Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Tina Bresser"'
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 6 (2020)
Retinitis pigmentosa (RP) represents genetically heterogeneous and clinically variable disease characterized by progressive degeneration of photoreceptors resulting in a gradual loss of vision. The autosomal dominant RP type 13 (RP13) has been linked
Externí odkaz:
https://doaj.org/article/4f11d4c3f57a478d8510b3f294da03ce
Autor:
Ann-Katrin Claudius, Steffen Erkelenz, Juliane Mundorf, Niels H. Gehring, Dimitrije Stanković, Volker Boehm, Mirka Uhlirova, Tina Bresser
Publikováno v:
Nucleic Acids Research
Pre-mRNA splicing catalyzed by the spliceosome represents a critical step in the regulation of gene expression contributing to transcriptome and proteome diversity. The spliceosome consists of five small nuclear ribonucleoprotein particles (snRNPs),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e10970a7d42a53256c2935550f320f34
https://doi.org/10.1093/nar/gkaa1274
https://doi.org/10.1093/nar/gkaa1274
Publikováno v:
The FEBS journalReferences. 289(15)
Cancer development has been linked to aberrant sensing and interpretation of mechanical cues and force-generating properties. Here, we show that upregulation of the actin crosslinking protein Cheerio (Cher), the fly ortholog of Filamin A (FLNA), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eacd157e13f0d001f3e62263d56efb23
https://pubmed.ncbi.nlm.nih.gov/35191183
https://pubmed.ncbi.nlm.nih.gov/35191183
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 6 (2020)
Retinitis pigmentosa (RP) represents genetically heterogeneous and clinically variable disease characterized by progressive degeneration of photoreceptors resulting in a gradual loss of vision. The autosomal dominant RP type 13 (RP13) has been linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eae530d018449dd370c0a3165b81f6e
http://dmm.biologists.org/content/13/6/dmm043174
http://dmm.biologists.org/content/13/6/dmm043174
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Retinitis pigmentosa (RP) represents genetically heterogeneous and clinically variable disease characterized by progressive degeneration of photoreceptors resulting in a gradual loss of vision. The autosomal dominant RP type 13 (RP13) has been linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21f01ecc69e72730be7b8a436add84d2
https://pubmed.ncbi.nlm.nih.gov/32424050
https://pubmed.ncbi.nlm.nih.gov/32424050
Publikováno v:
Nucleic Acids Research; 3/21/2024, Vol. 52 Issue 5, p2093-2111, 19p
Autor:
Külshammer, Eva1 (AUTHOR), Kilinc, Merve1 (AUTHOR), Csordás, Gábor1 (AUTHOR), Bresser, Tina1 (AUTHOR), Nolte, Hendrik1 (AUTHOR), Uhlirova, Mirka1 (AUTHOR) mirka.uhlirova@uni-koeln.de
Publikováno v:
FEBS Journal. Aug2022, Vol. 289 Issue 15, p4497-4517. 21p.
Autor:
Donohoe, Colin D.1, Csordás, Gábor1, Correia, Andreia1, Jindra, Marek2, Klein, Corinna3, Habermann, Bianca4, Uhlirova, Mirka1,5 mirka.uhlirova@uni-koeln.de
Publikováno v:
PLoS Genetics. 3/1/2018, Vol. 14 Issue 3, p1-32. 32p.
Autor:
Erkelenz, Steffen, Stanković, Dimitrije, Mundorf, Juliane, Bresser, Tina, Claudius, Ann-Katrin, Boehm, Volker, Gehring, Niels H, Uhlirova, Mirka
Publikováno v:
Nucleic Acids Research; 2/22/2021, Vol. 49 Issue 3, p1688-1707, 20p