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Nürnberg, Elina [Author] ; Hafner, Mathias [Degree supervisor]

Optimizing microscopy in three dimensions : optical clearing techniques for the study of hiPSC-derived neural spheroids and 3D cell cultures

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Heidelberg, 23 Apr. 2024
Neumaier, Michael [Author]; Giesler, Sophie [Author]; Ast, Volker [Author]; Römer, Mathis [Author]; Voß, Timo-Daniel [Author]; Reinz, Eileen [Author]; Costina, Victor [Author]; Schmelz, Martin [Author]; Nürnberg, Elina [Author]; Nittka, Stefanie [Author]; Leppä, Aino-Maija [Author]; Rudolf, Rüdiger [Author]; Trumpp, Andreas [Author]; Fuchs, Tina [Author]

Opsonization-independent antigen-specific recognition by myeloid phagocytes expressing monoclonal antibodies

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Sep 2023

Published in: Science advances ; 9(2023), 35, Artikel-ID eadg181, Seite 1-12
Martí, Yasmina; Nürnberg, Elina; Horschitz, Sandra; Hafner, Mathias; Schloss, Patrick; Meyer-Lindenberg, Andreas; Lau, Thorsten

Refinement of a neuronal differentiation protocol predominantly yields human iPS cell-derived dopaminergic neurons for the investigation of neurodegenerative pathomechanisms in vitro

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IOS Press, 2017

Published in: Journal of Cellular Biotechnology
Neumaier, Michael; Giesler, Sophie; Ast, Volker; Roemer, Mathis; Voß, Timo-Daniel; Reinz, Eileen; Costina, Victor; Schmelz, Martin; Nürnberg, Elina; Nittka, Stefanie; Leppä, Aino-Maija; Rudolf, Ruediger; Trumpp, Andreas; Fuchs, Tina

Opsonization-independent antigen-specific recognition by myeloid phagocytes expressing monoclonal antibodies

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American Association for the Advancement of Science (AAAS), 2023

Published in: Science Advances
Nürnberg, Elina; Vitacolonna, Mario; Klicks, Julia; von Molitor, Elena; Cesetti, Tiziana; Keller, Florian; Bruch, Roman; Ertongur-Fauth, Torsten; Riedel, Katja; Scholz, Paul; Lau, Thorsten; Schneider, Richard; Meier, Julia; Hafner, Mathias; Rudolf, Rüdiger

Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward

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Frontiers Media SA, 2020

Published in: Frontiers in Molecular Biosciences
Jabbari, Kamel; Bobbili, Dheeraj R.; Lal, Dennis; Reinthaler, Eva M.; Schubert, Julian; Wolking, Stefan; Sinha, Vishal; Motameny, Susanne; Thiele, Holger; Kawalia, Amit; Altmüller, Janine; Toliat, Mohammad Reza; Kraaij, Robert; van Rooij, Jeroen; Uitterlinden, André G.; Ikram, M. Arfan; Zara, Federico; Lehesjoki, Anna-Elina; Krause, Roland; Zimprich, Fritz; Sander, Thomas; Neubauer, Bernd A.; May, Patrick; Lerche, Holger;

Rare gene deletions in genetic generalized and Rolandic epilepsies

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Public Library of Science (PLoS), 2018

Published in: PLOS ONE
Lal, Dennis; Reinthaler, Eva M.; Dejanovic, Borislav; May, Patrick; Thiele, Holger; Lehesjoki, Anna-Elina; Schwarz, Günter; Riesch, Erik; Ikram, M. Arfan; Duijn, Cornelia M. van; Uitterlinden, Andre G.; Hofman, Albert; Steinböck, Hannelore; Gruber-Sedlmayr, Ursula; Neophytou, Birgit; Zara, Federico; Hahn, Andreas; Gormley, Padhraig; Becker, Felicitas; Weber, Yvonne G.; Cilio, Maria Roberta; Kunz, Wolfram S.; Krause, Roland; Zimprich, Fritz; [...]

Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

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Public Library of Science (PLoS), 2016

Published in: PLOS ONE
Huyghe, Jeroen R.; Van Laer, Lut; Hendrickx, Jan-Jaap; Fransen, Erik; Demeester, Kelly; Topsakal, Vedat; Kunst, Sylvia; Manninen, Minna; Jensen, Mona; Bonaconsa, Amanda; Mazzoli, Manuela; Baur, Manuela; Hannula, Samuli; Mäki-Torkko, Elina; Espeso, Angeles; Van Eyken, Els; Flaquer, Antonia; Becker, Christian; Stephens, Dafydd; Sorri, Martti; Orzan, Eva; Bille, Michael; Parving, Agnete; Pyykkö, Ilmari; [...]

Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment Trait

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Elsevier BV, 2008

Published in: The American Journal of Human Genetics
Galizia, Elizabeth C.; Myers, Candace T.; Leu, Costin; de Kovel, Carolien G. F.; Afrikanova, Tatiana; Cordero-Maldonado, Maria Lorena; Martins, Teresa G.; Jacmin, Maxime; Drury, Suzanne; Krishna Chinthapalli, V.; Muhle, Hiltrud; Pendziwiat, Manuela; Sander, Thomas; Ruppert, Ann-Kathrin; Møller, Rikke S.; Thiele, Holger; Krause, Roland; Schubert, Julian; Lehesjoki, Anna-Elina; Nürnberg, Peter; Lerche, Holger; Palotie, Aarno; Coppola, Antonietta; Striano, Salvatore; [...]

CHD2variants are a risk factor for photosensitivity in epilepsy

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Oxford University Press (OUP), 2015

Published in: Brain
Lemke, Johannes R; Lal, Dennis; Reinthaler, Eva M; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jähn, Johanna A; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Møller, Rikke S; Hjalgrim, Helle; Addis, Laura; [...]

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

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Springer Science and Business Media LLC, 2013

Published in: Nature Genetics
Leu, Costin; de Kovel, Carolien G.F.; Zara, Federico; Striano, Pasquale; Pezzella, Marianna; Robbiano, Angela; Bianchi, Amedeo; Bisulli, Francesca; Coppola, Antonietta; Giallonardo, Anna Teresa; Beccaria, Francesca; Trenité, Dorothée Kasteleijn‐Nolst; Lindhout, Dick; Gaus, Verena; Schmitz, Bettina; Janz, Dieter; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Kleefuß‐Lie, Ailing A.; Hallman, Kerstin; Kunz, Wolfram S.; Elger, Christian E.; Muhle, Hiltrud; [...]

Genome‐wide linkage meta‐analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

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Wiley, 2012

Published in: Epilepsia
Abou-Khalil, Bassel; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Balding, David J.; Bast, Thomas; Baum, Larry; Becker, Albert J.; Becker, Felicitas; Berghuis, Bianca; Berkovic, Samuel F.; Boysen, Katja E.; Bradfield, Jonathan P.; Brody, Lawrence C.; Buono, Russell J.; Campbell, Ellen; Cascino, Gregory D.; Catarino, Claudia B.; Cavalleri, Gianpiero L.; Cherny, Stacey S.; Chinthapalli, Krishna; Coffey, Alison J.; Compston, Alastair; Coppola, Antonietta; [...]

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

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Springer Science and Business Media LLC, 2018

Published in: Nature Communications
Niestroj, Lisa-Marie; Perez-Palma, Eduardo; Howrigan, Daniel P; Zhou, Yadi; Cheng, Feixiong; Saarentaus, Elmo; Nürnberg, Peter; Stevelink, Remi; Daly, Mark J; Palotie, Aarno; Lal, Dennis; Feng, Yen-Chen Anne; Howrigan, Daniel P; Abbott, Liam E; Tashman, Katherine; Cerrato, Felecia; Lal, Dennis; Churchhouse, Claire; Gupta, Namrata; Neale, Benjamin M; Berkovic, Samuel F; Lerche, Holger; Goldstein, David B; Lowenstein, Daniel H; [...]

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

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Oxford University Press (OUP), 2020

Published in: Brain
Stevelink, Remi; Campbell, Ciarán; Chen, Siwei; Abou-Khalil, Bassel; Adesoji, Oluyomi M.; Afawi, Zaid; Amadori, Elisabetta; Anderson, Alison; Anderson, Joseph; Andrade, Danielle M.; Annesi, Grazia; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Baker, Mark D.; Balagura, Ganna; Balestrini, Simona; Barba, Carmen; Barboza, Karen; Bartolomei, Fabrice; Bast, Thomas; Baum, Larry; Baumgartner, Tobias; Baykan, Betül; [...]

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

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Springer Science and Business Media LLC, 2023

Published in: Nature Genetics

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