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Anzahl der Publikationen: 36

Zeitschriftenartikel

Giusti, Sebastian A. ORCID logoORCID: https://orcid.org/0000-0002-0257-3027; Pino, Natalia S. ORCID logoORCID: https://orcid.org/0009-0001-6984-1751; Pannunzio, Camila; Ogando, Mora B. ORCID logoORCID: https://orcid.org/0000-0002-1453-2628; Armando, Natalia G. ORCID logoORCID: https://orcid.org/0000-0003-1379-4025; Garrett, Lillian ORCID logoORCID: https://orcid.org/0000-0003-4880-7076; Zimprich, Annemarie ORCID logoORCID: https://orcid.org/0000-0003-2078-6779; Becker, Lore ORCID logoORCID: https://orcid.org/0000-0002-6890-4984; Gimeno, Maria L.; Lukin, Jeronimo ORCID logoORCID: https://orcid.org/0000-0002-2284-7152; Merino, Florencia L. ORCID logoORCID: https://orcid.org/0000-0001-7247-2750; Pardi, M. Belen ORCID logoORCID: https://orcid.org/0000-0003-1942-7533; Pedroncini, Olivia ORCID logoORCID: https://orcid.org/0009-0009-0613-4126; Di Mauro, Giuliana C. ORCID logoORCID: https://orcid.org/0000-0001-5685-090X; Durner, Valerie Gailus; Fuchs, Helmut; Hrabe de Angelis, Martin ORCID logoORCID: https://orcid.org/0000-0002-7898-2353; Patop, Ines L. ORCID logoORCID: https://orcid.org/0000-0002-2929-0860; Turck, Christoph W. ORCID logoORCID: https://orcid.org/0000-0002-6585-8636; Deussing, Jan M. ORCID logoORCID: https://orcid.org/0000-0002-9329-5252; Vogt Weisenhorn, Daniela M. ORCID logoORCID: https://orcid.org/0000-0002-4566-6506; Jahn, Olaf ORCID logoORCID: https://orcid.org/0000-0002-3397-8924; Kadener, Sebastian; Hölter, Sabine M. ORCID logoORCID: https://orcid.org/0000-0003-4878-5241; Brose, Nils ORCID logoORCID: https://orcid.org/0000-0003-0938-8534; Giesert, Florian ORCID logoORCID: https://orcid.org/0000-0001-6825-8858; Wurst, Wolfgang ORCID logoORCID: https://orcid.org/0000-0003-4422-7410; Marin-Burgin, Antonia ORCID logoORCID: https://orcid.org/0000-0003-0684-9796 und Refojo, Damian ORCID logoORCID: https://orcid.org/0000-0002-9798-6413 (2024): A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli. In: Science Advances, Bd. 10, Nr. 21 [PDF, 5MB]

Leu, Chia-Luen; Lam, Daniel D.; Salminen, Aaro; Wefers, Benedikt; Becker, Lore; Garrett, Lillian; Rozman, Jan; Wurst, Wolfgang; de Angelis, Martin Hrabe; Hoelter, Sabine M.; Winkelmann, Juliane und Williams, Rhiannan H. (2024): A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice. In: Sleep, Bd. 47, Nr. 5

Maity-Kumar, Gandhari; Staender, Lisa; DeAngelis, Meri; Lee, Sooyeon; Molenaar, Anna; Becker, Lore; Garrett, Lillian; Amerie, Oana; Hoelter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Feuchtinger, Annette; Gailus-Durner, Valerie; Gárcia-Cáceres, Cristina; Othman, Ahmed E.; Brockmann, Caroline; Schoeffling, Vanessa I.; Beiser, Katja; Krude, Heiko; Mroz, Piotr A.; Hofmann, Susanna; Tuckermann, Jan; DiMarchi, Richard D.; de Angelis, Martin Hrabe; Tschoep, Matthias H.; Pfluger, Paul T. und Mueller, Timo D. (2022): Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome. In: Molecular Metabolism, Bd. 66, 101616 [PDF, 3MB]

