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Showing 1 to 6 of 6 for “"Meis"”.

  1. Gut Patterning In Development And Evolution: A Comparative Differential Transcriptomics Approach

    … urchin GRN featuring the interaction between Sp-Meis, an homeobox gene, and Sp-Lox protein has been revealed and the occupancy of Sp-Lox protein on Sp-Meis regulatory region has been demonstrated by ChIP-PCR. The comparison of the differentially expressed genes after Xlox and Cdx perturbation in …

    the-open-u Repository record for Gut Patterning In Development And Evolution: A Comparative Differential Transcriptomics Approach (opens in a new tab)

  2. Complete computational sequence characterization of mobile element variations in the human genome using meta-personal genome data

    … and in particular mobile elements insertions (MEIs). Moreover, almost all these methods can detect only the breakpoints of an occurred SV, sometimes with approximation, and do not provide complete sequences representing the SVs. The main objective of our research is to develop a set of computer …

    brock Repository record for Complete computational sequence characterization of mobile element variations in the human genome using meta-personal genome data (opens in a new tab)

  3. Diseño de herramientas para la determinación, evaluación y administración de los riesgos en la mediana empresa industrial salvadoreña.

    … La Mediana Empresa Industrial Salvadoreña (MEIS), para lograr su posicionamiento, necesita una reconversión y empleo de modernas herramientas que le permitan establecer sus objetivos, acordes a un nuevo pensamiento estratégico: misión, visión y valores básicos, y a sus recursos humanos, …

    u-elsalvador Repository record for Diseño de herramientas para la determinación, evaluación y administración de los riesgos en la mediana empresa industrial salvadoreña. (opens in a new tab)

  4. The Contribution of Structural Variants to 2,095 Molecular Phenotypes in 12,354 European Ancestry Individuals

    … 93% and 46% of deletions, inversions, reference MEIs and duplications have at least one SNP in high LD (r2>0.8)- suggesting that genotyping of the SVs is high quality. We evaluated the contribution of SVs on a comprehensive range of phenotypes available in the cohort. These traits include a range …

    cambridge Repository record for The Contribution of Structural Variants to 2,095 Molecular Phenotypes in 12,354 European Ancestry Individuals (opens in a new tab)

  5. Investigation of DNA methylation at the promoter region of the aralkylamine N-acetyltransferase (AANAT ) gene in South African children with Autism Spectrum Disorder

    … (zinc finger protein with interaction domain), MEIS1 (Meis homeobox 1) and ZIC1 (zinc finger protein of the cerebellum 1) were identified at or near to CpG 3. These three TFs have known gene ontology terms that relate to neurodevelopment. The age of participants did not correlate with DNAme, and …

    cape-town Repository record for Investigation of DNA methylation at the promoter region of the aralkylamine N-acetyltransferase (AANAT ) gene in South African children with Autism Spectrum Disorder (opens in a new tab)

  6. Studying the Patterning Mechanisms and Cell Fates during Limb Regeneration in Ambystoma mexicanum

    We studied patterning mechanisms and cell fates during limb regeneration in the axolotl. 1) It is crucial to understand the earliest events of patterning. Since it is technically challenging to study early events, we established single cell PCR. This new tool will allow us to obtain novel insight …

    qucosa-diss