Search results for "Chromosomes"

showing 10 items of 509 documents

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

2022

Abstract Background Cat eye syndrome (CES) is a rare chromosomal disease, with estimated incidence of about 1 in 100,000 live newborns. The classic triad of iris coloboma, anorectal malformations, and auricular abnormalities is present in 40% of patients, and other congenital defects may also be observed. The typical associated cytogenetic anomaly relies on an extra chromosome, derived from an inverted duplication of short arm and proximal long arm of chromosome 22, resulting in partial trisomy or tetrasomy of such regions (inv dup 22pter-22q11.2). Case presentation We report on a full-term newborn, referred to us soon after birth. Physical examination showed facial dysmorphisms, including …

Chromosome Aberrations...CholestasisHydrocortisoneCongenital hypopituitarismSupernumerary marker chromosomeChromosomes Human Pair 22Chromosome DisordersGeneral MedicineCESAneuploidyChromosome AberrationHypoglycemiaHypopituitarismColobomaEye AbnormalitieChromosome DisorderCholestasiCase reportHumansFemaleEye AbnormalitiesNeonatal hypoglycemiaItalian Journal of Pediatrics
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Investigations for fine mapping of amplifications in chromosome 3q26.3-28 frequently occurring in squamous cell carcinomas of the head and neck.

2002

<i>Objective:</i> Overrepresentations of chromosomal material on the long arm of chromosome 3 frequently occur in squamous cell carcinoma of the head and neck. This experimental study was conducted for further fine mapping of these overrepresentations by interphase fluorescence in situ hybridization (FISH) of tumor cells in cell lines. <i>Methods:</i> Seven cell lines derived from squamous cell carcinomas of the head and neck were investigated by comparative genomic hybridization to analyze unbalanced chromosomal aberrations. Overrepresentations of chromosomal material on the telomeric part of the long arm of chromsome 3 were further analyzed by interphase FISH using…

Chromosome AberrationsCancer Researchmedicine.diagnostic_testCellGene AmplificationChromosomeChromosome MappingGeneral MedicineBiologyMolecular biologymedicine.anatomical_structureOncologyChromosome 3Cell cultureHead and Neck NeoplasmsmedicineCarcinoma Squamous CellTumor Cells CulturedHumansBasal cellChromosomes Human Pair 3Head and neckIn Situ Hybridization FluorescenceComparative genomic hybridizationFluorescence in situ hybridizationOncology
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Eradicating Mosquitoes using Translocations: a First Field Experiment

1972

THEORETICAL considerations have led to the assumption that chromosomal translocations with ensuing semisterility could be used to control pests1–3. Inversions could have the same effect in animals and plants in which crossing over occurs in both sexes4. Many translocations of different type and with various degrees of sterility have been produced in the mosquito Culex pipiens5–8. Preliminary laboratory experiments with these translocations have shown that a cage population can be diminished and finally exterminated after a few generations by the release of translocation heterozygotes into the population9.

Chromosome AberrationsMaleGeneticseducation.field_of_studyMosquito ControlSex ChromosomesMultidisciplinarybiologyEcologyCulexSterilityField experimentfungiPopulationChromosomal translocationbiology.organism_classificationChromosomal crossoverCulexMosquito controlAnimalsNatural enemieseducationNature
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Insights into the annotated genome sequence of Methanoculleus bourgensis MS2(T), related to dominant methanogens in biogas-producing plants

2014

The final step of the biogas production process, the methanogenesis, is frequently dominated by members of the genus Methanoculleus. In particular, the species Methanoculleus bourgensis was identified to play a role in different biogas reactor systems. The genome of the type strain M. bourgensis MS2(T), originally isolated from a sewage sludge digestor, was completely sequenced to analyze putative adaptive genome features conferring competitiveness within biogas reactor environments to the strain. Sequencing and assembly of the M. bourgensis MS2(T) genome yielded a chromosome with a size of 2,789,773 bp. Comparative analysis of M. bourgensis MS2(T) and Methanoculleus marisnigri JR1 revealed…

Chromosomes ArchaealNitrogenMethanogenesisvirusesBioengineeringContext (language use)BiologyApplied Microbiology and BiotechnologyGenomeMethanomicrobialesBiogasGenome ArchaealBotanyNitrogen metabolismGeneWhole genome sequencingCompatible soluteGeneral Medicinebiology.organism_classificationequipment and suppliesArchaeaDNA ArchaealMethanoculleusMetagenomicsBiofuelsMetagenomeMethanomicrobiaceaeBiotechnology
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Eight million years of maintained heterozygosity in chromosome homologs of cercopithecine monkeys

2020

In the Cercopithecini ancestor two chromosomes, homologous to human chromosomes 20 and 21, fused to form the Cercopithecini specific 20/21 association. In some individuals from the genus Cercopithecus, this association was shown to be polymorphic for the position of the centromere, suggesting centromere repositioning events. We set out to test this hypothesis by defining the evolutionary history of the 20/21 association in four Cercopithecini species from three different genera. The marker order of the various 20/21 associations was established using molecular cytogenetic techniques, including an array of more than 100 BACs. We discovered that five different forms of the 20/21 association w…

Chromosomes Artificial BacterialHeterozygoteOld WorldCentromereSettore BIO/08 - AntropologiaGenomeChromosome PaintingEvolution MolecularLoss of heterozygosity03 medical and health sciences0302 clinical medicineChromosome DuplicationCentromereGeneticsHomologous chromosomeAnimalsHumansIn Situ Hybridization FluorescenceGenetics (clinical)030304 developmental biology0303 health sciencesChromosomes Heterozygosity Primates Evolution Heterozygous advantageCercopitheciniPhylogenetic treebiologyChromosomeHaplorhinibiology.organism_classificationBiological EvolutionChromosomes MammalianEvolutionary biologyKaryotyping030217 neurology & neurosurgery
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Immune evasion proteins of murine cytomegalovirus preferentially affect cell surface display of recently generated peptide presentation complexes.