Xie, Kan; Fuchs, Helmut; Scifo, Enzo; Liu, Dan; Aziz, Ahmad; Aguilar-Pimentel, Juan Antonio; Amarie, Oana Veronica; Becker, Lore; da Silva-Buttkus, Patricia; Calzada-Wack, Julia; Cho, Yi-Li; Deng, Yushuang; Edwards, A. Cole; Garrett, Lillian; Georgopoulou, Christina; Gerlini, Raffaele; Hoelter, Sabine M.; Klein-Rodewald, Tanja; Kramer, Michael; Leuchtenberger, Stefanie; Lountzi, Dimitra; Mayer-Kuckuk, Phillip; Nover, Lena L.; Oestereicher, Manuela A.; Overkott, Clemens; Pearson, Brandon L.; Rathkolb, Birgit; Rozman, Jan; Russ, Jenny; Schaaf, Kristina; Spielmann, Nadine; Sanz-Moreno, Adrian; Stoeger, Claudia; Treise, Irina; Bano, Daniele; Busch, Dirk H.; Graw, Jochen; Klingenspor, Martin; Klopstock, Thomas; Mock, Beverly A.; Salomoni, Paolo; Schmidt-Weber, Carsten; Weiergraber, Marco; Wolf, Eckhard; Wurst, Wolfgang; Gailus-Durner, Valerie; Breteler, Monique M. B.; Hrabe de Angelis, Martin und Ehninger, Dan (2022): Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice. In: Nature Communications, Bd. 13, Nr. 1, 6830 [PDF, 7MB]

Garrett, Lillian; Da Silva-Buttkus, Patricia; Rathkolb, Birgit; Gerlini, Raffaele; Becker, Lore; Sanz-Moreno, Adrian; Seisenberger, Claudia; Zimprich, Annemarie; Aguilar-Pimentel, Antonio; Amarie, Oana V.; Cho, Yi-Li; Kraiger, Markus; Spielmann, Nadine; Calzada-Wack, Julia; Marschall, Susan; Busch, Dirk; Schmitt-Weber, Carsten; Wolf, Eckhard; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hoelter, Sabine M. und de Angelis, Martin Hrabe (2022): Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk. In: Disease Models & Mechanisms, Bd. 15, Nr. 3, dmm049205 [PDF, 2MB]

Garrett, Lillian; Truembach, Dietrich; Spielmann, Nadine; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; De Angelis, Martin Hrabe und Hoelter, Sabine M. (2022): A rationale for considering heart/brain axis control in neuropsychiatric disease. In: Mammalian Genome, Bd. 34, Nr. 2: S. 331-350 [PDF, 7MB]

Biagosch, Caroline A.; Vidali, Silvia; Faerberboeck, Michael; Hensler, Svenja-Viola; Becker, Lore; Amarie, Oana V.; Aguilar-Pimentel, Antonio; Garrett, Lillian; Klein-Rodewald, Tanja; Rathkolb, Birgit; Zanuttigh, Enrica; Calzada-Wack, Julia; Silva-Buttkus, Patricia da; Rozman, Jan; Treise, Irina; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Janik, Dirk; Wurst, Wolfgang; Mayr, Johannes A.; Klopstock, Thomas; Meitinger, Thomas; Prokisch, Holger und Iuso, Arcangela (2021): A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse. In: Mammalian Genome, Bd. 32, Nr. 5: S. 332-349 [PDF, 3MB]

Vidali, Silvia; Gerlini, Raffaele; Thompson, Kyle; Urquhart, Jill E.; Meisterknecht, Jana; Aguilar-Pimentel, Juan Antonio; Amarie, Oana V.; Becker, Lore; Breen, Catherine; Calzada-Wack, Julia; Chhabra, Nirav F.; Cho, Yi-Li; Silva-Buttkus, Patricia da; Feichtinger, Rene G.; Gampe, Kristine; Garrett, Lillian; Hoefig, Kai P.; Hoelter, Sabine M.; Jameson, Elisabeth; Klein-Rodewald, Tanja; Leuchtenberger, Stefanie; Marschall, Susan; Mayer-Kuckuk, Philipp; Miller, Gregor; Oestereicher, Manuela A.; Pfannes, Kristina; Rathkolb, Birgit; Rozman, Jan; Sanders, Charlotte; Spielmann, Nadine; Stoeger, Claudia; Szibor, Marten; Treise, Irina; Walter, John H.; Wurst, Wolfgang; Mayr, Johannes A.; Fuchs, Helmut; Gaertner, Ulrich; Wittig, Ilka; Taylor, Robert W.; Newman, William G.; Prokisch, Holger; Gailus-Durner, Valerie und Hrabe de Angelis, Martin (2021): Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. In: EMBO Molecular Medicine, Bd. 13, Nr. 12, e14397

