Search results for " pair"

showing 10 items of 779 documents

Identification of a novel candidate locus for juvenile idiopathic arthritis at 14q13.2 in the Latvian population by association analysis with microsa…

2010

To identify novel juvenile idiopathic arthritis (JIA) susceptibility loci, a 270 kb genomic region encompassing FAM177A1, KIAA0391, and PSMA6 genes was genotyped in 97 oligoarthritis (JIoA) and 50 polyarthritis (JIpA) patients and 230 individuals without autoimmune disorders by five microsatellites (MS) previously described as HSMS markers of the 14q13.2 region. Direct sequencing revealed two variable components of the (CAA)(n)(A)(m) motif in HSMS602 marker (FAM177A1 gene). Repeat (AC)(5)AT(AC)(n) of the HSMS701 (KIAA0391 gene) was variable in the Latvian population only in its downstream part. Allele (AC)(5)AT(AC)(15) of HSMS701 was found to be strongly associated with JIA (p = 4.91 x 10(-…

MaleProteasome Endopeptidase ComplexGenetic LinkagePopulationPSMA6BiologyGenotypeGeneticsmedicineOdds RatioHumansGenetic Predisposition to DiseaseAlleleeducationMolecular BiologyAllelesGenetic associationGeneticsChromosomes Human Pair 14education.field_of_studyOligoarthritisPolymorphism GeneticCell BiologyGeneral Medicinemedicine.diseaseLatviaArthritis JuvenileGenetic markerGenetic LociCase-Control StudiesPolyarthritisFemaleMicrosatellite RepeatsDNA and cell biology
researchProduct

Search for a gene responsible for Floating-Harbor syndrome on chromosome 12q15q21.1.

2012

International audience; Floating-Harbor syndrome (FHS) is characterized by characteristic facial dysmorphism, short stature with delayed bone age, and expressive language delay. To date, the gene(s) responsible for FHS is (are) unknown and the diagnosis is only made on the basis of the clinical phenotype. The majority of cases appeared to be sporadic but rare cases following autosomal dominant inheritance have been reported. We identified a 4.7 Mb de novo 12q15-q21.1 microdeletion in a patient with FHS and intellectual deficiency. Pangenomic 244K array-CGH performed in a series of 12 patients with FHS failed to identify overlapping deletions. We hypothesized that FHS is caused by haploinsuf…

AdultHeart Septal Defects VentricularMaleCandidate geneFloating Harbor syndrome[SDV.GEN] Life Sciences [q-bio]/GeneticsHaploinsufficiencyBiologyBioinformaticsShort statureCraniofacial Abnormalities03 medical and health sciences12q15q21.1 microdeletion[SDV.BDD] Life Sciences [q-bio]/Development BiologyGeneticsmedicineHumansAbnormalities MultipleGenetic Predisposition to Disease[ SDV.BDD ] Life Sciences [q-bio]/Development BiologyChild[SDV.BDD]Life Sciences [q-bio]/Development BiologyGenetics (clinical)Growth Disorders030304 developmental biologySequence DeletionPhenocopyGenetics0303 health sciencesComparative Genomic Hybridization[SDV.GEN]Life Sciences [q-bio]/GeneticsChromosomes Human Pair 12Genetic heterogeneity030305 genetics & heredityChromosomeHigh-Throughput Nucleotide Sequencinghigh-throughput sequencingmedicine.disease3. Good healthPhenotypeFloating–Harbor syndromeChild PreschoolMutation (genetic algorithm)Femalemedicine.symptomHaploinsufficiency[ SDV.GEN ] Life Sciences [q-bio]/Genetics
researchProduct

Involvement of the long arm of chromosome 9 in medulloblastoma in an adult.

