Search Results - Rappold, Gudrun

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  1. 1
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    Inhibition of phosphodiesterase 10A by MP-10 rescues behavioral deficits and normalizes microglial morphology and synaptic pruning in a mouse model of FOXP1 syndrome by Fröhlich, Henning (Author) , Wang, Jing (Author) , Althammer, Ferdinand (Author) , Schubert, Tim (Author) , Kluck, Nina (Author) , Grinevich, Valéry (Author) , Schmitteckert, Stefanie (Author) , Schaaf, Christian P. (Author) , Rappold, Gudrun (Author) ,


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  2. 2
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    The role of genetics in inherited cardiac diseases by Rappold, Gudrun (Author) , Wollnik, Bernd (Author) ,


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  3. 3
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    Celebrating the 100th anniversary of the Japan Endocrine Society and international collaborations by Rappold, Gudrun (Author)


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  4. 4
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    10 years of international albinism awareness: United Nations celebrate an anniversary and a decade of collective progress, but challenges remain by Rappold, Gudrun (Author)


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  5. 5
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    Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations by Werren, Elizabeth A. (Author) , Peirent, Emily R. (Author) , Jantti, Henna (Author) , Guxholli, Alba (Author) , Srivastava, Kinshuk Raj (Author) , Orenstein, Naama (Author) , Narayanan, Vinodh (Author) , Wiszniewski, Wojciech (Author) , Dawidziuk, Mateusz (Author) , Gawlinski, Pawel (Author) , Umair, Muhammad (Author) , Khan, Amjad (Author) , Khan, Shahid Niaz (Author) , Geneviève, David (Author) , Lehalle, Daphné (Author) , van Gassen, K. L. I. (Author) , Giltay, Jacques C. (Author) , Oegema, Renske (Author) , van Jaarsveld, Richard H. (Author) , Rafiullah, Rafiullah (Author) , Rappold, Gudrun (Author) , Rabin, Rachel (Author) , Pappas, John G. (Author) , Wheeler, Marsha M. (Author) , Bamshad, Michael J. (Author) , Tsan, Yao-Chang (Author) , Johnson, Matthew B. (Author) , Keegan, Catherine E. (Author) , Srivastava, Anshika (Author) , Bielas, Stephanie L. (Author) ,


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  6. 6
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    Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 by Rädecke, Kristin (Author) , Gore, Ambuj (Author) , Burau, Karin (Author) , Laugsch, Magdalena (Author) , Köhler, Katrin (Author) , Rappold, Gudrun (Author) , Hoffmann, Sandra (Author) ,


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  7. 7
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    Identification of novel genes including NAV2 associated with isolated tall stature by Weiß, Birgit (Author) , Ott, Tim (Author) , Vick, Philipp (Author) , Lui, Julian C. (Author) , Röth, Ralph (Author) , Vogel, Sebastian (Author) , Waldmüller, Stephan (Author) , Hoffmann, Sandra (Author) , Baron, Jeffrey (Author) , Wit, Jan M. (Author) , Rappold, Gudrun (Author) ,


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  8. 8
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    Disrupted mitochondrial network drives deficits of learning and memory in a mouse model of FOXP1 haploinsufficiency by Wang, Jing (Author) , Rappold, Gudrun (Author) , Fröhlich, Henning (Author) ,


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  9. 9
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    Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome by Wang, Jing (Author) , Fröhlich, Henning (Author) , Torres, Felipe Bodaleo (Author) , Silva, Rangel Leal (Author) , Poschet, Gernot (Author) , Agarwal, Amit (Author) , Rappold, Gudrun (Author) ,


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  10. 10
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    Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome: a multicenter retrospective study by Berens, Sabrina (Author) , Dong, Yuanjun (Author) , Fritz, Nikola (Author) , Walstab, Jutta (Author) , D'Amato, Mauro (Author) , Zheng, Tenghao (Author) , Wahl, Verena (Author) , Boekstegers, Felix (Author) , Lorenzo Bermejo, Justo (Author) , Martinez, Cristina (Author) , Schmitteckert, Stefanie (Author) , Clevers, Egbert (Author) , Engel, Felicitas (Author) , Gauss, Annika (Author) , Herzog, Wolfgang (Author) , Spiller, Robin (Author) , Goebel-Stengel, Miriam (Author) , Mönnikes, Hubert (Author) , Andresen, Viola (Author) , Thomas, Frieling (Author) , Keller, Jutta (Author) , Pehl, Christian (Author) , Stein-Thöringer, Christoph (Author) , Clarke, Gerard (Author) , Dinan, Timothy G. (Author) , Quigley, Eamonn M. (Author) , Sayuk, Gregory (Author) , Simrén, Magnus (Author) , Tesarz, Jonas (Author) , Rappold, Gudrun (Author) , Oudenhove, Lukas van (Author) , Schaefert, Rainer (Author) , Niesler, Beate (Author) ,


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  11. 11
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    SHANK2 mutations impair apoptosis, proliferation and neurite outgrowth during early neuronal differentiation in SH-SY5Y cells by Unsicker, Christine (Author) , Cristian, Flavia-Bianca (Author) , Hahn, Manja von (Author) , Eckstein, Volker (Author) , Rappold, Gudrun (Author) , Berkel, Simone (Author) ,