Ung, Marie-Claire; Garrett, Lillian; Dalke, Claudia; Leitner, Valentin; Dragosa, Daniel; Hladik, Daniela; Neff, Frauke; Wagner, Florian; Zitzelsberger, Horst; Miller, Gregor; de Angelis, Martin Hrabe; Roessler, Ute; Vogt Weisenhorn, Daniela; Wurst, Wolfgang; Graw, Jochen und Hoelter, Sabine M. (2021): Dose-dependent long-term effects of a single radiation event on behaviour and glial cells. In: International Journal of Radiation Biology, Bd. 97, Nr. 2: S. 156-169 [PDF, 3MB]

Garrett, Lillian; Chang, Yoon Jeung; Niedermeier, Kristina M.; Heermann, Tamara; Enard, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Huttner, Wieland B.; Wurst, Wolfgang und Hoelter, Sabine M. (2020): A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons. In: Translational Psychiatry, Bd. 10, Nr. 1, 66 [PDF, 1MB]

Ignatova, Valentina V.; Stolz, Paul; Kaiser, Steffen; Gustafsson, Tobias H.; Lastres, Palma Rico; Sanz-Moreno, Adrian; Cho, Yi-Li; Amarie, Oana V.; Aguilar-Pimentel, Antonio; Klein-Rodewald, Tanja; Calzada-Wack, Julia; Becker, Lore; Marschall, Susan; Kraiger, Markus; Garrett, Lillian; Seisenberger, Claudia; Hoelter, Sabine M.; Borland, Kayla; Logt, Erik van de; Jansen, Pascal W. T. C.; Baltissen, Marijke P.; Valenta, Magdalena; Vermeulen, Michiel; Wurst, Wolfgang; Gailus-Durner, Valerie; Fuchs, Helmut; Hrabe de Angelis, Martin; Rando, Oliver J.; Kellner, Stefanie M.; Bultmann, Sebastian und Schneider, Robert (2020): The rRNA m(6)A methyltransferase METTL5 is involved in pluripotency and developmental programs. In: Genes & Development, Bd. 34: S. 715-729 [PDF, 4MB]

Lucienne, Marie; Aguilar-Pimentel, Juan Antonio; Amarie, Oana V.; Becker, Lore; Calzada-Wack, Julia; Silva-Buttkus, Patricia da; Garrett, Lillian; Holter, Sabine M.; Mayer-Kuckuk, Philipp; Rathkolb, Birgit; Rozman, Jan; Spielmann, Nadine; Treise, Irina; Busch, Dirk H.; Klopstock, Thomas; Schmidt-Weber, Carsten; Wolf, Eckhard; Wurst, Wolfgang; Forny, Merima; Mathis, Deborah; Fingerhut, Ralph; Froese, D. Sean; Gailus-Durner, Valerie; Fuchs, Helmut; Hrabe de Angelis, Martin und Baumgartner, Matthias R. (2020): In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduria. In: Biochimica et Biophysica Acta-Molecular Basis of Disease, Bd. 1866, Nr. 3, 165622 [PDF, 2MB]

Blechner, Christine; Becker, Lore; Fuchs, Helmut; Rathkolb, Birgit; Prehn, Cornelia; Adler, Thure; Calzada-Wack, Julia; Garrett, Lillian; Gailus-Durner, Valerie; Morellini, Fabio; Conrad, Susanne; Hoelter, Sabine M.; Wolf, Eckhard; Klopstock, Thomas; Adamski, Jerzy; Busch, Dirk; de Angelis, Martin Hrabe; Schmeisser, Michael J. und Windhorst, Sabine (2020): Physiological relevance of the neuronal isoform of inositol-1,4,5-trisphosphate 3-kinases in mice. In: Neuroscience Letters, Bd. 735, 135206

