Resultados de procura - Kerstin Becker
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Monoubiquitylation promotes mitochondrial p53 translocation por N D Marchenko, Sonja Wolff, Susan Erster, Kerstin Becker, Ute M. Moll
Publicado 2007Artigo -
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Safety of Dienogest and Other Hormonal Treatments for Endometriosis in Real-World Clinical Practice (VIPOS): A Large Noninterventional Study por Klaas Heinemann, Bruno Imthurn, Lena Marions, Christoph Gerlinger, Kerstin Becker, Sabine Moehner, Thomas Faustmann
Publicado 2020Artigo -
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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... por Suzanne Reed, Carol E. Koro, Julia DiBello, Kerstin Becker, Anja Bauerfeind, Christian Franke, Klaas Heinemann
Publicado 2021Artigo -
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Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomas por 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
Publicado 2016Artigo -
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A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease por 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
Publicado 2024Revisão -
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A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis por 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
Publicado 2017Artigo -
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Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length por 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
Publicado 2013Artigo -
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Expanding the genotypic spectrum of Perrault syndrome por 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
Publicado 2016Artigo -
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Wnt Signaling and Dupuytren's Disease por 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
Publicado 2011Artigo -
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Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With <i>BRCA</i>-Like Genomic Aberrations por 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
Publicado 2024Artigo -
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Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia por 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
Publicado 2018Artigo -
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The genomic landscape across 474 surgically accessible epileptogenic human brain lesions por 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
Publicado 2022Artigo -
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Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions por 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
Publicado 2024Artigo -
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The genomic and clinical landscape of fetal akinesia por 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
Publicado 2019Artigo -
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Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients por 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
Publicado 2015Artigo -
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Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome por 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
Publicado 2018Artigo
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Materias Relacionadas
Biology
Medicine
Genetics
Gene
Internal medicine
Bioinformatics
Computational biology
Disease
Mutation
Cancer research
Cell biology
Genome
Genotype
Pathology
Cancer
Genome-wide association study
Gynecology
Neuroscience
Oncology
Phenotype
Single-nucleotide polymorphism
Surgery
Allele
Apoptosis
Ataxia
Biochemistry
Chemotherapy
Confidence interval
Contracture
DNA