2009

CD8 T cells recognize infected cells by interaction of their T-cell receptor (TCR) with a cell surface presentation complex composed of a cognate antigenic peptide bound to a presenting allelic form of a major histocompatibility complex class I (MHC-I) glycoprotein (77, 85, 97, 98). The number of such “peptide receptors” per cell has been estimated to be on the order of 105 to 106 for each MHC-I allomorph (for a review, see reference 82). Viral antigenic peptides are generated within infected cells by proteolytic processing of viral proteins, usually in the proteasome, and associate with nascent MHC-I proteins in the endoplasmic reticulum (ER) before the peptide-MHC (pMHC) complexes travel …

Chromosomes Artificial BacterialMuromegalovirusImmunologyAntigen presentationchemical and pharmacologic phenomenaBiologyMajor histocompatibility complexMicrobiologyEpitopeMiceViral ProteinsAntigenVirologyCytotoxic T cellAnimalsCells CulturedDNA PrimersImmune EvasionBase SequenceAntigen processingT-cell receptorHistocompatibility Antigens Class IVirologyMice Inbred C57BLMutagenesisInsect Sciencebiology.proteinPathogenesis and ImmunityPeptidesCD8Journal of virology
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The human gene for mannan-binding lectin-associated serine protease-2 (MASP-2), the effector component of the lectin route of complement activation, …

2001

The proteases of the lectin pathway of complement activation, MASP-1 and MASP-2, are encoded by two separate genes. The MASP1 gene is located on chromosome 3q27, the MASP2 gene on chromosome 1p36.23-31. The genes for the classical complement activation pathway proteases, C1r and C1s, are linked on chromosome 12p13. We have shown that the MASP2 gene encodes two gene products, the 76 kDa MASP-2 serine protease and a plasma protein of 19 kDa, termed MAp19 or sMAP. Both gene products are components of the lectin pathway activation complex. We present the complete primary structure of the human MASP2 gene and the tight cluster that this locus forms with non-complement genes. A comparison of the …

Chromosomes Artificial BacterialTranscription GeneticGenetic LinkageRNA SplicingImmunologyMolecular Sequence DataBiologyGeneticsHumansPromoter Regions GeneticComplement ActivationGenetics (clinical)Mannan-binding lectinGeneticsComplement component 2Base SequenceCD69Serine EndopeptidasesC4AChromosome MappingCollectinsKLRB1Chromosomes Human Pair 1Lectin pathwayMannose-Binding Protein-Associated Serine ProteasesMultigene Familybiology.proteinCarrier ProteinsMASP2MASP1
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Two heterologously expressed Planobispora rosea proteins cooperatively induce Streptomyces lividans thiostrepton uptake and storage from the extracel…

2010

Abstract Background A bacterial artificial chromosomal library of Planobispora rosea, a genetically intractable actinomycete strain, was constructed using Escherichia coli-Streptomyces artificial chromosome (ESAC) and screened for the presence of genes known to be involved in the biosynthesis of antibiotics. Results One clone with a 40 kb insert showed antimicrobial activity against Gram positive bacteria. Insert sequence analysis and subcloning experiments revealed that the bioactivity was due to a 3.5 kb DNA fragment containing two open reading frames. These orfs encode two proteins with high similarity to a putative membrane protein of Streptomyces coelicolor and to the nogalamycin resis…

Chromosomes Artificial Bacteriallcsh:QR1-502BioengineeringApplied Microbiology and BiotechnologyThiostreptonlcsh:MicrobiologyMicrobiologychemistry.chemical_compoundOpen Reading FramesBacterial ProteinsActinomycetalesORFSCloning MolecularStreptomyces nogalaterPlanobispora rosea Streptomyces lividans heterologous expressionbiologyResearchNogalamycinStreptomyces coelicolorbiology.organism_classificationThiostreptonAnti-Bacterial AgentsComplementationSubcloningchemistryStreptomyces lividansActinomycetalesBiotechnologyMicrobial cell factories
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Interstitial deletion of the long arm of chromosome 1 (1q 25-32): Clinical and endocrine features with a long term follow-up

2003

Deletion of long arm of chromosome 1 (1q-) is a rare condition with malformations of many organs (central nervous system, heart, kidney, etc.). Authors describe a young girl characterised by 1q 25-32 deletion, with severe intra- and extrauterine growth retardation, facial dismorphisms, multiple organ malformations. The patient is followed for a long-term clinical and endocrine evaluation, with evidence of hypoplastic hypophysis and multiple endocrine deficiency.

Chromosomes Human Pair 1Abnormalities multiple geneticBrainHumansAbnormalities MultipleFemaleChromosome DeletionAbnormalities multiple diagnosiChildEndocrine System DiseasesChromosome deletion 1q 25-32Magnetic Resonance ImagingGrowth Disorders
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Chest Radiograph as Diagnostic Clue in a Floppy Infant

2016

Chromosomes Human Pair 14Male0301 basic medicineThoraxmedicine.medical_specialtymedicine.diagnostic_testbusiness.industryInfant NewbornThoraxUniparental Disomy030105 genetics & heredityRespiration ArtificialInfant newbornKAGAMI-OGATA SYNDROMESurgery03 medical and health sciencesPediatrics Perinatology and Child HealthmedicineHumansMuscle HypotoniaAbnormalities MultipleRadiologyChest radiographFloppy InfantbusinessThe Journal of Pediatrics
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