The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders

por Bacon, Claire, Rappold, Gudrun A.
Publicado 2012

Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder

por Niesler, Beate, Rappold, Gudrun A.
Publicado 2020

Distinct Phenotypes of Shank2 Mouse Models Reflect Neuropsychiatric Spectrum Disorders of Human Patients With SHANK2 Variants

por Eltokhi, Ahmed, Rappold, Gudrun, Sprengel, Rolf
Publicado 2018

A Track Record on SHOX: From Basic Research to Complex Models and Therapy

por Marchini, Antonio, Ogata, Tsutomu, Rappold, Gudrun A.
Publicado 2016

Disrupted Mitochondrial Network Drives Deficits of Learning and Memory in a Mouse Model of FOXP1 Haploinsufficiency

por Wang, Jing, Rappold, Gudrun A., Fröhlich, Henning
Publicado 2022

Inhibition of HDAC6 activity protects dopaminergic neurons from alpha-synuclein toxicity

por Francelle, Laetitia, Outeiro, Tiago F., Rappold, Gudrun A.
Publicado 2020

Complex Evolution of a Y-Chromosomal Double Homeobox 4 (DUX4)-Related Gene Family in Hominoids

por Schmidt, Julia, Kirsch, Stefan, Rappold, Gudrun A., Schempp, Werner
Publicado 2009

The Homeobox Transcription Factor HOXA9 Is a Regulator of SHOX in U2OS Cells and Chicken Micromass Cultures

por Durand, Claudia, Decker, Eva, Roeth, Ralph, Schneider, Katja U., Rappold, Gudrun
Publicado 2012

Molecular Characterization of Embryonic Stem Cell-Derived Cardiac Neural Crest-Like Cells Revealed a Spatiotemporal Expression of an Mlc-3 Isoform

por Schmitteckert, Stefanie, Ziegler, Cornelia, Rappold, Gudrun A., Niesler, Beate, Rolletschek, Alexandra
Publicado 2019

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders

por de Sena Cortabitarte, Ana, Berkel, Simone, Cristian, Flavia-Bianca, Fischer, Christine, Rappold, Gudrun A.
Publicado 2018

Alternative Splicing and Nonsense-Mediated RNA Decay Contribute to the Regulation of SHOX Expression

por Durand, Claudia, Roeth, Ralph, Dweep, Harsh, Vlatkovic, Irena, Decker, Eva, Schneider, Katja Ute, Rappold, Gudrun
Publicado 2011

SHANK2 mutations impair apoptosis, proliferation and neurite outgrowth during early neuronal differentiation in SH-SY5Y cells

por Unsicker, Christine, Cristian, Flavia-Bianca, von Hahn, Manja, Eckstein, Volker, Rappold, Gudrun A., Berkel, Simone
Publicado 2021

Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes

por Hoffmann, Sandra, Roeth, Ralph, Diebold, Sabrina, Gogel, Jasmin, Hassel, David, Just, Steffen, Rappold, Gudrun A.
Publicado 2021

Evidence for a Role of srGAP3 in the Positioning of Commissural Axons within the Ventrolateral Funiculus of the Mouse Spinal Cord

por Bacon, Claire, Endris, Volker, Andermatt, Irwin, Niederkofler, Vera, Waltereit, Robert, Bartsch, Dusan, Stoeckli, Esther T., Rappold, Gudrun
Publicado 2011

Sex Hormones Regulate SHANK Expression

por Berkel, Simone, Eltokhi, Ahmed, Fröhlich, Henning, Porras-Gonzalez, Diana, Rafiullah, Rafiullah, Sprengel, Rolf, Rappold, Gudrun A.
Publicado 2018

Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA)

por Muncke, Nadja, Niesler, Beate, Roeth, Ralph, Schön, Karin, Rüdiger, Heinz-Juergen, Goldmuntz, Elizabeth, Goodship, Judith, Rappold, Gudrun
Publicado 2005

Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome

por Wang, Jing, Fröhlich, Henning, Torres, Felipe Bodaleo, Silva, Rangel Leal, Poschet, Gernot, Agarwal, Amit, Rappold, Gudrun A.
Publicado 2022

RIC-3 Exclusively Enhances the Surface Expression of Human Homomeric 5-Hydroxytryptamine Type 3A (5-HT(3)A) Receptors Despite Direct Interactions with 5-HT3A, -C, -D, and -E Subuni...

por Walstab, Jutta, Hammer, Christian, Lasitschka, Felix, Möller, Dorothee, Connolly, Christopher N., Rappold, Gudrun, Brüss, Michael, Bönisch, Heinz, Niesler, Beate
Publicado 2010

Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism

por Vick, Philipp, Eberle, Birgit, Choukair, Daniela, Weiss, Birgit, Roeth, Ralph, Schneider, Isabelle, Paramasivam, Nagarajan, Bettendorf, Markus, Rappold, Gudrun A.
Publicado 2021

Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia

por Hoffmann, Sandra, Berger, Ina M., Glaser, Anne, Bacon, Claire, Li, Li, Gretz, Norbert, Steinbeisser, Herbert, Rottbauer, Wolfgang, Just, Steffen, Rappold, Gudrun
Publicado 2013