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JČU

University of South Bohemia in České Budějovice
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67 Projects, page 1 of 14
  • Funder: European Commission Project Code: 272562
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  • Funder: European Commission Project Code: 298186
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  • Funder: European Commission Project Code: 708255
    Overall Budget: 142,721 EURFunder Contribution: 142,721 EUR

    Increasing maternal age, a prevalent trend in developed countries, negatively influences oocyte quality and consequently female fertility – 5% of all couples experience fertility problems arising from a physiological source in the women. To develop novel approaches to prevent or treat infertility, a more complete understanding of oogenesis is required. The host laboratory has recently identified the Socs3 gene, to date associated only with roles in the immune system, as a novel strong candidate regulating oogenesis. The project exploits a genetic approach to ablate the Socs3 gene from the female germ-line and addresses the role of Socs3 gene during mouse oocyte maturation and fertilisation, e.g. in correct chromosomal segregation, followed by further detailed and cutting-edge functional characterisation. The results could lead to the identification of novel therapeutic targets to treat female infertility. Dr. Veselovska, coming from a world-renown institute, is joining a well-established early mammalian development orientated host group, within the Department of Molecular Biology at the University of South Bohemia. Synergies arising from this multidisciplinary proposal will benefit both host and applicant. In particular, Dr. Veselovska is bringing a wealth of highly relevant mouse oocyte experience and bioinformatics skills for genome-scale analyses that are currently an underrepresented skills set in the host laboratory and host institution, as well as her network of UK based collaborators. She will receive training that is both complementary to her current knowledge and skills and novel and highly contemporary in relation to the experimental approaches used. Consequently, the fellowship award will substantially further the Dr. Veselovska’s career ambitions to become an independent early mammalian developmental biologist within her native Central European region, and facilitate the under-represented exchange of ideas between Western and Eastern European countries.

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  • Funder: European Commission Project Code: 897949
    Overall Budget: 255,756 EURFunder Contribution: 255,756 EUR

    In all vertebrates, heart development is dependent on the interplay of several cell populations of distinct embryonic origin. One of these cell populations is the cardiac neural crest (CNC) which contributes to the outflow tract and spiral septum in amniotes. However, CNC cells also migrate to the ventricles and differentiate into cardiomyocytes both in zebrafish and in amniotes. Interestingly, recent results from one of the host lab have shown that CNC-derived cardiomyocytes in zebrafish have an extraordinary capacity for regeneration and that ablation of these cells blocks heart regeneration. Here, I will explore whether this regenerative capacity of cardiomyocytes is unique to zebrafish or represents an ancestral state of characters for vertebrates in general. The goal of the proposed research is to use phylogenetically important vertebrates (lamprey, sturgeon, and axolotl) to answer fundamental questions about the development of the CNC and its role in heart regeneration across vertebrates. Thus, we aim to i) examine the fate of CNC in three species; ii) determine the potential of CNC to differentiate into cardiomyocytes; iii) examine the gene expression profile of CNC cells and neural crest-derived cardiomyocytes; iv) ablate neural crest-derived cells and examine their function in heart regeneration.

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  • Funder: European Commission Project Code: 101110839
    Funder Contribution: 150,439 EUR

    Phytopathogenic bacteria are of substantial economic importance, threatening the quantity and quality of food production. Reducing crop losses from disease epidemics caused by bacterial pathogens is critical for the supply of agricultural produce. On the other hand, colonisation of plants with beneficial bacteria can stimulate plant growth by increasing the nutrient uptake by roots or prime plants for enhanced defense against biotic and abiotic stresses, which can help to improve (or bring new approaches to) efforts to reach sustainable agriculture. Cell-to-cell communication, which is ubiquitous in all biological systems, plays a critical role in plant-bacteria interaction. Recently it has been considered that one of the significant ways to achieve cell-to-cell communication is through extracellular vesicles (EVs). These cytosol-containing membrane spheres provide selection, storage, and protection against degradation of enclosed cargoes in a highly dynamic and environmental cue-responsive manner. EVs also offer the opportunity for directed cargo delivery to dedicated recipient cells and serve as a quick adaptation strategy to react to a changing environment [1]. This project proposal aims to shed light on the vesiculation process of phytobacteria and the role of EVs in plant-bacteria interactions. The missing detailed understanding of vesiculation and EVs' properties is a critical gap in our complete knowledge of cell-to-cell communication, especially in plant-bacteria interactions. At its completion, this project will lead to new insights into the crucial tool, cell-to-cell communication, contributing to the virulence of pathogenic phytobacteria and the mechanism for how bacterial symbionts promote plant growth and fitness.

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