14 human-rights positions at Institute of Bioorganic Chemistry Polish Academy of Sciences
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project objectives is to establish efficient and safe genome editing approaches to correct the SCD mutation. As part of this project, ICHB will develop and validate a new HDR-based method for precise
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: human genetics, Birt-Hogg-Dubé syndrome, Tuberous Sclerosis Complex, Hereditary Leiomyomatosis and Renal Cell Cancer, ultrasensitive next generation sequencing, somatic mutations, skin tumors, lung cysts
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amount of ca 4300 PLN (3800 PLN net) for the period of 19 months with a possible extension. Ph.D. students shall be subject to social insurance, pursuant to the article. 6 section 1 passage 7b of the act
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, and informatics to solve questions about synthesis, structure and function of nucleic acids, proteins and metabolites, as well as their mutual interactions. In our studies we use human model cell lines
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program, (3) chemical mapping of two large fragments of the 28S subunit of the human ribosomal RNA (rRNA). Both model rRNAs contain 5 and 13 pseudouridine residues, respectively. They are selected from
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datasets from different stages of neurodegeneration in AD will enable the development of an in silico model of neurodegeneration that will be further validated in human neuronal progenitors. Using RNA-based
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subject to social insurance, pursuant to the article. 6 section 1 passage 7b of the act of October 13th, 1998, on the social insurance system (Journal of Laws of 2019, items 300, 303, and 730). Requirements
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: biology. chemistry, and informatics to solve questions about synthesis, structure and function of nucleic acids, proteins and metabolites, as well as their mutual interactions. In our studies we use human
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of the EDITSCD project objectives is to establish efficient and safe genome editing approaches to correct the SCD mutation. As part of this project, ICHB will develop and validate a new HDR-based method
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: human genetics, Birt-Hogg-Dubé syndrome, Tuberous Sclerosis Complex, Hereditary Leiomyomatosis and Renal Cell Cancer, ultrasensitive next generation sequencing, somatic mutations, skin tumors, lung cysts