Αποτελέσματα αναζήτησης - Roland Krause
- Εμφανίζονται 1 - 20 Αποτελέσματα από 29
- Μετάβαση στην Επόμενη Σελίδα
-
1
-
2
-
3
-
4
70S-scanning initiation is a novel and frequent initiation mode of ribosomal translation in bacteria από Hiroshi Yamamoto, Daniela Wittek, Romi Gupta, Bo Qin, Takuya Ueda, Roland Krause, Kaori Yamamoto, Renate Albrecht, Markus Pech, Knud H. Nierhaus
Έκδοση 2016Artigo -
5
Identification of tightly regulated groups of genes during <i>Drosophila melanogaster</i> embryogenesis από Sean Hooper, Stéphanie Boué, Roland Krause, Lars Juhl Jensen, Christopher E. Mason, Murad Ghanim, Kevin P. White, Eileen E. M. Furlong, Peer Bork
Έκδοση 2007Artigo -
6
Mutation in the Transcriptional Regulator PhoP Contributes to Avirulence of Mycobacterium tuberculosis H37Ra Strain από Jong Seok Lee, Roland Krause, J. Schreiber, Hans‐Joachim Mollenkopf, Jane Kowall, Robert C. Stein, Bo‐Young Jeon, Jeong-Yeon Kwak, Min-Kyong Song, Juan Pablo Patron, Sabine Jörg, Kyoungmin Roh, Sang-Nae Cho, Stefan H. E. Kaufmann
Έκδοση 2008Artigo -
7
Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders από Katherine Crawford, Julie Xian, Katherine L. Helbig, Peter D. Galer, Shridhar Parthasarathy, David Lewis‐Smith, Michael C. Kaufman, Eryn Fitch, Shiva Ganesan, Margaret O’Brien, Veronica Codoni, Colin A. Ellis, Laura Conway, Deanne Taylor, Roland Krause, Ingo Helbig
Έκδοση 2021Artigo -
8
Ten simple rules for making training materials FAIR από Leyla García, Bérénice Batut, Melissa L. Burke, Mateusz Kuzak, Fotis Psomopoulos, Ricardo Arcila, Teresa K. Attwood, Niall Beard, Denise Carvalho‐Silva, Alexandros C. Dimopoulos, Victoria Domínguez Del Angel, Michel Dumontier, Kim Gurwitz, Roland Krause, Peter McQuilton, Loredana Le Pera, Sarah Morgan, Päivi Rauste, Allegra Via, Pascal Kahlem, Gabriella Rustici, Celia van Gelder, Patricia M. Palagi
Έκδοση 2020Editorial -
9
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy από Katri Silvennoinen, Nikola de Lange, Sara Zagaglia, Simona Balestrini, Ganna Androsova, Merel Wassenaar, Pauls Auce, Andreja Avberšek, Felicitas Becker, Bianca Berghuis, Ellen Campbell, Antonietta Coppola, Ben Francis, Stefan Wolking, Gianpiero L. Cavalleri, John Craig, Norman Delanty, Michael R. Johnson, Bobby P.C. Koeleman, Wolfram S. Kunz, Holger Lerche, Anthony G Marson, Terence J. O’Brien, Josemir W. Sander, Graeme J. Sills, Pasquale Striano, Federico Zara, Job van der Palen, Roland Krause, Chantal Depondt, Sanjay M. Sisodiya
Έκδοση 2019Artigo -
10
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders από Dennis Lal, Patrick May, Eduardo Pérez‐Palma, Kaitlin E. Samocha, Jack A. Kosmicki, Elise Robinson, Rikke S. Møller, Roland Krause, Peter Nürnberg, Sarah Weckhuysen, Peter De Jonghe, Renzo Guerrini, Lisa Marie Niestroj, Juliana Du, Carla Marini, James S. Ware, Mitja Kurki, Padhraig Gormley, Sha Tang, Sitao Wu, Saskia Biskup, Annapurna Poduri, Bernd A. Neubauer, Bobby P.C. Koeleman, Katherine L. Helbig, Yvonne G. Weber, Ingo Helbig, Amit R. Majithia, Aarno Palotie, Mark J. Daly
Έκδοση 2020Artigo -
11
