Search Results - Andreas W. Kuß

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  1. 1
    MicroRNAs in brain function and disease

    MicroRNAs in brain function and disease by Andreas W. Kuß, Wei Chen

    Published 2008
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  2. 2
    A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

    A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation by Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad, Farkhondeh Behjati, Andreas Tzschach, Hossein Najmabadi, Hans Hilger Ropers, Andreas W. Kuß

    Published 2008
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  3. 3
    CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait

    CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait by Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J. Alshalah, Claudia Mischung, Andreas W. Kuß, Nicholas Humphrey, Stefan Mundlos, Peter N. Robinson

    Published 2009
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  4. 4
    Cleavage of E-Cadherin and β-Catenin by Calpain Affects Wnt Signaling and Spheroid Formation in Suspension Cultures of Human Pluripotent Stem Cells

    Cleavage of E-Cadherin and β-Catenin by Calpain Affects Wnt Signaling and Spheroid Formation in Suspension Cultures of Human Pluripotent Stem Cells by Sarah A. Konze, Laura van Diepen, Anke Schröder, Ruth Olmer, Hanna Möller, Andreas Pich, Robert Weißmann, Andreas W. Kuß, Robert Zweigerdt, Falk F. R. Buettner

    Published 2014
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  5. 5
    A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay

    A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay by Cíntia Barros Santos-Rebouças, Natalia Fintelman‐Rodrigues, Lars Riff Jensen, Andreas W. Kuß, Márcia Gonçalves Ribeiro, Mário Campos, Jussara Mendonça dos Santos, Márcia Mattos Gonçalves Pimentel

    Published 2011
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  6. 6
    Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

    Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 by Kimia Kahrizi, Cougar Hao Hu, Masoud Garshasbi, Seyedeh Sedigheh Abedini, Shirin Ghadami, Roxana Kariminejad, Reinhard Ullmann, Wei Chen, H-Hilger Ropers, Andreas W. Kuß, Hossein Najmabadi, Andreas Tzschach

    Published 2010
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  7. 7
    Deciphering the Molecular Profile of Plaques, Memory Decline and Neuron Loss in Two Mouse Models for Alzheimer’s Disease by Deep Sequencing

    Deciphering the Molecular Profile of Plaques, Memory Decline and Neuron Loss in Two Mouse Models for Alzheimer’s Disease by Deep Sequencing by Yvonne Bouter, Tim Kacprowski, Robert Weißmann, Katharina Dietrich, Henning Borgers, Andreas Brauß, Christian Sperling, Oliver Wirths, Mario Albrecht, Lars R. Jensen, Andreas W. Kuß, Thomas A. Bayer

    Published 2014
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  8. 8
    Genetic rearrangements result in altered gene expression and novel fusion transcripts in Sézary syndrome

    Genetic rearrangements result in altered gene expression and novel fusion transcripts in Sézary syndrome by Katarzyna Iżykowska, Grzegorz K. Przybylski, Claudia Gand, Floriane Braun, Piotr Grabarczyk, Andreas W. Kuß, Karolina Olek‐Hrab, Armando N. Bastidas Torres, Maarten H. Vermeer, Willem H. Zoutman, Cornelis P. Tensen, Christian A. Schmidt

    Published 2017
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  9. 9
    Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability

    Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability by Luciana Musante, Lucia Püttmann, Kimia Kahrizi, Masoud Garshasbi, Hao Hu, Henning Stehr, Bettina Lipkowitz, Sabine Otto, Lars R. Jensen, Andreas Tzschach, Payman Jamali, Thomas F. Wienker, Hossein Najmabadi, Hans Hilger Ropers, Andreas W. Kuß

    Published 2017
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  10. 10
    ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions

    ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions by Hao Hu, Katinka Eggers, Wei Chen, Masoud Garshasbi, M. Mahdi Motazacker, Klaus Wrogemann, Kimia Kahrizi, Andreas Tzschach, Masoumeh Hosseini, Ideh Bahman, Tim Hucho, Martina Mühlenhoff, Rita Gerardy‐Schahn, Hossein Najmabadi, Hans‐Hilger Ropers, Andreas W. Kuß

    Published 2011
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  11. 11
    A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation

    A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation by Mohammad Mahdi Motazacker, Benjamin R. Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saeid Hosseini Amini, Chandan Goswami, Andreas Tzschach, Lars Riff Jensen, Dietmar Schmitz, Hans Hilger Ropers, Hossein Najmabadi, Andreas W. Kuß

    Published 2007
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  12. 12
    CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling

    CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling by Petro Starokadomskyy, Nathan Gluck, Haiying Li, Baozhi Chen, Mathew Wallis, Gabriel N. Maine, Xicheng Mao, Iram Waris Zaidi, Marco Y. Hein, Fiona J. McDonald, Steffen Lenzner, Agnes Zecha, Hans‐Hilger Ropers, Andreas W. Kuß, Julie McGaughran, Jozef Gécz, Ezra Burstein

