Search results for " 16"

showing 10 items of 871 documents

The gene encoding the transcriptional repressor BERF-1 maps to a region of conserved synteny on mouse chromosome 16 and human chromosome 3 and a rela…

1999

We have recently identified and characterized a Kruppel-like zinc finger protein (BERF-1), that functions as a repressor of β enolase gene transcription. By interspecific backcross analysis the gene encoding BERF-1 was localized 4.7 cM proximal to the <i>Mtv6</i> locus on mouse chromosome 16, and an isolated pseudogene was localized to mouse chromosome 8, about 5.3 cM distal to the D8Mit4 marker. Nucleotide sequence identity and chomosome location indicate that the gene encoding BERF-1 is the mouse homologue (<i>Zfp148</i>) of ZNF148 localized to human chromosome 3q21, a common translocation site in acute myeloid leukemia patients.

Genetic MarkersDNA ComplementaryTranscription GeneticKruppel-Like Transcription FactorsBiologyHybrid CellsPolymerase Chain ReactionGene Expression Regulation EnzymologicMiceChromosome 16GeneticsAnimalsHumansMolecular BiologyGenetics (clinical)Conserved SequenceSyntenyDNA PrimersGeneticsBase SequenceYY1Chromosome MappingTAF9Zinc FingersTCF4DNA-Binding ProteinsRepressor ProteinsChromosome 3GATAD2BPhosphopyruvate Hydratasecardiovascular systemChromosomes Human Pair 3Chromosome 22PseudogenesTranscription FactorsCytogenetics and cell genetics
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Autosomal dominant polycystic kidney disease—in vitro culture of cyst-lining epithelial cells

1992

The major form of autosomal dominant polycystic kidney disease (ADPKD) in humans is linked to the PKD1 gene on chromosome 16p. The identity of the gene and the underlying pathogenetic mechanisms are not yet defined. Cyst-lining epithelial cells derived from a polycystic kidney were successfully grown in culture and designated MZ-PKD-1 cells. By linkage analysis, the related pedigree of the nephrectomized patient could be linked to the PKD1 gene on chromosome 16p. Thus, these cells exhibit the genotype of a mutated PKD1 gene and represent an in vitro culture model for ADPKD involving chromosome 16p. The antigenic phenotype was characterized immunohistologically by epithelial differentiation …

Genetic MarkersPathologymedicine.medical_specialtyAutosomal dominant polycystic kidney diseaseHLA-C AntigensBiologyEpitheliumGenetic linkagemedicineHumansNorthern blotGeneCells CulturedHLA-A AntigensPKD1urogenital systemAntibodies MonoclonalGeneral MedicineMiddle AgedBlotting NorthernPolycystic Kidney Autosomal Dominantmedicine.diseaseImmunohistochemistryMolecular biologyPhenotypePedigreeBlotMicroscopy ElectronPhenotypeHLA-B AntigensCell cultureFemaleChromosomes Human Pair 16Virchows Archiv B Cell Pathology Including Molecular Pathology
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Geosphere-biosphere interactions in bio-activity volcanic lakes: Evidences from Hule and Rìo Cuarto (Costa Rica)

2014

Hule and R ́ıo Cuarto are maar lakes located 11 and 18 km N of Poa ́s volcano along a 27 km long fracture zone, in the Central Volcanic Range of Costa Rica. Both lakes are characterized by a stable thermic and chemical stratification and recently they were affected by fish killing events likely related to the uprising of deep anoxic waters to the surface caused by rollover phenomena. The vertical profiles of temperature, pH, redox potential, chemical and isotopic compositions of water and dissolved gases, as well as prokaryotic diversity estimated by DNA fingerprinting and massive 16S rRNA pyrosequencing along the water column of the two lakes, have highlighted that different bio-geochemica…

