Search results for "Chromosome 4"

showing 10 items of 11 documents

Reconstructing the Phylogeny of the Human Chromosome 4 Synteny using Comparative Karyology and Genomic Data Analysis

2010

Abstract This work focuses on the evolution of the architecture of human chromosome 4 (HSA4) through the analysis of chromosomal regions that have been conserved over time, and the comparison of regions that have been involved in different rearrangements in placental lineages. As with most elements of the human genome, HSA4 is considered to be evolutionarily stable. A more detailed analysis indicates that the syntenic association has been reshuffled by a series of rearrangements, yielding different chromosomes in various taxa. In its ancestral eutherian state, HSA4 has a syntenic association with HSA8p. We investigated the complex origin of this human chromosome using three different approa…

Comparative genomicsGeneticsChromosomeKaryotypeBiologySettore BIO/08 - AntropologiaMaximum parsimonyChromosome 4Evolutionary biologyGeneticsEnsemblHuman genomeComparative Chromosome painting Evolutionary breakpoints Human evolutionGeneral Agricultural and Biological SciencesSynteny
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Frequent chromosomal gains in recurrent juvenile nasopharyngeal angiofibroma.

2007

Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign tumor, mostly affecting adolescent males. Some patients develop recurrences after surgery independently of completeness of removal. Only very limited data concerning underlying chromosomal changes are available. We therefore analyzed samples of 22 JNAs, including six recurrences, with comparative genomic hybridization (CGH). Additionally, quantitative image cytometry was used for measurement of DNA aneuploidy in representative samples. Of the 13 primary JNAs without later recurrence, DNA gains were identified on autosomes in only two samples. Four patients with one or two recurrences were included in the study; for one of these, no…

OncologyAdultMaleCancer Researchmedicine.medical_specialtyAdolescentJuvenile nasopharyngeal angiofibromaBiologyBioinformaticsAngiofibromaBenign tumorInternal medicineGeneticsmedicineHumansChildMolecular BiologyGeneChromosome AberrationsAutosomeNucleic Acid HybridizationNasopharyngeal NeoplasmsGenomicsDna amplificationmedicine.diseasePrimary tumorChromosome 4Neoplasm Recurrence LocalComparative genomic hybridizationCancer genetics and cytogenetics
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The evolution of human synteny 4 by mapping sub-chromosomal specific probes in Primates

2014

Comparative cytogenetic data concerning the orthologue to human chromosome 4 in primates shows that this chromosome is conserved between humans and non-human primates. However, the degree of conservation is not as high as previously estimated. In primates it is as a rule a large submetacentric chromosome but many exceptions are known especially in taxa characterized by a high level of chromosomal rearrangements. The rearrangements that have been visualized by chromosome painting so far, which are mostly interchromosomal changes, are in fact only a fraction of the actual chromosomal changes that have occurred during evolution. Intrachromosome changes can be analysed through classical cytogen…

GeneticsChromosome engineeringchromosomal rearrangementbiologyHuman chromosome 4; chromosomal rearrangements; Platyrrhini Phylogeny; EvolutionEvolutionHuman chromosome 4CatarrhiniChromosomePlatyrrhiniSettore BIO/08 - Antropologiabiology.organism_classificationChromosome 4Evolutionary biologyPhylogeneticsCentromereGeneticsPlatyrrhini PhylogenyGeneral Agricultural and Biological SciencesSynteny
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Chromosome painting for cytogenetic monitoring of occupationally exposed and non-exposed groups of human individuals.

2001

The suitability of a three-color fluorescence in situ suppression hybridization technique was examined for monitoring five different groups of individuals: 30 occupied in radiology, 26 occupied in nuclear medicine or radiation physics, 32 patients with breast cancer, 26 occupied with military waste disposal, all presumably exposed to low doses of radiation or chemical mutagens and a non-exposed control group (N=29). The average frequency of breaks constituting the various aberrations did not significantly differ between the groups of medical radiation appliers and the control group. However, breast tumor patients and military waste disposers, as groups, showed a higher aberration rate than …

AdultMalemedicine.medical_specialtyHealth Toxicology and MutagenesisPopulationPhysiologyMutagenBiologymedicine.disease_causeChromosome PaintingBreast cancerOccupational ExposureGeneticsmedicineHumansLymphocyteseducationAgedGeneticsChromosome Aberrationseducation.field_of_studyCytogeneticsChromosomeMiddle Agedmedicine.diseaseChromosome 4Case-Control StudiesFemaleChromosome paintingWaste disposalMutation research
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4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization

2014

Abstract Background Microscopically chromosome rearrangements of the short arm of chromosome 4 include the two known clinical entities: partial trisomy 4p and deletions of the Wolf-Hirschhorn critical regions 1 and 2 (WHSCR-1 and WHSCR-2, respectively), which cause cranio-facial anomalies, congenital malformations and developmental delay/intellectual disability. Methods/results We report on clinical findings detected in a Chinese patient with a de novo 4p16.1-p15.32 duplication in association with a subtle 4p terminal deletion of 6 Mb in size. This unusual chromosome imbalance resulted in WHS classical phenotype, while clinical manifestations of 4p trisomy were practically absent. Conclusio…

GenotypeArray-CGHDevelopmental DisabilitiesTrisomy 4pChromosome DisordersTrisomyAsian PeopleChinese childrenGene duplicationmedicineHumansWolf–Hirschhorn syndromeOligonucleotide Array Sequence AnalysisGeneticsWolf-Hirschhorn syndromeGenome Humanbusiness.industryChromosomeGeneral Medicinemedicine.diseasePhenotypePenetranceDuplication/deletion 4pPhenotypeChromosome 4Child PreschoolPediatrics Perinatology and Child HealthFemaleNeurology (clinical)Chromosome DeletionChromosomes Human Pair 4HaploinsufficiencybusinessTrisomyEuropean Journal of Paediatric Neurology
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The mouseClq genes are clustered on chromosome 4 and show conservation of gene organization

