Einträge von Friedrich, Ulrike auf dem Publikationsserver
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Anzahl der Einträge: 13.
2022
Schmid, Verena, Wurzel, Alexander
, Wetzel, Christian H.
, Plössl, Karolina, Bruckmann, Astrid, Luckner, Patricia, Weber, Bernhard H. F. und Friedrich, Ulrike
(2022)
Retinoschisin and novel Na/K-ATPase interaction partners Kv2.1 and Kv8.2 define a growing protein complex at the inner segments of mammalian photoreceptors.
Cellular and Molecular Life Sciences 79 (8), S. 448.
Biasella, Fabiola, Strunz, Tobias
, Kiel, Christina
, Weber, Bernhard H. F. und Friedrich, Ulrike
(2022)
Vitronectin and Its Interaction with PAI-1 Suggests a Functional Link to Vascular Changes in AMD Pathobiology.
Cells 11 (11), S. 1766.
2020
Biasella, Fabiola, Plössl, Karolina
, Karl, Claudia, Weber, Bernhard H. F.
und Friedrich, Ulrike
(2020)
Altered Protein Function Caused by AMD-associated Variant rs704 Links Vitronectin to Disease Pathology.
Investigative Opthalmology & Visual Science 61 (14), S. 2.
Schmid, Verena, Plössl, Karolina, Schmid, Carina, Bernklau, Sarah, Weber, Bernhard H. F.
und Friedrich, Ulrike
(2020)
Retinoschisin and Cardiac Glycoside Crosstalk at the Retinal Na/K-ATPase.
Investigative Opthalmology & Visual Science 61 (5), S. 1-10.
2019
Ramchandran, Ramani, Plössl, Karolina
, Straub, Kristina, Schmid, Verena, Strunz, Franziska, Wild, Jens
, Merkl, Rainer, Weber, Bernhard H. F. und Friedrich, Ulrike
(2019)
Identification of the retinoschisin-binding site on the retinal Na/K-ATPase.
PLOS ONE 14 (5), e0216320.
2018
Plössl, Karolina, Schmid, Verena, Straub, Kristina
, Schmid, Carina, Ammon, Mirjam, Merkl, Rainer
, Weber, Bernhard H. F. und Friedrich, Ulrike
(2018)
Pathomechanism of mutated and secreted retinoschisin in X-linked juvenile retinoschisis.
Experimental Eye Research 177, S. 23-34.
Volltext nicht vorhanden.
, Schmid, Carina, Ammon, Mirjam, Merkl, Rainer
, Weber, Bernhard H. F. und Friedrich, Ulrike
(2018)
Pathomechanism of mutated and secreted retinoschisin in X-linked juvenile retinoschisis.
Experimental Eye Research 177, S. 23-34.
Volltext nicht vorhanden.
2017
Plössl, Karolina, Royer, Melanie, Bernklau, Sarah, Tavraz, Neslihan N., Friedrich, Thomas, Wild, Jens, Weber, Bernhard H. F.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
Plössl, Karolina, Royer, Melanie, Bernklau, Sarah, Tavraz, Neslihan N., Friedrich, Thomas, Wild, Jens, Weber, Bernhard H. F.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
Plössl, Karolina, Royer, Melanie, Bernklau, Sarah, Tavraz, Neslihan N., Friedrich, Thomas, Wild, Jens, Weber, Bernhard H. F.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
, Friedrich, Ulrike und Heldin, Carl-Henrik
(2017)
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization.
Molecular Biology of the Cell 28 (16), S. 2178-2189.
Volltext nicht vorhanden.
2016
Friedrich, Ulrike, Plössl, Karolina
und Weber, Bernhard H. F.
(2016)
The X-linked juvenile retinoschisis protein retinoschisin is a novel regulator of MAP kinase signaling and apoptosis in the retina.
Journal of Cellular and Molecular Medicine 2016, S. 1-13.
2015
Grassmann, Felix
, Friedrich, Ulrike, Fauser, Sascha, Schick, Tina, Milenkovic, Andrea, Schulz, Heidi L., von Strachwitz, Claudia N., Bettecken, Thomas, Lichtner, Peter, Meitinger, Thomas
, Arend, Nicole, Wolf, Armin, Haritoglou, Christos, Rudolph, Guenther, Chakravarthy, Usha
, Silvestri, Giuliana, McKay, Gareth J.
, Freitag-Wolf, Sandra, Krawczak, Michael
, Smith, R. Theodore, Merriam, John C., Merriam, Joanna E., Allikmets, Rando, Heid, Iris M. und Weber, Bernhard H. F.
(2015)
A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD).
NeuroMolecular Medicine 17 (2), S. 111-120.
Apaolaza, P. S., del Pozo-Rodríguez, A., Torrecilla, J.
, Rodríguez-Gascón, A., Rodríguez, J. M., Friedrich, Ulrike, Weber, Bernhard H. F.
und make_name_string expected hash reference
(2015)
Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model.
Journal of Controlled Release 217, S. 273-283.
Volltext nicht vorhanden.
, Rodríguez-Gascón, A., Rodríguez, J. M., Friedrich, Ulrike, Weber, Bernhard H. F.
und make_name_string expected hash reference
(2015)
Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model.
Journal of Controlled Release 217, S. 273-283.
Volltext nicht vorhanden.
Friedrich, Ulrike, Datta, Shyamtanu, Schubert, Thomas
, Plößl, Karolina, Schneider, Magdalena, Grassmann, Felix
, Fuchshofer, Rudolf
, Tiefenbach, Klaus-Jürgen, Längst, Gernot und Weber, Bernhard H. F.
(2015)
Synonymous variants in HTRA1 implicated in AMD susceptibility impair its capacity to regulate TGF-β signaling.
Human Molecular Genetics 24, S. 6361-6373.
Volltext nicht vorhanden.
, Plößl, Karolina, Schneider, Magdalena, Grassmann, Felix
, Fuchshofer, Rudolf
, Tiefenbach, Klaus-Jürgen, Längst, Gernot und Weber, Bernhard H. F.
(2015)
Synonymous variants in HTRA1 implicated in AMD susceptibility impair its capacity to regulate TGF-β signaling.
Human Molecular Genetics 24, S. 6361-6373.
Volltext nicht vorhanden.