Genetics and Molecular Biology (all)Aerobic bacterialcsh:MedicineMarine and Aquatic Sciencestrace elementsSettore BIO/19 - Microbiologia GeneraleBiochemistryWater columnBiochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)RNA Ribosomal 16SLimnologylcsh:SciencePhylogenyTotal organic carbonMultidisciplinarygeography.geographical_feature_categoryEcologyBiosphereBiogeochemistryHydrogen-Ion ConcentrationAnoxic watersMaarChemistryOceanographyPhysical SciencesMethaneOxidation-ReductionResearch ArticleFreshwater EnvironmentsCosta RicaSettore BIO/07 - EcologiaVolcanic EruptionsCarbon CycleHydrothermal VentsEnvironmental ChemistryMolecular Biology TechniquesSequencing TechniquesMolecular BiologygeographyVolcanic lakeBacterialcsh:RHigh Throughput SequencingEcology and Environmental SciencesOrganismsChemical CompoundsBiology and Life SciencesAquatic EnvironmentsCarbon DioxideArchaeaDNA FingerprintingOxygenLakesGeochemistryVolcanoAgricultural and Biological Sciences (all)Settore GEO/08 - Geochimica e VulcanologiaEarth SciencesEnvironmental sciencelcsh:QSurface water
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Coexistence of Wolbachia with Buchnera aphidicola and a Secondary Symbiont in the Aphid Cinara cedri

2004

ABSTRACT Intracellular symbiosis is very common in the insect world. For the aphid Cinara cedri , we have identified by electron microscopy three symbiotic bacteria that can be characterized by their different sizes, morphologies, and electrodensities. PCR amplification and sequencing of the 16S ribosomal DNA (rDNA) genes showed that, in addition to harboring Buchnera aphidicola , the primary endosymbiont of aphids, C. cedri harbors a secondary symbiont (S symbiont) that was previously found to be associated with aphids (PASS, or R type) and an α-proteobacterium that belongs to the Wolbachia genus. Using in situ hybridization with specific bacterial probes designed for symbiont 16S rDNA seq…

Genetics and Molecular BiologyBacterial genome sizeBiologyDNA RibosomalPolymerase Chain ReactionMicrobiologyBuchneraRNA Ribosomal 16SBotanyAnimalsSymbiosisMolecular BiologyRibosomal DNAPhylogenyGeneticsAphidBacteriocytefungifood and beveragesbiochemical phenomena metabolism and nutritionbiology.organism_classificationMicroscopy ElectronAphidsCinarabacteriaWolbachiaBuchneraWolbachiaSymbiotic bacteriaJournal of Bacteriology
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Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

2008

Contains fulltext : 69243.pdf (Publisher’s version ) (Closed access) Genetic contribution to the development of attention deficit hyperactivity disorder (ADHD) is well established. Seven independent genome-wide linkage scans have been performed to map loci that increase the risk for ADHD. Although significant linkage signals were identified in some of the studies, there has been limited replications between the various independent datasets. The current study gathered the results from all seven of the ADHD linkage scans and performed a Genome Scan Meta Analysis (GSMA) to identify the genomic region with most consistent linkage evidence across the studies. Genome-wide significant linkage (P(S…

Genetics and epigenetic pathways of disease [NCMLS 6]Genetic LinkageEuropean Continental Ancestry GroupMedizinGenome ScanBiologyNeuroinformatics [DCN 3]Mental health [NCEBP 9]Genetic determinismWhite PeopleArticleChromosomesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineGene mappingCognitive neurosciences [UMCN 3.2]Genetic linkageGenetic predispositionmedicinePerception and Action [DCN 1]Attention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersGenetics (clinical)030304 developmental biologyProbabilityLinkage (software)Genetics0303 health sciencesGenomeGenome HumanPair 16Chromosome Mappingmedicine.diseasePsychiatry and Mental healthGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityMeta-analysisLod ScoreFunctional Neurogenomics [DCN 2]030217 neurology & neurosurgeryChromosomes Human Pair 16HumanAmerican Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
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Genetics of Polyglandular Failure

2016

The rare autoimmune polyglandular failure syndromes (APS) comprise a juvenile (APS1) and an adult type (APS2 and 3). APS1 is caused by mutations in the autoimmune regulatory (AIRE) gene on chromosome 21 and is inherited in an autosomal recessive manner. Mutations in the AIRE gene impair self-tolerance and result in defect proteins causing autoimmune destruction of target organs. Genetic testing identifies patients with APS1. For APS2/3 disease susceptibility genes are the human leucocyte antigen on chromosome 6, the cytotoxic T lymphocyte antigen (chromosome 2), the protein tyrosine phosphatase nonreceptor type 22 (chromosome 1), the forkhead box P3 (X chromosome), and the interleukin-2 rec…

GeneticsCandidate geneChromosome 16AntigenChromosomeBiologyChromosome 21GeneX chromosomeChromosome 12
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Pseudo-exclusion from paternity due to maternal uniparental disomy 16.