Kollmus, Heike; Fuchs, Helmut; Lengger, Christoph; Haselimashhadi, Hamed; Bogue, Molly A.; Ostereicher, Manuela A.; Horsch, Marion; Adler, Thure; Aguilar-Pimentel, Juan Antonio; Amarie, Oana Veronica; Becker, Lore; Beckers, Johannes; Calzada-Wack, Julia; Garrett, Lillian; Hans, Wolfgang; Hoelter, Sabine M.; Klein-Rodewald, Tanja; Maier, Holger; Mayer-Kuckuk, Philipp; Miller, Gregor; Moreth, Kristin; Neff, Frauke; Rathkolb, Birgit; Racz, Ildiko; Rozman, Jan; Spielmann, Nadine; Treise, Irina; Busch, Dirk; Graw, Jochen; Klopstock, Thomas; Wolf, Eckhard; Wurst, Wolfgang; Yildirim, Ali Onder; Mason, Jeremy; Torres, Arturo; Balling, Rudi; Mehaan, Terry; Gailus-Durner, Valerie; Schughart, Klaus und de Angelis, Martin Hrabe (2020): A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes. In: Mammalian Genome, Bd. 31: S. 30-48 [PDF, 3MB]

Solga, Roxana; Behrens, Juliane; Ziemann, Anja; Riou, Adrien; Berwanger, Carolin; Becker, Lore; Garrett, Lillian; de Angelis, Martin Hrabe; Fischer, Lisa; Coras, Roland; Barkovits, Katalin; Marcus, Katrin; Mahabir, Esther; Eichinger, Ludwig; Schröder, Rolf; Noegel, Angelika A.; Clemen, Christoph S.; Aguilar-Pimentel, Antonio; Schmidt-Weber, Carsten; Klopstock, Thomas; Adler, Thure; Treisel, Irina; Busch, Dirk H.; Moreth, Kristin; Hoelter, Sabine M.; Zimprich, Annemarie; Wurst, Wolfgang; Amarie, Oana; Graw, Jochen; Rozman, Jan; Calzada-Wack, Julia; Racz, Ildiko; Rathkolb, Birgit; Wolf, Eckhard; Oestereicher, Manuela; Miller, Gregor; Lengger, Christoph; Maier, Holger; Stoeger, Claudia; Leuchtenberger, Stefanie; Gallus-Durner, Valerie und Fuchs, Helmut (2019): CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cells. In: European Journal of Cell Biology, Bd. 98, Nr. 5-8, UNSP 151046

Jensen, Lars R.; Garrett, Lillian; Hoelter, Sabine M.; Rathkolb, Birgit; Racz, Ildiko; Adler, Thure; Prehn, Cornelia; Hans, Wolfgang; Rozman, Jan; Becker, Lore; Aguilar-Pimentel, Juan Antonio; Puk, Oliver; Moreth, Kristin; Dopatka, Monika; Walther, Diego J.; Bohlen und Halbach, Viola von; Rath, Matthias; Delatycki, Martin; Bert, Bettina; Fink, Heidrun; Bluemlein, Katharina; Ralser, Markus; Dijck, Anke van; Kooy, Frank; Stark, Zornitza; Müller, Sabine; Scherthan, Harry; Gecz, Jozef; Wurst, Wolfgang; Wolf, Eckhard; Zimmer, Andreas; Klingenspor, Martin; Graw, Jochen; Klopstock, Thomas; Busch, Dirk; Adamski, Jerzy; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Bohlen und Halbach, Oliver von; Ropers, Hans-Hilger und Kuss, Andreas W. (2019): A mouse model for intellectual disability caused by mutations in the X-linked 2 '-O-methyltransferase Ftsj1 gene. In: Biochimica et Biophysica Acta-Molecular Basis of Disease, Bd. 1865, Nr. 9: S. 2083-2093

Dias, Mariana Castro; Coisne, Caroline; Baden, Pascale; Enzmann, Gaby; Garrett, Lillian; Becker, Lore; Hoelter, Sabine M.; de Angelis, Martin Hrabe; Deutsch, Urban; Engelhardt, Britta; Aguilar-Pimentel, Antonio; Adler, Thure; Busch, Dirk H.; Spielmann, Nadine; Moreth, Kristin; Hans, Wolfgang; Amarie, Oana; Graw, Jochen; Rozman, Jan; Radc, Ildiko; Neff, Frauke; Calzada-Wack, Julia; Rathkolb, Birgit; Wolf, Eckhard; Klopstock, Thomas; Wurst, Wolfgang; Beckers, Johannes; Oestereicher, Manuela; Miller, Gregor; Maier, Holger; Stoeger, Claudia; Leuchtenberger, Stefanie; Gailus-Durner, Valerie und Fuchs, Helmut (2019): Claudin-12 is not required for blood-brain barrier tight junction function. In: Fluids and Barriers of the Cns, Bd. 16, Nr. 1, 30 [PDF, 3MB]

