Search results for "chromosome"

showing 10 items of 1175 documents

Reconstitution of the Complement Function in C1q-Deficient (C1qa−/−) Mice with Wild-Type Bone Marrow Cells

2001

Abstract Besides Ab-independent and Ab-dependent activation of the complement classical pathway in host defense, C1q plays a key role in the processing of immune complexes and in the clearance of apoptotic cells. In humans, C1q deficiency leads to systemic lupus erythematosus-like symptoms in over 90% of the cases, thus making this defect a strong disease susceptibility factor. Similarly, C1q-deficient mice (C1qa−/−) develop systemic lupus erythematosus-like symptoms, such as autoantibodies and glomerulonephritis. We have previously provided evidence that C1q is produced by cells of the monocyte-macrophage lineage. In this study, we have tested whether transplantation of bone marrow cells w…

Malemedicine.medical_treatmentImmunologychemical and pharmacologic phenomenaHematopoietic stem cell transplantationBiologyMiceClassical complement pathwayImmune systemimmune system diseasesY ChromosomemedicineAnimalsLupus Erythematosus SystemicImmunology and AllergyTissue DistributionRNA Messengerskin and connective tissue diseasesBone Marrow TransplantationMice KnockoutLupus erythematosusComplement C1qHematopoietic Stem Cell TransplantationGlomerulonephritismedicine.diseaseMice Inbred C57BLTransplantationKineticsmedicine.anatomical_structureImmunologyFemaleBone marrowStem cellThe Journal of Immunology
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14q13.1-21.1 deletion encompassing the HPE8 locus in an adolescent with intellectual disability and bilateral microphthalmia, but without holoprosenc…

2011

Interstitial deletions involving 14q13.1q21.1 are rare. In the literature at least 10 cases involving this region have been described and all patients showed a phenotype within the holoprosencephaly (HPE) spectrum. Previous studies suggested the HPE8 region as a candidate locus for HPE at 14q13. We report an adolescent with a 14q13.1q21.1 deletion encompassing the HPE8 region associated with intellectual disability (ID), bilateral microphthalmia, and coloboma, without cerebral anomalies typical of HPE. Except for ocular defects (i.e., microphthalmia, coloboma) consistent with HPE-type anomalies, the minor facial dysmorphia was not suggestive for HPE and the absence of cerebral anomalies sho…

Malemusculoskeletal diseasescongenital hereditary and neonatal diseases and abnormalitiesCandidate geneAdolescentID/MCA deletion syndromeLocus (genetics)MicrophthalmiamicroformSettore MED/38 - Pediatria Generale E SpecialisticaHoloprosencephalyIntellectual DisabilityIntellectual disabilityGeneticsmedicineHumansMicrophthalmoschromosome 14q deletionIn Situ Hybridization FluorescenceGenetics (clinical)Sequence DeletionChromosomes Human Pair 14GeneticsComparative Genomic HybridizationColobomabiologybusiness.industryNPAS3Faciesmedicine.diseaseeye diseasesDevelopmental disorderPhenotypeholoprosencephalySettore MED/03 - Genetica MedicaGenetic Lociarray-CGHbiology.proteinbusinessAmerican Journal of Medical Genetics Part A
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Sex reversal from functional disomy of Xp: Prenatal and post-mortem findings.

2008

Translocations involving the short arms of the X and Y chromosomes are uncommon and are often associated with anomalies in gonadal development. Segmental duplications of the X chromosome interfere with the formation of the testis in patients with a 46,XY karyotype. The gene products located within the duplicated segment, when present in double dose, may affect on male sex development. We report on a fetus with karyotype 46,XY,der (14)t(X;14) (p10;p10)dn. Attached to chromosome 14 is the entire short arm of the X chromosome. Therefore, the fetus is affected with a disomy of Xp, resulting in complete male to female sex reversal, as well as other structural defects. To the best of our knowledg…

Malesex severalDisorders of Sex DevelopmentChromosomal translocationBiologysex reversal • Xp disomy • DAX1 gene • multiple congenital anomaliesTranslocation GeneticChromosome PaintingSettore MED/38 - Pediatria Generale E SpecialisticaPregnancyPrenatal DiagnosisGene duplicationGeneticsHumansAbnormalities MultipleGenetics (clinical)X chromosomeSex Chromosome AberrationsSegmental duplicationUltrasonographyGeneticsChromosome AberrationsChromosomes Human Pair 14FetusChromosomes Human XSex ChromosomesInfant NewbornChromosomeKaryotypeSex reversalChromosome BandingPhenotypeSettore MED/03 - Genetica MedicaKaryotypingTetralogy of FallotFemaledisomy XpDandy-Walker Syndrome
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All-Food-Seq (AFS): a quantifiable screen for species in biological samples by deep DNA sequencing.

