Search results for "Cytogenetic"

showing 10 items of 159 documents

Spermatocyte chromosome analysis of Helicella virgata (Pulmonata: Helicidae): silver-stained and C-banded chromosomes.

1991

Chromosome numbers of the snail Helicella virgata from the fields of Castellammare del Golfo (Sicily) are n = 26 and 2n = 52. Silver-staining analyses of testicular cells suggest that both mitotic and meiotic chromosomes are involved in nucleolus organization. A within-individual variability in NOR-banding pattern is present in each of the 20 specimens analyzed.

Malemedicine.medical_specialtySnailsMitosisChromosomesHelicidaeMeiosisSpermatocytesOxazinesGeneticsmedicineAnimalsSpermatogenesisMolecular BiologyGenetics (clinical)GeneticsbiologyStaining and LabelingCytogeneticsChromosomeKaryotypeNucleolus organizationbiology.organism_classificationMolecular biologyChromosome BandingMeiosisKaryotypingHelicellaNucleolus organizer regionBiotechnologyThe Journal of heredity
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Karyological studies in Coris julis (Pisces, Labridae).

1988

In the present investigation the diploid number 2n = 48 (NF = 58) has been determined for females, primary males, and secondary males of Coris julis from the Gulf of Palermo. Differentiated sex chromosomes have not been observed in the population under study.

Malemedicine.medical_specialtyeducation.field_of_studySex ChromosomesbiologyCorisPopulationCytogeneticsFishesZoologyKaryotypePlant ScienceGeneral Medicinebiology.organism_classificationDiploidyInsect ScienceKaryotypingGeneticsmedicineAnimalsAnimal Science and ZoologyFemalePloidyeducationMetaphaseGenetica
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Relationships of the Woody Medicago Species (Section Dendrotelis) Assessed by Molecular Cytogenetic Analyses

2008

†Background and Aims The organization of rDNA genes in the woody medic species from the agronomically important Medicago section Dendrotelis was analysed to gain insight into their taxonomic relationships, to assess the levels of infraspecific variation concerning ribosomal loci in a restricted and fragmented insular species (M. citrina) and to assess the nature of its polyploidy. †Methods Fluorescence in situ hybridization (FISH) was used for physical mapping of 5S and 45S ribosomal DNA genes in the three species of section Dendrotelis (M. arborea, M. citrina, M. strasseri) and the related M. marina from section Medicago. Genomic in situ hybridization (GISH) was used to assess the genomic …

Medicagomedicine.diagnostic_testbiologyDNA Plantfood and beveragesMedicago arboreaLocus (genetics)Plant ScienceOriginal Articlesbiology.organism_classificationDNA RibosomalChromosomes PlantPolyploidyPolyploidBotanyCytogenetic AnalysismedicineMedicagoPloidyRibosomal DNAIn Situ Hybridization FluorescenceFluorescence in situ hybridizationHybrid
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Chromosome analysis of Bothus podas (Pisces, Pleuronectiformes) from the Mediterranean Sea

1993

A modal diploid number 2n=38 has been determined in both sexes of the pleuronectiform Bothus podas from the Gulf of Palermo (Mediterranean). An XX-XY sex-determining mechanism presumably occurs in this species. Application of silver staining (NORs) along with G- and C-banding techniques showed that secondary constrictions occurring in a large metacentric pair were variable in length in different fish. Polymorphisms of these areas seem to have a genetic, rather than transcriptional, basis.

Mediterranean climatemedicine.medical_specialtyCytogeneticsZoologyKaryotypeAquatic ScienceBiologyMediterranean seaChromosome analysisBothus podasmedicinePloidyNucleolus organizer regionEcology Evolution Behavior and SystematicsJournal of Fish Biology
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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
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Systematics of Mepraia (Hemiptera-Reduviidae): cytogenetic and molecular variation.

