Anzahl der Publikationen: 13
Zeitschriftenartikel
Yan, Jie; Guenter, Alexander; Das, Soumyaparna; Muehlfriedel, Regine; Michalakis, Stylianos; Jiao, Kangwei; Seeliger, Mathias W. und Paquet-Durand, Francois
(2022):
Inherited Retinal Degeneration: PARP-Dependent Activation of Calpain Requires CNG Channel Activity.
In: Biomolecules, Bd. 12, Nr. 3, 455
Stieglitz, Marc S.; Fenske, Stefanie; Hammelmann, Verena; Becirovic, Elvir; Schöttle, Verena; Delorme, James E.; Schöll-Weidinger, Martha; Mader, Robert; Deussing, Jan; Wolfer, David P.; Seeliger, Mathias W.; Albrecht, Urs; Wotjak, Carsten T.; Biel, Martin; Michalakis, Stylianos und Wahl-Schott, Christian
(2018):
Disturbed Processing of Contextual Information in HCN3 Channel Deficient Mice.
In: Frontiers in Molecular Neuroscience, Bd. 10, 436
[PDF, 4MB]
Petersen-Jones, Simon M.; Occelli, Laurence M.; Winkler, Paige A.; Lee, Winston; Sparrow, Janet R.; Tsukikawa, Mai; Boye, Sanford L.; Chiodo, Vince; Capasso, Jenina E.; Becirovic, Elvir; Schön, Christian; Seeliger, Mathias W.; Levin, Alex V.; Michalakis, Stylianos; Hauswirth, William W. und Tsang, Stephen H.
(2018):
Patients and animal models of CNG beta 1-deficient retinitis pigmentosa support gene augmentation approach.
In: Journal of Clinical Investigation, Bd. 128, Nr. 1: S. 190-206
[PDF, 23MB]
Schön, Christian; Sothilingam, Vithiyanjali; Mühlfriedel, Regine; Garrido, Marina Garcia; Beck, Susanne C.; Tanimoto, Naoyuki; Wissinger, Bernd; Paquet-Durand, Francois; Biel, Martin; Michalakis, Stylianos und Seeliger, Mathias W.
(2017):
Gene Therapy Successfully Delays Degeneration in a Mouse Model of PDE6A-Linked Retinitis Pigmentosa (RP43).
In: Human Gene therapy, Bd. 28, Nr. 12: S. 1180-1188
Mühlfriedel, Regine; Tanimoto, Naoyuki; Schön, Christian; Sothilingam, Vithiyanjali; Garrido, Marina Garcia; Beck, Susanne C.; Huber, Gesine; Biel, Martin; Seeliger, Mathias W. und Michalakis, Stylianos
(2017):
AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects.
In: Frontiers in Neuroscience, Bd. 11, 292
[PDF, 5MB]
Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali; Koch, Susanne; Schludi, Verena; Krause, Stefanie; Zeitz, Christina; Audo, Isabelle; Lancelot, Marie-Elise; Hamel, Christian; Meunier, Isabelle; Preising, Markus N.; Friedburg, Christoph; Lorenz, Birgit; Zabouri, Nawal; Haverkamp, Silke; Garcia Garrido, Marina; Tanimoto, Naoyuki; Seeliger, Mathias W.; Biel, Martin und Wahl-Schott, Christian A.
(2017):
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014).
In: Human Molecular Genetics, Bd. 26, Nr. 2: S. 466
Schön, Christian; Asteriti, Sabrina; Koch, Susanne; Sothilingam, Vithiyanjali; Garrido, Marina Garcia; Tanimoto, Naoyuki; Herms, Jochen; Seeliger, Mathias W.; Cangiano, Lorenzo; Biel, Martin und Michalakis, Stylianos
(2016):
Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia.
In: Human Molecular Genetics, Bd. 25, Nr. 6: S. 1165-1175
Schön, Christian; Hoffmann, Nadine A.; Ochs, Simon M.; Burgold, Steffen; Filser, Severin; Steinbach, Sonja; Seeliger, Mathias W.; Arzberger, Thomas; Goedert, Michel; Kretzschmar, Hans A.; Schmidt, Boris und Herms, Jochen
(2012):
Long-term in vivo imaging of fibrillar tau in the retina of P301S transgenic mice.
In: PLOS ONE
7(12), e53547
[PDF, 7MB]
Fischer, M. Dominik; Huber, Gesine; Beck, Susanne C.; Tanimoto, Naoyuki; Muehlfriedel, Regine; Fahl, Edda; Grimm, Christian; Wenzel, Andreas; Remé, Charlotte E.; van de Pavert, Serge A.; Wijnholds, Jan; Pacal, Marek; Bremner, Rod und Seeliger, Mathias W.
(2009):
Noninvasive, in vivo assessment of mouse retinal structure using optical coherence tomography.
In: PLOS ONE
4(10), e7507
[PDF, 1MB]
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