Genome-wide association meta-analyses of drug-resistant epilepsy από Costin Leu, Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed, Caitlin A. Bennett, Lina Jönsson, Unnur Unnsteinsdóttir, Andrea Jorgensen, Gianpiero L. Cavalleri, Norman Delanty, John Craig, Chantal Depondt, Michael R. Johnson, Bobby P.C. Koeleman, Emadeldin Hassanin, Maryam Omidvar, Roland Krause, Holger Lerche, Anthony G Marson, Terence J. O’Brien, Josemir W. Sander, Graeme J. Sills, Pasquale Striano, Federico Zara, Hreinn Stefánsson, Hreinn Stefánsson, Patrick May, Benjamin M. Neale, Dennis Lal, Samuel F. Berkovic, Sanjay M. Sisodiya
Έκδοση 2025Revisão -
12
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features από Cristina Elena Niturad, Dorit Lev, Vera M. Kalscheuer, Agnieszka Charzewska, Julian Schubert, Tally Lerman‐Sagie, Hester Y. Kroes, Renske Oegema, Monica Traverso, Nicola Specchio, Maria Lassota, Jamel Chelly, Odeya Bennett-Back, Nirit Carmi, Tal Koffler-Brill, Michele Iacomino, Marina Trivisano, Giuseppe Capovilla, Pasquale Striano, Magdalena Nawara, Sylwia Rzońca, Ute Fischer, Melanie Bienek, Corinna Jensen, Hao Hu, Hölger Thiele, Janine Altmüller, Roland Krause, Patrick May, Felicitas Becker, Rudi Balling, Saskia Biskup, Stefan A. Haas, Peter Nürnberg, Koen L.I. van Gassen, Holger Lerche, Federico Zara, Snezana Maljevic, Esther Leshinsky‐Silver
Έκδοση 2017Artigo -
13
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy από Steffen Syrbe, Ulrike B. S. Hedrich, Erik Riesch, Tania Djémié, Stephan A. Müller, Rikke S. Møller, Bridget H. Maher, Laura Hernandez‐Hernandez, Matthis Synofzik, Hande Çağlayan, Mutluay Arslan, José M. Serratosa, Michael Nothnagel, Patrick May, Roland Krause, H. Löffler, Katja Detert, Thomas Dorn, Heinrich Vogt, Günter Krämer, Lüdger Schöls, Primus E. Mullis, Tarja Linnankivi, Anna-Elina Lehesjoki, Katalin Štěrbová, Dana Craiu, Dorota Hoffman‐Zacharska, Christian Korff, Yvonne G. Weber, Maja Steinlin, Sabina Gallati, Astrid Bertsche, Matthias K. Bernhard, Andreas Merkenschlager, Wieland Kieß, Michael Gonzalez, Stephan Züchner, Aarno Palotie, Arvid Suls, Peter De Jonghe, Ingo Helbig, Saskia Biskup, Markus Wolff, Snezana Maljevic, Rebecca Schüle, Sanjay M. Sisodiya, Sarah Weckhuysen, Holger Lerche, Johannes R. Lemke
Έκδοση 2015Artigo -
14
<i>CHD2</i>variants are a risk factor for photosensitivity in epilepsy από Elizabeth Galizia, Candace T. Myers, Costin Leu, Carolien G. F. de Kovel, Tatiana Afrikanova, María Lorena Cordero-Maldonado, Teresa G. Martins, Maxime Jacmin, Suzanne Drury, Krishna Chinthapalli, Hiltrud Muhle, Manuela Pendziwiat, Thomas Sander, Ann-Kathrin Ruppert, Rikke S. Møller, Hölger Thiele, Roland Krause, Julian Schubert, Anna-Elina Lehesjoki, Peter Nürnberg, Holger Lerche, Aarno Palotie, Antonietta Coppola, Salvatore Striano, Luigi Del Gaudio, C. R. Boustred, Amy L. Schneider, Nicholas Lench, Bosanka Jocić-Jakubi, Athanasios Covanis, Giuseppe Capovilla, Pierangelo Veggiotti, Marta Piccioli, Pasquale Parisi, Laura Cantonetti, Lynette G. Sadleir, Saul A. Mullen, Samuel F. Berkovic, Ulrich Stephani, Ingo Helbig, Alexander D. Crawford, Camila V. Esguerra, Dorothee Kasteleijn‐Nolst Trenité, Bobby P.C. Koeleman, Heather C. Mefford, Ingrid E. Scheffer, Sanjay M. Sisodiya
Έκδοση 2015Artigo -
15
