Search results for "Allele"

showing 10 items of 1006 documents

Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments

2004

The most common mutation in the USH2A gene (Usherin), 2299delG, causes both typical Usher (USH) syndrome type II and atypical USH syndrome, two autosomal recessive disorders, characterised by moderate to severe sensorineural hearing loss and retinitis pigmentosa (RP). Furthermore, the C759F mutation in the USH2A gene has been described in 4.5% of patients with nonsyndromic recessive RP. We have investigated the presence of the 2299delG and/or the C759F mutations in 191 unrelated Spanish patients with different syndromic and nonsyndromic retinal diseases, or with nonsyndromic hearing impairment. The 2299delG mutation was observed in patients with clinical signs of USHII or of atypical USH sy…

GenotypeHearing Loss SensorineuralEye diseaseDNA Mutational AnalysisMutation MissenseGenetic analysisGene FrequencyGenotypeRetinitis pigmentosaotorhinolaryngologic diseasesGeneticsmedicineHumansAlleleAllelesPolymorphism Single-Stranded ConformationalGenetics (clinical)Sequence DeletionGeneticsExtracellular Matrix Proteinsbusiness.industryDNAmedicine.diseasePhenotypePhenotypeSpainMutation (genetic algorithm)Sensorineural hearing lossbusinessRetinitis PigmentosaEuropean Journal of Human Genetics
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MHC class II genes influence the susceptibility to chronic active hepatitis C

1997

Chronic hepatitis C develops in more than 70% of hepatitis C virus infected subjects. Viral factors influence the disease course, but little is known about the importance of host factors.Frequencies of major histocompatibility complex (MHC) class I and class II antigens were analyzed in two groups of patients with chronic hepatitis C virus infection and in control subjects. MHC class I typing was done by standard microlymphocytotoxicity assays. DRB1 and DQA1 genotyping was done by PCR based typing methods.DRB1*0301 was found in 26 of 75 patients with chronic hepatitis C virus infection (34.7%) and in 12 of 101 control subjects (11.9%) (relative risk 3.9; p0.001). Homozygosity for this allel…

GenotypeHepatitis C virusGenes MHC Class IIBiologymedicine.disease_causePolymerase Chain ReactionHLA-DQ alpha-ChainsVirusMHC Class II GeneReference ValuesHLA-DQ AntigensMHC class ImedicineHumansGenetic Predisposition to DiseaseAllelesAntilymphocyte SerumHepatitis ChronicHepatitisMHC class IIHepatologyHistocompatibility Antigens Class IHomozygoteHistocompatibility Antigens Class IIHLA-DR AntigensHepatitis Cmedicine.diseaseHepatitis CVirologyHistocompatibilityImmunologyDisease Progressionbiology.proteinDisease SusceptibilityHLA-DRB1 ChainsJournal of Hepatology
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Human SPG11 cerebral organoids reveal cortical neurogenesis impairment

2018

Abstract Spastic paraplegia gene 11(SPG11)-linked hereditary spastic paraplegia is a complex monogenic neurodegenerative disease that in addition to spastic paraplegia is characterized by childhood onset cognitive impairment, thin corpus callosum and enlarged ventricles. We have previously shown impaired proliferation of SPG11 neural progenitor cells (NPCs). For the delineation of potential defect in SPG11 brain development we employ 2D culture systems and 3D human brain organoids derived from SPG11 patients’ iPSC and controls. We reveal that an increased rate of asymmetric divisions of NPCs leads to proliferation defect, causing premature neurogenesis. Correspondingly, SPG11 organoids appe…

GenotypeHereditary spastic paraplegiaNeurogenesisFluorescent Antibody TechniqueBiology03 medical and health sciencesGlycogen Synthase Kinase 3GeneticsOrganoidmedicineSpasticHumansMolecular BiologyGenetics (clinical)Allelesbeta CateninCerebral Cortex0303 health sciences030305 genetics & heredityNeurogenesisProteinsGeneral MedicineHuman brainmedicine.diseaseNeural stem cellnervous system diseasesOrganoidsmedicine.anatomical_structurePhenotypeMutationGeneral ArticleDisease SusceptibilityParaplegiaCognition DisordersNeuroscienceNeural developmentBiomarkersHuman Molecular Genetics
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Taste, movement, and death: varying effects of new prospero mutants during Drosophila development

