Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Roel Smeets"'
Publikováno v:
Journal of Cultural Analytics, Vol 6, Iss 3 (2021)
This essay responds to a lack of scholarly attention for conflict as a narrative mechanism since the formalist models of Vladimir Propp and Algirdas Julien Greimas. Building on recent developments within cultural analytics, the essay argues for a new
Externí odkaz:
https://doaj.org/article/93bea8842dee4cdd9fdef5ffd42597ae
Publikováno v:
Journal of Cultural Analytics, Vol 4, Iss 2 (2019)
Literary history is no longer written in books alone. As literary reception thrivesin blogs, Wikipedia entries, Amazon reviews, and Goodreads profiles, the Webhas become a key platform for the exchange of information on literature.
Externí odkaz:
https://doaj.org/article/f594cd7e6c2f44958fa4646eafdb25e7
Autor:
Roel Smeets
Publikováno v:
Nederlandse Letterkunde. 27:251-253
Autor:
Nurulamin Abu Bakar, Angel Ashikov, Jaime Moritz Brum, Roel Smeets, Marjan Kersten, Karin Huijben, Wee Teik Keng, Carlos Eduardo Speck‐Martins, Daniel Rocha de Carvalho, Isabela Maria Pinto Oliveira de Rizzo, Walquiria Domingues de Mello, Rebecca Heiner‐Fokkema, Kathleen Gorman, Stephanie Grunewald, Helen Michelakakis, Marina Moraitou, Diego Martinelli, Monique van Scherpenzeel, Mirian Janssen, Lonneke de Boer, Lambertus P. van den Heuvel, Christian Thiel, Dirk J. Lefeber
Publikováno v:
Journal of Inherited Metabolic Disease, 45, 769-781
Journal of Inherited Metabolic Disease, 45, 4, pp. 769-781
Journal of Inherited Metabolic Disease, 45(4), 769-781. SPRINGER
Journal of Inherited Metabolic Disease, 45, 4, pp. 769-781
Journal of Inherited Metabolic Disease, 45(4), 769-781. SPRINGER
Contains fulltext : 282651.pdf (Publisher’s version ) (Open Access) Congenital disorders of glycosylation type 1 (CDG-I) comprise a group of 27 genetic defects with heterogeneous multisystem phenotype, mostly presenting with nonspecific neurologica
Autor:
Roel Smeets
Publikováno v:
Elements in Digital Literary Studies. Cambridge : Cambridge University Press
Elements in Digital Literary Studies
Elements in Digital Literary Studies
This Element sheds a new light on the ubiquitous yet complex notion of mimesis. By systematically comparing the social dynamics of the Dutch population at a given time with the social dynamics of characters in Dutch literary fiction published in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611adbb8fed266a430bb3a2c1800fed0
https://repository.ubn.ru.nl/handle/2066/252223
https://repository.ubn.ru.nl/handle/2066/252223
Autor:
Roel Smeets
Fiction has a major social impact, not least because it co-shapes the image that society has of various social groups. Drawing on a collection of 170 contemporary Dutch-language novels, Character Constellations presents a range of data-driven, statis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acec8dbcae768d6399a81a4c6f8e6d6e
https://doi.org/10.11116/9789461664136
https://doi.org/10.11116/9789461664136
Autor:
Helleke Braber, Jeroen Dera, Jos Joosten, Maarten Steenmeijer, Lieke Deinsen, Nina Geerdink, Paul Hulsenboom, Maaike Koffeman, Gaston Franssen, Rob Schoor, Gwennie Debergh, Sander Bax, Linda Ackersmans, Jack McMartin, Laurens Ham, Roel Smeets, Betram Mourits
For many, literature and marketing are considered opposite phenomena. This book discusses cases in which the two are closely connected. It argues that literature is subject to the same mechanisms as other commercial products: our experience of litera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d888821855c928267c4e33793b1fb1
http://hdl.handle.net/2066/232876
http://hdl.handle.net/2066/232876
Autor:
Roel Smeets
Item does not contain fulltext 252 p.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3321f4150c633cf58e4ea60108581eb
https://repository.ubn.ru.nl/handle/2066/252827
https://repository.ubn.ru.nl/handle/2066/252827
Autor:
Angel, Ashikov, Nurulamin, Abu Bakar, Xiao-Yan, Wen, Marco, Niemeijer, Glentino, Rodrigues Pinto Osorio, Koroboshka, Brand-Arzamendi, Linda, Hasadsri, Hana, Hansikova, Kimiyo, Raymond, Dorothée, Vicogne, Nina, Ondruskova, Marleen E H, Simon, Rolph, Pfundt, Sharita, Timal, Roel, Beumers, Christophe, Biot, Roel, Smeets, Marjan, Kersten, Karin, Huijben, Peter T A, Linders, Geert, van den Bogaart, Sacha A F T, van Hijum, Richard, Rodenburg, Lambertus P, van den Heuvel, Francjan, van Spronsen, Tomas, Honzik, Francois, Foulquier, Monique, van Scherpenzeel, Dirk J, Lefeber, Wamelink, Mirjam, Brunner, Han, Mundy, Helen, Michelakakis, Helen, van Hasselt, Peter, van de Kamp, Jiddeke, Martinelli, Diego, Morkrid, Lars, Brocke Holmefjord, Katja, Hertecant, Jozef, Alfadhel, Majid, Carpenter, Kevin, Te Water Naude, Johann
Publikováno v:
CDG group 2018, ' Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation ', Human Molecular Genetics, vol. 27, no. 17, pp. 3029-3045 . https://doi.org/10.1093/hmg/ddy213
Human Molecular Genetics, 27(17), 3029-3045. Oxford University Press
Human Molecular Genetics, 27, 3029-3045
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (17), pp.3029-3045. ⟨10.1093/hmg/ddy213⟩
Human Molecular Genetics, 27(17), 3029. Oxford University Press
Human Molecular Genetics, 27, 17, pp. 3029-3045
Human Molecular Genetics, 2018, 27 (17), pp.3029-3045. ⟨10.1093/hmg/ddy213⟩
Human Molecular Genetics, 27(17), 3029-3045. Oxford University Press
Human Molecular Genetics, 27, 3029-3045
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (17), pp.3029-3045. ⟨10.1093/hmg/ddy213⟩
Human Molecular Genetics, 27(17), 3029. Oxford University Press
Human Molecular Genetics, 27, 17, pp. 3029-3045
Human Molecular Genetics, 2018, 27 (17), pp.3029-3045. ⟨10.1093/hmg/ddy213⟩
Genomics methodologies have significantly improved elucidation of Mendelian disorders. The combination with high-throughput functional-omics technologies potentiates the identification and confirmation of causative genetic variants, especially in sin