyGenetics(clinical)educationAllelesHistory AncientGenetics (clinical)Historical record030304 developmental biologyGenetics0303 health scienceseducation.field_of_studyChromosomes Human YGeography030305 genetics & heredityEmigration and Immigrationlanguage.human_languageGenealogyGenetics PopulationHaplotypeslanguagePhoenician
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Y-chromosome STR haplotypes from a Western Mediterranean population sample

2001

Nine Y-chromosome STRs were investigated in a male population sample from the Western Mediterranean region of Valencia (Eastern Spain). Complete nine Y-chromosomal STRs haplotypes were obtained in 140 individuals, among which 113 different haplotypes were observed. The most common haplotype was shared by 5% of the sample, while 99 haplotypes were unique. The gene diversity was 0.9892 and the discrimination capacity was 0.8071. Significant population differences were observed with respect to other Iberian populations, such as the Basques and Northern Portugueses.

MaleMediterranean climatemedicine.medical_specialtyPopulationPopulation geneticsMinisatellite RepeatsBiologyY chromosomePolymerase Chain ReactionPathology and Forensic MedicineGene FrequencyY ChromosomemedicineHumanseducationGeneticseducation.field_of_studyHaplotypeCytogeneticsDiscriminant AnalysisGenetic VariationDNA FingerprintinghumanitiesHaplotypesDNA profilingSpainEvolutionary biologyMicrosatelliteLawForensic Science International
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Mitochondrial DNA effects on fitness in Drosophila subobscura

2011

We tested different fitness components on a series of conspecific mtDNA haplotypes, detected by RFLPs in Drosophila subobscura. Additionally, haplotype VIII, endemic to the Canary Islands, was tested upon its own native nuclear DNA background and upon that of the rest of mtDNAs tested herein. We found that both nuclear and mitochondrial DNA can have a significant effect upon their hosts' fitness, and that negative selection is one of the mechanisms that can intervene in this species' mtDNA haplotype pattern. We discuss the importance of this mechanism in relation to genetic drift, in the form of periodic population bottlenecks, and how the latter can enhance the former. We also detected a s…

MaleMitochondrial DNALongevityGenetic FitnessBiologyDNA MitochondrialGenetic driftGenetic variationHybrid VigorGeneticsAnimalsSelection GeneticGenetics (clinical)Cell NucleusGeneticsGenetic DriftHaplotypeGenetic VariationDrosophila subobscuraNuclear DNAFertilityHaplotypesSpainEvolutionary biologyMutationOriginal ArticleDrosophilaFemaleGenetic FitnessRestriction fragment length polymorphismWolbachiaHeredity
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Assortative mating and fertility in two Drosophila subobscura strains with different mitochondrial DNA haplotypes.

2003

The mating pattern and female fertility on the two main mitochondrial DNA haplotypes (I and II) of Drosophila subobscura were studied, in an attempt to find possible differences between them in relation to sexual selection or isolation that could explain the populational dynamics and the co-existence of these two strains in nature. The mating pattern indicated an assortative mating in population cages, where couples of the same haplotype, mainly those of haplotype I, mated more often. However, the significations detected in laboratory conditions disappeared in wild populations, where random mating was the rule. The female fertility also showed differences in the laboratory compared to the w…

MaleMitochondrial DNAmedia_common.quotation_subjectPopulationPopulation DynamicsFertilityPlant ScienceBiologyDNA MitochondrialSexual Behavior AnimalGeneticsAnimalsMatingSelection Geneticeducationmedia_commonGeneticseducation.field_of_studyAssortative matingHaplotypeGeneral MedicineDrosophila subobscuraFertilityHaplotypesEvolutionary biologySpainInsect ScienceSexual selectionAnimal Science and ZoologyDrosophilaFemaleGenetica
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Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia

2014

Idiopathic achalasia is characterized by a failure of the lower esophageal sphincter to relax due to a loss of neurons in the myenteric plexus(1,2). This ultimately leads to massive dilatation and an irreversibly impaired megaesophagus. We performed a genetic association study in 1,068 achalasia cases and 4,242 controls and fine-mapped a strong MHC association signal by imputing classical HLA haplotypes and amino acid polymorphisms. An eight-residue insertion at position 227-234 in the cytoplasmic tail of HLA-DQ beta 1 (encoded by HLA-DQB1*05:03 and HLA-DQB1*06:01) confers the strongest risk for achalasia (P = 1.73 x 10(-19)). In addition, two amino acid substitutions in the. extracellular …

MaleModels MolecularAchalasiaImmunogeneticsBiologyMajor histocompatibility complexPolymorphism Single Nucleotidedigestive systemHLA-DQ alpha-ChainsHLA-DQ AntigensHLA-DQotorhinolaryngologic diseasesGeneticsmedicineHLA-DQ beta-ChainsHumansGenetic Predisposition to DiseaseEsophagusAllelesGenetic Association StudiesGenetic associationGeneticsAchalasiaMotility disorderASSOCIATIONmedicine.diseasedigestive system diseasesEsophageal AchalasiaINSIGHTSLogistic Modelsmedicine.anatomical_structureAmino Acid SubstitutionHaplotypesCase-Control StudiesImmunologybiology.proteinFemaleIdiopathic achalasiageneticMHCNature Genetics
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Genome-wide patterns of selection in 230 ancient Eurasians

2015

Mathieson, Iain et al.

