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  1. Schmitt, Ramona [Author]; Tscheuschler, Anke [Author]; Meffert-Laschinski, Philipp [Author]; Uffelmann, Xenia [Author]; Discher, Philipp [Author]; Fuchs, Jana [Author]; Kreibich, Maximilian [Author]; Peyronnet, Remi [Author]; Kari, Fabian Alexander [Author]

    A potential key mechanism in ascending aortic aneurysm development: Detection of a linear relationship between MMP-14/TIMP-2 ratio and active MMP-2

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    San Francisco, California, US: Public Library of Science (PLoS), 2019

    Published in: PLOS ONE ; 14, 2 (2019), e0212859$z1932-6203

  2. Barthe, Christoph [Author]; Gericke, Jan [Author]; Allgayer, Angelika [Author]; Appl, Ekkehard [Author]; Bartel, Louisa [Author]; Diemer, Herbert [Author]; Feilcke, Burkhard [Author]; Fischer, Thomas [Author]; Geilhorn, Alexandra [Author]; Glaser, Michael [Author]; Gmel, Duscha [Author]; Graf, Jürgen Peter [Author]; Greven, Michael [Author]; Hadamitzky, Anke [Author]; Heil, Henning [Author]; Henrichs, Simon [Author]; Jakobs, Sebastian [Author]; Krehl, Christoph [Author]; Lohse, Kai [Author]; Maur, Lothar [Author]; Mayer, Herbert [Author]; Moldenhauer, Gerwin M. [Author]; Paul, Carsten Otto Georg [Author]; Peterson, Ines [Author]; [...] ; Barthe, Christoph [Editor]; Gericke, Jan [Editor]

    Karlsruher Kommentar zur Strafprozessordnung : mit GVG, EGGVG und EMRK - [9., neu bearbeitete Auflage]

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    München: C.H. Beck, 2023

    Published in: Beck-online ; Bücher

  3. Hannich, Rolf [Author]; Appl, Ekkehard [Author]; Bartel, Louisa [Author]; Barthe, Christoph [Author]; Bruns, Michael [Author]; Diemer, Herbert [Author]; Feilcke, Burkhard [Author]; Fischer, Thomas [Author]; Gericke, Jan [Author]; Gmel, Duscha [Author]; Graf, Jürgen Peter [Author]; Greger, Anette [Author]; Greven, Michael [Author]; Griesbaum, Rainer [Author]; Hadamitzky, Anke [Author]; Jakobs, Sebastian [Author]; Krehl, Christoph [Author]; Kuckein, Jürgen-Detlef [Author]; Lohse, Kai [Author]; Maul, Heinrich [Author]; Maur, Lothar [Author]; Mayer, Herbert [Author]; Moldenhauer, Gerwin M. [Author]; Paul, Carsten Otto Georg [Author]; [...] ; Hannich, Rolf [Editor]

    Karlsruher Kommentar zur Strafprozessordnung : mit GVG, EGGVG und EMRK - [8., neu bearbeitete Auflage]

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    München: C.H. Beck, 2019

    Published in: Beck-online ; Bücher

  4. Geiger, Pamina Xenia Charlotte [Author] ; Reuning, Ute [Degree supervisor]; Schmitt, Manfred [Degree supervisor]; Rummeny, Ernst J. [Degree supervisor]

    Einfluss des Metastasierungssuppressors KAI1 CD 82 auf das Integrin αvβ3-vermittelte Migrations- und <em>spreading</em>-Verhalten humaner Ovarialkarzinomzellen

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    München: Universitätsbibliothek der TU München, 2012

  6. Schmitt, Ramona; Tscheuschler, Anke; Laschinski, Philipp; Uffelmann, Xenia; Discher, Philipp; Fuchs, Jana; Kreibich, Maximilian; Peyronnet, Remi; Kari, Fabian A.

    A potential key mechanism in ascending aortic aneurysm development: Detection of a linear relationship between MMP-14/TIMP-2 ratio and active MMP-2

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    Public Library of Science (PLoS), 2019

    Published in: PLOS ONE, 14 (2019) 2, Seite e0212859

  7. Gatzweiler, Charlotte; Ridinger, Johannes; Herter, Sonja; Gerloff, Xenia F.; ElHarouni, Dina; Berker, Yannick; Imle, Roland; Schmitt, Lukas; Kreth, Sina; Stainczyk, Sabine; Ayhan, Simay; Najafi, Sara; Krunic, Damir; Frese, Karen; Meder, Benjamin; Reuss, David; Fiesel, Petra; Schramm, Kathrin; Blattner-Johnson, Mirjam; Jones, David T. W.; Banito, Ana; Westermann, Frank; Oppermann, Sina; Milde, Till; [...]

