Search results for "Polymorphism"

showing 10 items of 1968 documents

European traditional tomatoes galore: a result of farmers' selection of a few diversity-rich loci

2022

A comprehensive collection of 1254 tomato accessions, corresponding to European traditional and modern varieties, early domesticated varieties, and wild relatives, was analyzed by genotyping by sequencing. A continuous genetic gradient between the traditional and modern varieties was observed. European traditional tomatoes displayed very low genetic diversity, with only 298 polymorphic loci (95% threshold) out of 64 943 total variants. European traditional tomatoes could be classified into several genetic groups. Two main clusters consisting of Spanish and Italian accessions showed higher genetic diversity than the remaining varieties, suggesting that these regions might be independent seco…

LDQTLPhysiologySLCFruit morphologyMicrobiologiaPlant SciencePortes-lès-ValenceSLLquantitative trait locusSolanum lycopersicumsingle nucleotide polymorphismCrop evolution; diversification; fruit morphology; genome-wide association study; genotyping by sequencing; selection; single nucleotide polymorphismGWASLSLSolanum pimpinellifolium HM ClauseCrop evolutionFarmersSPSolanum lycopersicum var. cerasiformeTomàquets--Conreuminimum allele frequencyMAFPhenotypeDiversificationGenotyping by sequencinglong shelf-lifeGenome-wide association studydiversificationSNPselectionprincipal coordinate analysesGBSFrance Crop evolutionPolymorphism Single Nucleotidegenotyping by sequencingLife ScienceHumansPCoA:Enginyeria agroalimentària::Agricultura::Producció vegetal [Àrees temàtiques de la UPC]SelectionAllelesfruit morphologyGenetic VariationEcologia[SDV.BV.AP]Life Sciences [q-bio]/Vegetal Biology/Plant breedingPlant BreedingSolanum lycopersicum L. var. lycopersicumlinkage disequilibriumTomatoes--VarietiesGenome-Wide Association StudyJ Exp Bot
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Genome-Wide Association Analysis in Primary Sclerosing Cholangitis

2010

Background & Aims We aimed to characterize the genetic susceptibility to primary sclerosing cholangitis (PSC) by means of a genome-wide association analysis of single nucleotide polymorphism (SNP) markers. Methods A total of 443,816 SNPs on the Affymetrix SNP Array 5.0 (Affymetrix, Santa Clara, CA) were genotyped in 285 Norwegian PSC patients and 298 healthy controls. Associations detected in this discovery panel were re-examined in independent case-control panels from Scandinavia (137 PSC cases and 368 controls), Belgium/The Netherlands (229 PSC cases and 735 controls), and Germany (400 cases and 1832 controls). Results The strongest associations were detected near HLA-B at chromosome 6p21…

LOCIMacrophage Stimulating 1 (Hepatocyte Growth Factor-Like)Genome-wide association studySUSCEPTIBILITYGene FrequencyHLA AntigensRisk FactorsHEPATOCELLULAR-CARCINOMAOdds RatioBileBiliary TractINCREASED RISKOligonucleotide Array Sequence AnalysisGastroenterologyMULTIPLE-SCLEROSISCROHNS-DISEASEEuropePhenotypeULCERATIVE-COLITISInflammation MediatorsSNP arrayCholangitis SclerosingSingle-nucleotide polymorphismLocus (genetics)Human leukocyte antigenBiologyPolymorphism Single NucleotideRisk AssessmentCell LinePrimary sclerosing cholangitisGlypicansGenetic predispositionmedicineHumansGenetic Predisposition to DiseaseGene SilencingACID RECEPTOR TGR5Genetic associationInflammationChi-Square DistributionHepatologyGene Expression ProfilingGlypican 6medicine.diseaseGENEG-Protein-Coupled Bile Acid Receptor 1Case-Control StudiesImmunologyColitis UlcerativeGenome-Wide Association StudyINFLAMMATORY-BOWEL-DISEASEGastroenterology
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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

