Projects per year
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 1 Finished
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RiboCure (Anbahnung)
Breitenbach-Koller, H. (Principal Investigator) & Friedrich, A. (Co-Investigator)
1/03/18 → 28/02/19
Project: Research
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RiboScreenTM Technology Delivers a Ribosomal Target and a Small-Molecule Ligand for Ribosome Editing to Boost the Production Levels of Tropoelastin, the Monomeric Unit of Elastin
Wimmer, B., Schernthaner, J., Edobor, G., Friedrich, A., Poeltner, K., Temaj, G., Wimmer, M., Kronsteiner, E., Pichler, M., Gercke, H., Huber, R., Kaefer, N., Rinnerthaler, M., Karl, T., Krauß, J., Mohr, T., Gerner, C., Hintner, H., Breitenbach, M. & Bauer, J. W. & 6 others, , 1 Aug 2024, In: International Journal of Molecular Sciences. 25, 15, 8430.Research output: Contribution to journal › Article › peer-review
Open Access -
Emerging Personalized Opportunities for Enhancing Translational Readthrough in Rare Genetic Diseases and Beyond
Wagner, R. N., Wießner, M., Friedrich, A., Zandanell, J., Breitenbach-Koller, H. & Bauer, J. W., 23 Mar 2023, In: International Journal of Molecular Sciences. 24, 7, 6101.Research output: Contribution to journal › Review article › peer-review
Open Access -
Drug Development for Target Ribosomal Protein rpL35/uL29 for Repair of LAMB3R635X in Rare Skin Disease Epidermolysis Bullosa
Rathner, A., Rathner, P., Friedrich, A., Wießner, M., Kitzler, C. M., Schernthaner, J., Karl, T., Krauß, J., Lottspeich, F., Mewes, W., Hintner, H., Bauer, J. W., Breitenbach, M., Müller, N., Breitenbach-Koller, H. & von Hagen, J., 2021, In: Skin Pharmacology and Physiology. 34, 4, p. 167-182 16 p.Research output: Contribution to journal › Article › peer-review
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Tailored gene expression at the ribosome: Correction of the mutationLAMB3R635X in Epidermolysis bullosa
Breitenbach-Koller, H., Moßhammer, C., Friedrich, A., Rathner, A., Rathner, P. & Edobor, G., 2021, From Molecular Machines to Translation Medicine.Research output: Chapter in Book/Report/Conference proceeding/Legal commentary › Conference contribution
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A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia
Zanni, G., Kalscheuer, V., Friedrich, A., Barresi, S., Alfieri, P., M, M. M., Haas, S., Piccini, G., Karl, T., Klauck, S., Bellacchio, E., Emma, F., Cappa, M., Bertini, E. & Breitenbach-Koller, H., 2015, In: HUMAN MUTATION. p. 1155-1158Research output: Contribution to journal › Article › peer-review
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Small molecule binding to human ribosomal protein L35 and translational repair of mutant skin protein Lamb3 PTC in rare disease Epidermolysis bullosa
Breitenbach-Koller, H. (Presenter) & Friedrich, A. (Presenter)
16 Sept 2019 → 18 Sept 2019Activity: Talk or presentation › Poster presentation › science to science / art to art
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Customized translational repair of skin protein Lamb3 PTC mutation in rare disease Epidermolysis bullosa
Breitenbach-Koller, H. (Presenter) & Friedrich, A. (Presenter)
2019 → …Activity: Talk or presentation › Poster presentation › science to science / art to art
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Poster: Ribosomal proteins as drug targets for PTC repair in rare disease epidermolysis bullosa (eb).
Friedrich, A. (Presenter)
13 Dec 2018Activity: Talk or presentation › Poster presentation › science to science / art to art
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Poster: Customized protein therapy for PTC repair in rare disease epidermolysis bullosa (eb).
Friedrich, A. (Presenter)
11 Nov 2018 → 14 Nov 2018Activity: Talk or presentation › Poster presentation › science to science / art to art
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Symposium, in der Vortragsreihe des Projekts Proteinsynthese nach Maß.
Friedrich, A. (Speaker)
24 Oct 2018Activity: Talk or presentation › Oral presentation › science to science / art to art