2013

Background DNA-based methods like PCR efficiently identify and quantify the taxon composition of complex biological materials, but are limited to detecting species targeted by the choice of the primer assay. We show here how untargeted deep sequencing of foodstuff total genomic DNA, followed by bioinformatic analysis of sequence reads, facilitates highly accurate identification of species from all kingdoms of life, at the same time enabling quantitative measurement of the main ingredients and detection of unanticipated food components. Results Sequence data simulation and real-case Illumina sequencing of DNA from reference sausages composed of mammalian (pig, cow, horse, sheep) and avian (c…

MeatMethodology ArticleChromosome MappingHigh-Throughput Nucleotide SequencingSequence Analysis DNABiosurveillanceSpecies SpecificityIlluminaCalibrationDatabases GeneticFood QualityNext-generation sequencingAnimalsHumansMetagenomicsSpecies identificationReal-time PCRBMC genomics
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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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Chromosomal location polymorphism of major rDNA sites in two Mediterranean populations of the killifih Aphanius fasciatus (Pisces: Cyprinodontidae)

2005

The chromosomes of the Mediterranean killifish, Aphanius fasciatus from two populations, the Lagoon of Venice (LV, 15 specimens) and the Lagoon ‘Stagnone di Marsala’ (Sicily) (SM, 48 specimens), have been investigated using conventional Ag-staining and fluorescent in situ hybridization (FISH) with 18S rDNA probe. The two methods revealed variation in the number of major rDNA sites ranging from 8 to 14 (LV) and from 1 to 4 (SM) per individual. The fact that each individual possessed its own number of sites implies that observed variation was structural. Moreover, overlapping of silver staining and FISH patterns demonstrated that all ribosomal genes were transcriptionally active in each speci…

Mediterranean climateMaleSilverAphanius fasciatuAphaniusGeneral Physics and AstronomyZoologyrDNABiologyDNA RibosomalChromosomesKaryotype polymorphismMediterranean seaStructural BiologyPolymorphism (computer science)FundulidaeNucleolus Organizer RegionAnimalsGeneral Materials Science18s rdnaKillifishIn Situ Hybridization FluorescenceGeneticsPolymorphism GeneticStaining and LabelingCell BiologyRibosomal RNAbiology.organism_classificationGenetics PopulationItalyKaryotypingMediterranean seaFemaleIn situ hybridizationMediterranean killifish
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Population structure in the Méditerranean basin: a Y chromosome perspective

2006

The Mediterranean region has been characterised by a number of pre-historical and historical demographic events whose legacy on the current genetic landscape is still a matter of debate. In order to investigate the degree of population structure across the Mediterranean, we have investigated Y chromosome variation in a large dataset of Mediterranean populations, 11 of which are first described here. Our analyses identify four main clusters in the Mediterranean that can be labelled as North Africa, Arab, Central-East and West Mediterranean. In particular, Near Eastern samples tend to separate according to the presence of Arab Y chromosome lineages, suggesting that the Arab expansion played a…

Mediterranean climateMaledemographyhaplotypeSouthern EuropegenotypeUEPsPopulation geneticsVariation (Genetics)ArabMediterraneanMediterranean BasinArab; article; cluster analysis; demography; gene locus; genetic linkage; genetic variability; genotype; haplotype; human; male; North Africa; population genetics; population structure; priority journal; Southern Europe; Y chromosome Chromosomes Human Y; Ethnic Groups; Genetics Population; Humans; Male; Mediterranean Region; Variation (Genetics)genetic linkagegenetic variabilityEthnicity[SDV.BDD]Life Sciences [q-bio]/Development BiologyGenetics (clinical)Genetics0303 health scienceseducation.field_of_studyEcologyMediterranean Region030305 genetics & heredityarticlepriority journalMediterranean; Population genetic structure; STRs; UEPs; Y chromosomeY-chromosome population genetics ArabYgene locusPopulationPopulationEthnic GroupsBiologyY chromosomeChromosomes03 medical and health sciencesGenetic variationGeneticsHumansPopulation genetic structureGenetic variabilityhumaneducation030304 developmental biology[SDV.GEN]Life Sciences [q-bio]/GeneticsChromosomes Human YY chromosomeHaplotypeGenetic Variationpopulation geneticspopulation structureSettore MED/43 - MEDICINA LEGALENorth AfricaSettore BIO/18 - GeneticaGenetics PopulationSTRscluster analysis
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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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Distribution of gamma‐tubulin differs in primary and secondary oocytes of Ephestia kuehniella (Pyralidae, Lepidoptera)

1996

In a previous study, barrel-shaped spindles were found in metaphase I oocytes of Ephestia kuehniella (Pyralidae, Lepidoptera). Aster microtubules (MTs) were missing (Wolf, 1993 : Cell Motil Cytoskeleton 24 :200-204). This points to an acentriolar organization of the spindle apparatus. The present study was aimed at the question of whether gamma-tubulin, a newly detected member of the tubulin superfamily that has often been identified in microtubule-organizing centers, plays a role in the nucleation of MTs in meiotic spindles of the moth. To this end, the distribution of gamma-tubulin was examined in oocytes of E. kuehniella using an antibody against gamma-tubulin in combination with indirec…

Meiosis IImacromolecular substancesCell BiologyAster (cell biology)BiologySpindle pole bodySpindle apparatusCell biologyMeiosisBotanyGeneticsHomologous chromosomeSpindle organizationDevelopmental BiologyAnaphaseMolecular Reproduction and Development
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