Search results for "chromosome"

showing 10 items of 1175 documents

Age at diagnosis is an important prognostic factor in Philadelphia-negative Myeloproliferative Neoplasms

2019

Oncologymedicine.medical_specialtyPrognostic factorPrognosiMEDLINEAge at diagnosisPhiladelphia chromosomeMyeloproliferative DisordersInternal medicinemedicineBiomarkers TumorHumansAge FactorPhiladelphia ChromosomeAge of OnsetMyeloproliferative DisorderPhiladelphia negativeMyeloproliferative Disordersbusiness.industryAge FactorsHematologyGeneral Medicinemedicine.diseasePrognosisAge of onsetbusinessHuman
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Post-transplant consolidation based on combination of lenalidomide and proteasome inhibitors in multiple myeloma

2021

Multiple myeloma (MM) is a hematological malignancy due to uncontrolled proliferation of neoplastic plasma cells in the bone marrow, associated to chromosomal instability and cytogenetic abnormalities, which could have an impact on prognosis. Response to treatment and survival of newly diagnosed myeloma patients is heterogeneous, with median overall survival ranging from two to more than ten years, due to clinical and biological factors. To warrant long-term control of disease, several strategies have been proposed in the last years, including short-term high-dose of treatment, named as consolidation, before maintenance. This review will discuss the role of consolidation in the current myel…

Oncologymedicine.medical_specialtyTime FactorsDisease030204 cardiovascular system & hematologyRisk Assessment03 medical and health sciences0302 clinical medicineRisk FactorsInternal medicineChromosome instabilityAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansImmunologic FactorsLenalidomideMultiple myelomaLenalidomide030219 obstetrics & reproductive medicinebusiness.industryGeneral Medicinemedicine.diseaseResponse to treatmentProgression-Free SurvivalPost transplantConsolidation Chemotherapymedicine.anatomical_structureProteasomeBone marrowMultiple MyelomabusinessProteasome InhibitorsStem Cell Transplantationmedicine.drugPanminerva Medica
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Cloning of branched chain amino acid biosynthesis genes and assays of alpha-acetolactate synthase activities in Leuconostoc mesenteroides subsp. crem…

1999

Abstract A genomic library from Leuconostoc mesenteroides subsp. cremoris (Lmc) in Escherichia coli was screened for α-acetolactate synthase (ALS) activity using a phenotypic test detecting the production of acetolactate or related C 4 derivatives (diacetyl, acetoin or 2,3-butanediol) in the culture. Four recombinant E. coli clones, with plasmids containing overlapping DNA fragments and displaying anabolic ALS activity, were selected. This activity is encoded by an ilvB gene belonging to a putative operon which contains genes highly similar to the genes of the branched chain amino acid (BCAA) operon of Lactococcus lactis subsp. lactis. This putative BCAA operon is not functional as the ilvA…

OperonBranched-chain amino acidMolecular Sequence DataRestriction MappingMolecular cloningMicrobiologychemistry.chemical_compoundPlasmidLeucineOperonAmino Acid SequenceCloning MolecularIsoleucineMolecular BiologyGeneAcetolactate synthasebiologyBase SequenceLactococcus lactisValineGeneral MedicineSequence Analysis DNAbiology.organism_classificationPhysical Chromosome MappingMolecular biologyAcetolactate SynthaseBiochemistrychemistryLeuconostoc mesenteroidesGenes Bacterialbiology.proteinbacteriaAmino Acids Branched-ChainLeuconostocResearch in microbiology
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Vehicles, replicators, and intercellular movement of genetic information: evolutionary dissection of a bacterial cell.

2012

Prokaryotic biosphere is vastly diverse in many respects. Any given bacterial cell may harbor in different combinations viruses, plasmids, transposons, and other genetic elements along with their chromosome(s). These agents interact in complex environments in various ways causing multitude of phenotypic effects on their hosting cells. In this discussion I perform a dissection for a bacterial cell in order to simplify the diversity into components that may help approach the ocean of details in evolving microbial worlds. The cell itself is separated from all the genetic replicators that use the cell vehicle for preservation and propagation. I introduce a classification that groups different r…

Order (biology)Article SubjectChromosome (genetic algorithm)Evolutionary biologyevoluutioZoologyta1181Biologyhorisontaalinen geeniliikenneBacterial cell structureResearch Articlehorizontal genetic movementbakteerit
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A first comparative map of copy number variations in the sheep genome.