2003

0022-3034 (Print) Comparative Study Journal Article Research Support, Non-U.S. Gov't; The PGal4 transposon inserted upstream of the pan-neural gene prospero (pros) causes several neural and behavioral defects in the Voila(1) strain. The precise excision of the transposon simultaneously rescued all these defects whereas its unprecise excision created new pros(V) alleles, including the null allele pros(V17). Here, we describe the relationship between the genetic structure of pros locus, larval locomotion, and larval gustatory response. These two behaviors showed varying degrees of variation depending upon the pros allele. We also found a good relation between behavioral alteration, the level …

GenotypeNerve Tissue Proteins/*genetics/metabolismeducationLethalMovement/*physiologyTaste/*geneticsDrosophila melanogaster/embryology/genetics/growth & developmentReaction TimeAnimalsDrosophila ProteinsNeuromuscular Junction/genetics/growth & development/metabolismSouthernLarva/genetics/*growth & developmentAllelesNonmammalianNuclear Proteins/*genetics/metabolismBlottingDevelopmental/physiologyImmunohistochemistryhumanitiesGenomics/methodsDeathInvertebrate/chemistryGene Expression RegulationGenesEmbryoMutationDNA Transposable ElementsGangliaInsectTranscription Factors
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Historical and biological determinants of genetic diversity in the highly endemic triploid sea lavender Limonium dufourii (Plumbaginaceae)

2007

14 páginas, 5 figuras, 2 tablas.

GenotypePopulationBiologyPlant conservationGenetic diversityEvolution MolecularCritically endangeredPlumbaginaceaeHalophytesAlloploidyGenetic variationGeneticsAlleleMicrosatelliteseducationAllelesEcology Evolution Behavior and Systematicseducation.field_of_studyGenetic diversityGeographyEcologyGenetic VariationSequence Analysis DNASpainGenetic markerEvolutionary biologyGenetic structureHybridization GeneticMicrosatelliteApomixisGenome PlantMicrosatellite RepeatsMolecular Ecology
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Genotypic analysis at multiple loci across Kaposi's sarcoma herpesvirus (KSHV) DNA molecules: clustering patterns, novel variants and chimerism

2001

Abstract Background: the genomes of human Kaposi's sarcoma-associated herpesvirus (KSHV) display several levels of DNA sequence heterogeneity and subgrouping that show distinctive clustering patterns in related human populations. The four major subtype patterns for the hypervariable ORF-K1 protein correlate closely with the principal diasporas resulting from the migration of modern humans out of East Africa and suggest that KSHV is an ancient human virus that is transmitted primarily in a familial fashion with consequent very low recombination rates. However, chimeric genomes have also been detected, especially with regard to the presence of P versus M alleles of the ORF-K15 gene. Objective…

GenotypePopulationMolecular Sequence DataGenome ViralBiologyGenomeDNA sequencingMiddle EastOpen Reading FramesAfrica NorthernViral Envelope ProteinsVirologyGenotypemedicineHumansAmino Acid SequenceAlleleeducationCladeKaposi's sarcomaGeneSarcoma KaposiAllelesPhylogenyGeneticsRecombination Geneticeducation.field_of_studyAcquired Immunodeficiency SyndromeKoreaMembrane Proteinsmedicine.diseaseEuropeInfectious DiseasesHerpesvirus 8 HumanNorth AmericaSequence Alignment
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Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.

2014

Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with breast cancer risk. To clarify the role of CASP8 in breast cancer susceptibility, we carried out dense genotyping of this region in the Breast Cancer Association Consortium (BCAC). Single-nucleotide polymorphisms (SNPs) spanning a 1 Mb region around CASP8 were genotyped in 46 450 breast cancer cases and 42 600 controls of European origin from 41 studies participating in the BCAC as part of a custom genotyping array experiment (iCOGS). Missing genotypes and SNPs were imputed and, after quality exclusions, 501 typed and 1232 imputed SNPs were included in logistic regressionmodels adjusting for stud…