    Published 2013
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  13. 13
    Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis

    Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis by Bernd Timmermann, Martin Kerick, Christina Roehr, Axel Fischer, Melanie Isau, Stefan Boerno, Andrea Wunderlich, Christian Barmeyer, Petra Seemann, Jana Koenig, Michael Lappé, Andreas W. Kuß, Masoud Garshasbi, Lars Bertram, Kathrin Trappe, Martin Werber, Bernhard G. Herrmann, Kurt Zatloukal, Hans Lehrach, Michal R. Schweiger

    Published 2010
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  14. 14
    Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

    Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene by Joanna Walczak‐Sztulpa, Jonathan Eggenschwiler, Daniel P. S. Osborn, Desmond Brown, Francesco Emma, Claus Klingenberg, Raoul C. M. Hennekam, Giuliano Torre, Masoud Garshasbi, Andreas Tzschach, Małgorzata Szczepańska, Marian Krawczyński, Jacek Zachwieja, Danuta Zwołińska, Philip L. Beales, Hans‐Hilger Ropers, Anna Latos‐Bieleńska, Andreas W. Kuß

    Published 2010
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  15. 15
    Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

    Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability by Lia Abbasi‐Moheb, Sara Mertel, Melanie Gonsior, Leyla Nouri-Vahid, Kimia Kahrizi, Sebahattin Çirak, Dagmar Wieczorek, Mohammad Mahdi Motazacker, Sahar Esmaeeli-Nieh, Kirsten Cremer, Robert Weißmann, Andreas Tzschach, Masoud Garshasbi, Seyedeh Sedigheh Abedini, Hossein Najmabadi, Hans‐Hilger Ropers, Stephan J. Sigrist, Andreas W. Kuß

    Published 2012
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  16. 16
    Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)

    Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG) by Christina T. Thiesler, Samanta Cajic, Dirk Hoffmann, Christian Thiel, Laura van Diepen, René Hennig, Malte Sgodda, Robert Weiβmann, Udo Reichl, Doris Steinemann, Ulf Diekmann, Nicolas Huber, Astrid Oberbeck, Tobias Cantz, Andreas W. Kuß, Christian Körner, Axel Schambach, Erdmann Rapp, Falk F. R. Buettner

    Published 2016
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  17. 17
    Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

    Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation by Asif Mir, Liana Kaufman, Abdul Noor, M. Mahdi Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Rafiq, Rosanna Weksberg, Tanveer Nasr, Farooq Naeem, Andreas Tzschach, Andreas W. Kuß, Gisele E. Ishak, Dan Doherty, Hans‐Hilger Ropers, A. James Barkovich, Hossein Najmabadi, Muhammad Ayub, John B. Vincent

    Published 2009
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  18. 18
    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability by Muhammad Rafiq, Andreas W. Kuß, Lucia Puettmann, Abdul Noor, Annapoorani Ramiah, Ghazanfar Ali, Hao Hu, Nadir Ali Kerio, Yong Xiang, Masoud Garshasbi, Muzammil Ahmad Khan, Gisele E. Ishak, Rosanna Weksberg, Reinhard Ullmann, Andreas Tzschach, Kimia Kahrizi, Khalid Mahmood, Farooq Naeem, Muhammad Ayub, Kelley W. Moremen, John B. Vincent, Hans Hilger Ropers, Muhammad Ansar, Hossein Najmabadi

    Published 2011
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  19. 19
    Novel tRNA-like transcripts from the NEAT1-MALAT1 genomic region critically influence human innate immunity and macrophage functions

    Novel tRNA-like transcripts from the NEAT1-MALAT1 genomic region critically influence human innate immunity and macrophage functions by Martina Gast, Vanasa Nageswaran, Andreas W. Kuß, Ana Tzvetkova, Xiaomin Wang, Liliana H. Mochmann, Pegah Ramezani-Rad, Stefan Weiß, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang Hoffmann, Uwe Völker, Stefan Felix, Marcus Dörr, Antje Beling, Carsten Skurk, D Leistner, Bernhard Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C. Poller, Filip K. Świrski, Arash Haghikia, Wolfgang Poller

    Published 2022
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  20. 20
    Novel tRNA-like transcripts from the NEAT1-MALAT1 genomic region critically influence human innate immunity and macrophage functions

    Novel tRNA-like transcripts from the NEAT1-MALAT1 genomic region critically influence human innate immunity and macrophage functions by Martina Gast, Vanasa Nageswaran, Andreas W. Kuß, Ana Tzvetkova, Xiaomin Wang, Liliana H. Mochmann, Pegah Ramezani-Rad, Stefan Weiß, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang Hoffmann, Uwe Völker, Stefan Felix, Marcus Dörr, Antje Beling, Carsten Skurk, D Leistner, Bernhard Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C. Poller, Filip K. Świrski, Arash Haghikia, Wolfgang Poller

    Published 2022
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