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Susann Schweiger

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Sybille Krauss; Maciej Lalowski; Désiree Rutschow; Rainer Schneider; Clemens Achmüller; Sylvia Boesch; Changwei Chen; Stephanie Dorn; Nadine Griesche; Ewa Jastrzebska; Erich Wanker; Susann Schweiger
Translation of HTT mRNA with expanded CAG repeats is regulated by the MID1-PP2A protein complex.
Beatriz Aranda-Orgillés; Changwei Chen; Antonios I Karagiannidis; Andrea Köhler; Sven Krause; David Lilley; Stefan Roepcke; Désirée Rutschow; Rainer Schneider; Timothy Wilson; Raphael Zeller; Susann Schweiger
Protein phosphatase 2A (PP2A)-specific ubiquitin ligase MID1 is a sequence-dependent regulator of translation efficiency controlling 3-phosphoinositide-dependent protein kinase-1 (PDPK-1).
Eva Kickstein; Sybille Krauss; Paul Thornhill; Désirée Rutschow; Raphael Zeller; John Sharkey; Ritchie Williamson; Melanie Fuchs; Andrea Köhler; Hartmut Glossmann; Rainer Schneider; Calum Sutherland; Susann Schweiger
Biguanide metformin acts on tau phosphorylation via mTOR/protein phosphatase 2A (PP2A) signaling.

