Anzahl der Einträge: 9.
Artikel
Nachtigal, Anna-Lena,
Milenkovic, Andrea,
Brandl, Caroline ,
Schulz, Heidi L.,
Duerr, Lisa M. J.,
Lang, Gabriele E.,
Reiff, Charlotte,
Herrmann, Philipp,
Kellner, Ulrich und
Weber, Bernhard H. F.
(2020)
Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies.
International Journal of Molecular Sciences 21 (5), S. 1597.
Volltext nicht vorhanden.
Milenkovic, Andrea,
Schmied, Denise,
Tanimoto, Naoyuki,
Seeliger, Mathias W.,
Sparrow, Janet R. und
Weber, Bernhard H. F.
(2019)
The Y227N mutation affects bestrophin-1 protein stability and impairs sperm function in a mouse model of Best vitelliform macular dystrophy.
Biology Open.
Volltext nicht vorhanden.
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.
Milenkovic, Andrea,
Brandl, C.,
Milenkovic, Vladimir M.,
Jendryke, T.,
Sirianant, L.,
Wanitchakool, P.,
Zimmermann, S. und
Weber, Bernhard H. F.
(2015)
Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells.
Proc Natl Acad Sci U S A (PNAS) 112 (20), E2630-E2639.
Volltext nicht vorhanden.
Brandl, Caroline,
Zimmermann, Stephanie J.,
Milenkovic, Vladimir M.,
Rosendahl, S. M.,
Grassmann, Felix,
Milenkovic, Andrea,
Hehr, Ute,
Federlin, Marianne,
Wetzel, Christian H.,
Helbig, Horst und
Weber, Bernhard H. F.
(2014)
In-Depth Characterisation of Retinal Pigment Epithelium (RPE) Cells Derived from Human Induced Pluripotent Stem Cells (hiPSC).
NeuroMolecular Medicine 16, S. 551-564.
Friedrich, U.,
Myers, C. A.,
Fritsche, L. G.,
Milenkovic, Andrea,
Wolf, A.,
Corbo, J. C. und
Weber, Bernhard H. F.
(2011)
Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
Human Molecular Genetics 20, S. 1387-1399.
Volltext nicht vorhanden.
Diese Liste wurde erzeugt am Thu May 2 16:03:20 2024 CEST.