MaleMultifactorial InheritanceArchaeogeneticsAsiaPopulationBiologyGenomeArticleBone and Bones03 medical and health sciences0302 clinical medicineHumansSelection GeneticeducationHistory AncientSelection (genetic algorithm)030304 developmental biologyGenetics0303 health scienceseducation.field_of_studyMultidisciplinaryNatural selectionancient DNA; prehistory; Eurasia; natural selectionGenome HumanPigmentationImmunityAgricultureDNASequence Analysis DNA15. Life on landBody HeightDiet3. Good healthEuropeGenetics PopulationAncient DNAHaplotypesEvolutionary biologyHuman genomeAdaptation030217 neurology & neurosurgery
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Gender-Specific Association of a Perilipin Gene Haplotype with Obesity Risk in a White Population

2004

Objective: Perilipin is a class of protein-coating lipid droplets in adipocytes and steroidogenic cells. Our purpose was to examine the association between common single-nucleotide polymorphisms (SNPs) at the perilipin (PLIN) locus and obesity, as well as related phenotypes, in unrelated American adults. Research Methods and Procedures: Four PLIN SNPs (PLIN 6209T>C, 11482G>A, 13041A>G, and 14995A>T) were typed in 734 white subjects (373 men and 361 women) attending a residential lifestyle intervention program. The baseline anthropometric and biochemical measures were used. Obesity was defined as BMI ≥ 30 kg/m2. Results: Multivariate analysis demonstrated that, in women, two of the SNPs (130…

MalePerilipin-1medicine.medical_specialtyWaistGenotypeEndocrinology Diabetes and MetabolismMedicine (miscellaneous)Single-nucleotide polymorphismPolymorphism Single NucleotideWhite PeopleBody Mass IndexEndocrinologyWaist–hip ratioInternal medicinemedicineHumansGenetic Predisposition to DiseaseObesityAnalysis of VarianceSex CharacteristicsWaist-Hip Ratiobusiness.industryHaplotypePublic Health Environmental and Occupational HealthDNAOdds ratioMiddle AgedPhosphoproteinsmedicine.diseaseObesityEndocrinologyAdipose TissueHaplotypesBody CompositionLinear ModelsPerilipinFemaleCarrier ProteinsbusinessBody mass indexFood ScienceObesity Research
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A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia.

2001

Abstract The elucidation of the molecular basis of hyperphenylalaninemia in various world populations (PKU Consortium Database: http://www.mcgill.ca/pahdb/) has revealed a remarkable molecular heterogeneity at the locus encoding for phenylalanine hydroxylase. As a consequence, genotyping of HPA patients has prompted the establishment of an impressive number of mutation detection protocols. In spite of the large variety of methods proposed so far, no comprehensive strategy has been yet developed for the detection of PAH gene mutations. Therefore, new approaches, combining the advantages of individual methods are required, especially in populations with a high number of PAH gene mutations. In…

MalePhenylalanine hydroxylaseGenotypeDNA Mutational AnalysisLocus (genetics)Gene mutationMolecular heterogeneityPolymerase Chain ReactionHyperphenylalaninemiaPhenylketonuriasmedicineHumansMutation detectionGenetic TestingMolecular BiologyGenotypingSicilyReverse dot blotGeneticsbiologyGenetic VariationNucleic Acid HybridizationPhenylalanine HydroxylaseCell BiologyExonsmedicine.diseasePedigreeHaplotypesMutationbiology.proteinFemaleOligonucleotide ProbesMolecular and cellular probes
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Y-chromosome haplotypes in Italy: the GEFI collaborative database

2001

Abstract A sample of 1176 males from 10 Italian regions have been typed for DYS19, DYS389-I, DYS389-II, DYS390, DYS391, DYS392, DYS393, and DYS385. Individual haplotype data are available on line. A low degree of variation is present among regions. Use of this database is specifically recommended for forensic applications in Italy.

MalePopulation dataDatabases FactualDatabaseHaplotypePopulation geneticsSettore MED/43 - MEDICINA LEGALEcomputer.software_genreY chromosomePathology and Forensic MedicineGenetics PopulationGeographyHaplotypesItalyShort tandem repeatsY ChromosomePopulation dataHumansMicrosatelliteY haplotypeLawcomputerY-chromosome
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