2009

The haematophagous insects of the subfamily Triatominae (Hemiptera-Reduviidae) have great epidemiological importance as vectors of Trypanosoma cruzi, the causative agent of Chagas disease. Mepraia was originally described as a monotypic genus comprised of Mepraia spinolai, distributed along coastal areas of northern Chile (from Region I to the Metropolitan Region). Recently, some M. spinolai populations have been ranked as a new species named Mepraia gajardoi. Several populations along the distribution range of the genus were sampled, and genetic differentiation was studied based upon the analysis of three molecular markers: cytogenetics (karyotype and chromosome behaviour during meiosis us…

Microbiology (medical)SystematicsMaleMitochondrial DNAMolecular Sequence DataMicrobiologyPolymerase Chain ReactionMepraiaCytogeneticsIntergenic regionGeneticsAnimalsChagas DiseaseChileGonadsMolecular BiologyRibosomal DNAEcology Evolution Behavior and SystematicsPhylogenyGeneticsPolymorphism GeneticbiologyMolecular epidemiologyBase SequenceGeographyChromosomebiology.organism_classificationInsect VectorsInfectious DiseasesReduviidaeEvolutionary biologyDNA IntergenicFemaleTriatominaeSequence AlignmentInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
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Ribosomal DNA 18S-28S sequence Probe Mapping on Primate Genome: evolutionary insights

2017

Molecular cytogenetics phylogenySettore BIO/08 - Antropologia
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Primate Cytogenetics and Comparative Genomics

2006

This volume is a collection of contributions of a Florentine post congress symposium on "Primate Cytogenetics and Comparative Genomics" held on occasion of the XX International Primatological Congress (Turin in 2004). Comparative Molecular Cytogenetics and Genomics are two rapidly expanding fields. Researchers from Italy, Germany, Spain, United States and Japan meet in Florence to discuss over a two day period recent advances and summarize the current state of the science.

Molecular cytogeneticsComparative genomicsmedicine.medical_specialtyHistoryeducationCytogeneticsmedicineLibrary scienceState of the sciencehealth care economics and organizations
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Eradication of Culex pipiens fatigans through Cytoplasmic Incompatibility

1967

Culex pipiens fatigans is the chief vector of filariasis in south-east Asia. Urbanization has often caused the numbers of this mosquito—and with it the danger of filariasis infection—to increase alarmingly1. The natural vigour, tolerance and fast development of resistance to insecticides of this mosquito necessitate the development of other control methods, and cytoplasmic incompatibility2 seems to be an ideal means.

MultidisciplinaryPesticide resistancefungiZoologyMyanmarBiologymedicine.diseaseInsect ControlFilariasisCulex pipiens fatigansToxicologyCulexCytogeneticsSexual Behavior AnimalGenetics PopulationInsecticide resistanceVector (epidemiology)parasitic diseasesmedicineAnimalsNatural enemiesControl methodsCytoplasmic incompatibilityNature
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DNMT3A mutations Predict for Inferior Outcome in NPM1-Wildtype and Molecular Unfavorable Cytogenetically-Normal Acute Myeloid Leukemia: A Study of th…

2011

Abstract Abstract 415 Background: Alteration of DNA methylation, a hallmark of epigenetic modification, is currently discussed as one important pathomechanism in leukemogenesis. Using a next-generation sequencing approach, a frameshift mutation of the gene encoding the DNA methyltransferase (DNMT3A) in an acute myeloid leukemia (AML) case was identified. DNMT3A catalyses the addition of a methyl group to the cytosine residue of CpG dinucleotides, thereby affecting promoter methylation status and gene expression. Subsequent sequencing analysis in an independent cohort of 288 AML patients (pts) revealed DNMT3A mutations (DNMT3Amut) in 22% of the pts; mutations were associated with intermediat…

MutationNPM1medicine.medical_specialtyImmunologyCytogeneticsMyeloid leukemiaCell BiologyHematologyBiologymedicine.disease_causeBiochemistryIDH2Molecular biologyFrameshift mutationCEBPAmedicineMissense mutationBlood
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