Zobrazeno 1 - 10
of 255
pro vyhledávání: '"Suls, Arvid"'
Autor:
Boeren, Marlies, de Vrij, Nicky, Ha, My K., Valkiers, Sebastiaan, Souquette, Aisha, Gielis, Sofie, Kuznetsova, Maria, Schippers, Jolien, Bartholomeus, Esther, Van den Bergh, Johan, Michels, Nele, Aerts, Olivier, Leysen, Julie, Bervoets, An, Lambert, Julien, Leuridan, Elke, Wens, Johan, Peeters, Karin, Emonds, Marie-Paule, Elias, George, Vandamme, Niels, Jansens, Hilde, Adriaensen, Wim, Suls, Arvid, Vanhee, Stijn, Hens, Niel, Smits, Evelien, Van Damme, Pierre, Thomas, Paul G., Beutels, Philippe, Ponsaerts, Peter, Van Tendeloo, Viggo, Delputte, Peter, Laukens, Kris, Meysman, Pieter, Ogunjimi, Benson
Publikováno v:
In Cell Reports 23 April 2024 43(4)
Akademický článek
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Autor:
Vandoren, Romi, Boeren, Marlies, Schippers, Jolien, Bartholomeus, Esther, Mullan, Kerry, Michels, Nele, Aerts, Olivier, Leysen, Julie, Bervoets, An, Lambert, Julien, Leuridan, Elke, Wens, Johan, Peeters, Karin, Emonds, Marie-Paule, Jansens, Hilde, Casanova, Jean-Laurent, Bastard, Paul, Suls, Arvid, Tendeloo, Viggo Van, Ponsaerts, Peter
Publikováno v:
Journal of Infectious Diseases; 9/15/2024, Vol. 230 Issue 3, p706-715, 10p
Autor:
Ha, My Kieu, Bartholomeus, Esther, Van Os, Luc, Dandelooy, Julie, Leysen, Julie, Aerts, Olivier, Siozopoulou, Vasiliki, De Smet, Eline, Gielen, Jan, Guerti, Khadija, De Maeseneer, Michel, Herregods, Nele, Lechkar, Bouchra, Wittoek, Ruth, Geens, Elke, Claes, Laura, Zaqout, Mahmoud, Dewals, Wendy, Lemay, Annelies, Tuerlinckx, David, Weynants, David, Vanlede, Koen, van Berlaer, Gerlant, Raes, Marc, Verhelst, Helene, Boiy, Tine, Van Damme, Pierre, Jansen, Anna C., Meuwissen, Marije, Sabato, Vito, Van Camp, Guy, Suls, Arvid, Werff ten Bosch, Jutte Van der, Dehoorne, Joke, Joos, Rik, Laukens, Kris, Meysman, Pieter, Ogunjimi, Benson
Supplementary Material 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116fca362fb7cb2e144c4acb57de19a6
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Coppola, Antonietta, Cellini, Elena, Stamberger, Hannah, Saarentaus, Elmo, Cetica, Valentina, Lal, Dennis, Djémié, Tania, Bartnik-Glaska, Magdalena, Ceulemans, Berten, Cross, J. Helen, Deconinck, Tine, De Masi, Salvatore, Dorn, Thomas, Guerrini, Renzo, Hoffman-Zacharska, Dorotha, Kooy, Frank, Lagae, Lieven, Lench, Nicholas, Lemke, Johannes R., Lucenteforte, Ersilia, Madia, Francesca, Mefford, Heather C., Morrogh, Deborah, Nuernberg, Peter, Palotie, Aarno, Schoonjans, An-Sofie, Striano, Pasquale, Szczepanik, Elzbieta, Tostevin, Anna, Vermeesch, Joris R., Van Esch, Hilde, Van Paesschen, Wim, Waters, Jonathan J., Weckhuysen, Sarah, Zara, Federico, De Jonghe, Peter, Sisodiya, Sanjay M., Marini, Carla, Lehesjioki, Anna-Elina, Craiu, Dana, Talvik, Tiina, Caglayan, Hande, Serratosa, Jose, Sterbova, Katalin, Moller, Rikke S., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne, Helbig, Ingo, von Spiczak, Sarah, Barba, Carmen, Bogaerts, Anneleen, Boni, Antonella, Galizia, Elisabeth Caruana, Chiari, Sara, Clementella, Claudia, Di Gacomo, Gianpiero, Ferrari, Annarita, Guarducci, Silvia, Giglio, Sabrina, Holmgren, Philip, Leu, Costin, Mari, Francesco, Melani, Federico, Novara, Francesca, Pantaleo, Marilena, Peeters, Elke, Pisano, Tiziana, Rosati, Anna, Sander, Josemir, Schoeler, Natasha, Stankiewicz, Pawel, Striano, Salvatore, Suls, Arvid, Traverso, Monica, Vandeweyer, Geert, Van Dijck, Anke, Zuffardi, Orsetta
Publikováno v:
Epilepsia
OBJECTIVE: Copy number variations (CNVs) represent a significant genetic risk for several neurodevelopmental disorders including epilepsy. As knowledge increases, reanalysis of existing data is essential. Reliable estimates of the contribution of CNV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d64720a02b7a8989ae51ed67af125bf5
https://lirias.kuleuven.be/handle/123456789/636103
https://lirias.kuleuven.be/handle/123456789/636103
Autor:
