Search results for "comparative"

showing 10 items of 1371 documents

Biofonctionnements des sols tropicaux et mode de gestion des terres

2000

L'effet de deux peuplements de nématodes phytoparasites a été étudié en conditions contrôlées sur la croissance du mil (#Pennisetum glaucum$). Les plants de mil (cv. IKMV 8201) ont été cultivés en pots sur du col collecté au Sud du Sénégal dans un champ cultivé (sol cultivé) et dans une jachère de 17 ans (sol de jachère). La moitié du sol de chacun des prélèvements à été stérilisée. Pour compenser l'effet de la stérilisation, six cycles de cultures de mil de deux mois ont été faits avant l'expérimentation. A l'issu de cette période, trois espèces ont été observées sur le sol cultivé non stérilisé : #Scutellonema cavanessi$, #Tylenchorhynchus gladiolatus$ et #Ditylenchus myceliophagus$, dans…

CARACTERISTIQUE PHYSIQUEBIOMASSEMILSOL CULTIVEDIVERSITE SPECIFIQUE[SDV.SA.SDS]Life Sciences [q-bio]/Agricultural sciences/Soil studyJACHERENEMATODE PHYTOPARASITEPOUVOIR PATHOGENEMETHODE DE LUTTEETUDE COMPARATIVE[SDV.SA.SDS] Life Sciences [q-bio]/Agricultural sciences/Soil studyLUTTE BIOLOGIQUEComputingMilieux_MISCELLANEOUSCARACTERISTIQUE CHIMIQUE
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RECONSTRUCTION OF GENOMIC REARRANGEMENTS IN AFRICAN DORMICE (RODENTIA-GLIRIDAE) BY CROSS-SPECIES CHROMOSOME PAINTING AND HUMAN SYNTENIC ASSOCIATION A…

2008

ABSTRACT

COMPARATIVE GENOMICS PRIMATE/RODENTIACHROMOSOME PAINTING PHYLOGENY CHROMOSOME PAINTING DORMICE GRAPHIURINAE COMPARATIVE CYTOGENETICSSettore BIO/08 - Antropologia
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A Comparative Analysis of Copy Number Variation of the Sheep and Goat Genomes

2010

Recent studies have shown that copy number variants (CNVs) are important sources of variability of mammalian genomes. We applied a cross species array comparative genome hybridization (aCGH) experiment using as reference the cattle genome to investigate, for the first time, variability in the sheep and goat genomes derived from copy number variation and identified 431 and 358 CNVs, respectively. A comparison of these results to those obtained in other mammals for similar experiments is reported. The identified CNVs could be important in determining phenotypic and production differences between and within breeds. Further studies will be carried out to evaluate the identified CNVs from both f…

COMPARATIVE GENOMICSSettore AGR/17 - Zootecnica Generale E Miglioramento Geneticocongenital hereditary and neonatal diseases and abnormalitiescomparative analysis CNV sheep goatendocrine system diseasesSHEEPmental disordersGOATGENOMESCOPY NUMBER VARIATION
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A comparative study on campus sustainability in higher education sector in Hong Kong and Finland

2015

This thesis presents a comparative study examining the practices of campus sustainability in Higher Education Sectors between Hong Kong and Finland. Campus sustainability is a trend during the last decade as a result of numerous declarations and meetings for sustainable development in Higher education all over the world. In this thesis, the investigated areas are focused on environmental sustainability and Social sustainability. This study used the content analysis method to analyze public available documents from the selected fifteen Higher education institutions in Hong Kong and Finland. The first stage was a description of the current overall situations of campus sustainability in the tw…

Campus sustainabilityVertaileva tutkimuscontent analysiskampuksetkestävä kehitysenergiatehokkuusGreen CampusHongkongHigher EducationyliopistoalueetEnergy efficiencySuomiSustainability teaching and researchyliopistotcomparative study
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Les inégalités d’accès à l’enseignement supérieur des jeunes: Analyse comparative de trois systèmes éducatifs : Suisse, Canada et France

2017

CanadaInégalité d'accès à l'éducation[SHS.EDU] Humanities and Social Sciences/EducationJeuneAnalyse comparativeFranceSystème éducatifSuisseEnseignement supérieur
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Biopiracy and the right to self-determination of indigenous peoples.

