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Revision as of 12:30, 14 October 2020 by DG Regio (talk | contribs) (‎Changed label, description and/or aliases in 1 language: remove_english_label)
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Project in Poland financed by DG Regio
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English
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Project in Poland financed by DG Regio

    Statements

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    2,949,970.0 zloty
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    707,992.80 Euro
    13 January 2020
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    2,949,970.0 zloty
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    707,992.80 Euro
    13 January 2020
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    100.0 percent
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    1 November 2016
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    30 April 2020
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    UNIWERSYTET IM. ADAMA MICKIEWICZA W POZNANIU
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    Q2513981 (Deleted Item)
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    Malfunctioning DNA repair lead to an accumulation of mutations, which frequently results in cancer. The Nucleotide Excision Repair (NER) pathway removes a DNA lesions caused by UV light, cigarette smoke and chemical mutagens. NER is highly conserved, and studying the simpler NER in bacteria provides key insight into human NER. I propose an interdisciplinary approach to understand the mechanistic details of bacterial NER in living cells. I will use a combination of cutting-edge single-molecule methods to elucidate how DNA is repaired inside living cells. I will use super-resolution microscopy combined to study the behaviour of individual NER proteins. To complement this, conventional biochemistry, cell biology, genetics, smFRET assays, FCS and TIRF microscopy will be used. Together, this will provide a comprehensive understanding of the bacterial NER pathway, and constitute the first steps toward my ultimate goal, which is to understand how human cells repair DNA. (Polish)
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    Malfunctioning DNA repair lead to an accumulation of mutations, which frequently results in cancer. The Nucleotide Excision Repair (NER) pathway removes a DNA lesions caused by UV light, cigarette smoke and chemical mutagens. NER is highly conserved, and studying the simpler NER in bacteria provides key insight into human NER. I propose an interdisciplinary approach to understand the mechanistic details of bacterial NER in living cells. I will use a combination of cutting-edge single-molecule methods to elucidate how DNA is repaired inside living cells. I will use super-resolution microscopy combined to study the behaviour of individual NER proteins. To complement this, conventional Biochemistry, cell biology, genetics, SmFRET assays, FCS and tirf microscopy will be used. Together, this will provide a comprehensive understanding of the bacterial NER pathway, and constitute the first steps towards my ultimate goal, which is to understand how human cells repair DNA. (English)
    14 October 2020
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    Identifiers

    POIR.04.04.00-00-1CA9/16
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