Vetrivel, Sharmilee; Tiso, Natascia; Kuegler, Andrea; Irmler, Martin; Horsch, Marion; Beckers, Johannes; Hladik, Daniela; Giesert, Florian; Gailus-Durner, Valerie; Fuchs, Helmut; Sabrautzki, Sibylle; Angelis, Martin Hrabe de; Graw, Jochen; Adler, Thure; Treise, Irina; Busch, Dirk H.; Aguilar-Pimentel, Antonio; Ollert, Markus; Götz, Alexander; Amarie, Oana; Stoeger, Tobias; Schulz, Holger; Becker, Lore; Klopstock, Thomas; Schrewe, Anja; Spielmann, Nadine; Bekeredjian, Raffi; Garrett, Lillian; Hoelter, Sabine M.; Zimprich, Annemarie; Wurst, Wolfgang; Mayer-Kuckuk, Philipp; Hans, Wolfgang; Rozman, Jan; Klingenspor, Martin; Neff, Frauke; Silva-Buttkus, Patricia da; Calzada-Wack, Julia; Racz, Ildiko; Zimmer, Andreas; Rathkolb, Birgit; Wolf, Eckhard; Prehn, Cornelia; Adamski, Jerzy; Oestereicher, Manuela; Miller, Gregor; Steinkamp, Ralph; Lengger, Christoph; Maier, Holger; Stoeger, Claudia und Leuchtenberger, Stefanie (2019): Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia. In: Experimental Eye Research, Bd. 188, UNSP 107632 [PDF, 7MB]

Segal, Joanna; Muelleder, Michael; Krüger, Antje; Adler, Thure; Scholze-Wittler, Manuela; Becker, Lore; Calzada-Wack, Julia; Garrett, Lillian; Hoelter, Sabine M.; Rathkolb, Birgit; Rozman, Jan; Racz, Ildiko; Fischer, Ralf; Busch, Dirk H.; Neff, Frauke; Klingenspor, Martin; Klopstock, Thomas; Grüning, Nana-Maria; Michel, Steve; Lukaszewska-McGreal, Beata; Voigt, Ingo; Hartmann, Ludger; Timmermann, Bernd; Lehrach, Hans; Wolf, Eckhard; Wurst, Wolfgang; Gailus-Durner, Valerie; Fuchs, Helmut; de Angelis, Martin H.; Schrewe, Heinrich; Yuneva, Mariia und Ralser, Markus (2019): Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency. In: Journal of Inherited Metabolic Disease, Bd. 42, Nr. 5: S. 839-849 [PDF, 3MB]

Clemen, Christoph S.; Winter, Lilli; Strucksberg, Karl-Heinz; Berwanger, Carolin; Türk, Matthias; Kornblum, Cornelia; Florin, Alexandra; Aguilar-Pimentel, Juan Antonio; Amarie, Oana Veronica; Becker, Lore; Garrett, Lillian; Hans, Wolfgang; Moreth, Kristin; Neff, Frauke; Pingen, Laura; Rathkolb, Birgit; Rácz, Ildikó; Rozman, Jan; Treise, Irina; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Vorgerd, Matthias; Eichinger, Ludwig und Schröder, Rolf (2018): The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? In: Biochemical and Biophysical Research Communications, Bd. 503, Nr. 4: S. 2770-2777

