Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lena Zobel"'
Autor:
Surabhi Kandaswamy, Lena Zobel, Bina John, Sathiyavedu Thyagarajan Santhiya, Jacqueline Bogedein, Gerhard K. H. Przemeck, Valérie Gailus-Durner, Helmut Fuchs, Martin Biel, Martin Hrabĕ de Angelis, Jochen Graw, Stylianos Michalakis, Oana Veronica Amarie
Publikováno v:
Cell Death Discovery, Vol 8, Iss 1, Pp 1-12 (2022)
Abstract Retinitis pigmentosa is a group of progressive inherited retinal dystrophies that may present clinically as part of a syndromic entity or as an isolated (nonsyndromic) manifestation. In an Indian family suffering from retinitis pigmentosa, w
Externí odkaz:
https://doaj.org/article/64371217682f4adeb05ba3804086516f
Autor:
Laurence M. Occelli, Lena Zobel, Jonathan Stoddard, Johanna Wagner, Nathaniel Pasmanter, Janice Querubin, Lauren M. Renner, Rene Reynaga, Paige A. Winkler, Kelian Sun, Luis Felipe L.P. Marinho, Catherine R. O’Riordan, Amy Frederick, Andreas Lauer, Stephen H. Tsang, William W. Hauswirth, Trevor J. McGill, Martha Neuringer, Stylianos Michalakis, Simon M. Petersen-Jones
Publikováno v:
Molecular Therapy.
Autor:
Helmut Pein, Alexander L. Gerbes, Johanna Pachmayr, Martin Müller, Martina Meßner, Simon Rothenfußer, Andreas Koeberle, Georg J. Arnold, Thomas Fröhlich, Angelika M. Vollmar, Alexandra K. Kiemer, Maximilian A. Ardelt, Sabine Schmitt, Carina Ortler, Lena Zobel, Petra Huber-Cantonati, Lars M. Koenig, Hans Zischka
Publikováno v:
FASEB J. 34, 11860-11882 (2020)
Sorafenib represents the current standard of care for patients with advanced-stage hepatocellular carcinoma (HCC). However, acquired drug resistance occurs frequently during therapy and is accompanied by rapid tumor regrowth after sorafenib therapy t
Autor:
Amy Frederick, Stylianos Michalakis, Maximilian Gerhardt, Martin Biel, Lena Zobel, Simon M. Petersen-Jones, Johanna Wagner, Catherine R. O'Riordan
Publikováno v:
Hum Gene Ther
Retinitis pigmentosa type 45 (RP45) is an autosomal-recessively inherited blinding disease caused by mutations in the cyclic nucleotide-gated channel subunit beta 1 (CNGB1) gene. In this study, we developed and tested a novel gene supplementation the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::290e1dd9d81615ee55f493376c9f4b36
https://europepmc.org/articles/PMC8819509/
https://europepmc.org/articles/PMC8819509/