The association between frailty and MRI features of cerebral small vessel disease από Ilse Kant, Henk J. M. M. Mutsaerts, Simone J.T. van Montfort, Myriam G. Jaarsma‐Coes, Theodoor D. Witkamp, Georg Winterer, Claudia Spies, Jeroen Hendrikse, Arjen J. C. Slooter, Jeroen de Bresser, Franz Paul Armbruster, Axel Böcher, Diana Boraschi, Friedrich Borchers, Giacomo Della Camera, Edwin van Dellen, Ina Diehl, Thomas Dschietzig, Insa Feinkohl, Ariane Fillmer, Jürgen Gallinat, Bettina Hafen, Katarina Hartmann, Karsten Heidtke, Anja Helmschrodt, Paola Italiani, Bernd Ittermann, Roland Krause, Marion Kronabel, Simone Kühn, Gunnar Lachmann, Daniela Melillo, David Menon, Laura Moreno-López, Rudolf Mörgeli, Peter Nürnberg, Kwaku Ofosu, Maria Olbert, Malte Pietzsch, Tobias Pischon, Jacobus Preller, Jana Ruppert, Reinhard Schneider, Emmanuel A. Stamatakis, Simon Weber, Marius Weyer, Stefan Winzeck, Alissa Wolf, Fatima Yürek, Norman Zacharias
Έκδοση 2019Artigo -
16
<i>CHD2</i> myoclonic encephalopathy is frequently associated with self-induced seizures από Rhys H. Thomas, Lin Mei Zhang, Gemma L. Carvill, John S. Archer, Sinéad B. Heavin, Simone Mandelstam, Dana Craiu, Samuel F. Berkovic, Deepak Gill, Heather C. Mefford, Ingrid E. Scheffer, Aarno Paalotie, Anna‐Elina Lehesjoki, Bobby P.C. Koeleman, Carla Marini, Christel Depienne, Dana Craiu, Deb K. Pal, Dorota Hoffman‐Zacharska, Eric LeGuern, Federico Zara, Felix Rosenow, Hande Çağlayan, Helle Hjalgrim, Hiltrud Muhle, Holger Lerche, Ingo Helbig, Johanna Jähn, Johannes R. Lemke, José M. Serratosa, Kaja Kristine Selmer, Karl Martin Klein, Katalin Štěrbová, Manuela Pendziwiat, Nina Barišić, Padhraig Gormley, Pasquale Striano, Patrick May, Peter De Jonghe, Renzo Guerrini, Rikke S. Møller, Roland Krause, Rudi Balling, Sanjay M. Sisodiya, Sarah von Spiczak, Sarah Weckhuysen, Stéphanie Baulac, Arvid Suls, Tania Djémié, Tiina Talvik, Ulrich Stephani, Vladimı́r Komárek, Yvonne G. Weber
Έκδοση 2015Artigo -
17
The Human Phenotype Ontology in 2021 από Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu, Leigh Carmody, David Lewis‐Smith, Nicole Vasilevsky, Daniel Daniš, Ganna Balagura, Gareth Baynam, Amy Brower, Tiffany J Callahan, Christopher G. Chute, Johanna L Est, Peter D. Galer, Shiva Ganesan, Matthias Griese, Matthias Haimel, Júlia Pázmándi, Marc Hanauer, Nomi L. Harris, M. J. Hartnett, Maximilian Hastreiter, Fabian Hauck, Yongqun He, Tim Jeske, Hugh Kearney, Gerhard Kindle, Christoph Klein, Katrin Knoflach, Roland Krause, David Lagorce, Julie A. McMurry, Jillian A. Miller, Monica Muñoz‐Torres, Rebecca L. Peters, Christina Rapp, Ana Rath, Shahmir A Rind, Avi Z. Rosenberg, Michael M. Segal, Markus G. Seidel, Damian Smedley, Tomer Talmy, Yarlalu Thomas, Samuel Agyei Wiafe, Julie Xian, Zafer Yüksel, Ingo Helbig, Chris Mungall, Melissa Haendel, Peter N. Robinson
Έκδοση 2020Artigo -
18
