Torthaí cuardaigh - Kerstin Becker

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  1. 1
    A role of HAUSP in tumor suppression in a human colon carcinoma xenograft model

    A role of HAUSP in tumor suppression in a human colon carcinoma xenograft model de réir Kerstin Becker, Natalia Marchenko, Gustavo Palacios, Ute M. Moll

    Foilsithe / Cruthaithe 2008
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  2. 2
    Monoubiquitylation promotes mitochondrial p53 translocation

    Monoubiquitylation promotes mitochondrial p53 translocation de réir N D Marchenko, Sonja Wolff, Susan Erster, Kerstin Becker, Ute M. Moll

    Foilsithe / Cruthaithe 2007
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  3. 3
    Safety of Dienogest and Other Hormonal Treatments for Endometriosis in Real-World Clinical Practice (VIPOS): A Large Noninterventional Study

    Safety of Dienogest and Other Hormonal Treatments for Endometriosis in Real-World Clinical Practice (VIPOS): A Large Noninterventional Study de réir Klaas Heinemann, Bruno Imthurn, Lena Marions, Christoph Gerlinger, Kerstin Becker, Sabine Moehner, Thomas Faustmann

    Foilsithe / Cruthaithe 2020
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  4. 4
    Stress-mediated nuclear stabilization of p53 is regulated by ubiquitination and importin-α3 binding

    Stress-mediated nuclear stabilization of p53 is regulated by ubiquitination and importin-α3 binding de réir N D Marchenko, Walter Hanel, Dun Li, Kerstin Becker, Nancy C. Reich, Ute M. Moll

    Foilsithe / Cruthaithe 2009
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  5. 5
    Three-Dimensional Cell Growth Confers Radioresistance by Chromatin Density Modification

    Three-Dimensional Cell Growth Confers Radioresistance by Chromatin Density Modification de réir Katja Storch, Iris Eke, Kerstin Borgmann, Mechthild Krause, Christian Richter, Kerstin Becker, Evelin Schröck, Nils Cordes

    Foilsithe / Cruthaithe 2010
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  6. 6
    Real world data on symptomology and diagnostic approaches of 27,840 women living with endometriosis

    Real world data on symptomology and diagnostic approaches of 27,840 women living with endometriosis de réir Kerstin Becker, Klaas Heinemann, Bruno Imthurn, Lena Marions, Sabine Moehner, Christoph Gerlinger, Marco Serrani, Thomas Faustmann

    Foilsithe / Cruthaithe 2021
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  7. 7
    Prospective controlled cohort study on the safety of a monophasic oral contraceptive containing nomegestrol acetate (2.5mg) and 17β-oestradiol (1.5mg) (PRO-E2 study): risk of venous and arterial thromboembolism

    Prospective controlled cohort study on the safety of a monophasic oral contraceptive containing nomegestrol acetate (2.5mg) and 17β-oestradiol (1.5mg) (PRO-E2 study): risk of venou... de réir Suzanne Reed, Carol E. Koro, Julia DiBello, Kerstin Becker, Anja Bauerfeind, Christian Franke, Klaas Heinemann

    Foilsithe / Cruthaithe 2021
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  8. 8
    Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomas

    Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomas de réir Khalil Abou‐El‐Ardat, Michael Seifert, Kerstin Becker, Sophie Eisenreich, Matthias Lehmann, Karl Hackmann, Andreas Rump, Gerrit A. Meijer, Beatriz Carvalho, Achim Temme, Gabriele Schackert, Evelin Schröck, Dietmar Krex, Barbara Klink

    Foilsithe / Cruthaithe 2016
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  9. 9
    A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease

    A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease de réir Sophie A. Riesmeijer, Zoha Kamali, Michael Ng, Dmitriy Drichel, Bram Piersma, Kerstin Becker, T. B. Layton, Jagdeep Nanchahal, Michael Nothnagel, Ahmad Vaez, Hans Christian Hennies, Paul M. N. Werker, Dominic Furniss, Ilja M. Nolte

    Foilsithe / Cruthaithe 2024
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  10. 10
    A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis

    A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis de réir Michael Ng, Dipti Thakkar, Lorraine Southam, Paul M. N. Werker, Roel A. Ophoff, Kerstin Becker, Michael Nothnagel, André Franke, Peter Nürnberg, Ana Isabel Espirito-Santo, David Izadi, Hans Christian Hennies, Jagdeep Nanchahal, Eleftheria Zeggini, Dominic Furniss

    Foilsithe / Cruthaithe 2017
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  11. 11
    Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length

    Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length de réir Katja‐Martina Eckl, Rotem Tidhar, Holger Thiele, Vinzenz Oji, Ingrid Haußer, Susanne Brodesser, Marie-Luise Preil, Aysel Önal-Akan, Friedrich Stock, Dietmar Müller, Kerstin Becker, Ramona Casper, Gudrun Nürnberg, Janine Altmüller, Peter Nürnberg, Heiko Traupe, Anthony H. Futerman, Hans Christian Hennies

    Foilsithe / Cruthaithe 2013
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  12. 12
    Expanding the genotypic spectrum of Perrault syndrome

    Expanding the genotypic spectrum of Perrault syndrome de réir Leigh Demain, Jill Urquhart, James O’Sullivan, Simon G. Williams, Sanjeev S. Bhaskar, Emma M. Jenkinson, Charles Marques Lourenço, Arvid Heiberg, Simon H. S. Pearce, Stavit A. Shalev, Wyatt W. Yue, Sabrina MacKinnon, Kevin J. Munro, Ruth Newbury‐Ecob, Kerstin Becker, M.J. Kim, Raymond T. O. Keefe, William G. Newman

    Foilsithe / Cruthaithe 2016
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  13. 13
    Wnt Signaling and Dupuytren's Disease

    Wnt Signaling and Dupuytren's Disease de réir Guido H. Dolmans, Paul M. N. Werker, Hans Christian Hennies, Dominic Furniss, Eleonora A. Festen, Lude Franke, Kerstin Becker, Pieter van der Vlies, Bruce H. R. Wolffenbuttel, Sigrid Tinschert, Mohammad R. Toliat, Michael Nothnagel, André Franke, Norman Klopp, H. E. Wichmann, Peter Nürnberg, Henk Giele, Roel A. Ophoff, Cisca Wijmenga

    Foilsithe / Cruthaithe 2011
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  14. 14
    Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With <i>BRCA</i>-Like Genomic Aberrations

    Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With <i>BRCA</i>-Like Genomic Aberrations de réir Philip C. Schouten, Sandra Schmidt, Kerstin Becker, Hölger Thiele, Peter Nürnberg, Lisa Richters, Corinna Ernst, Isabelle Treilleux, Jacques Médioni, Florian Heitz, Carmela Pisano, Yolanda García García, Edgar Petru, Sakari Hietanen, Nicoletta Colombo, Ignace Vergote, Shoji Nagao, Sabine C. Linn, Éric Pujade-Lauraine, Isabelle Ray‐Coquard, Philipp Harter, Eric Hahnen, Rita K. Schmutzler

    Foilsithe / Cruthaithe 2024
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  15. 15
    Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia

    Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia de réir Sharissa L. Latham, Nadja Ehmke, P. Reinke, Manuel H. Taft, Dorothee Eicke, Theresia Reindl, Werner Stenzel, Michael J. Lyons, Michael J. Friez, Jennifer A. Lee, Ramona Hecker, Michael C. Frühwald, Kerstin Becker, Teresa Neuhann, Denise Horn, Evelin Schröck, Indra Niehaus, Katharina Sarnow, Konrad Grützmann, Luzie Gawehn, Barbara Klink, Andreas Rump, Christine Chaponnier, Constança Figueiredo, Ralf Knöfler, Dietmar J. Manstein, Nataliya Di Donato

    Foilsithe / Cruthaithe 2018
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  16. 16
    The genomic landscape across 474 surgically accessible epileptogenic human brain lesions

