Voluntary wheel running in mice increases the rate of neurogenesis without affecting anxiety-related behaviour in single tests

Por Garrett Lillian, Lie D, Hrabé de Angelis Martin, Wurst Wolfgang, Hölter Sabine M
Publicado em 2012-06-01

Voluntary wheel running in mice increases the rate of neurogenesis without affecting anxiety-related behaviour in single tests

Por Garrett, Lillian, Lie, D Chichung, Hrabé de Angelis, Martin, Wurst, Wolfgang, Hölter, Sabine M
Publicado em 2012

A robust and reliable non-invasive test for stress responsivity in mice

Por Zimprich, Annemarie, Garrett, Lillian, Deussing, Jan M., Wotjak, Carsten T., Fuchs, Helmut, Gailus-Durner, Valerie, de Angelis, Martin Hrabě, Wurst, Wolfgang, Hölter, Sabine M.
Publicado em 2014

Conditional Reduction of Adult Born Doublecortin-Positive Neurons Reversibly Impairs Selective Behaviors

Por Garrett, Lillian, Zhang, Jingzhong, Zimprich, Annemarie, Niedermeier, Kristina M., Fuchs, Helmut, Gailus-Durner, Valerie, Hrabě de Angelis, Martin, Vogt Weisenhorn, Daniela, Wurst, Wolfgang, Hölter, Sabine M.
Publicado no Front Behav Neurosci (2015)

Interplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiation

Por Deng, Tao, Postnikov, Yuri, Zhang, Shaofei, Garrett, Lillian, Becker, Lore, Rácz, Ildikó, Hölter, Sabine M., Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, de Angelis, Martin Hrabe, Bustin, Michael
Publicado no Nucleic Acids Res (2017)

Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function

Por Sun, Minxuan, Hölter, Sabine M., Stepan, Jens, Garrett, Lillian, Genius, Just, Kremmer, Elisabeth, Hrabě de Angelis, Martin, Wurst, Wolfgang, Lie, D. Chichung, Bally-Cuif, Laure, Eder, Matthias, Rujescu, Dan, Graw, Jochen
Publicado em 2013

RNase H2 Loss in Murine Astrocytes Results in Cellular Defects Reminiscent of Nucleic Acid-Mediated Autoinflammation

Por Bartsch, Kareen, Damme, Markus, Regen, Tommy, Becker, Lore, Garrett, Lillian, Hölter, Sabine M, Knittler, Katharina, Borowski, Christopher, Waisman, Ari, Glatzel, Markus, Fuchs, Helmut, Gailus-Durner, Valerie, Hrabe de Angelis, Martin, Rabe, Björn
Publicado no Front Immunol (2018)

The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing

Por Vogl, Christian, Butola, Tanvi, Haag, Natja, Hausrat, Torben J, Leitner, Michael G, Moutschen, Michel, Lefèbvre, Philippe P, Speckmann, Carsten, Garrett, Lillian, Becker, Lore, Fuchs, Helmut, Hrabe de Angelis, Martin, Nietzsche, Sandor, Kessels, Michael M, Oliver, Dominik, Kneussel, Matthias, Kilimann, Manfred W, Strenzke, Nicola
Publicado no EMBO Rep (2017)

Abnormal Brain Iron Metabolism in Irp2 Deficient Mice Is Associated with Mild Neurological and Behavioral Impairments

Por 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, de Angelis, Martin Hrabě, Romney, Steven J., Leibold, Elizabeth A.
Publicado em 2014

Meis1: effects on motor phenotypes and the sensorimotor system in mice

Por Salminen, Aaro V., Garrett, Lillian, Schormair, Barbara, Rozman, Jan, Giesert, Florian, Niedermeier, Kristina M., Becker, Lore, Rathkolb, Birgit, Rácz, Ildikó, Klingenspor, Martin, Klopstock, Thomas, Wolf, Eckhard, Zimmer, Andreas, Gailus-Durner, Valérie, Torres, Miguel, Fuchs, Helmut, Hrabě de Angelis, Martin, Wurst, Wolfgang, Hölter, Sabine M., Winkelmann, Juliane
Publicado no Dis Model Mech (2017)

Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1(I27N) mutant mice

Por 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, Valérie, Hrabe de Angelis, Martin, Wolf, Eckhard, Aigner, Bernhard
Publicado no J Biomed Sci (2017)

Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders

Por Blanco, Sandra, Dietmann, Sabine, Flores, Joana V, Hussain, Shobbir, Kutter, Claudia, Humphreys, Peter, Lukk, Margus, Lombard, Patrick, Treps, Lucas, Popis, Martyna, Kellner, Stefanie, Hölter, Sabine M, Garrett, Lillian, Wurst, Wolfgang, Becker, Lore, Klopstock, Thomas, Fuchs, Helmut, Gailus-Durner, Valerie, Hrabĕ de Angelis, Martin, Káradóttir, Ragnhildur T, Helm, Mark, Ule, Jernej, Gleeson, Joseph G, Odom, Duncan T, Frye, Michaela
Publicado em 2014

Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3(L423P) Mutant Mice

Por 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, Vargas Panesso, Ingrid Liliana, Vernaleken, Alexandra, Zimmer, Andreas, Fuchs, Helmut, Gailus-Durner, Valérie, Hrabě de Angelis, Martin, Wolf, Eckhard, Aigner, Bernhard
Publicado no PLoS One (2016)

Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss

Por Schludi, Martin H., Becker, Lore, Garrett, Lillian, Gendron, Tania F., Zhou, Qihui, Schreiber, Franziska, Popper, Bastian, Dimou, Leda, Strom, Tim M., Winkelmann, Juliane, von Thaden, Anne, 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, de Angelis, Martin Hrabe, Klopstock, Thomas, Arzberger, Thomas, Edbauer, Dieter
Publicado no Acta Neuropathol (2017)

A Broad Phenotypic Screen Identifies Novel Phenotypes Driven by a Single Mutant Allele in Huntington’s Disease CAG Knock-In Mice

Por Hölter, Sabine M., Stromberg, Mary, Kovalenko, Marina, Garrett, Lillian, Glasl, Lisa, Lopez, Edith, Guide, Jolene, Götz, Alexander, Hans, Wolfgang, Becker, Lore, Rathkolb, Birgit, Rozman, Jan, Schrewed, Anja, Klingenspor, Martin, Klopstock, Thomas, Schulz, Holger, Wolf, Eckhard, Wursta, Wolfgang, Gillis, Tammy, Wakimoto, Hiroko, Seidman, Jonathan, MacDonald, Marcy E., Cotman, Susan, Gailus-Durner, Valérie, Fuchs, Helmut, de Angelis, Martin Hrabě, Lee, Jong-Min, Wheeler, Vanessa C.
Publicado em 2013

Viable Ednra(Y129F) mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation

Por Sabrautzki, Sibylle, Sandholzer, Michael A., Lorenz-Depiereux, Bettina, Brommage, Robert, Przemeck, Gerhard, Vargas Panesso, Ingrid L., 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, de Angelis, Martin Hrabě
Publicado no Mamm Genome (2016)

Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract risk

Por Dalke, Claudia, Neff, Frauke, Bains, Savneet Kaur, Bright, Scott, Lord, Deborah, Reitmeir, Peter, Rößler, Ute, Samaga, Daniel, Unger, Kristian, Braselmann, Herbert, Wagner, Florian, Greiter, Matthias, Gomolka, Maria, Hornhardt, Sabine, Kunze, Sarah, Kempf, Stefan J., Garrett, Lillian, Hölter, Sabine M., Wurst, Wolfgang, Rosemann, Michael, Azimzadeh, Omid, Tapio, Soile, Aubele, Michaela, Theis, Fabian, Hoeschen, Christoph, Slijepcevic, Predrag, Kadhim, Munira, Atkinson, Michael, Zitzelsberger, Horst, Kulka, Ulrike, Graw, Jochen
Publicado no Radiat Environ Biophys (2018)

Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data

Por André, Viola, Gau, 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, Valérie, Brielmeier, Markus, Fuchs, Helmut, Hrabé de Angelis, Martin
Publicado no PLoS Biol (2018)

High Mobility Group N Proteins Modulate the Fidelity of the Cellular Transcriptional Profile in a Tissue- and Variant-specific Manner

Por Kugler, Jamie E., Horsch, Marion, Huang, Di, Furusawa, Takashi, Rochman, Mark, Garrett, Lillian, Becker, Lore, Bohla, Alexander, Hölter, Sabine M., Prehn, Cornelia, Rathkolb, Birgit, Racz, Ildikó, Aguilar-Pimentel, Juan Antonio, Adler, Thure, Adamski, Jerzy, Beckers, Johannes, Busch, Dirk H., Eickelberg, Oliver, Klopstock, Thomas, Ollert, Markus, Stöger, Tobias, Wolf, Eckhard, Wurst, Wolfgang, Yildirim, Ali Önder, Zimmer, Andreas, Gailus-Durner, Valérie, Fuchs, Helmut, Hrabě de Angelis, Martin, Garfinkel, Benny, Orly, Joseph, Ovcharenko, Ivan, Bustin, Michael
Publicado em 2013

Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon

Por Spieler, Derek, Kaffe, Maria, Knauf, Franziska, Bessa, José, Tena, Juan J., Giesert, Florian, Schormair, Barbara, Tilch, Erik, Lee, Heekyoung, Horsch, Marion, Czamara, Darina, Karbalai, Nazanin, von Toerne, Christine, Waldenberger, Melanie, Gieger, Christian, Lichtner, Peter, Claussnitzer, Melina, Naumann, Ronald, Müller-Myhsok, Bertram, Torres, Miguel, Garrett, Lillian, Rozman, Jan, Klingenspor, Martin, Gailus-Durner, Valérie, Fuchs, Helmut, Hrabě de Angelis, Martin, Beckers, Johannes, Hölter, Sabine M., Meitinger, Thomas, Hauck, Stefanie M., Laumen, Helmut, Wurst, Wolfgang, Casares, Fernando, Gómez-Skarmeta, Jose Luis, Winkelmann, Juliane
Publicado em 2014