2012

BACKGROUND: High plasma HDL cholesterol is associated with reduced risk of myocardial infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes are randomly assigned at meiosis, are independent of non-genetic confounding, and are unmodified by disease processes, mendelian randomisation can be used to test the hypothesis that the association of a plasma biomarker with disease is causal. METHODS: We performed two mendelian randomisation analyses. First, we used as an instrument a single nucleotide polymorphism (SNP) in the endothelial lipase gene (LIPG Asn396Ser) and tested this SNP in 20 studies (20,913 myocardial infarction cases, 95,407 controls). Se…

LOCIMyocardial Infarction030204 cardiovascular system & hematologychemistry.chemical_compound0302 clinical medicineHigh-density lipoproteinGene Frequencyplasma HDL cholesterol ; mendelian randomisation ; MIHDL cholesterolsingle nucleotide polymorphismRisk FactorsGENETIC-VARIANTSARTERY-DISEASEProspective StudiesMyocardial infarction0303 health sciencesHDL cholesterol; myocardial infarction; single nucleotide polymorphismISCHEMIC CARDIOVASCULAR-DISEASEGeneral Medicine3. Good healthCardiologylipids (amino acids peptides and proteins)medicine.medical_specialtyDalcetrapibSingle-nucleotide polymorphismPolymorphism Single Nucleotide03 medical and health sciencesInternal medicinemedicineHumansCORONARY-HEART-DISEASEGenetic Predisposition to DiseaseMETAANALYSIS030304 developmental biologyBLOOD CHOLESTEROLbusiness.industryCholesterolCholesterol HDLCase-control studyCholesterol LDLLipaseOdds ratioMendelian Randomization Analysismedicine.diseaseENDOTHELIAL LIPASEATHEROSCLEROSISchemistryCase-Control StudiesbusinessHIGH-DENSITY-LIPOPROTEINBiomarkersEvacetrapibThe Lancet
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Comparison of the polymorphs and solvates of two analogous fungicides—a case study of the applicability of a supramolecular synthon approach in cryst…

2011

The polymorphism and solvate formation of thiophanate-ethyl (TE), a fungicidal active, were investigated by solvent crystallization and compared to a close analogue, thiophanate-methyl (TM). Four polymorphs and seven solvates of TE were found and structurally compared with the previously found two polymorphs and fourteen solvates of TM by analyzing the hydrogen bonding patterns and using fingerprint plots, packing coefficients and lattice energies. TE and TM have the same functional groups that can build identical supramolecular synthons. Despite the strong similarities, the polymorphs and solvates of the two actives show significant differences in hydrogen bonding and packing. The results …

Lattice energycrystal formHydrogen bondChemistrySynthonSupramolecular chemistrypolymorfiaGeneral ChemistryCondensed Matter PhysicsCrystal engineeringsolvaattipolymorphismlaw.inventionSolventCrystallographykidemuotosolvatePolymorphism (materials science)lawGeneral Materials ScienceCrystallizationta116CrystEngComm
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The differential diagnoses of uterine leiomyomas and leiomyosarcomas using DNA and RNA sequencing.

2019

BACKGROUND: Although uterine leiomyomas and leiomyosarcomas are considered biologically unrelated tumors, they share morphologic and histologic characteristics that complicate their differential diagnosis. The long-term therapeutic option for leiomyoma is laparoscopic myomectomy with morcellation, particularly for patients who wish to preserve their fertility. However, because of the potential dissemination of undiagnosed or hidden leiomyosarcoma from morcellation, there is a need to develop a preoperative assessment of malignancy risk. OBJECTIVE: Through an integrated comparative genomic and transcriptomic analysis, we aim to identify differential genetic targets in leiomyomas vs leiomyosa…

LeiomyosarcomaAdultLeiomyosarcomaDNA Copy Number Variationsmedicine.disease_causeMalignancyPolymorphism Single NucleotideDNA sequencinggenomic/transcriptomic profileuterine leiomyosarcomaDiagnosis Differential03 medical and health sciences0302 clinical medicineGene DuplicationmedicineHumans030212 general & internal medicineCopy-number variationGeneAgedMutation030219 obstetrics & reproductive medicineuterine leiomyomaLeiomyomabusiness.industrySequence Analysis RNAGene Expression ProfilingObstetrics and GynecologyHigh-Throughput Nucleotide SequencingGenomicsSequence Analysis DNAMiddle Agedmedicine.diseaseBRCA2body regionsLeiomyomaUterine NeoplasmsCancer researchFGFR4FemaleDifferential diagnosisGene FusionbusinessROS1DNA/RNA sequencingGene DeletionAmerican journal of obstetrics and gynecology
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Functional analysis of the -2548G/A leptin gene polymorphism in breast cancer cells