1996

Mouse complement component C1q is a serum glycoprotein which consists of six A chains, six B chains and six C chains. The three polypeptides are 223, 228, and 217 residues long, respectively, and are encoded by three genes. DNA probes for mouse C1q A, B, and C chains were hybridized to Southern blots of DNA obtained from various inbred mouse strains. On the basis of fragment length polymorphisms, two different alleles of each of the genes could be identified. The distribution of these alleles was determined in the BXD and LXPL recombinant inbred strain series. Comparison with previously reported strain distribution patterns shows that the genes encoding mouseClq map to the same locus on dis…

GeneticsChromosome 4Complementary DNAImmunologyGene clusterGeneticsGenomic libraryRecombinant inbred strainLocus (genetics)BiologyGeneMolecular biologySouthern blotImmunogenetics
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Pattern of secondary genomic changes in pancreatic tumors ofTgfα/Trp53+/−transgenic mice

2003

Trp53+/− mice overexpressing Tgfα in a pancreas-specific manner represent a well-established animal model for pancreatic cancer. In this study we analyzed 38 pancreatic adenocarcinomas of these mice for secondary genomic changes by comparative genomic hybridization (CGH), loss of heterozygosity (LOH) analysis, real-time PCR, and methylation-specific analysis. CGH screening of the tumors revealed a recurrent pattern of genomic changes. In more than 50% of the tumors, chromosome 11 was affected. The gain of the proximal part spans about 16 cM, including the genes for Egfr, Rel, and Stk10. The distal part of chromosome 11, which contains the Trp53 locus, was deleted. LOH analysis proved that a…

Cancer ResearchLocus (genetics)Biologymedicine.diseaseMolecular biologyLoss of heterozygosityChromosome 15Chromosome 4CDKN2APancreatic cancerDNA methylationGeneticsmedicineComparative genomic hybridizationGenes, Chromosomes and Cancer
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A region on human chromosome 4 (q35.1→qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis

2005

Human papillomavirus (HPV) types 16 and 18 are known to play a major role in cervical carcinogenesis. Additional genetic alterations are required for the development and progression of cervical cancer. Previously, we showed that the introduction of an entire human chromosome 4 into HPV-immortalized cells by microcell-mediated chromosome transfer (MMCT) can induce senescence in cell hybrids. In the present study, we established eight new murine donor cell lines harboring different fragments of the human chromosome 4. These were tested for their ability to induce senescence by MMCT into HPV16-immortalized keratinocytes (HPK II) and cervical carcinoma cells (HeLa). By exclusion, we could ident…

KeratinocytesSenescenceCancer ResearchChromosome TransferUterine Cervical NeoplasmsLocus (genetics)Hybrid CellsBiologyPolymerase Chain ReactionLoss of heterozygosityGeneticsmedicineHumansAlleleCellular SenescenceIn Situ Hybridization FluorescenceSequence DeletionChromosome AberrationsCervical cancermedicine.diagnostic_testChromosome Mappingmedicine.diseaseMolecular biologyChromosome 4FemaleChromosomes Human Pair 4Microsatellite RepeatsFluorescence in situ hybridizationGenes, Chromosomes and Cancer
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The chromosomes of 16 molluscan species

1982

Abstract Chromosome numbers were determined for two species of Placophora, eleven species of Gastropoda, one species of Pelecypoda and two species of Cephalopoda. No heterotypic or supernumerary chromosome resulted from the analysis of meiotic and, when possible, of mitotic chromosomes. For this reason no positive evidence emerges for the presence of differentiated sex chromosome pairs. Data available seem to indicate that evolution within the Mollusca phylum has been accompanied by a decrease in both chromosome number and DNA content (according to Hinegardner, 1974), if we consider subclasses, orders and families (apart from the subclass Prosobranchia). On the contrary the primitive class …

Chromosome 17 (human)B chromosomeChromosome 4Chromosome 16Chromosome 3Chromosome 18ZoologyAnimal Science and ZoologyBiologySmall supernumerary marker chromosomeChromosome 12Bolletino di zoologia
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Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies IL6R Polymorphism in Relation to Atrial Fibrillation The National Hear…

2011

Background— The genetic background of atrial fibrillation (AF) in whites and African Americans is largely unknown. Genes in cardiovascular pathways have not been systematically investigated. Methods and Results— We examined a panel of approximately 50 000 common single-nucleotide polymorphisms (SNPs) in 2095 cardiovascular candidate genes and AF in 3 cohorts with participants of European (n=18 524; 2260 cases) or African American descent (n=3662; 263 cases) in the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource. Results in whites were followed up in the German Competence Network for AF (n=906, 468 cases). The top result was assessed in relation to incident i…

medicine.medical_specialtyCandidate geneINTERLEUKIN-6ATHEROSCLEROSIS RISKSingle-nucleotide polymorphismVARIANTSDISEASEINFLAMMATIONDESIGNsingle nucleotide polymorphismInternal medicinecohort studyGeneticsmedicineatrial fibrillationCHROMOSOME 4Q25Genetics (clinical)Geneticsbusiness.industryHazard ratioAtrial fibrillationrace/ethnicitymedicine.diseaseC-REACTIVE PROTEINEUROPEAN ANCESTRYISCHEMIC-STROKERelative riskCohortepidemiologyCardiology and Cardiovascular MedicinebusinessCandidate Gene AnalysisCohort study
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