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  12. 12
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    Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control by Hoffmann, Sandra (Author) , Schmitteckert, Stefanie (Author) , Rädecke, Kristin (Author) , Rheinert, David (Author) , Diebold, Sabrina (Author) , Röth, Ralph (Author) , Weiß, Birgit (Author) , Granzow, Martin (Author) , Niesler, Beate (Author) , Griesbeck, Anne (Author) , Eckstein, Volker (Author) , Zimmermann, Wolfram-Hubertus (Author) , Just, Steffen (Author) , Rappold, Gudrun (Author) ,


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  13. 13
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    Evidence that non-syndromic familial tall stature has an oligogenic origin including ciliary genes by Weiß, Birgit (Author) , Röth, Ralph (Author) , Hinderhofer, Katrin (Author) , Rappold, Gudrun (Author) ,


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  14. 14
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    Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes by Hoffmann, Sandra (Author) , Röth, Ralph (Author) , Hassel, David (Author) , Rappold, Gudrun (Author) ,


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  15. 15
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    Expression profiling of rectal biopsies suggests altered enteric neuropathological traits in Parkinson’s disease patients by Cossais, François (Author) , Schaeffer, Eva (Author) , Heinzel, Sebastian (Author) , Zimmermann, Jessica (Author) , Niesler, Beate (Author) , Röth, Ralph (Author) , Rappold, Gudrun (Author) , Scharf, Amelie (Author) , Zorenkov, Dmitri (Author) , Lange, Christina (Author) , Barrenschee, Martina (Author) , Margraf, Nils Gerd (Author) , Ellrichmann, Mark (Author) , Berg, Daniela (Author) , Böttner, Martina (Author) , Wedel, Thilo (Author) ,


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  16. 16
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    Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder by Niesler, Beate (Author) , Rappold, Gudrun (Author) ,


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  17. 17
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    Parkinson mice show functional and molecular changes in the gut long before motoric disease onset by Gries, Manuela (Author) , Christmann, Anne (Author) , Schulte, Steven (Author) , Weyland, Maximilian (Author) , Rommel, Stephanie (Author) , Martin, Monika (Author) , Baller, Marko (Author) , Röth, Ralph (Author) , Schmitteckert, Stefanie (Author) , Unger, Marcus (Author) , Liu, Yang (Author) , Sommer, Frederik (Author) , Mühlhaus, Timo (Author) , Schroda, Michael (Author) , Timmermans, Jean-Pierre (Author) , Pintelon, Isabel (Author) , Rappold, Gudrun (Author) , Britschgi, Markus (Author) , Lashuel, Hilal (Author) , Menger, Michael D. (Author) , Laschke, Matthias W. (Author) , Niesler, Beate (Author) , Schäfer, Karl Herbert (Author) ,


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  18. 18
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    The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome by Mohr, Sandra (Author) , Fritz, Nikola (Author) , Hammer, Christian (Author) , Martínez, Cristina (Author) , Berens, Sabrina (Author) , Schmitteckert, Stefanie (Author) , Wahl, Verena (Author) , Schmidt, Malin (Author) , Houghton, Lesley A. (Author) , Goebel-Stengel, Miriam (Author) , Kabisch, Maria (Author) , Götze, Dorothea (Author) , Milovač, Irina (Author) , D’Amato, Mauro (Author) , Zheng, Tenghao (Author) , Röth, Ralph (Author) , Mönnikes, Hubert (Author) , Engel, Felicitas (Author) , Gauss, Annika (Author) , Tesarz, Jonas (Author) , Raithel, Martin (Author) , Andresen, Viola (Author) , Frieling, Thomas (Author) , Keller, Jutta (Author) , Pehl, Christian (Author) , Stein-Thöringer, Christoph (Author) , Clarke, Gerard (Author) , Kennedy, Paul J. (Author) , Cryan, John F. (Author) , Dinan, Timothy G. (Author) , Quigley, Eamonn M. M. (Author) , Spiller, Robin (Author) , Beltrán, Caroll (Author) , Madrid, Ana María (Author) , Torres, Verónica (Author) , Arce, Edith Pérez de (Author) , Herzog, Wolfgang (Author) , Mayer, Emeran A. (Author) , Sayuk, Gregory (Author) , Gazouli, Maria (Author) , Karamanolis, George (Author) , Kapur-Pojskič, Lejla (Author) , Bustamante, Mariona (Author) , Rabionet, Raquel (Author) , Estivil, Xavier (Author) , Franke, André (Author) , Lieb, Wolfgang (Author) , Boeckxstaens, Guy (Author) , Wouters, Mira M. (Author) , Simrén, Magnus (Author) , Rappold, Gudrun A. (Author) , Vicario, Maria (Author) , Santos, Javier (Author) , Schaefert, Rainer (Author) , Lorenzo Bermejo, Justo (Author) , Niesler, Beate (Author) ,


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  19. 19
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    Wenn die Intelligenz beeinträchtigt ist by Rappold, Gudrun (Author)


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  20. 20
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    Protect minorities in genetic research: letter by Lipphardt, Veronika (Author) , Rappold, Gudrun (Author) , Surdu, Mihai (Author) ,


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