Andreas Kuss - Dissemin

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All papers authored by Andreas Kuss

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2021 Karsten Cirksena

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, Hermann J. Hütte

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, Aleksandra Shcherbakova

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, Thomas Thumberger

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, Lars Riff Jensen

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, Alina Friedrich, Daniel Todt

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, Andreas W. Kuss

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, Thomas Ruppert

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, Joachim Wittbrodt

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, Falk F. R. Buettner

The C-Mannosylome of Human Induced Pluripotent Stem Cells Implies a Role for ADAMTS16 C-Mannosylation in Eye Development

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Monica M. Sheffer

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, Henrik Krehenwinkel

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, Andreas W. Kuss

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, Lars Jensen, Corinna Jensen, Rosemary G. Gillespie

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, Katharina J. Hoff

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Chromosome-level reference genome of the European wasp spiderArgiope bruennichi: a resource for studies on range expansion and evolutionary adaptation

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F. Kliewe, A. W. Kuss

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, F. Siegerist, S. Schröder, S. Schordan, N. Artelt, F. Kindt, K. Amann, M. T. Lindenmeyer, K. Endlich, N. Endlich

Studies on the Role of the Transcription Factor Tcf21 in the Transdifferentiation of Parietal Epithelial Cells into Podocyte-Like Cells

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2020 Neetika Nath

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, Stefan Weiss, Ana Tzvetkova, Lars R. Jensen

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, Lars Kaderali

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, Matthias Port, Harry Scherthan, Andreas W. Kuss

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Genome-Wide DNA Alterations in X-Irradiated Human Gingiva Fibroblasts

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Masoud Garshasbi, Mahdi Mahmoudi

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, Ehsan Razmara

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, Mahdi Vojdanian, Saeed Aslani, Elham Farhadi, Lars Riff Jensen

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, Seyed Masoud Arzaghi, Shiva Poursani, Amirreza Bitaraf

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, Milad Eidi, Elika Esmaeilzadeh Gharehdaghi, Andreas Walter Kuss

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, Ahmadreza Jamshidi

Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS

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2019 Lars R. Jensen, Lillian Garrett, Sabine M. Hölter, Birgit Rathkolb, Ildikó Rácz, Thure Adler, Cornelia Prehn, Wolfgang Hans, Jan Rozman, Lore Becker

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, Juan Antonio Aguilar-Pimentel, Oliver Puk, Kristin Moreth, Monika Dopatka, Diego J. Walther and 27 other authors

A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene

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Martina Gast, Bernhard H. Rauch, Arash Haghikia, Shinichi Nakagawa, Jan Haas, Andrea Stroux, David Schmidt, Paul Schumann, Stefan Weiss, Lars Jensen, Adelheid Kratzer, Nicolle Kraenkel, Christian Müller, Daniela Börnigen, Tetsuro Hirose and 8 other authors

Long noncoding RNA NEAT1 modulates immune cell functions and is suppressed in early onset myocardial infarction patients

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2018 Nicole Endlich, Tim Lange

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, Jana Kuhn, Paul Klemm, Ahmed M. Kotb, Florian Siegerist

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, Frances Kindt, Maja T. Lindenmeyer, Clemens D. Cohen, Andreas W. Kuss

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, Neetika Nath, Rainer Rettig, Uwe Lendeckel, Uwe Zimmermann, Kerstin Amann and 2 other authors

BDNF : mRNA expression in urine cells of patients with chronic kidney disease and its role in kidney function

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Laura van Diepen, Falk F. R. Buettner

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, Oliver von Bohlen und Halbach

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, Dirk Hoffmann, Viola von Bohlen und Halbach, Christina T. Thiesler, Oliver von Bohlen und Halbach, Viola von Bohlen und Halbach, Lars R. Jensen

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, Doris Steinemann, Simon Edvardson, Orly Elpeleg, Axel Schambach, Rita Gerardy-Schahn, Andreas W. Kuss

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A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency

