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Mathias W. Seeliger

university of gottingen

64H指数
255论文数
1.3W被引数
收录论文 78
发表时间
Quantitative proteomics identifies potential molecular adaptations in mouse models of congenital stationary night blindness type 2定量蛋白质组学鉴定先天性静止性夜盲症2型的潜在分子适应性改变小鼠模型
err2025-11-10
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errOAAI
errMatthias Ganglberger; Lucia Zanetti; Anna-Sophia Egger; Alexander Günter; Bettina Wagner; Soumaya Belhadj; Regine Mühlfriedel; Dagmar Knoflach; Emilio Casanova; Thomas Rülicke; Mathias W. Seeliger; Marcel Kwiatkowski; Hartwig Seitter; Alexandra Koschak
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APOSTEL-R Recommendations for Reporting Retinal Optical Coherence Tomography Studies in Rodents
err2025-11-01
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PREAI
errOertel, Frederike Cosima; Cabrera Debuc, Delia; Calabresi, Peter A.; Chen, Mei; Cordano, Christian; Dietrich, Michael; Feltgen, Nicolas; Gramlich, Oliver; Green, Ari J.; Groh, Janos; Huang, Su-Chun; Knier, Benjamin; Korn, Thomas; Leocani, Letizia; Loewenstein, Anat; van Oterendorp, Christian; Peto, Tunde; Schippling, Sven; Schmetterer, Leopold; Schmitz-Valckenberg, Steffen; Seeliger, Mathias W.; Shindler, Kenneth S.; Schuman, Joel S.; Sindi, Mustafa; Tufail, Adnan; Wang, Jui-Kai; Wolf, Sebastian; You, Yuyi; Zinkernagel, Martin; Lagreze, Wolf; Albrecht, Philipp
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Mural Cell SRF Controls Pericyte Migration, Vessel Patterning and Blood Flow
err2022-08-05
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errOAAI
errOrlich, Michael M.; Dieguez-Hurtado, Rodrigo; Muehlfriedel, Regine; Sothilingam, Vithiyanjali; Wolburg, Hartwig; Oender, Cansu Ebru; Woelffing, Pascal; Betsholtz, Christer; Gaengel, Konstantin; Seeliger, Mathias; Adams, Ralf H.; Nordheim, Alfred
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Three-year results of phase I retinal gene therapy trial for CNGA3-mutated achromatopsia: results of a non randomised controlled trial
err2021-05-18
err49
PREAI
errReichel, Felix Friedrich; Michalakis, Stylianos; Wilhelm, Barbara; Zobor, Ditta; Muehlfriedel, Regine; Kohl, Susanne; Weisschuh, Nicole; Sothilingam, Vithiyanjali; Kuehlewein, Laura; Kahle, Nadine; Seitz, Immanuel; Paquet-Durand, Francois; Tsang, Stephen H.; Martus, Peter; Peters, Tobias; Seeliger, Mathias; Bartz-Schmidt, Karl Ulrich; Ueffing, Marius; Zrenner, Eberhard; Biel, Martin; Wissinger, Bernd; Fischer, Dominik
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A retinal model of cerebral malaria
err2019-03-05
err13
errOAAI
errPaquet-Durand, Francois; Beck, Susanne C.; Das, Soumyaparna; Huber, Gesine; Chang, Le; Schubert, Timm; Tanimoto, Naoyuki; Garcia-Garrido, Marina; Muehlfriedel, Regine; Bolz, Sylvia; Hoffmann, Wolfgang; Schraermeyer, Ulrich; Mordmueller, Benjamin; Seeliger, Mathias W.
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Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina
err2018-04-13
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errOAAI
errBeck, Susanne C.; Karlstetter, Marcus; Garrido, Marina Garcia; Feng, Yuxi; Dannhausen, Katharina; Muehlfriedel, Regine; Sothilingam, Vithiyanjali; Seebauer, Britta; Berger, Wolfgang; Hammes, Hans-Peter; Seeliger, Mathias W.; Langmann, Thomas
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Disturbed Processing of Contextual Information in HCN3 Channel Deficient Mice
err2018-01-09
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errOAAI
errStieglitz, Marc S.; Fenske, Stefanie; Hammelmann, Verena; Becirovic, Elvir; Schoettle, Verena; Delorme, James E.; Schoell-Weidinger, Martha; Mader, Robert; Deussing, Jan; Wolfer, David P.; Seeliger, Mathias W.; Albrecht, Urs; Wotjak, Carsten T.; Biel, Martin; Michalakis, Stylianos; Wahl-Schott, Christian
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The absence of angiopoietin-2 leads to abnormal vascular maturation and persistent proliferative retinopathy
err2017-11-24
err21
PREAI
errFeng, Yuxi; vom Hagen, Franziska; Wang, Yumei; Beck, Susanne; Schreiter, Kay; Pfister, Frederick; Hoffmann, Sigrid; Wagner, Patrick; Seeliger, Mathias; Molema, Grietje; Deutsch, Urban; Hammes, Hans-Peter
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Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach
err2017-11-20
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errOAAI
errPetersen-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; Schon, Christian; Seeliger, Mathias W.; Levin, Alex V.; Michalakis, Stylianos; Hauswirth, William W.; Tsang, Stephen H.
