Search results for " Polymorphism."

showing 10 items of 1006 documents

DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome short tandem repeats

2001

Abstract During the past few years the DNA commission of the International Society of Forensic Genetics has published a series of documents providing guidelines and recommendations concerning the application of DNA polymorphisms to the problems of human identification. This latest report addresses a relatively new area, namely Y-chromosome polymorphisms, with particular emphasis on short tandem repeats (STRs). This report addresses nomenclature, use of allelic ladders, population genetics and reporting methods.

Genetics0303 health sciencesDna polymorphismCommissionBiologyY chromosomeGenealogyPathology and Forensic MedicineForensic science03 medical and health sciencesIssues ethics and legal aspects0302 clinical medicineMicrosatelliteIdentification (biology)030216 legal & forensic medicineForensic genetics030304 developmental biologyLegal Medicine
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic inf…

2018

AbstractHumans vary substantially in their willingness to take risks. In a combined sample of over one million individuals, we conducted genome-wide association studies (GWAS) of general risk tolerance, adventurousness, and risky behaviors in the driving, drinking, smoking, and sexual domains. We identified 611 approximately independent genetic loci associated with at least one of our phenotypes, including 124 with general risk tolerance. We report evidence of substantial shared genetic influences across general risk tolerance and risky behaviors: 72 of the 124 general risk tolerance loci contain a lead SNP for at least one of our other GWAS, and general risk tolerance is moderately to stro…

Genetics0303 health sciencesGabaergic neurotransmissionSingle-nucleotide polymorphismGenome-wide association studyBiologyPhenotype03 medical and health sciences0302 clinical medicineSNPGene030217 neurology & neurosurgery030304 developmental biologyGenetic association
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Mycobacterium tuberculosiscomplex lineage 5 exhibits high levels of within-lineage genomic diversity and differing gene content compared to the type …

2020

AbstractPathogens of theMycobacterium tuberculosiscomplex (MTBC) are considered monomorphic, with little gene content variation between strains. Nevertheless, several genotypic and phenotypic factors separate the different MTBC lineages (L), especially L5 and L6 (traditionally termedMycobacterium africanum), from each other. However, genome variability and gene content especially of L5 and L6 strains have not been fully explored and may be potentially important for pathobiology and current approaches for genomic analysis of MTBC isolates, including transmission studies.We compared the genomes of 358 L5 clinical isolates (including 3 completed genomes and 355 Illumina WGS (whole genome seque…

Genetics0303 health sciencesLineage (genetic)030306 microbiologySequence assemblySingle-nucleotide polymorphismBiologybiology.organism_classificationGenome3. Good health03 medical and health sciencesMycobacterium tuberculosis complexGeneMycobacterium africanum030304 developmental biologyReference genome
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Sequence analyses of S10-spcoperon among 16SrV group phytoplasmas: phylogenetic relationships and identification of discriminating single nucleotide …

2012

Phytoplasmas are cell-wall less, uncultivable bacteria, belonging to the class Mollicutes. They parasitise both plant hosts and insect vectors, but knowledge of their biological and molecular properties is limited. In particular, analyses of 16S rDNA nucleotide sequences revealed that 16SrV group phytoplasma strains identified in grapevine plants are closely related, but associated with distinct ecologies. In this work, we investigated the evolutionary relationships of eight representative 16SrV phytoplasma strains by sequencing 15 ribosomal protein (rp) genes positioned within the S10-spc operon. Phylogenetic analyses of concatenated nucleotide and amino acid sequences underscored that 16S…

Genetics0303 health sciencesPhylogenetic tree030306 microbiologySingle-nucleotide polymorphismGrapevine yellowsBiologybiology.organism_classification03 medical and health sciencesPhytoplasmaCandidatusMultilocus sequence typingFlavescence doréeAgronomy and Crop ScienceGene030304 developmental biologyAnnals of Applied Biology
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2015

Hearing loss and individual differences in normal hearing both have a substantial genetic basis. Although many new genes contributing to deafness have been identified, very little is known about genes/variants modulating the normal range of hearing ability. To fill this gap, we performed a two-stage meta-analysis on hearing thresholds (tested at 0.25, 0.5, 1, 2, 4, 8 kHz) and on pure-tone averages (low-, medium- and high-frequency thresholds grouped) in several isolated populations from Italy and Central Asia (total N = 2636). Here, we detected two genome-wide significant loci close to PCDH20 and SLC28A3 (top hits: rs78043697, P = 4.71E-10 and rs7032430, P = 2.39E-09, respectively). For bot…

Genetics0303 health sciencesSequence analysisHearing lossGenome-wide association studySingle-nucleotide polymorphismGeneral MedicineBiologyGenome03 medical and health sciences0302 clinical medicineGenotypeotorhinolaryngologic diseasesGeneticsmedicinemedicine.symptomMolecular BiologyGene030217 neurology & neurosurgeryGenetics (clinical)Imputation (genetics)030304 developmental biologyHuman Molecular Genetics
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Meta-analysis and imputation refines the association of 15q25 with smoking quantity.

