Anzahl der Einträge: 6.
Artikel
Meindl, Katrin ,
Issler, Naomi,
Afonso, Sara Cerqueira,
Cebrian-Serrano, Alberto,
Müller-Decker, Karin,
Sterner, Christina,
Othmen, Helga,
Tegtmeier, Ines,
Witzgall, Ralph ,
Klootwijk, Enriko D.,
Davies, Benjamin,
Kleta, Robert und
Warth, Richard
(2023)
A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.
Frontiers in Cell and Developmental Biology 11.
Triebelhorn, Julian ,
Cardon, Iseline ,
Kuffner, Kerstin,
Bader, Stefanie,
Jahner, Tatjana,
Meindl, Katrin ,
Rothhammer-Hampl, Tanja ,
Riemenschneider, Markus J.,
Drexler, Konstantin,
Berneburg, Mark,
Nothdurfter, Caroline,
Manook, André,
Brochhausen, Christoph,
Baghai, Thomas C.,
Hilbert, Sven ,
Rupprecht, Rainer,
Milenkovic, Vladimir M. und
Wetzel, Christian H.
(2022)
Induced neural progenitor cells and iPS-neurons from major depressive disorder patients show altered bioenergetics and electrophysiological properties.
Molecular Psychiatry.
Issler, Naomi,
Afonso, Sara,
Weissman, Irith,
Jordan, Katrin,
Cebrian-Serrano, Alberto,
Meindl, Katrin,
Dahlke, Eileen,
Tziridis, Konstantin,
Yan, Guanhua,
Robles-López, José M.,
Tabernero, Lydia ,
Patel, Vaksha,
Kesselheim, Anne,
Klootwijk, Enriko D.,
Stanescu, Horia C.,
Dumitriu, Simona,
Iancu, Daniela,
Tekman, Mehmet,
Mozere, Monika,
Jaureguiberry, Graciana,
Outtandy, Priya,
Russell, Claire,
Forst, Anna-Lena,
Sterner, Christina,
Heinl, Elena-Sofia,
Othmen, Helga,
Tegtmeier, Ines,
Reichold, Markus,
Schiessl, Ina Maria ,
Limm, Katharina,
Oefner, Peter,
Witzgall, Ralph,
Fu, Lifei,
Theilig, Franziska,
Schilling, Achim,
Shuster Biton, Efrat,
Kalfon, Limor,
Fedida, Ayalla,
Arnon-Sheleg, Elite,
Ben Izhak, Ofer,
Magen, Daniella,
Anikster, Yair,
Schulze, Holger,
Ziegler, Christine,
Lowe, Martin,
Davies, Benjamin,
Böckenhauer, Detlef,
Kleta, Robert,
Falik Zaccai, Tzipora C. und
Warth, Richard
(2022)
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
Journal of the American Society of Nephrology 33 (4), S. 732-745.
Issler, Naomi,
Afonso, Sara Cerqueira,
Weissman, Irith,
Jordan, Katrin,
Cebrian-Serrano, Alberto,
Meindl, Katrin,
Dahlke, Eileen,
Tziridis, Konstantin,
Yan, Guanhua,
Robles-López, José M.,
Tabernero, Lydia ,
Patel, Vaksha,
Kesselheim, Anne,
Klootwijk, Enriko D.,
Stanescu, Horia C.,
Dumitriu, Simona,
Iancu, Daniela,
Tekman, Mehmet,
Mozere, Monika,
Jaureguiberry, Graciana,
Outtandy, Priya,
Russell, Claire,
Forst, Anna-Lena,
Sterner, Christina,
Heinl, Elena-Sofia,
Othmen, Helga,
Tegtmeier, Ines,
Reichold, Markus,
Schiessl, Ina Maria ,
Limm, Katharina,
Oefner, Peter J.,
Witzgall, Ralph,
Fu, Lifei,
Theilig, Franziska,
Schilling, Achim,
Shuster Biton, Efrat,
Kalfon, Limor,
Fedida, Ayalla,
Arnon-Sheleg, Elite,
Ben Izhak, Ofer,
Magen, Daniella,
Anikster, Yair,
Schulze, Holger,
Ziegler, Christine,
Lowe, Martin,
Davies, Benjamin,
Böckenhauer, Detlef,
Kleta, Robert,
Falik Zaccai, Tzipora C. und
Warth, Richard
(2022)
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
Journal of the American Society of Nephrology 33.
Volltext nicht vorhanden.
Kuffner, Kerstin,
Triebelhorn, Julian,
Meindl, Katrin,
Benner, Christoph,
Manook, André,
Sudria-Lopez, Daniel,
Siebert, Ramona,
Nothdurfter, Caroline,
Baghai, Thomas C.,
Drexler, Konstantin,
Berneburg, Mark,
Rupprecht, Rainer,
Milenkovic, Vladimir M. und
Wetzel, Christian H.
(2020)
Major Depressive Disorder is Associated with Impaired Mitochondrial Function in Skin Fibroblasts.
Cells 9 (4), S. 884.
Hochschulschrift der Universität Regensburg
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