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AAV-Mediated Gene Supplementation Therapy in Achromatopsia Type 2: Preclinical Data on Therapeutic Time Window and Long-Term Effects
err2017-05-24
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errOAAI
errMuehlfriedel, Regine; Tanimoto, Naoyuki; Schoen, Christian; Sothilingam, Vithiyanjali; Garrido, Marina Garcia; Beck, Susanne C.; Huber, Gesine; Biel, Martin; Seeliger, Mathias W.; Michalakis, Stylianos
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Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014)
err2017-03-10
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errOAAI
errMichalakis, 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; Garrido, Marina Garcia; Tanimoto, Naoyuki; Seeliger, Mathias W.; Biel, Martin; Wahl-Schott, Christian A.
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Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 Mutation
err2017-01-23
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errStojic, Aleksandar; Fairless, Richard; Beck, Susanne C.; Sothilingam, Vithiyanjali; Weissgerber, Petra; Wissenbach, Ulrich; Gimmy, Valerie; Seeliger, Mathias W.; Flockerzi, Veit; Diem, Ricarda; Williams, Sarah K.
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Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia
err2016-01-05
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errOAAI
errSchoen, Christian; Asteriti, Sabrina; Koch, Susanne; Sothilingam, Vithiyanjali; Garrido, Marina Garcia; Tanimoto, Naoyuki; Herms, Jochen; Seeliger, Mathias W.; Cangiano, Lorenzo; Biel, Martin; Michalakis, Stylianos
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Retinal functional alterations in mice lacking intermediate filament proteins glial fibrillary acidic protein and vimentin
err2015-08-06
err30
PREAI
errWunderlich, Kirsten A.; Tanimoto, Naoyuki; Grosche, Antje; Zrenner, Eberhart; Pekny, Milos; Reichenbach, Andreas; Seeliger, Mathias W.; Pannicke, Thomas; Perez, Maria-Thereza
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Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype
err2015-07-17
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errOAAI
errSothilingam, Vithiyanjali; Garrido, Marina Garcia; Jiao, Kangwei; Buena-Atienza, Elena; Sahaboglu, Ayse; Trifunovic, Dragana; Balendran, Sukirthini; Koepfli, Tanja; Muehlfriedel, Regine; Schoen, Christian; Biel, Martin; Heckmann, Angelique; Beck, Susanne C.; Michalakis, Stylianos; Wissinger, Bernd; Seeliger, Mathias W.; Paquet-Durand, Francois
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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
err2015-06-01
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errOAAI
errKohl, Susanne; Zobor, Ditta; Chiang, Wei-Chieh; Weisschuh, Nicole; Staller, Jennifer; Menendez, Irene Gonzalez; Chang, Stanley; Beck, Susanne C.; Garrido, Marina Garcia; Sothilingam, Vithiyanjali; Seeliger, Mathias W.; Stanzial, Franco; Benedicenti, Francesco; Inzana, Francesca; Heon, Elise; Vincent, Ajoy; Beis, Jill; Strom, Tim M.; Rudolph, Guenther; Roosing, Susanne; den Hollander, Anneke I.; Cremers, Frans P. M.; Lopez, Irma; Ren, Huanan; Moore, Anthony T.; Webster, Andrew R.; Michaelides, Michel; Koenekoop, Robert K.; Zrenner, Eberhart; Kaufman, Randal J.; Tsang, Stephen H.; Wissinger, Bernd; Lin, Jonathan H.
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Electroretinographic assessment of rod- and cone-mediated bipolar cell pathways using flicker stimuli in mice
err2015-06-01
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errOAAI
errTanimoto, Naoyuki; Sothilingam, Vithiyanjali; Kondo, Mineo; Biel, Martin; Humphries, Peter; Seeliger, Mathias W.
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