2011

article i nfo We carried out a cross species cattle-sheep array comparative genome hybridization experiment to identify copy number variations (CNVs) in the sheep genome analysing ewes of Italian dairy or dual-purpose breeds (Bagnolese, Comisana, Laticauda, Massese, Sarda, and Valle del Belice) using a tiling oligonucleotide array with ~385,000 probes designed on the bovine genome. We identified 135 CNV regions (CNVRs; 24 reported in more than one animal) covering ~10.5 Mb of the virtual sheep genome referred to the bovine genome (0.398%) with a mean and a median equal to 77.6 and 55.9 kb, respectively. A comparative analysis between the identified sheep CNVRs and those reported in cattle a…

Ovis ariesDNA Copy Number VariationsRuminantSheep breedsaCGH; Comparative map; Copy number variation; Ovis aries; Ruminants; Sheep breedsGenomicsOvis arieBiologyGenomeChromosomesSettore AGR/17 - Zootecnica Generale E Miglioramento Genetico03 medical and health sciencesaCGHChromosome regionsGeneticsAnimalsCopy-number variationGene030304 developmental biologyOligonucleotide Array Sequence AnalysisGeneticsCOMPARATIVE MAPPING0303 health sciencesComparative Genomic HybridizationGenomeSheepCopy number variation0402 animal and dairy scienceComparative Genome HybridizationChromosome Mapping04 agricultural and veterinary sciencesRuminantsbiology.organism_classification040201 dairy & animal scienceBovine genomeSardaCattleComparative mapGenomics
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Antioxidant therapy counteracts the disturbing effects of diamide and maternal ageing on meiotic division and chromosomal segregation in mouse oocytes

1998

This study aims (i) to ascertain whether oxidative-stress-induced disturbances in chromosomal distribution in the metaphase-II spindle of mouse oocytes can be counteracted by supplementing culture medium with antioxidants; and (ii) to determine whether supplemental intake of antioxidants neutralizes the disturbing effects of maternal ageing on segregation of chromosomes during the first meiotic division and distribution of chromosomes in the metaphase-II spindle. (i): Germinal vesicle oocytes from unstimulated 10-12 week old mice were matured in vitro in the presence or absence of diamide and/or dithiothreitol. Metaphase-II oocytes were fixed and stained with 4',6-diamidino-2-phenylindole (…

OvulationAgingEmbryologymedicine.medical_treatmentAneuploidyAscorbic AcidBiologyAntioxidantsChromosomesAndrologyMiceMeiosisGeneticsmedicineAnimalsVitamin EMolecular BiologyMetaphaseMetaphaseDiamideGerminal vesicleVitamin EObstetrics and GynecologyKaryotypeCell BiologyAneuploidyOxidantsmedicine.diseaseOocyteAscorbic acidMice Inbred C57BLDithiothreitolMeiosisOxidative Stressmedicine.anatomical_structureReproductive MedicineBiochemistryDietary SupplementsMice Inbred CBAOocytesFemaleMaternal AgeDevelopmental BiologyMolecular Human Reproduction
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Phylogenomics of species from four genera of New World monkeys by flow sorting and reciprocal chromosome painting

2007

Abstract Background The taxonomic and phylogenetic relationships of New World monkeys (Platyrrhini) are difficult to distinguish on the basis of morphology and because diagnostic fossils are rare. Recently, molecular data have led to a radical revision of the traditional taxonomy and phylogeny of these primates. Here we examine new hypotheses of platyrrhine evolutionary relationships by reciprocal chromosome painting after chromosome flow sorting of species belonging to four genera of platyrrhines included in the Cebidae family: Callithrix argentata (silvered-marmoset), Cebuella pygmaea (pygmy marmoset), Callimico goeldii (Goeldi's marmoset) and Saimiri sciureus (squirrel monkey). This is t…

PLATYRRHINE MONKEYSPRIMATE PHYLOGENYMOLECULAR PHYLOGENYMITOCHONDRIAL-DNAPygmy marmosetZOO-FISHZoologyPlatyrrhiniDIVERGENCE TIMESChromosome PaintingEvolution MolecularANCESTRAL KARYOTYPEbiology.animalCebidaeAnimalsChromosomes HumanHumansPhylogenyEcology Evolution Behavior and SystematicsChromosome 13biologyCallimico goeldiiResearchSquirrel monkeySaimiri sciureusMarmosetIN-SITU HYBRIDIZATIONFlow Cytometrybiology.organism_classificationEVOLUTIONPlatyrrhiniEvolutionary biologyKaryotypingGENOMIC REARRANGEMENTSphylogenomics Primates molecular cytogeneticsBMC Evolutionary Biology
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KARYOTYPE EVOLUTION IN PRIMATES AND RODENTS. PHYLOGENETIC RELATIONSHIP AND CHROMOSOMAL SIGNATURES BY COMPARATIVE CYTOGENETIC APPROACHES