2009

Leptin is overexpressed in human breast tumors and is produced by breast cancer cells in response to obesity-related stimuli. The leptin promoter polymorphism Lep-2548G/A can be associated with increased leptin secretion by adipocytes and elevated cancer risk. However, molecular mechanisms underlying the link between Lep-2548G/A and breast cancer have never been addressed. Lep-2548G/A is proximal to a binding site for the transcriptional factor Sp1. Furthermore nucleolin, a transcriptional repressor, can bind Sp1 or its consensus site. Consequently, we focused on the impact of Lep-2548G/A on Sp1- and nucleolin-dependent leptin transcription in breast cancer cells. The Lep-2548G/A was identi…

LeptinChromatin ImmunoprecipitationCancer Researchmedicine.medical_specialtyGenotypeSp1 Transcription FactorBlotting WesterneducationAdipokineBreast NeoplasmsBiologyBody Mass IndexBreast cancerInternal medicineTumor Cells CulturedmedicineHumansHypoglycemic AgentsInsulinObesityRNA MessengerPromoter Regions Genetichealth care economics and organizationsPolymorphism GeneticLeptin receptorReverse Transcriptase Polymerase Chain ReactionLeptinRNA-Binding ProteinsCancerPhosphoproteinsmedicine.diseaseEndocrinologyOncologyCancer researchImmunohistochemistryBreast diseaseNucleolinhormones hormone substitutes and hormone antagonistsInternational Journal of Cancer
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Aerobic Fitness Does Not Modify the Effect of FTO Variation on Body Composition Traits

2012

Purpose Poor physical fitness and obesity are risk factors for all cause morbidity and mortality. We aimed to clarify whether common genetic variants of key energy intake determinants in leptin (LEP), leptin receptor (LEPR), and fat mass and obesity-associated (FTO) are associated with aerobic and neuromuscular performance, and whether aerobic fitness can alter the effect of these genotypes on body composition. Methods 846 healthy Finnish males of Caucasian origin were genotyped for FTO (rs8050136), LEP (rs7799039) and LEPR (rs8179183 and rs1137101) single nucleotide polymorphisms (SNPs), and studied for associations with maximal oxygen consumption, body fat percent, serum leptin levels, wa…

LeptinMaleAnatomy and PhysiologyLiikuntatiede - Sport and fitness sciencesMuscle FunctionsEpidemiologyRespiratory SystemPhysical fitnesslcsh:MedicineCardiovascular SystemBody Mass Indexlcsh:ScienceMusculoskeletal SystemMultidisciplinaryIGF1VO2 maxAdipose TissueGenetic EpidemiologyBody CompositionCirculatory PhysiologyReceptors LeptinMuscleMedicinePublic HealthWaist CircumferenceBehavioral and Social Aspects of HealthResearch ArticleAdultmedicine.medical_specialtyWaistAlpha-Ketoglutarate-Dependent Dioxygenase FTOBiologyPolymorphism Single NucleotideOxygen ConsumptionInternal medicineGeneticsmedicineHumansAerobic exerciseRespiratory PhysiologySports and Exercise MedicineMuscle SkeletalExerciseBiologyGenetic Association StudiesAerobic capacityLeptin receptorbusiness.industrylcsh:RProteinsnutritional and metabolic diseasesHuman Geneticsmedicine.diseaseObesityOikeuslääketiede ja muut lääketieteet - Forensic science and other medical sciencesEndocrinologylcsh:QPreventive MedicinebusinessBody mass indexPLoS ONE
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Genetic variations of leptin and leptin receptor are associated with body composition changes in response to physical training

