5 research outputs found

    Modelling fixed plant and algal dynamics in rivers

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    EThOS - Electronic Theses Online ServiceGBUnited Kingdo

    Delta Dynamic Integrated Emulator Model

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    The aim of the ESPA Deltas project was to provide policy makers with the knowledge and tools to enable them to evaluate the effects of policy decisions on ecosystem services and people&#39;s livelihoods. In another word, to link science to policy at the landscape scale. ESPA Deltas investigated the south-west coastal zone of Bangladesh through a transdisciplinary lens. The Delta Dynamic Integrated Emulator Model (&Delta;DIEM) is essentially a trans-disciplinary framework designed to analyse linkages between ecosystem services, livelihoods, well-being and governance in coastal Bangladesh. It is designed to support the delta planning in Bangladesh. It is a tightly coupled platform driven by climatic and environmental change, demographic changes, economic changes, household decisions and governance and estimating the resulting wellbeing and poverty of the coastal population. &Delta;DIEM has built-in water-based structural and policy interventions (e.g. embankment changes, new crops, subsidies, loan structures, etc.) that enables consistent model runs within a robust scenario framework. Thus, development trajectories and their trade-offs can be quantified.</span

    Leptin gene (TTTC)n microsatellite polymorphism in pre-eclampsia and HELLP syndrome

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    Background: Leptin plays an important role in energy homeostasis. There is polymorphism on the leptin (LEP) gene. Our aim was to compare the tetranucleotide repeat (TTTC)n polymorphism in the 3′-flanking region in the LEP gene on DNA samples from patients with pre-eclampsia (PE), hemolysis, elevated liver enzymes, and low platelet (HELLP) syndrome and healthy pregnant controls. Methods: Blood samples were collected from healthy pregnant women (n=88), patients with PE (n=79) and HELLP (n=77) syndrome. Fluorescent PCR and DNA fragment analysis was performed from the isolated DNA for the detection of (TTTC) repeats. The electrophoretograms were evaluated and patients were assigned to two groups; class I low (&#60;190 bp) or class II high (≥190 bp) PCR fragments. Results: We observed similar distributions of the class I and class II (TTTC) alleles in the groups studied (class I allele: healthy pregnant 58.5%; severe pre-eclamptic 58.3%; HELLP syndrome 52.6%). We detected a higher frequency of the II/II genotype in HELLP syndrome patients (32.4%) compared to healthy controls (22.7%). However, the difference was not statistically significant. Conclusions: In an ethnically homogenous population, the LEP gene (TTTC) microsatellite polymorphism in the 3′-flanking region does not show a significant difference in the allele and genotype distribution in healthy pregnant, pre-eclamptic and HELLP syndrome patients. Furthermore, we recommend a new classification of the class I and class II alleles based on the distribution of the (TTTC) microsatellites. Clin Chem Lab Med 2009;47:1033–7.Peer Reviewe

    Leptin gene (TTTC)n microsatellite polymorphism in pre-eclampsia and HELLP syndrome

    No full text
    Background: Leptin plays an important role in energyhomeostasis. There is polymorphism on the leptin(LEP) gene. Our aim was to compare the tetranucleo-tide repeat (TTTC)npolymorphism in the 39-flankingregion in theLEPgene on DNA samples from patientswith pre-eclampsia (PE), hemolysis, elevated liverenzymes, and low platelet (HELLP) syndrome andhealthy pregnant controls.Methods: Blood samples were collected from healthypregnant women (ns88), patients with PE (ns79) andHELLP (ns77) syndrome. Fluorescent PCR and DNAfragment analysis was performed from the isolatedDNA for the detection of (TTTC) repeats. The electro-phoretograms were evaluated and patients wereassigned to two groups; class I low (-190 bp) or classII high (G190 bp) PCR fragments.Results: We observed similar distributions of the classI and class II (TTTC) alleles in the groups studied(class I allele: healthy pregnant 58.5%; severe pre-eclamptic 58.3%; HELLP syndrome 52.6%). We detect-ed a higher frequency of the II/II genotype in HELLPsyndrome patients (32.4%) compared to healthy con-trols (22.7%). However, the difference was not statis-tically significant.Conclusions: In an ethnically homogenous popula-tion, the LEP gene (TTTC) microsatellite polymor-phism in the 3 9 -flanking region does not show asignificant difference in the allele and genotype dis-tribution in healthy pregnant, pre-eclamptic andHELLP syndrome patients. Furthermore, we recom-mend a new classification of the class I and class II alleles based on the distribution of the (TTTC) microsatellites
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