Longitudinal multi-omics analysis identifies early blood-based predictors of anti-TNF therapy response in inflammatory bowel disease από Neha Mishra, Konrad Aden, Johanna I. Blase, Nathan Baran, Dora Bordoni, Florian Tran, Claudio Conrad, Diana Avalos, Charlot Jaeckel, Michael Scherer, Signe Bek Sørensen, Silja Hvid Overgaard, Berenice Schulte, Susanna Nikolaus, Guillaume Rey, Gilles Gasparoni, Paul Lyons, Joachim L. Schultze, Jörn Walter, Vibeke Andersen, Aggelos Banos, George Βertsias, Marc Beyer, Dimitrios T. Boumpas, Axel Finckh, André Franke, Michel Georges, Wei Gu, Robert Häsler, Mohamad Jawhara, Amy Kenyon, Christina Kratsch, Roland Krause, Gordan Lauc, Massimo Mangino, Gioacchino Natoli, Marek Ostaszewski, Marija Pezer, Jeroen Raes, Souad Rahmouni, Marilou Ramos‐Pamplona, Benedikt Reiz, Elisa Rosati, Despina Sanoudou, Venkata Satagopam, Reinhard Schneider, Jonas Schulte-Schrepping, Prodromos Sidiropoulos, Kenneth G. C. Smith, Timothy D. Spector, Doris Vandeputte, Sara Vieira‐Silva, Aleksandar Vojta, Stefanie Warnat‐Herresthal, Vlatka Zoldoš, Emmanouil T. Dermitzakis, Stefan Schreiber, Philip Rosenstiel
Έκδοση 2022Artigo -
19
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual parti... από Remi Stevelink, Dania Al‐Toma, Floor E. Jansen, Herm J. Lamberink, Ali A. Asadi‐Pooya, Mohsen Farazdaghi, Gonçalo Cação, Sita Jayalakshmi, Anuja Patil, Çiğdem Özkara, Şenay Aydın, Joanna Gesche, Christoph P. Beier, Linda J. Stephen, Martin J. Brodie, Gopeekrishnan Unnithan, Ashalatha Radhakrishnan, Julia Höfler, Eugen Trinka, Roland Krause, Emanuele Cerulli Irelli, Carlo Di Bonaventura, Jerzy P. Szaflarski, Laura E. Hernández‐Vanegas, Monica L. Moya-Alfaro, Yingying Zhang, Dong Zhou, Nicola Pietrafusa, Nicola Specchio, Giorgi Japaridze, Sándor Beniczky, Mubeen Janmohamed, Patrick Kwan, Marte Syvertsen, Kaja Kristine Selmer, Bernd J. Vorderwülbecke, Martin Holtkamp, Lakshminarayanapuram Gopal Viswanathan, Sanjib Sinha, Betül Baykan, Ebru Altındağ, Felix von Podewils, Juliane Schulz, Udaya Seneviratne, Alejandro Viloria‐Alebesque, Ioannis Karakis, Wendyl D’Souza, Josemir W. Sander, Bobby P.C. Koeleman, Willem M. Otte, Kees P. J. Braun
Έκδοση 2022Revisão -
20
The Human Phenotype Ontology in 2017 από Sebastian Köhler, Nicole Vasilevsky, Mark Engelstad, Erin D. Foster, Julie A. McMurry, Ségolène Aymé, Gareth Baynam, Susan M. Bello, Cornelius F. Boerkoel, Kym M. Boycott, Michael Brudno, Orion J. Buske, Patrick F. Chinnery, Valentina Cipriani, Laureen E. Connell, Hugh Dawkins, Laura E. DeMare, A. Devereau, Bert B.A. de Vries, Helen V. Firth, Kathleen Freson, Daniel Greene, Ada Hamosh, Ingo Helbig, Courtney Hum, Johanna Jähn, Roger James, Roland Krause, Stanley J. F. Laulederkind, Hanns Lochmüller, Gholson J. Lyon, Soichi Ogishima, Annie Olry, Willem H. Ouwehand, Nikolas Pontikos, Ana Rath, Franz Schaefer, Richard H. Scott, Michael M. Segal, Panagiotis I. Sergouniotis, Richard Sever, Cynthia L. Smith, Volker Straub, Rachel Thompson, C. Turner, Ernest Turro, Marijcke W. M. Veltman, Tom Vulliamy, Jing Yu, Julie von Ziegenweidt, Andreas Zankl, Stephan Züchner, Tomasz Żemojtel, Julius O.B. Jacobsen, Tudor Groza, Damian Smedley, Chris Mungall, Melissa Haendel, Peter N. Robinson
Έκδοση 2016Revisão
Εργαλεία αναζήτησης:
Σχετικά θέματα
Biology
Gene
Genetics
Medicine
Computational biology
Epilepsy
Bioinformatics
Neuroscience
Phenotype
Genome
Internal medicine
Psychiatry
Computer science
Copy-number variation
Disease
Encephalopathy
Missense mutation
Pathology
Programming language
Botany
Epistemology
Exome
Exome sequencing
Genome-wide association study
Genotype
Identification (biology)
Mutation
Philosophy
Physics
Single-nucleotide polymorphism