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  1. Dichanz, Horst [Editor]; Hauer, Nadine [Editor]; Hölzle, Peter [Editor]; Horn, Imme [Editor] ; Bundeszentrale für Politische Bildung

    Antisemitismus in Medien

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    Bonn: Bundeszentrale für Politische Bildung, 1997

    Published in: Arbeitshilfen für die politische Bildung

  2. Hauer, Georg [Author]; Naumann, Nadine [Author]; Harte, Patrick [Author]

    Digital transformation challenges successful enterprises : an exploration of the collaboration of marketing and sales department in German organizations

    2021

    Published in: Innovation & management review ; 18(2021), 2, Seite 164-174

  3. Hauer, Nadine N. [Author]; Popp, Bernt [Author]; Taher, Leila [Author]; Vogl, Carina [Author]; Dhandapany, Perundurai S. [Author]; Büttner, Christian [Author]; Uebe, Steffen [Author]; Sticht, Heinrich [Author]; Ferrazzi, Fulvia [Author]; Ekici, Arif Bülent [Author]; De Luca, Alessandro [Author]; Klinger, Patrizia [Author]; Kraus, Cornelia [Author]; Zweier, Christiane [Author]; Wiesener, Antje [Author]; Abou Jamra, Rami [Author]; Kunstmann, Erdmute [Author]; Rauch, Anita [Author]; Wieczorek, Dagmar [Author]; Jung, Anna-Marie [Author]; Rohrer, Tilman [Author]; Zenker, Martin [Author]; Dörr, Helmuth-Günther [Author]; Reis, André [Author];

    Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature

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    2019

    Published in: The journal of biological chemistry ; 27(2019), 7, Seite 1061-1071

  4. Montalbano, Antonino; Juergensen, Lonny; Fukami, Maki; Thiel, Christian T; Hauer, Nadine H; Roeth, Ralph; Weiss, Birgit; Naiki, Yasuhiro; Ogata, Tsutomu; Hassel, David; Rappold, Gudrun A.

    Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature

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    Springer Science and Business Media LLC, 2018

    Published in: European Journal of Human Genetics

  5. Lochner, Matthias; Bérard, Marion; Sawa, Shinichiro; Hauer, Siona; Gaboriau-Routhiau, Valérie; Fernandez, Tahia Diana; Snel, Johannes; Bousso, Philippe; Cerf-Bensussan, Nadine; Eberl, Gérard

    Restricted Microbiota and Absence of Cognate TCR Antigen Leads to an Unbalanced Generation of Th17 Cells

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    The American Association of Immunologists, 2011

    Published in: The Journal of Immunology

  6. Zahnleiter, Diana; Hauer, Nadine N.; Kessler, Kristin; Uebe, Steffen; Sugano, Yuya; Neuhauss, Stephan C.F.; Giessl, Andreas; Ekici, Arif B.; Blessing, Holger; Sticht, Heinrich; Dörr, Helmuth-Günther; Reis, André; Thiel, Christian T.

    MAP4-Dependent Regulation of Microtubule Formation Affects Centrosome, Cilia, and Golgi Architecture as a Central Mechanism in Growth Regulation

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    Hindawi Limited, 2015

    Published in: Human Mutation

  7. Rüchel, Nadine; Oldenburg, Marina; Janssen, Stefan; Pandyra, Aleksandra A.; Liu, Wei; Vasileiou, Eleni; Hein, Daniel; Jepsen, Vera Helena; Fischer, Ute; Picard, Daniel; Kögler, Gesine; Hauer, Julia; Auer, Franziska; Beer, Angelina; Adams, Ortwin; MacKenzie, Colin; Jaeger, Martin; Netea, Mihai G.; Borkhardt, Arndt; Gössling, Katharina L.

    Cytokine Hyperresponsiveness in Children With ETV6::RUNX1-positive Acute Lymphoblastic Leukemia After Challenge With Common Pathogens

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    Wiley, 2023

    Published in: HemaSphere

  8. Hauer, Nadine N.; Popp, Bernt; Taher, Leila; Vogl, Carina; Dhandapany, Perundurai S.; Büttner, Christian; Uebe, Steffen; Sticht, Heinrich; Ferrazzi, Fulvia; Ekici, Arif B.; De Luca, Alessandro; Klinger, Patrizia; Kraus, Cornelia; Zweier, Christiane; Wiesener, Antje; Jamra, Rami Abou; Kunstmann, Erdmute; Rauch, Anita; Wieczorek, Dagmar; Jung, Anna-Marie; Rohrer, Tilman R.; Zenker, Martin; Doerr, Helmuth-Guenther; Reis, André;

    Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature

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    Springer Science and Business Media LLC, 2019

    Published in: European Journal of Human Genetics

  9. Tiosano, Dov; Baris, Hagit N.; Chen, Anlu; Hitzert, Marrit M.; Schueler, Markus; Gulluni, Federico; Wiesener, Antje; Bergua, Antonio; Mory, Adi; Copeland, Brett; Gleeson, Joseph G.; Rump, Patrick; van Meer, Hester; Sival, Deborah A.; Haucke, Volker; Kriwinsky, Josh; Knaup, Karl X.; Reis, André; Hauer, Nadine N.; Hirsch, Emilio; Roepman, Ronald; Pfundt, Rolph; Thiel, Christian T.; Wiesener, Michael S.; [...]

    Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction

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    Public Library of Science (PLoS), 2019

    Published in: PLOS Genetics

  10. Hauer, Nadine N.; Popp, Bernt; Schoeller, Eva; Schuhmann, Sarah; Heath, Karen E.; Hisado-Oliva, Alfonso; Klinger, Patricia; Kraus, Cornelia; Trautmann, Udo; Zenker, Martin; Zweier, Christiane; Wiesener, Antje; Abou Jamra, Rami; Kunstmann, Erdmute; Wieczorek, Dagmar; Uebe, Steffen; Ferrazzi, Fulvia; Büttner, Christian; Ekici, Arif B.; Rauch, Anita; Sticht, Heinrich; Dörr, Helmuth-Günther; Reis, André; Thiel, Christian T.

    Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature

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    Elsevier BV, 2018

    Published in: Genetics in Medicine

  11. Hauer, Nadine N.; Sticht, Heinrich; Boppudi, Sangamitra; Büttner, Christian; Kraus, Cornelia; Trautmann, Udo; Zenker, Martin; Zweier, Christiane; Wiesener, Antje; Jamra, Rami Abou; Wieczorek, Dagmar; Kelkel, Jaqueline; Jung, Anna-Maria; Uebe, Steffen; Ekici, Arif. B; Rohrer, Tilman; Reis, André; Dörr, Helmuth-Günther; Thiel, Christian T.

    Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature

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    Springer Science and Business Media LLC, 2017

    Published in: Scientific Reports

  12. Begemann, Anaïs; Sticht, Heinrich; Begtrup, Amber; Vitobello, Antonio; Faivre, Laurence; Banka, Siddharth; Alhaddad, Bader; Asadollahi, Reza; Becker, Jessica; Bierhals, Tatjana; Brown, Kathleen E.; Bruel, Ange-Line; Brunet, Theresa; Carneiro, Maryline; Cremer, Kirsten; Day, Robert; Denommé-Pichon, Anne-Sophie; Dyment, Dave A.; Engels, Hartmut; Fisher, Rachel; Goh, Elaine S.; Hajianpour, M.J.; Haertel, Lucia Ribeiro Machado; Hauer, Nadine; [...]

    New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics

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    Elsevier BV, 2021

    Published in: Genetics in Medicine