2010

Smoking is a leading global cause of disease and mortality(1). We established the Oxford-GlaxoSmithKline study (Ox-GSK) to perform a genome-wide meta-analysis of SNP association with smoking-related behavioral traits. Our final data set included 41,150 individuals drawn from 20 disease, population and control cohorts. Our analysis confirmed an effect on smoking quantity at a locus on 15q25 (P = 9.45 x 10(-19)) that includes CHRNA5, CHRNA3 and CHRNB4, three genes encoding neuronal nicotinic acetylcholine receptor subunits. We used data from the 1000 Genomes project to investigate the region using imputation, which allowed for analysis of virtually all common SNPs in the region and offered a …

Genetics0303 health scienceseducation.field_of_study/dk/atira/pure/subjectarea/asjc/1300/1311PopulationSingle-nucleotide polymorphismGenome-wide association studyLocus (genetics)BiologyArticle3. Good health03 medical and health sciences0302 clinical medicineGenome-Wide Association; Nicotine Dependence; Lung-Cancer; Susceptibility Locus; Risk-Factors; Disease; Genes; SNPS; Colaus StudyGeneticsSNP1000 Genomes ProjectAlleleeducation030217 neurology & neurosurgeryImputation (genetics)genome-wide association study; smoking initiation; smoking quantity030304 developmental biologyNature genetics
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Association of JAK-STAT pathway related genes with lymphoma risk: results of a European case-control study (EpiLymph)

2011

Previous studies have suggested an important role for the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signalling pathway in tumour development. Therefore, we explored genetic variants in JAK-STAT pathway associated genes with lymphoma risk. In samples of the EpiLymph case-control study we genotyped 1536 single nucleotide polymorphisms (SNPs) using GoldenGate BeadArray™ Technology (Illumina, San Diego, CA, USA). Here, we report the associations between selected SNPs and haplotypes of the JAK-STAT pathway and risk of Hodgkin lymphoma (HL), B-cell non-Hodgkin lymphoma (B-NHL) and most frequent B-NHL subtypes. Among 210 relevant JAK-STAT pathway-related SNPs, polymo…

Genetics0303 health sciencesmedicine.medical_specialtyHematologyHaplotypeJAK-STAT signaling pathwaySingle-nucleotide polymorphismHematologyBiologymedicine.diseaseLymphomaSTAT5A03 medical and health sciences0302 clinical medicineimmune system diseaseshemic and lymphatic diseases030220 oncology & carcinogenesisInternal medicineIL12ACancer researchmedicineSNP030304 developmental biologyBritish Journal of Haematology
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Genetic characterisation of CSN2 gene in Girgentana goat breed

2014

Among calcium sensitive caseins, β-casein is the most abundant in goat milk, representing up to 50% of total casein content. The goat β-casein locus has been widely investigated and at least ten alleles have been identified in different goat breeds. The aim of this work was to investigate the polymorphisms of β-casein gene in Girgentana dairy goat breed in order to assess the genotype distribution and evaluate how frequencies have changed during the last 10 years, as genotype is known to influence technological and nutritional milk properties. Sequencing analysis and alignment of the obtained sequences of β-casein exon 7, showed the presence of C, C1, and A strong alleles, and 0' null allel…

Genetics040301 veterinary sciences0402 animal and dairy scienceCSN2 locus Genetic polymorphisms Genetic evolution Girgentana goat breedLocus (genetics)04 agricultural and veterinary sciencesBiology040201 dairy & animal scienceNull alleleBreed0403 veterinary scienceExonSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoCaseinGenotypeAnimal Science and Zoologylcsh:Animal cultureAlleleGenelcsh:SF1-1100
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Identification of SNPs in the promoter of β-lactoglobulin gene in three Sicilian goat breeds

2009

The aim of this work was to sequence the full-length promoter region of the caprine β-lactoglobulin (β-lg) gene in three Sicilian goat breeds (Girgentana, Maltese, and Derivata di Siria), in order to identify polymorphisms, to search for transcription factors (TFs) sites, and to check if polymorphisms found lay within TFs binding sites. The promoter region of β-lg gene in Sicilian goat breeds showed high level of polymorphism due to the presence of 31 SNPs. Binding sites for several TFs were found within the goat β-lg promoter and within regions conserved between ovine and caprine species. Two SNPs were detected within TFs binding sites, such as MPBF and NF-I. Further st…

Genetics040301 veterinary sciencesfungigenetic processes0402 animal and dairy scienceβ-lactoglobulin Promoter Goat SNPs.β-lactoglobulin Promoter Goat SNPsSingle-nucleotide polymorphismPromoter04 agricultural and veterinary sciencesBiology040201 dairy & animal scienceCaprine species0403 veterinary scienceSettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoPolymorphism (computer science)Gene expressionAnimal Science and Zoologynatural scienceslcsh:Animal cultureBinding siteGeneTranscription factorlcsh:SF1-1100
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Are polymorphisms of the β3 -adrenoceptor gene associated with an altered bladder function?

2012

Aims As the presence of a Trp64Arg polymorphism of the gene encoding the β3-adrenoceptor (B3AR) has been linked to the presence of overactive bladder, we investigated whether additional polymorphisms are detectable in this gene and explore their relationships parameters related to lower urinary tract function. Methods The coding region and adjacent stretches of the B3AR gene was sequenced in 91 patients. In total, 1015 patients from a single academic hospital were genotyped for the presence of two single nucleotide polymorphisms. Symptom scores and parameters from pressure-flow studies were analyzed relative to genotype in the B3AR gene. Results No frequent novel polymorphisms were detected…

GeneticsAdrenergic receptorbusiness.industryUrology030232 urology & nephrologySingle-nucleotide polymorphismmedicine.disease03 medical and health sciences0302 clinical medicineOveractive bladder030220 oncology & carcinogenesisGenotypeMedicineCoding regionNeurology (clinical)Gene polymorphismAllelebusinessGeneNeurourology and Urodynamics
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