Bartholomeus, Esther, Neuter, Nicolas De, Lemay, Annelies, Pattyn, Luc, Tuerlinckx, David, Weynants, David, Lede, Koen Van, Gerlant Van Berlaer, Bulckaert, Dominique, Boiy, Tine, Auwera, Ann Vander, Raes, Marc, Linden, Dimitri Van Der, Verhelst, Helene, Steijn, Susanne Van, Jonckheer, Tijl, Dehoorne, Joke, Joos, Rik, Jansens, Hilde, Suls, Arvid, Damme, Pierre Van, Laukens, Kris, Mortier, Geert, Meysman, Pieter, Benson Ogunjimi
Additional file 12: Additional Results. Gene expression differences between enteroviral and bacterial meningitis including the neuroborreliosis case.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e431254ef1b2b6f227e150396a4cf2
Autor:
Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, Partoens, Michele, Balak, Chris, Belnap, Newell, Claasen, Ana, Courtright, Amanda, de Both, Matt, Huentelman, Matthew J., Naymik, Marcus, Richholt, Ryan, Siniard, Ashley L., Szelinger, Szabolcs, Craig, David W., Schrauwen, Isabelle, Afawi, Zaid, Balling, Rudi, Baulac, Stephanie, Barisic, Nina, Caglayan, Hande S., Craiu, Dana, Guerrero-Lopez, Rosa, Guerrini, Renzo, Hjalgrim, Helle, Jahn, Johanna, Klein, Karl Martin, Leguern, Eric, Lemke, Johannes R., Lerche, Holger, Marini, Carla, Moller, Rikke S., Muhle, Hiltrud, Rosenow, Felix, Serratosa, Jose, Suls, Arvid, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Zara, Federico, De Jonghe, Peter
Publikováno v:
Nature Communications
Nature communications
Siekierska, A, Stamberger, H, Deconinck, T, Oprescu, S N, Partoens, M, Zhang, Y, Sourbron, J, Adriaenssens, E, Mullen, P, Wiencek, P, Hardies, K, Lee, J S, Giong, H K, Distelmaier, F, Elpeleg, O, Helbig, K L, Hersh, J, Isikay, S, Jordan, E, Karaca, E, Kecskes, A, Lupski, J R, Kovacs-Nagy, R, May, P, Narayanan, V, Pendziwiat, M, Ramsey, K, Rangasamy, S, Shinde, D N, Spiegel, R, Timmerman, V, von Spiczak, S, Helbig, I, C4RCD Research Group, Møller, R S, Hjalgrim, H, AR working group of the EuroEPINOMICS RES Consortium, Weckhuysen, S, Francklyn, C, Antonellis, A, de Witte, P A M & De Jonghe, P 2019, ' Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish ', Nature Communications, vol. 10, 708 . https://doi.org/10.1038/s41467-018-07953-w
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Nature communications
Siekierska, A, Stamberger, H, Deconinck, T, Oprescu, S N, Partoens, M, Zhang, Y, Sourbron, J, Adriaenssens, E, Mullen, P, Wiencek, P, Hardies, K, Lee, J S, Giong, H K, Distelmaier, F, Elpeleg, O, Helbig, K L, Hersh, J, Isikay, S, Jordan, E, Karaca, E, Kecskes, A, Lupski, J R, Kovacs-Nagy, R, May, P, Narayanan, V, Pendziwiat, M, Ramsey, K, Rangasamy, S, Shinde, D N, Spiegel, R, Timmerman, V, von Spiczak, S, Helbig, I, C4RCD Research Group, Møller, R S, Hjalgrim, H, AR working group of the EuroEPINOMICS RES Consortium, Weckhuysen, S, Francklyn, C, Antonellis, A, de Witte, P A M & De Jonghe, P 2019, ' Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish ', Nature Communications, vol. 10, 708 . https://doi.org/10.1038/s41467-018-07953-w
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Aminoacyl tRNA synthetases (ARSs) link specific amino acids with their cognate transfer RNAs in a critical early step of protein translation. Mutations in ARSs have emerged as a cause of recessive, often complex neurological disease traits. Here we r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3097b073091d6148ed9e1c5e935f26a
https://mediatum.ub.tum.de/1544105
https://mediatum.ub.tum.de/1544105
Autor:
Lieselot Croes, Beyens, Matthias, Fransen, Erik, Ibrahim, Joe, Berghe, Wim Vanden, Suls, Arvid, Peeters, Marc, Pauwels, Patrick, Camp, Guy Van, Beeck, Ken Op De
Table S1. Mean difference in DFNA5 methylation between the paired tumor and normal breast sample in 79 patients for every of the 22 CpGs. Figure S1. DFNA5 methylation (in the gene promoter and in the gene body) and expression (microarray and RNA-seq)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d65e20d514dddb9ac30837ec0f053858