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 2012

A rationale for considering heart/brain axis control in neuropsychiatric disease

por Garrett, Lillian, Trümbach, Dietrich, Spielmann, Nadine, Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Hrabě de Angelis, Martin, Hölter, Sabine M.
Publicado 2022

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 2014

Claudin-12 is not required for blood–brain barrier tight junction function

por Castro Dias, Mariana, Coisne, Caroline, Baden, Pascale, Enzmann, Gaby, Garrett, Lillian, Becker, Lore, Hölter, Sabine M., Hrabě de Angelis, Martin, Deutsch, Urban, Engelhardt, Britta
Publicado 2019

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 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 2017

A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons

por Garrett, Lillian, Chang, Yoon Jeung, Niedermeier, Kristina M., Heermann, Tamara, Enard, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Angelis, Martin Hrabě de, Huttner, Wieland B., Wurst, Wolfgang, Hölter, Sabine M.
Publicado 2020

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 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 2018

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 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 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 2017

Knockout mouse models as a resource for the study of rare diseases

por da Silva-Buttkus, Patricia, Spielmann, Nadine, Klein-Rodewald, Tanja, Schütt, Christine, Aguilar-Pimentel, Antonio, Amarie, Oana V., Becker, Lore, Calzada-Wack, Julia, Garrett, Lillian, Gerlini, Raffaele, Kraiger, Markus, Leuchtenberger, Stefanie, Östereicher, Manuela A., Rathkolb, Birgit, Sanz-Moreno, Adrián, Stöger, Claudia, Hölter, Sabine M., Seisenberger, Claudia, Marschall, Susan, Fuchs, Helmut, Gailus-Durner, Valerie, Hrabě de Angelis, Martin
Publicado 2023

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 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 2016

Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk

por 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, Hölter, Sabine M., Hrabě de Angelis, Martin
Publicado 2022

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 2017

A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse

por 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, da Silva-Buttkus, Patricia, Rozman, Jan, Treise, Irina, Fuchs, Helmut, Gailus-Durner, Valerie, de Angelis, Martin Hrabě, Janik, Dirk, Wurst, Wolfgang, Mayr, Johannes A., Klopstock, Thomas, Meitinger, Thomas, Prokisch, Holger, Iuso, Arcangela
Publicado 2021

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 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 2016