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Martina Gast, Bernhard H. Rauch, Shinichi Nakagawa, Arash Haghikia, Andrzej Jasina, Jan Haas, Neetika Nath, Lars Jensen, Andrea Stroux, Andreas Böhm, Julian Friebel, Ursula Rauch, Carsten Skurk, Stefan Blankenberg

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, Tanja Zeller and 5 other authors

Immune system-mediated atherosclerosis caused by deficiency of long non-coding RNAMALAT1in ApoE−/−mice

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Neetika Nath, Jennifer Esche, Jessica Müller, Lars R. Jensen, Matthias Port, Mario Stanke, Lars Kaderali, Harry Scherthan, Andreas W. Kuss

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Exome Sequencing Discloses Ionizing-radiation-induced DNA Variants in the Genome of Human Gingiva Fibroblasts:

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Anne Steininger, Grit Ebert, Benjamin V. Becker, Chalid Assaf, Markus Möbs

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, Christian A. Schmidt, Piotr Grabarczyk, Lars R. Jensen, Grzegorz K. Przybylski

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, Matthias Port, Andreas W. Kuss

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, Reinhard Ullmann

Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line

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Nicole Endlich, Felix Kliewe

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, Frances Kindt, Katharina Schmidt, Ahmed M. Kotb, Nadine Artelt, Maja T. Lindenmeyer, Clemens D. Cohen, Franziska Döring, Andreas W. Kuss

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, Kerstin Amann, Marcus J. Moeller, Nazanin Kabgani, Antje Blumenthal, Karlhans Endlich

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The transcription factor Dach1 is essential for podocyte function

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2017 Katarzyna Iżykowska, Grzegorz K. Przybylski

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, Claudia Gand, Floriane C. Braun, Piotr Grabarczyk, Andreas W. Kuss

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, Karolina Olek-Hrab, Armando N. Bastidas Torres, Armando N. Bastidas Torres, Maarten H. Vermeer, Willem H. Zoutman, Cornelis P. Tensen, Christian A. Schmidt

Genetic rearrangements result in altered gene expression and novel fusion transcripts in Sézary syndrome

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Luciana Musante, Lucia Püttmann, Kimia Kahrizi, Masoud Garshasbi, Hao Hu, Henning Stehr, Bettina Lipkowitz, Sabine Otto, Lars R. Jensen, Andreas Tzschach, Payman Jamali, Thomas Wienker, Hossein Najmabadi, Hans Hilger Ropers, Andreas W. Kuss

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

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2016 Robert Weissmann, Tim Kacprowski, Michel Peper, Jennifer Esche, Lars R. Jensen, Laura van Diepen, Matthias Port, Andreas W. Kuss

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, Harry Scherthan

Transcriptome Alterations In X-Irradiated Human Gingiva Fibroblasts:

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Jonathan Bertram, Leif Koschützke, Jörg P. Pfannmöller, Jennifer Esche, Laura van Diepen, Andreas W. Kuss

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, Bianca Hartmann, Dusan Bartsch, Martin Lotze, Oliver von Bohlen und Halbach

Morphological and behavioral characterization of adult mice deficient for SrGAP3

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Sahar Esmaeeli-Nieh, Michaela Fenckova, Iain M. Porter, M. Mahdi Motazacker, Porter Im, Motazacker Mm, Bonnie Nijhof, Anna Castells-Nobau

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, Zoltan Asztalos, Robert Weißmann, Farkhondeh Behjati, Harry Scherthan, Seyed Morteza Sayfati, Andreas Tzschach, H. Hilger Ropers and 8 other authors

BOD1 Is Required for Cognitive Function in Humans and Drosophila

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Birgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, Linea Melchior, Nanette Mol Debes, Lars Riff Jensen, Camilla Groth, Csaba Barta, Liselotte Skov, Peter Nagy

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, Luca Farkas, Thomas Werge, Karen Brøndum-Nielsen, Renata Rizzo, Iordanis Karagiannidis and 21 other authors

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

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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 M. B. Huber, Astrid Oberbeck, Tobias Cantz

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, Andreas W. Kuss

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and 4 other authors

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

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