    The genomic landscape across 474 surgically accessible epileptogenic human brain lesions de réir Javier A. López-Rivera, Costin Leu, Marie Macnee, Jean Khoury, Lucas Hoffmann, Roland Coras, Katja Kobow, Nisha Bhattarai, Eduardo Pérez‐Palma, Hajo M. Hamer, Sebastian Brandner, Karl Rössler, Christian G. Bien, Thilo Kalbhenn, Tom Pieper, Till Hartlieb, Elizabeth Butler, Giulio Genovese, Kerstin Becker, Janine Altmüller, Lisa-Marie Niestroj, Lisa Ferguson, Robyn M. Busch, Peter Nürnberg, Imad Najm, Ingmar Blümcke, Dennis Lal

    Foilsithe / Cruthaithe 2022
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  17. 17
    Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions

    Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions de réir Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão, Fabian Kilpert, Georg Sebastian Hönes, Sabine Kaya, Christopher Schröder, Andreas Thieme, Marc Sturm, Joohyun Park, Agatha Schlüter, Montserrat Ruíz, Moisés Morales de la Prida, Carlos Casasnovas, Kerstin Becker, Ulla Roggenbuck, Sonali Pechlivanis, Frank J. Kaiser, Matthis Synofzik, Thomas Wirth, Mathieu Anheim, Tobias B. Haack, Paul J. Lockhart, Karl‐Heinz Jöckel, Aurora Pujol, Stephan Klebe, Dagmar Timmann, Christel Depienne

    Foilsithe / Cruthaithe 2024
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  18. 18
    The genomic and clinical landscape of fetal akinesia

    The genomic and clinical landscape of fetal akinesia de réir Matthias Pergande, Susanne Motameny, Özkan Özdemir, Mona Kreutzer, Haicui Wang, Hülya‐Sevcan Daimagüler, Kerstin Becker, Mert Karakaya, Harald Ehrhardt, Nursel Elçioğlu, Slavica Ostojić, Cho‐Ming Chao, Amit Kawalia, Özgür Duman, Anne Koy, Andreas Hahn, Jens Reimann, Katharina Schoner, Anne Schänzer, Jens H. Westhoff, Eva Maria Christina Schwaibold, Mireille Cossée, Marion Imbert‐Bouteille, Harald von Pein, Göknur Haliloğlu, Haluk Topaloğlu, Janine Altmüller, Peter Nürnberg, Hölger Thiele, Raoul Heller, Sebahattin Çırak

    Foilsithe / Cruthaithe 2019
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  19. 19
    Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients

    Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients de réir Katharina König, Martin Peifer, Jana Fassunke, Michaela A. Ihle, Helen Künstlinger, Carina Heydt, Katrin Stamm, Rebecca Roth, Claudia Vollbrecht, Marc Bos, Masyar Gardizi, Matthias Scheffler, Lucia Nogová, Frauke Leenders, Kerstin Albus, Lydia Meder, Kerstin Becker, Alexandra Florin, Ursula Rommerscheidt‐Fuss, Janine Altmüller, Michael Kloth, Peter Nürnberg, Thomas Henkel, Sven-Ernö Bikár, Martin L. Sos, William J. Geese, Lewis C. Strauss, Yon‐Dschun Ko, Ulrich Gerigk, Margarete Odenthal, Thomas Zander, Jürgen Wolf, Sabine Merkelbach‐Bruse, Reinhard Buettner, Lukas C. Heukamp

    Foilsithe / Cruthaithe 2015
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  20. 20
    Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

    Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome de réir Shereen G. Ghosh, Kerstin Becker, He Huang, Tracy Dixon‐Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al‐Gazali, Quinten Waisfisz, Haicui Wang, Keith K. Vaux, Valentina Stanley, Andreea Manole, Uğur Akpulat, Marjan M. Weiss, Stéphanie Efthymiou, Michael G. Hanna, Carlo Minetti, Pasquale Striano, Livia Pisciotta, Elisa De Grandis, Janine Altmüller, Lisa Weixler, Peter Nürnberg, Hölger Thiele, Uluç Yiş, Tuncay Derya Okur, Ayşe Polat, Nafise Amiri, Mohammad Doosti, Ehsan Ghayoor Karimani, Mehran Beiraghi Toosi, Gabriel Haddad, Mert Karakaya, Brunhilde Wirth, Johanna M. van Hagen, Nicole I. Wolf, Reza Maroofian, Henry Houlden, Sebahattin Çırak, Joseph G. Gleeson

    Foilsithe / Cruthaithe 2018
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