Fuchs, Helmut; Aguilar-Pimentel, Juan Antonio; Amarie, Oana V.; Becker, Lore; Calzada-Wack, Julia; Cho, Yi-Li; Garrett, Lillian; Hölter, Sabine M.; Irmler, Martin; Kistler, Martin; Kraiger, Markus; Mayer-Kuckuk, Philipp; Moreth, Kristin; Rathkolb, Birgit; Rozman, Jan; Silva Buttkus, Patricia da; Treise, Irina; Zimprich, Annemarie; Gampe, Kristine; Hutterer, Christine; Stoeger, Claudia; Leuchtenberger, Stefanie; Maier, Holger; Miller, Manuel; Scheideler, Angelika; Wu, Moya; Beckers, Johannes; Bekeredjian, Raffi; Brielmeier, Markus; Busch, Dirk H.; Klingenspor, Martin; Klopstock, Thomas; Ollert, Markus; Schmidt-Weber, Carsten; Stoeger, Tobias; Wolf, Eckhard; Wurst, Wolfgang; Yildirim, Ali Oender; Zimmer, Andreas; Gailus-Durner, Valerie und Hrabe de Angelis, Martin (2018): Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic. In: Behavioural Brain Research, Bd. 352: S. 187-196

Zimprich, Annemarie; Ostereicher, Manuela A.; Becker, Lore; Dirscherl, Petra; Ernst, Luise; Fuchs, Helmut; Gailus-Durner, Valerie; Garrett, Lillian; Giesert, Florian; Glasl, Lisa; Hummel, Angelika; Rozman, Jan; Hrabe de Angelis, Martin; Vogt-Weisenhorn, Daniela; Wurst, Wolfgang und Hölter, Sabine M. (2018): Analysis of locomotor behavior in the German Mouse Clinic. In: Journal of Neuroscience Methods, Bd. 300: S. 77-91

Andre, Viola; Gaut, Christine; Scheideler, Angelika; Aguilar-Pimentel, Juan A.; Amarie, Oana V.; Becker, Lore; Garrett, Lillian; Hans, Wolfgang; Hölter, Sabine M.; Janik, Dirk; Moreth, Kristin; Neff, Frauke; Östereicher, Manuela; Racz, Ildiko; Rathkolb, Birgit; Rozman, Jan; Bekeredjian, Raffi; Graw, Jochen; Klingenspor, Martin; Klopstock, Thomas; Ollert, Markus; Schmidt-Weber, Carsten; Wolf, Eckhard; Wurst, Wolfgang; Gailus-Durner, Valerie; Brielmeier, Markus; Fuchs, Helmut und Hrabe de Angelis, Martin (2018): Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.
In: PLOS Biology 16(4), e2005019 [PDF, 5MB]

Garrett, Lillian; Becker, Lore; Rozman, Jan; Puk, Oliver; Stoeger, Tobias; Yildirim, Ali Onder; Bohla, Alexander; Eickelberg, Oliver; Hans, Wolfgang; Prehn, Cornelia; Adamski, Jerzy; Klopstock, Thomas; Racz, Ildiko; Zimmer, Andreas; Klingenspor, Martin; Fuchs, Helmut; Gailus-Durner, Valerie; Wurst, Wolfgang; Hrabe de Angelis, Martin; Graw, Jochen und Hölter, Sabine M. (2018): Fgf9(Y162C) Mutation Alters Information Processing and Social Memory in Mice. In: Molecular Neurobiology, Bd. 55, Nr. 6: S. 4580-4595

Heermann, Tamara; Garrett, Lillian; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Graw, Jochen und Holter, Sabine M. (2018): Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in Mice. In: Molecular Neurobiology: S. 1-16

Zimprich, Annemarie; Mroz, Gabi; Meyer zu Reckendorf, Christopher; Anastasiadou, Sofia; Förstner, Philip; Garrett, Lillian; Hölter, Sabine M.; Becker, Lore; Rozman, Jan; Prehn, Cornelia; Rathkolb, Birgit; Moreth, Kristin; Wurst, Wolfgang; Klopstock, Thomas; Klingenspor, Martin; Adamski, Jerzy; Wolf, Eckhard; Bekeredjian, Raffi; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin und Knöll, Bernd (2017): Serum Response Factor (SRF) Ablation Interferes with Acute Stress-Associated Immediate and Long-Term Coping Mechanisms. In: Molecular Neurobiology, Bd. 54, Nr. 10: S. 8242-8262