2010

Leptin regulates body weight, metabolism, and tissue adaptations to environmental stressors. We examined the association of single nucleotide polymorphism (SNP) of leptin promoter G-2548A (rs7799039) and leptin receptor Gln223Arg (rs1137101) with body composition, plasma leptin levels, and peak oxygen uptake (VO(2)peak) in response to 8 weeks of physical training in 48 male military conscripts. AA homozygotes of leptin promoter SNP-2548 showed higher body fat and BMI values than G allele carriers. Acute exercise decreased leptin levels in G allele carriers, but increased in AA homozygotes. Physical training significantly decreased BMI values and also a tendency for decreased plasma leptin l…

LeptinMalemedicine.medical_specialtyGenotypeClinical BiochemistrySingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideBiochemistryBody Mass IndexYoung AdultOxygen ConsumptionInternal medicinemedicineHumansAllelePromoter Regions GeneticExerciseAllelesLeptin receptorLeptinHomozygotedigestive oral and skin physiologyVO2 maxCell BiologyGeneral MedicineEndocrinologyBlood chemistryHormone receptorBody CompositionReceptors LeptinBody mass indexhormones hormone substitutes and hormone antagonistsCell Biochemistry and Function
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Coordination isomerism in spin crossover (SCO) materials

2021

International audience; A new series of three spin crossover (SCO) Fe(II) complexes based on a cyanocarbanion and on the neutral quinolin-8-amine (aqin) ligands, [Fe(aqin)2(tcnsme)2] (1), [Fe(aqin)2(tcnset)2] (2), and [Fe(aqin)2(tcnspr)2] (3), has been studied. The three complexes display similar molecular structures consisting of discrete [Fe(aqin)2(tcnsR)2] complexes [R = Me (1), Et (2), and Pr (3)]. Infrared spectroscopy and magnetic studies, performed on the three complexes, revealed the presence of similar SCO behaviors which strongly differ by their transition temperatures [234 K (1) < 266 K (2) < 360 K (3)]. The increase of the transition temperatures when passing from 1 to 3 may be …

Ligand field theoryMaterials scienceMolecular magnetic propertiesGeneral Physics and AstronomyInfrared spectroscopyElectron donor02 engineering and technologyCrystal structure01 natural scienceschemistry.chemical_compoundIsomerism[CHIM.ANAL]Chemical Sciences/Analytical chemistrySpin crossover0103 physical sciences[CHIM]Chemical SciencesPolymorphismInfrared spectroscopyAlkylLigand fields010302 applied physicschemistry.chemical_classificationCrystal structureTransition temperature[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyIntermolecular forcesMaterials scienceCoordination isomerismCrystallographychemistry0210 nano-technologyJournal of Applied Physics
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New Reactivity of 4‐Amino‐3,5‐bis(pyridin‐2‐yl)‐1,2,4‐triazole: Synthesis and Structure of a Mononuclear Species, a Dinuclear Species, and a Novel Te…

2007

Reactions of Ni(O 2 CMe) 2 ·4H 2 O or NiCl 2 ·6H 2 O, 4-amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole (abpt) and NaN 3 or KSCN in different molar ratios heated under reflux or hydrothermal conditions generate a mononuclear species with dimorphous phases, a dinuclear species incorporating an in situ deaminated [bpt-H] - ligand and a tetranuclear rectangle box incorporating an unprecedented μ:η 1 :η 2 :η 1 coordination mode of the deprotonated [abpt-H] - ligand. Structural analysis reveals that a pair of [Ni 2 (μ 1,1 -N 3 )(μ-OAc)] motifs in [Ni 4 (abpt) 2 -(abpt-H)(N3) 5 (Ο 2 CMe) 2 ]·5H 2 O (1) are bridged by two abpt and one [abpt-H] - units into a rectangle box. [Ni 2 (bpt-H) 2 -(SCN) 2 (H 2…

LigandStereochemistryChemistry124-Triazolechemistry.chemical_elementMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographyNickelDeprotonationFerromagnetismPolymorphism (materials science)AntiferromagnetismEuropean Journal of Inorganic Chemistry
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