Zobrazeno 1 - 6
of 6
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