Schludi, Martin H.; Becker, Lore; Garrett, Lillian; Gendron, Tania F.; Zhou, Qihui; Schreiber, Franziska; Popper, Bastian; Dimou, Leda; Strom, Tim M.; Winkelmann, Juliane; Thaden, Anne von; Rentzsch, Kristin; May, Stephanie; Michaelsen, Meike; Schwenk, Benjamin M.; Tan, Jing; Schoser, Benedikt; Dieterich, Marianne; Petrucelli, Leonard; Hölter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Klopstock, Thomas; Arzberger, Thomas und Edbauer, Dieter (2017): Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss. In: Acta Neuropathologica, Bd. 134, Nr. 2: S. 241-254

Deng, Tao; Postnikov, Yuri; Zhang, Shaofei; Garrett, Lillian; Becker, Lore; Racz, Ildiko; Hoelter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin und Bustin, Michael (2017): Interplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiation. In: Nucleic Acids Research, Bd. 45, Nr. 6: S. 3031-3045

Kumar, Sudhir; Rathkolb, Birgit; Sabrautzki, Sibylle; Krebs, Stefan; Kemter, Elisabeth; Becker, Lore; Beckers, Johannes; Bekeredjian, Raffi; Brommage, Robert; Calzada-Wack, Julia; Garrett, Lillian; Hölter, Sabine M.; Horsch, Marion; Klingenspor, Martin; Klopstock, Thomas; Moreth, Kristin; Neff, Frauke; Rozman, Jan; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabe de Angelis, Martin; Wolf, Eckhard und Aigner, Bernhard (2017): Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1(I27N) mutant mice. In: Journal of Biomedical Science 24:57 [PDF, 870kB]

Salminen, Aaro V.; Garrett, Lillian; Schormair, Barbara; Rozman, Jan; Giesert, Florian; Niedermeier, Kristina M.; Becker, Lore; Rathkolb, Birgit; Racz, Ildiko; Klingenspor, Martin; Klopstock, Thomas; Wolf, Eckhard; Zimmer, Andreas; Gailus-Durner, Valerie; Torres, Miguel; Fuchs, Helmut; Hrabe de Angelis, Martin; Wurst, Wolfgang; Hölter, Sabine M. und Winkelmann, Juliane (2017): Meis1: effects on motor phenotypes and the sensorimotor system in mice. In: Disease Models & Mechanisms, Bd. 10, Nr. 8: S. 981-991

Sabrautzki, Sibylle; Sandholzer, Michael A.; Lorenz-Depiereux, Bettina; Brommage, Robert; Przemeck, Gerhard; Panesso, Ingrid L. Vargas; Vernaleken, Alexandra; Garrett, Lillian; Baron, Katharina; Yildirim, Ali O.; Rozman, Jan; Rathkolb, Birgit; Gau, Christine; Hans, Wolfgang; Hoelter, Sabine M.; Marschall, Susan; Stoeger, Claudia; Becker, Lore; Fuchs, Helmut; Gailus-Durner, Valerie; Klingenspor, Martin; Klopstock, Thomas; Lengger, Christoph; Stefanie, Leuchtenberger; Wolf, Eckhard; Strom, Tim M.; Wurst, Wolfgang und Hrabě de Angelis, Martin (2016): Viable Ednra (Y129F) mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation. In: Mammalian Genome, Bd. 27, Nr. 11-12: S. 587-598

Fuchs, Helmut; Sabrautzki, Sibylle; Przemeck, Gerhard K. H.; Leuchtenberger, Stefanie; Lorenz-Depiereux, Bettina; Becker, Lore; Rathkolb, Birgit; Horsch, Marion; Garrett, Lillian; Östereicher, Manuela A.; Hans, Wolfgang; Abe, Koichiro; Sagawa, Nobuho; Rozman, Jan; Vargas-Panesso, Ingrid L.; Sandholzer, Michael; Lisse, Thomas S.; Adler, Thure; Aguilar-Pimentel, Juan Antonio; Calzada-Wack, Julia; Ehrhard, Nicole; Elvert, Ralf; Gau, Christine; Hölter, Sabine M.; Micklich, Katja; Moreth, Kristin; Prehn, Cornelia; Puk, Oliver; Racz, Ildiko; Stoeger, Claudia; Vernaleken, Alexandra; Michel, Dian; Diener, Susanne; Wieland, Thomas; Adamski, Jerzy; Bekeredjian, Raffi; Busch, Dirk H.; Favor, John; Graw, Jochen; Klingenspor, Martin; Lengger, Christoph; Maier, Holger; Neff, Frauke; Ollert, Markus; Stoeger, Tobias; Yildirim, Ali Önder; Strom, Tim M.; Zimmer, Andreas; Wolf, Eckhard; Wurst, Wolfgang; Klopstock, Thomas; Beckers, Johannes; Gailus-Durner, Valerie und Hrabé de Angelis, Martin (2016): The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations. In: G3-Genes Genomes Genetics, Bd. 6, Nr. 12: S. 4035-4046