Genotyping TechniquesResearch Support U.S. Gov't P.H.S.CASP8 and FADD-Like Apoptosis Regulating ProteinGenome-wide association studyP.H.S.Medical and Health SciencesBreast and Ovarian Cancer Susceptibility (BOCS) StudyMedizinische FakultätGenetics(clinical)Non-U.S. Gov'tGenetics (clinical)GeneticsGenetics & HeredityvariantsCaspase 8Research Support Non-U.S. Gov'tAssociation Studies ArticlesGeneral MedicineBiological Sciencesddc:Chromosomes Human Pair 2kConFab InvestigatorsFemaleGENICA NetworkAustralian Ovarian Cancer Study GroupEuropean Continental Ancestry GroupNon-P.H.S.Single-nucleotide polymorphismBreast Neoplasms-BiologyResearch SupportPolymorphism Single NucleotideWhite PeopleN.I.H.Breast cancerResearch Support N.I.H. ExtramuralSDG 3 - Good Health and Well-beingmedicineGeneticsJournal ArticleHumansGenetic Predisposition to Diseaseddc:610geneGenotyping TechniquesGenotypingMolecular BiologyGenetic associationdiseaseExtramuralProteinsOdds ratiomedicine.diseasesusceptibility lociMinor allele frequencyCase-Control Studiesgenome-wide associationenhancersU.S. Gov'tcasp8Research Support U.S. Gov't Non-P.H.S.Genome-Wide Association Study
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Population genetic analysis of bi-allelic structural variants from low-coverage sequence data with an expectation-maximization algorithm

2014

Background Population genetics and association studies usually rely on a set of known variable sites that are then genotyped in subsequent samples, because it is easier to genotype than to discover the variation. This is also true for structural variation detected from sequence data. However, the genotypes at known variable sites can only be inferred with uncertainty from low coverage data. Thus, statistical approaches that infer genotype likelihoods, test hypotheses, and estimate population parameters without requiring accurate genotypes are becoming popular. Unfortunately, the current implementations of these methods are intended to analyse only single nucleotide and short indel variation…

GenotypingGenotypePopulation geneticsPopulationPopulation geneticsBiologyBiochemistryReference biasStructural variation03 medical and health sciences0302 clinical medicineStructural BiologyGenotypeStatisticsHumans1000 Genomes ProjecteducationMolecular BiologyAlleles030304 developmental biologySampling biasGenetic associationGeneticsLikelihood Functions0303 health scienceseducation.field_of_studyGenomePolymorphism GeneticGenètica de poblacionsApplied MathematicsHigh-Throughput Nucleotide SequencingGenomicsComputer Science ApplicationsGenotype frequencyGenetics PopulationStructural variationSoftwareAlgorithms030217 neurology & neurosurgeryMaximum likelihood
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Preliminary identification of self-incompatibility genotypes of Sicilian almond landraces

2018

Sicily is the main almond producer in Italy. The almond tree is one of the main protagonists of the Sicilian agrarian landscape, especially in the winter, when the bare branches are covered by white or pinkish flowers. Its presence is particularly significant in the province of Agrigento, in Syracuse and in Ragusa areas, where the almond nut is used for fresh consumption and for the preparation of typical sweets. The extremely rich Sicilian almond germplasm can be useful for genetic improvement, since many local landraces possess aromatic characteristics of the nuts of high value. Self-incompatibility in this species is gametophytic and controlled by a multi-allelic S locus, coding for the …

GermplasmBreeding programConservationBreedingHorticultureBiologyPrunus dulcimedicine.disease_causelanguage.human_languageSelf-incompatibilitySettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreePrunus dulcisHorticulturePCRPollinatorS-allelePollenmedicinelanguageIdentification (biology)CultivarSicilianActa Horticulturae
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Genetic relationships, structure and parentage simulation among the olive tree (Olea europaea L. subsp. europaea) cultivated in Southern Italy reveal…

2013

In this work, we assess both the morphological and genetic diversity of 68 important olive cultivars from three Southern Italian regions: Calabria, Campania and Sicily. Twenty-five phenotypic traits were evaluated and 12 simple sequence repeat (SSR) markers were analysed. All SSR primers were polymorphic and reliable. The total number of alleles per locus varied from 5 to 19 with an average number of 13.1 and a mean polymorphic information content (PIC) of 0.81. These results suggested high genetic diversity within these three olive germplasm collections. Morphological traits also showed significant variability amongst cultivars. Two cases of identity were found and ten statistically signif…

GermplasmGenetic diversityGenetic relationshipDendrogramUPGMAfood and beveragesOliveForestryPhenotypic traitHorticultureBiologySSRSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeGenetic structureBotanyGeneticsMantel testMorphological characterisationAlleleGenetic structureMolecular Biology
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