Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jonathan D Windster"'
Autor:
Laura E Kuil, Katherine C MacKenzie, Clara S Tang, Jonathan D Windster, Thuy Linh Le, Anwarul Karim, Bianca M de Graaf, Robert van der Helm, Yolande van Bever, Cornelius E J Sloots, Conny Meeussen, Dick Tibboel, Annelies de Klein, René M H Wijnen, Jeanne Amiel, Stanislas Lyonnet, Maria-Mercè Garcia-Barcelo, Paul K H Tam, Maria M Alves, Alice S Brooks, Robert M W Hofstra, Erwin Brosens
Publikováno v:
PLoS Genetics, Vol 17, Iss 8, p e1009698 (2021)
Hirschsprung disease (HSCR) is a complex genetic disease characterized by absence of ganglia in the intestine. HSCR etiology can be explained by a unique combination of genetic alterations: rare coding variants, predisposing haplotypes and Copy Numbe
Externí odkaz:
https://doaj.org/article/1c07ad4d76c24f9488439c5f30f264c2
Autor:
Laura E. Kuil, Naomi J.M. Kakiailatu, Jonathan D. Windster, Eric Bindels, Joke T.M. Zink, Gaby van der Zee, Robert M.W. Hofstra, Iain T. Shepherd, Veerle Melotte, Maria M. Alves
Publikováno v:
iScience, Vol 26, Iss 7, Pp 107070- (2023)
Summary: The enteric nervous system (ENS) regulates many gastrointestinal functions including peristalsis, immune regulation and uptake of nutrients. Defects in the ENS can lead to severe enteric neuropathies such as Hirschsprung disease (HSCR). Zebr
Externí odkaz:
https://doaj.org/article/b7ec781be7a740e7809fef44bcc8fbf0
Autor:
Almira Zada, Laura E. Kuil, Bianca M. de Graaf, Naomi Kakiailatu, Jonathan D. Windster, Alice S. Brooks, Marjon van Slegtenhorst, Barbara de Koning, René M. H. Wijnen, Veerle Melotte, Robert M. W. Hofstra, Erwin Brosens, Maria M. Alves
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Background: Pediatric Intestinal Pseudo-obstruction (PIPO) is a congenital enteric disorder characterized by severe gastrointestinal (GI) dysmotility, without mechanical obstruction. Although several genes have been described to cause this disease, m
Externí odkaz:
https://doaj.org/article/88f91001bc774e99be4b2759acc6def2
Autor:
Jonathan D Windster, Andrea Sacchetti, Gerben J Schaaf, Eric MJ Bindels, Robert MW Hofstra, Rene MH Wijnen, Cornelius EJ Sloots, Maria M Alves
Publikováno v:
EMBO Reports, 24(4):e55789. Wiley-Blackwell
Efficient isolation of neurons and glia from the human enteric nervous system (ENS) is challenging because of their rare and fragile nature. Here, we describe a staining panel to enrich ENS cells from the human intestine by fluorescence-activated cel
Autor:
Tjitske M van der Zanden, Matthijs de Hoog, Saskia N. de Wildt, Jonathan D. Windster, I. Heleen van der Sijs, Joost van Rosmalen
Publikováno v:
Paediatric Drugs, 22, 2, pp. 229-239
Paediatric Drugs
Paediatric Drugs, 22, 229-239. Adis
Paediatric Drugs, 22, 229-239
Paediatric Drugs
Paediatric Drugs, 22, 229-239. Adis
Paediatric Drugs, 22, 229-239
Objectives The structured digital dosing guidelines of the web-based Dutch Paediatric Formulary provided the opportunity to develop an integrated paediatric dose calculator. In a simulated setting, we tested the ability of this calculator to reduce c
Autor:
Alice S. Brooks, Robert van der Helm, Bianca M. de Graaf, Erwin Brosens, Conny J.H.M. Meeussen, Laura E. Kuil, Robert M.W. Hofstra, Thuy Linh Le, Anwarul Karim, Annelies de Klein, Rene M. H. Wijnen, Cornelius E. J. Sloots, Paul K.H. Tam, Maria M. Alves, Yolande van Bever, Clara S. Tang, Maria-Mercè Garcia-Barceló, Jeanne Amiel, Jonathan D. Windster, Katherine C. MacKenzie, Dick Tibboel, Stanislas Lyonnet
Publikováno v:
PLoS Genetics, Vol 17, Iss 8, p e1009698 (2021)
PLoS Genetics, 17(8):1009698. Public Library of Science
PLoS Genetics
PLoS Genetics, 17(8):1009698. Public Library of Science
PLoS Genetics
Hirschsprung disease (HSCR) is a complex genetic disease characterized by absence of ganglia in the intestine. HSCR etiology can be explained by a unique combination of genetic alterations: rare coding variants, predisposing haplotypes and Copy Numbe
Autor:
Miriam G. Mooij, J van Rosmalen, Dick Tibboel, SN de Wildt, Lidwien M. Hanff, Jonathan D. Windster
Publikováno v:
Archives of Disease in Childhood. 104:e45.2-e45
BackgroundThe disposition of orally prescribed drugs in critically ill children may be affected critical illness in in addition to age, resulting in erratic effects and safety. We aimed to study oral drug prescribing in the neonatal and pediatric int
Autor:
Barbara A. E. de Koning, Wouter H. Vaes, Jonathan D. Windster, Saskia N. de Wildt, Joost van Rosmalen, Bianca D van Groen, Dick Tibboel, Miriam G. Mooij, Heleen M. Wortelboer, Evita van de Steeg
Publikováno v:
Drug Metabolism and Disposition, 44, 1005-13
Drug Metabolism and Disposition, 44, 7, pp. 1005-13
Drug Metabolism and Disposition, 7, 44, 1005-1013
Drug Metabolism & Disposition, 44(7), 1005-1013. American Society for Pharmacology and Experimental Therapeutics
Drug Metabolism and Disposition, 44, 7, pp. 1005-13
Drug Metabolism and Disposition, 7, 44, 1005-1013
Drug Metabolism & Disposition, 44(7), 1005-1013. American Society for Pharmacology and Experimental Therapeutics
Human hepatic membrane-embedded transporter proteins are involved in trafficking endogenous and exogenous substrates. Even though impact of transporters on pharmacokinetics is recognized, little is known on maturation of transporter protein expressio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22b434a996814d6d61242a199f7dcb18
http://hdl.handle.net/2066/171296
http://hdl.handle.net/2066/171296