2009

PRIMATES RODENTIA CHROMOSOME EVOLUTIONSettore BIO/08 - Antropologia
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Common variants conferring risk of schizophrenia

2009

Schizophrenia is a complex disorder, caused by both genetic and environmental factors and their interactions. Research on pathogenesis has traditionally focused on neurotransmitter systems in the brain, particularly those involving dopamine. Schizophrenia has been considered a separate disease for over a century, but in the absence of clear biological markers, diagnosis has historically been based on signs and symptoms. A fundamental message emerging from genome-wide association studies of copy number variations (CNVs) associated with the disease is that its genetic basis does not necessarily conform to classical nosological disease boundaries. Certain CNVs confer not only high relative ris…

Pair 6/geneticsGenetics and epigenetic pathways of disease [NCMLS 6]Genome-wide association studyAetiology screening and detection [ONCOL 5]1Q21.1Major Histocompatibility Complex/geneticsMajor Histocompatibility ComplexTranscription Factor 40302 clinical medicineChemicals And Cas Registry NumbersPerception and Action [DCN 1]Copy-number variationPOPULATIONGeneticsPair 18/genetics0303 health scienceseducation.field_of_studyGenomeHuman/geneticsMultidisciplinaryBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsSchizophrenia/*genetics/immunologyGenetic Predisposition to Disease/*genetics3. Good healthDNA-Binding ProteinsNeurogranin/geneticsDISEASESChromosomes Human Pair 6Single Nucleotide/*geneticsFunctional Neurogenomics [DCN 2]Zinc finger protein 804AHumanGenetic MarkersPsychosisGenotypePopulationTranscription Factors/geneticsSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideChromosomesPair 11/geneticsArticleChromosomes; Human; Pair 11/genetics; Pair 18/genetics; Pair 6/genetics; DNA-Binding Proteins/genetics; Genetic Markers/genetics; Genetic Predisposition to Disease/*genetics; Genome; Human/genetics; Genome-Wide Association Study; Genotype; Humans; Major Histocompatibility Complex/genetics; Neurogranin/genetics; Polymorphism; Single Nucleotide/*genetics; Schizophrenia/*genetics/immunology; Transcription Factors/geneticsGenomic disorders and inherited multi-system disorders [IGMD 3]Molecular epidemiology [NCEBP 1]03 medical and health sciencesTranslational research [ONCOL 3]medicineHumansSNPGenetic Predisposition to DiseasePolymorphismGENOME-WIDE ASSOCIATIONeducation030304 developmental biologyGenetic associationGenetic Markers/geneticsHereditary cancer and cancer-related syndromes [ONCOL 1]Genome HumanChromosomes Human Pair 11MEMORYmedicine.diseaseGENENEUROGRANINDELETIONSSchizophreniabiology.proteinNeurograninChromosomes Human Pair 18DNA-Binding Proteins/geneticsMENTAL-RETARDATIONSCAN030217 neurology & neurosurgeryGenome-Wide Association StudyTranscription Factors
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Microsatellite Instability in Colorectal Cancer: Time to Stop Hiding!

2011

Colorectal cancer (CRC) is the second cause of cancer-related death worldwide. Surgery constitutes the primary therapy for these tumors, together with chemotherapy that is usually recommended in patients with metastatic primary CRC. Although molecularly distinct entities arising from different physiopathogenic mechanisms - microsatellite (MSI) and chromosomal instability (also called microsatellite stable, MSS) - have been characterized in CRC, there is still no specific therapeutic approach that takes into account disease’s molecular heterogeneity [1]. MSI is observed in 1015% of sporadic CRCs. MSI CRCs displayed particular morphologic features, with greater predilection for the right colo…

Pathologymedicine.medical_specialtyChemotherapyColorectal cancermedicine.medical_treatmentMicrosatellite instabilityDiseaseBiologymedicine.diseasedigestive system diseasesTherapeutic approachOncologyChromosome instabilityCancer researchmedicineMicrosatelliteAnimalsHumansIn patientMicrosatellite InstabilityHSP110 Heat-Shock ProteinsColorectal NeoplasmsneoplasmsEditorial CommentsOncotarget
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