1997

Abstract Medulloblastoma is the most common primitive neuroectodermal tumor (PNET) in children, but is very rare in adults. An isochromosome for the long arms of 17, i(17q), is found in about 30% of pediatric cases. Cytogenetic studies in adults are very scarce; only six cases have been described cytogenetically: three cases had normal karyotype, two were studied partially, and another presented only two clonal structural anomalies: del(9)(q12) and del(11)(q22). We studied the chromosomes from medulloblastoma in a 27-year-old woman and found one hypotetraploid stemline with clonal alterations. In the structural anomalies, chromosomes 3, 9, 12, and i(17q) were involved. Chromosome 9 presente…

MedulloblastomaAdultCancer Researchmedicine.medical_specialtyPathologyAdult MedulloblastomaIsochromosomeCytogeneticsChromosome 9KaryotypeAnatomyBiologymedicine.diseasePrimitive neuroectodermal tumorKaryotypingGeneticsmedicineHumansHistopathologyFemaleChromosome DeletionCerebellar NeoplasmsChromosomes Human Pair 9Molecular BiologyMedulloblastomaCancer genetics and cytogenetics
researchProduct

Evidence against linkage of schizophrenia to chromosome 5q11-q13 markers in systematically ascertained families.

1992

Ten pedigrees systematically ascertained in Germany were tested for linkage to chromosome 5q11-q13. In order to replicate the previous report by Sherrington et al (1988), families with a bipolar family member were omitted from the lod score calculations, all diagnoses were based upon Research Diagnostic Criteria, and four different models of the affection status were calculated, including the model for which Sherrington et al calculated the highest lod scores. None of the families investigated showed a positive lod score. Using multipoint linkage analyses, we were able to exclude the region for which a positive linkage has been reported.

Linkage (software)GeneticsGenetic Markerscongenital hereditary and neonatal diseases and abnormalitiesGenetic LinkageResearch Diagnostic CriteriaPedigree chartmedicine.diseaseFamily memberChromosome (genetic algorithm)Psychotic DisordersSchizophreniamedicineSchizophreniaChromosomes Human Pair 5HumansFamilyLymphocytesLod ScorePsychologyBiological PsychiatryLod scoresLod scoreBiological psychiatry
researchProduct

Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent

1994

The Friedreich's ataxia locus (FRDA) maps on chromosome 9q13. Genetic data, obtained from a small number of recombination events, indicated that the FRDA locus might be located centromeric to the D9S15/D9S5 linkage group, the most probable order being cen-FRDA-D9S5-D9S111-D9S15-D9S110-qter. Recently, new centromeric markers have been reported. Analysis of these markers allowed us to localize the recombination breakpoint in some of the recombinant families. However, only one proximal recombination has been found with these markers. To increase the genetic information from FRDA families, we have analyzed the centromeric markers FR1, FR2, FR7, FR8, and FR5 in patients homozygous by descent. Th…

GeneticsAtaxiaConsanguineous familyHaplotypeCentromereGenetic dataChromosome MappingLocus (genetics)BiologyPedigreeMeiosisFriedreich AtaxiaGeneticsmedicineHumansIn patientmedicine.symptomChromosomes Human Pair 9Genetics (clinical)RecombinationBiomarkers
researchProduct

Extractive Spectrophotometric Determination of Ondansetron by Ion-Pair Formation with Bromocresol Green

1996

Abstract An empirical spectrophotometric procedure for the determination of the antiemetic ondansetron is carried out. The method is based on the formation of a 1:1 ion pair with bromocresol green in the pH range over 3.2 – 4.4, extraction into chloroform layer and spectrophotometric measurement at 420.8 nm. The calibration graph is linear over the range 0.1 – 20 μg ml−1 ondansetron, with a relative standard deviation of 2.7%; the influence of foreign substances is also studied. The method is applied to ondansetron determination in human urine.

ChromatographyChloroformBromocresol greenmedicine.diagnostic_testCalibration curveBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Ion pairsBiochemistryAnalytical ChemistryOndansetronchemistry.chemical_compoundchemistrySpectrophotometryElectrochemistrymedicineQuantitative analysis (chemistry)Spectroscopymedicine.drugAnalytical Letters
researchProduct

Analytical Approach Determining the Optimal Length of Paired Drip Laterals in Uniformly Sloped Fields

2015

Microirrigation plants, if properly designed, allow for water use efficiency to be optimized and high values of emission uniformity to be obtained in the field. Disposing paired laterals, for which two distribution pipes extend in opposite directions from a common manifold, can contribute to reducing the initial investment cost that represents a limiting factor for small-scale farmers of developing countries where in the last decade, the diffusion of such irrigation systems has been increasing. The objective of this paper is to propose an analytical approach to evaluate the maximum lengths of paired drip laterals for any uniform ground slope, respecting the criteria to maintain emitter flow…