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All Publications

2013: Sybille Krauss; Maciej Lalowski; Désiree Rutschow; Rainer Schneider; Clemens Achmüller; Sylvia Boesch; Changwei Chen; Stephanie Dorn; Nadine Griesche; Ewa Jastrzebska; Erich Wanker; Susann Schweiger
Translation of HTT mRNA with expanded CAG repeats is regulated by the MID1-PP2A protein complex.
Nature communications 2013;4():1511.
2011: Beatriz Aranda-Orgillés; Changwei Chen; Antonios I Karagiannidis; Andrea Köhler; Sven Krause; David Lilley; Stefan Roepcke; Désirée Rutschow; Rainer Schneider; Timothy Wilson; Raphael Zeller; Susann Schweiger
Protein phosphatase 2A (PP2A)-specific ubiquitin ligase MID1 is a sequence-dependent regulator of translation efficiency controlling 3-phosphoinositide-dependent protein kinase-1 (PDPK-1).
The Journal of biological chemistry 2011;286(46):39945-57.
2010: Eva Kickstein; Sybille Krauss; Paul Thornhill; Désirée Rutschow; Raphael Zeller; John Sharkey; Ritchie Williamson; Melanie Fuchs; Andrea Köhler; Hartmut Glossmann; Rainer Schneider; Calum Sutherland; Susann Schweiger
Biguanide metformin acts on tau phosphorylation via mTOR/protein phosphatase 2A (PP2A) signaling.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(50):21830-5.
2008: Nadya al Yacoub; Malgorzata Romanowska; Sybille Krauss; Susann Schweiger; John Foerster
PPARdelta is a type 1 IFN target gene and inhibits apoptosis in T cells.
The Journal of investigative dermatology 2008;128(8):1940-9.
2008: Beatriz Aranda-Orgillés; Alexander Trockenbacher; Jennifer Winter; Johanna Aigner; Andrea Köhler; Ewa Jastrzebska; Joachim Stahl; Eva-Christina Müller; Albrecht Otto; Erich E Wanker; Rainer Schneider; Susann Schweiger
The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex.
Human genetics 2008;123(2):163-76.
2008: Beatriz Aranda-Orgillés; Johanna Aigner; Melanie Kunath; Rudi Lurz; Rainer Schneider; Susann Schweiger
Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A.
PloS one 2008;3(10):e3507.
2008: Jennifer Winter; Stefan Roepcke; Sven Krause; Eva-Christina Müller; Albrecht Otto; Martin Vingron; Susann Schweiger
Comparative 3'UTR analysis allows identification of regulatory clusters that drive Eph/ephrin expression in cancer cell lines.
PloS one 2008;3(7):e2780.
2008: Joyce So; Ines Müller; Melanie Kunath; Susanne Herrmann; Reinhard Ullmann; Susann Schweiger
Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.
American journal of medical genetics. Part A 2008;146A(1):103-9.
2008: Malgorzata Romanowska; Nadya al Yacoub; Henrik Seidel; Susanne Donandt; Hannah Gerken; Sandra Phillip; Nathalie Haritonova; Metin Artuc; Susann Schweiger; Wolfram Sterry; John Foerster
PPARdelta enhances keratinocyte proliferation in psoriasis and induces heparin-binding EGF-like growth factor.
The Journal of investigative dermatology 2008;128(1):110-24.
2007: Jennifer Winter; Melanie Kunath; Stefan Roepcke; Sven Krause; Rainer Schneider; Susann Schweiger
Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1.
BMC molecular biology 2007;8():105.
2006: Olivier Hagens; Eleonora Minina; Susann Schweiger; Hans-Hilger Ropers; Vera Kalscheuer
Characterization of FBX25, encoding a novel brain-expressed F-box protein.
Biochimica et biophysica acta 2006;1760(1):110-8.
2006: Sarah A Shoichet; Laurence Duprez; Olivier Hagens; Vicki Waetzig; Corinna Menzel; Thomas Herdegen; Susann Schweiger; Bernard Dan; Esther Vamos; Hans-Hilger Ropers; Vera Kalscheuer
Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy.
Human genetics 2006;118(5):559-67.
2005: Ilse Wieland; William Reardon; Sibylle Jakubiczka; Brunella Franco; Wolfram Kress; Catherine Vincent-Delorme; Patrick Thierry; Matt Edwards; Rainer König; Cristina Rusu; Susann Schweiger; Elizabeth Thompson; Sigrid Tinschert; Fiona Stewart; Peter Wieacker
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS).
Human mutation 2005;26(2):113-8.
2005: John Foerster; Ilja Nolte; Judith Junge; Marcel Bruinenberg; Susann Schweiger; Katja Spaar; Gerrit van der Steege; Claudia Ehlert; Marcel Mulder; Vera Kalscheuer; Elisa Blumenthal-Barby; Jennifer Winter; Philip Seeman; Markward Ständer; Wolfram Sterry; Gerard te Meerman
Haplotype sharing analysis identifies a retroviral dUTPase as candidate susceptibility gene for psoriasis.
The Journal of investigative dermatology 2005;124(1):99-102.
2005: Joyce So; Vanessa Suckow; Zofia Kijas; Vera Kalscheuer; Bettina Moser; Jennifer Winter; Marieke Baars; Helen V Firth; Peter Lunt; Ben Hamel; Peter Meinecke; Claude Moraine; Sylvie Odent; Albert Schinzel; Jasper van der Smagt; koenraad devriendt; Beate Albrecht; Gabriele Gillessen-Kaesbach; Ineke van der Burgt; Fred Petrij; Laurence Faivre; Julie McGaughran; Fiona McKenzie; John M Opitz; Timothy Cox; Susann Schweiger
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.
American journal of medical genetics. Part A 2005;132A(1):1-7.
2004: Jennifer Winter; Tanja Lehmann; Sybille Krauss; Alexander Trockenbacher; Zofia Kijas; John Foerster; Vanessa Suckow; Marie-Laure Yaspo; Andreas E Kulozik; Vera Kalscheuer; Rainer Schneider; Susann Schweiger
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing.
Human genetics 2004;114(6):541-52.
2004: John Foerster; Ilja Nolte; Susann Schweiger; Claudia Ehlert; Marcel Bruinenberg; Katja Spaar; Gerrit van der Steege; Marcel Mulder; Vera Kalscheuer; Bettina Moser; Zofia Kijas; Petra Seeman; Markward Ständer; Wolfram Sterry; Gerard te Meerman
Evaluation of the IRF-2 gene as a candidate for PSORS3.
The Journal of investigative dermatology 2004;122(1):61-4.
2003: Christina Zeitz; Harry Scherthan; Susanne Freier; Silke Feil; Vanessa Suckow; Susann Schweiger; Wolfgang Berger
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.
Investigative ophthalmology & visual science 2003;44(10):4184-91.
2003: Susann Schweiger; Rabih Chaoui; Cornelia Tennstedt; Katarina Lehmann; Stefan Mundlos; Sigrid Tinschert
Antenatal onset of cortical hyperostosis (Caffey disease): case report and review.
American journal of medical genetics. Part A 2003;120A(4):547-52.
2003: Susann Schweiger; Rainer Schneider
The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome.
BioEssays : news and reviews in molecular, cellular and developmental biology 2003;25(4):356-66.
2003: Jennifer Winter; Tanja Lehmann; Vanessa Suckow; Zofia Kijas; Andreas E Kulozik; Vera Kalscheuer; Ben Hamel; koenraad devriendt; John M Opitz; Steffen Lenzner; Hans-Hilger Ropers; Susann Schweiger
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome.
Human genetics 2003;112(3):249-54.
2003: Luciana Musante; Hans G Kehl; Frank Majewski; Peter Meinecke; Susann Schweiger; Gabriele Gillessen-Kaesbach; Dagmar Wieczorek; Georg Klaus Hinkel; Sigrid Tinschert; Maria Hoeltzenbein; Hans-Hilger Ropers; Vera Kalscheuer
Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome.
European journal of human genetics : EJHG 2003;11(2):201-6.
2002: Elke Raderschall; Karen Stout; Susanne Freier; Vanessa Suckow; Susann Schweiger; Thomas Haaf
Elevated levels of Rad51 recombination protein in tumor cells.
Cancer research 2002;62(1):219-25.
2001: Alexander Trockenbacher; Vanessa Suckow; John Foerster; Jennifer Winter; S Krauss; Hans-Hilger Ropers; Rainer Schneider; Susann Schweiger
MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation.
Nature genetics 2001;29(3):287-94.
1999: Susann Schweiger; John Foerster; Tanja Lehmann; Vanessa Suckow; Y A Muller; G Walter; T Davies; H Porter; H van Bokhoven; P W Lunt; P Traub; Hans-Hilger Ropers
The Opitz syndrome gene product, MID1, associates with microtubules.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(6):2794-9.
1999: C Rinderle; HM Christensen; Susann Schweiger; Hans Lehrach; Marie-Laure Yaspo
AIRE encodes a nuclear protein co-localizing with cytoskeletal filaments: altered sub-cellular distribution of mutants lacking the PHD zinc fingers.
Human molecular genetics 1999;8(2):277-90.
1997: NA Quaderi; Susann Schweiger; K Gaudenz; Brunella Franco; Elena I Rugarli; Wolfgang Berger; G J Feldman; M Volta; Gennaro Andolfi; S Gilgenkrantz; Robert W Marion; Raoul Hennekam; John M Opitz; Maximilian Muenke; Hans-Hilger Ropers; Andrea Ballabio
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.
Nature genetics 1997;17(3):285-91.