Kumar, Sudhir; Rathkolb, Birgit; Kemter, Elisabeth; Sabrautzki, Sibylle; Michel, Dian; Adler, Thure; Becker, Lore; Beckers, Johannes; Busch, Dirk H.; Garrett, Lillian; Hans, Wolfgang; Hölter, Sabine M.; Horsch, Marion; Klingenspor, Martin; Klopstock, Thomas; Rácz, Ildikó; Rozman, Jan; Panesso, Ingrid Liliana Vargas; Vernaleken, Alexandra; Zimmer, Andreas; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Wolf, Eckhard und Aigner, Bernhard (2016): Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3(L423P) Mutant Mice.
In: PLOS ONE 11(3), e0150472 [PDF, 1MB]

Zumbrennen-Bullough, Kimberly B.; Becker, Lore; Garrett, Lillian; Hölter, Sabine M.; Calzada-Wack, Julia; Mossbrugger, Ilona; Quintanilla-Fend, Leticia; Racz, Ildiko; Rathkolb, Birgit; Klopstock, Thomas; Wurst, Wolfgang; Zimmer, Andreas; Wolf, Eckhard; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabé de Angelis, Martin; Romney, Steven J. und Leibold, Elizabeth A. (2014): Abnormal Brain Iron Metabolism in Irp2 Deficient Mice Is Associated with Mild Neurological and Behavioral Impairments.
In: PLOS ONE 9(6), e98072 [PDF, 5MB]

Kraus, Petra; Sivakamasundari, V; Yu, Hong Bing; Xing, Xing; Lim, Siew Lan; Adler, Thure; Pimentel, Juan Antonio Aguilar; Becker, Lore; Bohla, Alexander; Garrett, Lillian; Hans, Wolfgang; Hölter, Sabine M.; Janas, Eva; Moreth, Kristin; Prehn, Cornelia; Puk, Oliver; Rathkolb, Birgit; Rozman, Jan; Adamski, Jerzy; Bekeredjian, Raffi; Busch, Dirk H.; Graw, Jochen; Klingenspor, Martin; Klopstock, Thomas; Neff, Frauke; Ollert, Markus; Stoeger, Tobias; Yildrim, Ali Önder; Eickelberg, Oliver; Wolf, Eckhard; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Hrabě de Angelis, Martin; Lufkin, Thomas und Stanton, Lawrence W. (2014): Pleiotropic Functions for Transcription Factor Zscan10.
In: PLOS ONE 9(8), e104568 [PDF, 3MB]

Staropoli, John F.; Haliw, Larissa; Biswas, Sunita; Garrett, Lillian; Hölter, Sabine M.; Becker, Lore; Skosyrski, Sergej; Silva-Buttkus, Patricia da; Calzada-Wack, Julia; Neff, Frauke; Rathkolb, Birgit; Rozman, Jan; Schrewe, Anja; Adler, Thure; Puk, Oliver; Sun, Minxuan; Favor, Jack; Racz, Ildikó; Bekeredjian, Raffi; Busch, Dirk H.; Graw, Jochen; Klingenspor, Martin; Klopstock, Thomas; Wolf, Eckhard; Wurst, Wolfgang; Zimmer, Andreas; Lopez, Edith; Harati, Hayat; Hill, Eric; Krause, Daniela S.; Guide, Jolene; Dragileva, Ella; Gale, Evan; Wheeler, Vanessa C.; Boustany, Rose-Mary; Brown, Diane E.; Breton, Sylvie; Ruether, Klaus; Gailus-Durner, Valérie; Fuchs, Helmut; Hrabé de Angelis, Martin und Cotman, Susan L. (2012): Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system.
In: PLOS ONE 7(6), e38310 [PDF, 4MB]

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