2018

Abstract Background: Since over thirty years, I work on the unclear legal situation of in which indigenous peoples find themselves today in the beginning mainly in the USA and later also in Canada, Australia and New Zealand. The status of indigenous people and native nations is characterized as a mixture of national and international law. Hypothesis/Purpose: To clarify the status of indigenous people it is necessary to analyze and interpret carefully hundreds of old treaties, international declarations and covenants, national statutes and jurisprudence, especially the old leading decisions of the US-Supreme Court. Such an analysis and interpretation should prove that indigenous people have …

CanadaUnited NationsPharmaceutical ScienceTheftIndigenousStatute03 medical and health sciences0302 clinical medicinePopulation GroupsPolitical scienceDrug DiscoveryComparative lawHumansTreaty030304 developmental biologyPharmacology0303 health sciencesAustraliaDeclaration on the Rights of Indigenous PeoplesBiodiversityInternational lawIndigenous rightsUnited StatesComplementary and alternative medicine030220 oncology & carcinogenesisLawPersonal AutonomyIndians North AmericanMolecular MedicineMinority rightsNew ZealandPhytomedicine : international journal of phytotherapy and phytopharmacology
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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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Frequent deletion ofCDKN2Aand recurrent coamplification ofKIT,PDGFRA, andKDRin fibrosarcoma of bone-An array comparative genomic hybridization study

2009

Very little is known about the genetics of fibrosarcoma (FS) of bone. We applied array comparative genomic hybridization (CGH) to identify genes and genomic regions with potential role in the pathogenesis of this tumor. Seventeen patients with FS of bone were included in the study. Array CGH analysis was carried out in 13 fresh frozen tissue specimens from 11 of these patients (nine primary tumors and four local recurrences). DNA was extracted and hybridizations were performed on Agilent 244K CGH oligoarrays. The data were analyzed using Agilent DNA Analytics Software. The number of changes per patient ranged from 0 to 132 (average = 43). Losses were most commonly detected at 6q, 8p, 9p, 10…

Cancer ResearchPDGFRBPDGFRABiologymedicine.diseaseCHD1LCDKN2AGene duplicationDNA methylationGeneticsmedicineCancer researchFibrosarcomaComparative genomic hybridizationGenes, Chromosomes and Cancer
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Genomic Abnormalities Acquired in the Blastic Transformation of Splenic Marginal Zone B-cell Lymphoma

2003

Among 20 cases of typical splenic marginal zone lymphoma (SMZL), two cases had blastic transformation. The genetic mechanisms underlying the morphologic transformation were investigated by comparing genetic changes in initial and blastic phases. A complex karyotype including trisomy of 3q and genomic gain of 17q22-q24 was seen in both cases at diagnosis. However, the extra copy of 3q was lost during the transformation process in both tumors. Additionally, the Karpas 1718 cell line, which was derived from a patient with transformed SMZL and carried a trisomy of 3q, also evidenced the spontaneous loss of the extra 3q during the culturing process. Other acquired abnormalities observed exclusiv…

Cancer ResearchPathologymedicine.medical_specialtyLymphoma B-CellTrisomyChromosomal translocationBiologyComplex KaryotypeTumor Cells CulturedmedicineChromosomes HumanHumansSplenic marginal zone lymphomaChromosome AberrationsLymphoma Non-HodgkinSplenic NeoplasmsHematologymedicine.diseaseTransformation (genetics)OncologyKaryotypingDisease ProgressionB-Cell Non-Hodgkin LymphomaChromosomes Human Pair 3Chromosome DeletionAbnormalityBlast CrisisTrisomyChromosomes Human Pair 17Comparative genomic hybridizationLeukemia & Lymphoma
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Preclinical xenograft models of human sarcoma show nonrandom loss of aberrations

2011

BACKGROUND: Human tumors transplanted into immunodeficient mice (xenografts) are good preclinical models, and it is important to identify possible systematic changes during establishment and passaging in mice. METHODS: High-resolution microarray-based comparative genomic hybridization (array CGH) was used to investigate how well a series of sarcoma xenografts, including 9 patient/xenograft pairs and 8 early versus late xenograft passage pairs, represented the patient tumor from which they originated. RESULTS: In all analyses, the xenografts were more similar to their tumor of origin than other xenografts of the same type. Most changes in aberration patterns were toward a more normal genome …

Cancer ResearchPathologymedicine.medical_specialtyMicroarraybiologyCancerPDGFRAbiology.organism_classificationmedicine.diseaseTransplantationNude mouseOncologyTumor progressionmedicineSarcomaComparative genomic hybridizationCancer
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