OptimizationField (physics)Low-flow irrigation systemsDrip irrigationMechanicsAnalytical techniquesAgricultural and Biological Sciences (miscellaneous)Drip irrigation systems paired laterals designTrickle irrigation; Optimization; Analytical techniquesSettore AGR/08 - Idraulica Agraria E Sistemazioni Idraulico-ForestaliGeotechnical engineeringTrickle irrigationWater Science and TechnologyCivil and Structural EngineeringMathematicsJournal of Irrigation and Drainage Engineering
researchProduct

FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates

2000

Accumulating evidence suggests that haploinsufficiency of a dosage-sensitive gene(s) in human chromosome 9p24.3 is responsible for the failure of testicular development and feminisation in XY patients with monosomy for 9p. We have used molecular cytogenetic methods to characterise the sex-reversing 9p deletions in two XY females. Fluorescence in situ hybridisation (FISH) with YACs from the critical 9p region containing an evolutionarily conserved sex-determining gene, DMRT1, is a very fast and reliable assay for patient screening. Comparative YAC mapping on great ape and Old and New World monkey chromosomes demonstrated that the critical region was moved from an interstitial position on the…

MonosomyX ChromosomeDisorders of Sex DevelopmentChromosome BreakpointsChromosomal translocationBiologyY chromosomePolymerase Chain ReactionTranslocation GeneticY ChromosomeGeneticsmedicineAnimalsHumansChromosomes Artificial YeastIn Situ Hybridization FluorescenceGenetics (clinical)X chromosomeChromosomal inversionGeneticsChromosome MappingChromosomeKaryotypemedicine.diseaseCebidaeKaryotypingFemaleChromosome DeletionChromosomes Human Pair 9Transcription FactorsEuropean Journal of Human Genetics
researchProduct

A measurement of the inclusive b → sγ branching ratio

1998

The flavour changing neutral current decay b --> s gamma has been detected in hadronic Z decays collected by ALEPH at LEP. The signal is isolated in lifetime-tagged b (b) over bar events by the presence of a hard photon associated with a system of high momentum and high rapidity hadrons. The background processes are normalised from the data themselves. The inclusive branching ratio is measured to be (3.11 +/- 0.80(stat) +/- 0.72(syst)) x 10(-4), consistent with the Standard Model expectation via penguin processes. (C) 1998 Published by Elsevier Science B.V. All rights reserved. The flavour changing neutral current decay b → sγ has been detected in hadronic Z decays collected by ALEPH at …

Nuclear and High Energy PhysicsParticle physicsPhotonelectron positron. colliding beamselectron positron. annihilationElectron–positron annihilationquark. pair productionHadronlepStandard ModelquarkALEPH ExperimentNuclear physicsRapidityALEPH experimentPhysicselectron positronNeutral currentquark. radiative decayBranching fractionPhysicsHigh Energy Physics::PhenomenologyALEPH Experiment; lepquark. branching ratioHigh Energy Physics::Experimentexperimental results
researchProduct

Vector current conservation and neutrino emission from singlet-paired baryons in neutron stars

2006

Neutrino emission caused by singlet Cooper pairing of baryons in neutron stars is recalculated by accurately taking into account for conservation of the vector weak currents. The neutrino emissivity via the vector weak currents is found to be several orders of magnitude smaller than that obtained before by different authors. This makes unimportant the neutrino radiation from singlet pairing of protons or hyperons.

PhysicsNuclear and High Energy PhysicsParticle physicsProtonAstrophysics::High Energy Astrophysical PhenomenaAstrophysics (astro-ph)Nuclear TheoryHigh Energy Physics::PhenomenologyHyperonFOS: Physical sciencesAstrophysics::Cosmology and Extragalactic AstrophysicsAstrophysicsPartícules (Física nuclear)BaryonNuclear physicsHigh Energy Physics - PhenomenologyNeutron starHigh Energy Physics - Phenomenology (hep-ph)PairingHigh Energy Physics::ExperimentNeutrinoCooper pairNeutrino oscillationNuclear ExperimentPhysics Letters B
researchProduct