1998

The investigation of a case of disputed paternity revealed indirect exclusion of the alleged father in the haptoglobin system and in the DNA single-locus system D16S309/Hinf I (MS205). The paternity index for the non-exclusion systems was > 10(6). Since both exclusion systems (HP and MS205) are located on chromosome 16, we investigated 10 microsatellite loci covering this chromosome with 10-20 cM resolution. Analysis of the child's chromosome showed only alleles of maternal origin and lack of inheritance of paternal alleles for five informative loci. The markers close to the centromere of chromosome 16 were heterozygous, whereas distal loci were either heterozygous or homozygous for materna…

GeneticsChromosome AberrationsMalePaternity IndexHaptoglobinsChromosomePaternityUniparental HeterodisomyBiologyPolymerase Chain ReactionPathology and Forensic MedicineChromosome 16NondisjunctionNondisjunction GeneticCentromereMicrosatelliteHumansFemaleAlleleChildAllelesChromosomes Human 16-18Microsatellite RepeatsInternational journal of legal medicine
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Reciprocal translocation t(1;18)(p32;q21) in a patient with some phenotypical anomalies

1987

The authors report on a case of 1;18 translocation and request contact with any colleagues who have observed similar cases.

GeneticsEyelashesChromosomal translocationBiologyPhenotypeMolecular medicineTranslocation GeneticHuman geneticsPhenotypeChromosomes Human Pair 1GeneticsHumansFemaleEyebrowsMetabolic diseaseChildChromosomes Human Pair 16Genetics (clinical)Human Genetics
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Phylogenetic relationships within the family Halomonadaceae based on comparative 23S and 16S rRNA gene sequence analysis.

2010

A phylogenetic study of the family Halomonadaceae was carried out based on complete 16S rRNA and 23S rRNA gene sequences. Several 16S rRNA genes of type strains were resequenced, and 28 new sequences of the 23S rRNA gene were obtained. Currently, the family includes nine genera (Carnimonas, Chromohalobacter, Cobetia, Halomonas, Halotalea, Kushneria, Modicisalibacter, Salinicola and Zymobacter). These genera are phylogenetically coherent except Halomonas, which is polyphyletic. This genus comprises two clearly distinguished clusters: group 1 includes Halomonas elongata (the type species) and the species Halomonas eurihalina, H. caseinilytica, H. halmophila, H. sabkhae, H. almeriensis, H. hal…

GeneticsHalomonasPhylogenetic treebiologyMolecular Sequence DataGenes rRNAGeneral MedicineSequence Analysis DNARibosomal RNAbiology.organism_classificationMicrobiologyDNA RibosomalBacterial Typing TechniquesHalomonadaceaeType speciesHalomonadaceaeRNA Ribosomal 23SSpecies Specificity23S ribosomal RNARNA Ribosomal 16SRibosomal DNAHalomonas salariaEcology Evolution Behavior and SystematicsPhylogenyInternational journal of systematic and evolutionary microbiology
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On the Specificity of PCR Detection of Listeria monocytogenes in Food: a Comparison of Published Primers

2002

A total of nine pairs of primers, seven previously published and two newly developed, have been assayed for PCR detection of Listeria monocytogenes in food. They have been tested for specificity on a total of 72 strains including reference and food isolates belonging to L. monocytogenes and other species in the genus. First of all, a polyphasic approach has been carried out in order to establish a reference strain collection. They were biochemically and genetically characterized by API-Lis and randomly amplified polymorphic DNA PCR (RAPD-PCR), respectively. Random amplification of DNA was performed with M13, T7 and T3 universal primers and a data bank was created to compile the RAPD pattern…

GeneticsSequence analysisUPGMARibosomal RNABiology16S ribosomal RNAmedicine.disease_causeListeria monocytogenesSensitivity and SpecificityApplied Microbiology and BiotechnologyMicrobiologyRandom Amplified Polymorphic DNA TechniqueMicrobiologylaw.inventionRAPDListeria monocytogeneslawRNA Ribosomal 16SFood MicrobiologymedicinePrimer (molecular biology)PhylogenyEcology Evolution Behavior and SystematicsPolymerase chain reactionDNA PrimersSystematic and Applied Microbiology
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