    Functional Therapeutic Target Validation Using Pediatric Zebrafish Xenograft Models

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    MDPI AG, 2022

    Published in: Cancers, 14 (2022) 3, Seite 849

  8. Nizon, Mathilde; Cogne, Benjamin; Vallat, Jean-Michel; Joubert, Madeleine; Liet, Jean-Michel; Simon, Laure; Vincent, Marie; Küry, Sébastien; Boisseau, Pierre; Schmitt, Sébastien; Mercier, Sandra; Bénéteau, Claire; Larrose, Catherine; Coste, Marianne; Latypova, Xénia; Péréon, Yann; Mussini, Jean-Marie; Bézieau, Stéphane; Isidor, Bertrand

    Two novel variants in CNTNAP1 in two siblings presenting with congenital hypotonia and hypomyelinating neuropathy

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    Springer Science and Business Media LLC, 2017

    Published in: European Journal of Human Genetics, 25 (2017) 1, Seite 150-152

  9. Sigaud, Romain; Rösch, Lisa; Gatzweiler, Charlotte; Benzel, Julia; von Soosten, Laura; Peterziel, Heike; Selt, Florian; Najafi, Sara; Ayhan, Simay; Gerloff, Xenia F; Hofmann, Nina; Büdenbender, Isabel; Schmitt, Lukas; Foerster, Kathrin I; Burhenne, Jürgen; Haefeli, Walter E; Korshunov, Andrey; Sahm, Felix; van Tilburg, Cornelis M; Jones, David T W; Pfister, Stefan M; Knoerzer, Deborah; Kreider, Brent L; Sauter, Max; [...]

    The first-in-class ERK inhibitor ulixertinib shows promising activity in mitogen-activated protein kinase (MAPK)-driven pediatric low-grade glioma models

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    Oxford University Press (OUP), 2023

    Published in: Neuro-Oncology, 25 (2023) 3, Seite 566-579

  10. Isidor, Bertrand; Küry, Sébastien; Rosenfeld, Jill A.; Besnard, Thomas; Schmitt, Sébastien; Joss, Shelagh; Davies, Sally J; Roger Lebel, Robert; Henderson, Alex; Schaaf, Christian P.; Streff, Haley E.; Yang, Yaping; Jain, Vani; Chida, Nodoka; Latypova, Xenia; Caignec, Cédric Le; Cogné, Benjamin; Mercier, Sandra; Vincent, Marie; Colin, Estelle; Bonneau, Dominique; Denommé, Anne-Sophie; Parent, Philippe; Gilbert-Dussardier, Brigitte; [...]

    De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment GeneCHAMP1Cause Syndromic Intellectual Disability

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    Hindawi Limited, 2016

    Published in: Human Mutation, 37 (2016) 4, Seite 354-358

  11. Petrovski, Slavé; Küry, Sébastien; Myers, Candace T.; Anyane-Yeboa, Kwame; Cogné, Benjamin; Bialer, Martin; Xia, Fan; Hemati, Parisa; Riviello, James; Mehaffey, Michele; Besnard, Thomas; Becraft, Emily; Wadley, Alexandrea; Politi, Anya Revah; Colombo, Sophie; Zhu, Xiaolin; Ren, Zhong; Andrews, Ian; Dudding-Byth, Tracy; Schneider, Amy L.; Wallace, Geoffrey; Rosen, Aaron B.I.; Schelley, Susan; Enns, Gregory M.; [...]

    Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

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    Elsevier BV, 2016

    Published in: The American Journal of Human Genetics, 98 (2016) 5, Seite 1001-1010

  12. Küry, Sébastien; Besnard, Thomas; Ebstein, Frédéric; Khan, Tahir N.; Gambin, Tomasz; Douglas, Jessica; Bacino, Carlos A.; Craigen, William J.; Sanders, Stephan J.; Lehmann, Andrea; Latypova, Xénia; Khan, Kamal; Pacault, Mathilde; Sacharow, Stephanie; Glaser, Kimberly; Bieth, Eric; Perrin-Sabourin, Laurence; Jacquemont, Marie-Line; Cho, Megan T.; Roeder, Elizabeth; Denommé-Pichon, Anne-Sophie; Monaghan, Kristin G.; Yuan, Bo; Xia, Fan; [...]

    De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder

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    Elsevier BV, 2017

    Published in: The American Journal of Human Genetics, 100 (2017) 2, Seite 352-363

  13. Küry, Sébastien; Besnard, Thomas; Ebstein, Frédéric; Khan, Tahir N.; Gambin, Tomasz; Douglas, Jessica; Bacino, Carlos A.; Craigen, William J.; Sanders, Stephan J.; Lehmann, Andrea; Latypova, Xénia; Khan, Kamal; Pacault, Mathilde; Sacharow, Stephanie; Glaser, Kimberly; Bieth, Eric; Perrin-Sabourin, Laurence; Jacquemont, Marie-Line; Cho, Megan T.; Roeder, Elizabeth; Denommé-Pichon, Anne-Sophie; Monaghan, Kristin G.; Yuan, Bo; Xia, Fan; [...]

    De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder

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    Elsevier BV, 2017

    Published in: The American Journal of Human Genetics, 100 (2017) 4, Seite 689

  14. Küry, Sébastien; van Woerden, Geeske M.; Besnard, Thomas; Proietti Onori, Martina; Latypova, Xénia; Towne, Meghan C.; Cho, Megan T.; Prescott, Trine E.; Ploeg, Melissa A.; Sanders, Stephan; Stessman, Holly A.F.; Pujol, Aurora; Distel, Ben; Robak, Laurie A.; Bernstein, Jonathan A.; Denommé-Pichon, Anne-Sophie; Lesca, Gaëtan; Sellars, Elizabeth A.; Berg, Jonathan; Carré, Wilfrid; Busk, Øyvind Løvold; van Bon, Bregje W.M.; Waugh, Jeff L.; Deardorff, Matthew; [...]

    De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

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    Elsevier BV, 2017

    Published in: The American Journal of Human Genetics, 101 (2017) 5, Seite 768-788