Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Remco, van Dijk"'
Autor:
Doret de Rooij, Miriam van de Watering, Remco van Dijk, Thijs Veenstra, Rolf Appels, Corien Swaan, Aura Timen
Publikováno v:
BMC Public Health, Vol 23, Iss 1, Pp 1-13 (2023)
Abstract Background Long-lasting crises, such as the COVID-19 pandemic, require proper interim evaluation in order to optimize response. The World Health Organization and the European Center for Disease Control have recently promoted the in(tra)-acti
Externí odkaz:
https://doaj.org/article/8ebda7996f10439fac5565ba0e0731c8
Autor:
Sem J. Aronson, Robert S. Bakker, Sascha Moenis, Remco van Dijk, Giulia Bortolussi, Fanny Collaud, Xiaoxia Shi, Suzanne Duijst, Lysbeth ten Bloemendaal, Giuseppe Ronzitti, Andrés F. Muro, Federico Mingozzi, Ulrich Beuers, Piter J. Bosma
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 250-258 (2020)
Potency assessment of clinical-grade vector lots is crucial to support adeno-associated virus (AAV) vector release and is required for future marketing authorization. We have developed and validated a cell-based, quantitative potency assay that detec
Externí odkaz:
https://doaj.org/article/edb7a29586e044c8b082be4c5aa3a2dd
Autor:
Remco van Dijk, Sem J. Aronson, Dirk R. de Waart, Stan F. van de Graaf, Suzanne Duijst, Jurgen Seppen, Ronald Oude Elferink, Ulrich Beuers, Piter J. Bosma
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract We aimed to identify potent biliverdin reductase (BVRA) inhibitors as a novel concept for the treatment of severe unconjugated hyperbilirubinemia. 1280 FDA-approved compounds were screened in vitro for their ability to inhibit human and rat
Externí odkaz:
https://doaj.org/article/d12f4548a8564f6a914ed21b89937903
Autor:
Giuseppe Ronzitti, Giulia Bortolussi, Remco van Dijk, Fanny Collaud, Severine Charles, Christian Leborgne, Patrice Vidal, Samia Martin, Bernard Gjata, Marcelo Simon Sola, Laetitia van Wittenberghe, Alban Vignaud, Philippe Veron, Piter J Bosma, Andres F Muro, Federico Mingozzi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 3, Iss C (2016)
Crigler-Najjar syndrome is a severe metabolic disease of the liver due to a reduced activity of the UDP Glucuronosyltransferase 1A1 (UGT1A1) enzyme. In an effort to translate to the clinic an adeno-associated virus vector mediated liver gene transfer
Externí odkaz:
https://doaj.org/article/b411908592d443658eb6cd43556b216e
Autor:
Giulia Bortolussi, Giuseppe Ronzitti, Lysbeth ten Bloemendaal, Piter J. Bosma, Andrés F. Muro, Robert S. Bakker, Xiaoxia Shi, Remco van Dijk, Federico Mingozzi, Fanny Collaud, Suzanne Duijst, Sem J. Aronson, Ulrich Beuers, Sascha Moenis
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss, Pp 250-258 (2020)
Molecular Therapy-Methods & Clinical Development
Molecular therapy. Methods & clinical development, 18, 250-258. Nature Publishing Group
Molecular Therapy-Methods & Clinical Development
Molecular therapy. Methods & clinical development, 18, 250-258. Nature Publishing Group
Potency assessment of clinical-grade vector lots is crucial to support adeno-associated virus (AAV) vector release and is required for future marketing authorization. We have developed and validated a cell-based, quantitative potency assay that detec
Autor:
Sem J, Aronson, Robert S, Bakker, Sascha, Moenis, Remco, van Dijk, Giulia, Bortolussi, Fanny, Collaud, Xiaoxia, Shi, Suzanne, Duijst, Lysbeth, Ten Bloemendaal, Giuseppe, Ronzitti, Andrés F, Muro, Federico, Mingozzi, Ulrich, Beuers, Piter J, Bosma
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Potency assessment of clinical-grade vector lots is crucial to support adeno-associated virus (AAV) vector release and is required for future marketing authorization. We have developed and validated a cell-based, quantitative potency assay that detec
Autor:
Vincent A. van der Mark, Isabel Mayayo-Peralta, Piter J. Bosma, Ulrich Beuers, Sem J. Aronson, Nevin Oruc, Rob J. de Knegt, Remco van Dijk, Anja A. Kattentidt-Mouravieva
Publikováno v:
Journal of hepatology, 63(6), 1525-1529. Elsevier
Journal of Hepatology, 63(6), 1525-1529. Elsevier
Journal of Hepatology, 63(6), 1525-1529. Elsevier
Crigler-Najjar syndrome presents as severe unconjugated hyper-bilirubinemia and is characteristically caused by a mutation in the UGT1A1 gene, encoding the enzyme responsible for bilirubin glucuronidation. Here we present a patient with Crigler-Najja
Autor:
Dirk R. de Waart, Sem J. Aronson, Ulrich Beuers, Ronald P.J. Oude Elferink, Stan F.J. van de Graaf, Remco van Dijk, Piter J. Bosma, Suzanne Duijst, Jurgen Seppen
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Scientific Reports
Scientific reports, 7(1). Nature Publishing Group
Scientific Reports
Scientific reports, 7(1). Nature Publishing Group
We aimed to identify potent biliverdin reductase (BVRA) inhibitors as a novel concept for the treatment of severe unconjugated hyperbilirubinemia. 1280 FDA-approved compounds were screened in vitro for their ability to inhibit human and rat BVRA acti
Autor:
Zoë Castricum, Remco van Dijk, Wouter J. de Jonge, Casper Marsman, Kam S. Ho-Mok, Coen C. Paulusma, Mohammed Ghiboub, Vincent A. van der Mark, Jing Zhao, Johan K. Hiralall, Ronald P.J. Oude Elferink
Publikováno v:
Cellular and Molecular Life Sciences
P4-ATPases are lipid flippases that catalyze the transport of phospholipids to create membrane phospholipid asymmetry and to initiate the biogenesis of transport vesicles. Here we show, for the first time, that lipid flippases are essential to dampen
Autor:
Thomas M. van Gulik, Hennie Bikker, Mark Feist, Pieter C. F. Stokkers, Piter J. Bosma, Ulrich Beuers, Johan S. Laméris, Remco van Dijk, Andreas E. Kremer, Wouter L. Smit, Dirk J. Gouma, Valentine Enemuo, Bram D.J. van den Elzen, Peter L.M. Jansen
Publikováno v:
Liver international, 35(4), 1478-1488. Wiley-Blackwell
Liver International, 35(4), 1478-1488. Wiley
Liver International, 35(4), 1478-1488. Wiley
Background & Aims Hepatocellular secretory failure induced by drugs, toxins or transient biliary obstruction may sometimes persist for months after removal of the initiating factor and may then be fatal without liver transplantation. We characterized