Bijvelds MJ - Search Results

1

Cystic fibrosis: toward personalized therapies.

Ikpa PT, Bijvelds MJ, de Jonge HR. Ikpa PT, et al. Among authors: bijvelds mj. Int J Biochem Cell Biol. 2014 Jul;52:192-200. doi: 10.1016/j.biocel.2014.02.008. Epub 2014 Feb 20. Int J Biochem Cell Biol. 2014. PMID: 24561283 Review.

2

No indications for altered essential fatty acid metabolism in two murine models for cystic fibrosis.

Werner A, Bongers ME, Bijvelds MJ, de Jonge HR, Verkade HJ. Werner A, et al. Among authors: bijvelds mj. J Lipid Res. 2004 Dec;45(12):2277-86. doi: 10.1194/jlr.M400238-JLR200. Epub 2004 Oct 1. J Lipid Res. 2004. PMID: 15466369 Free article.

3

Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events.

Bijvelds MJ, Bronsveld I, Havinga R, Sinaasappel M, de Jonge HR, Verkade HJ. Bijvelds MJ, et al. Am J Physiol Gastrointest Liver Physiol. 2005 Apr;288(4):G646-53. doi: 10.1152/ajpgi.00295.2004. Epub 2004 Nov 4. Am J Physiol Gastrointest Liver Physiol. 2005. PMID: 15528257 Free article.

4

Activation of CFTR by ASBT-mediated bile salt absorption.

Bijvelds MJ, Jorna H, Verkade HJ, Bot AG, Hofmann F, Agellon LB, Sinaasappel M, de Jonge HR. Bijvelds MJ, et al. Am J Physiol Gastrointest Liver Physiol. 2005 Nov;289(5):G870-9. doi: 10.1152/ajpgi.00226.2005. Epub 2005 Jul 21. Am J Physiol Gastrointest Liver Physiol. 2005. PMID: 16037545 Free article.

5

Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat.

Norez C, Noel S, Wilke M, Bijvelds M, Jorna H, Melin P, DeJonge H, Becq F. Norez C, et al. FEBS Lett. 2006 Apr 3;580(8):2081-6. doi: 10.1016/j.febslet.2006.03.010. Epub 2006 Mar 10. FEBS Lett. 2006. PMID: 16546175 Free article.

6

Cholesterol depletion and genistein as tools to promote F508delCFTR retention at the plasma membrane.

Lim CH, Bijvelds MJ, Nigg A, Schoonderwoerd K, Houtsmuller AB, de Jonge HR, Tilly BC. Lim CH, et al. Among authors: bijvelds mj. Cell Physiol Biochem. 2007;20(5):473-82. doi: 10.1159/000107531. Cell Physiol Biochem. 2007. PMID: 17762174

7

Activation of intestinal Cl- secretion by lubiprostone requires the cystic fibrosis transmembrane conductance regulator.

Bijvelds MJ, Bot AG, Escher JC, De Jonge HR. Bijvelds MJ, et al. Gastroenterology. 2009 Sep;137(3):976-85. doi: 10.1053/j.gastro.2009.05.037. Epub 2009 May 18. Gastroenterology. 2009. PMID: 19454284

8

Effect of antibiotic treatment on fat absorption in mice with cystic fibrosis.

Wouthuyzen-Bakker M, Bijvelds MJ, de Jonge HR, De Lisle RC, Burgerhof JG, Verkade HJ. Wouthuyzen-Bakker M, et al. Among authors: bijvelds mj. Pediatr Res. 2012 Jan;71(1):4-12. doi: 10.1038/pr.2011.4. Pediatr Res. 2012. PMID: 22289844 Free PMC article.

9

Ursodeoxycholate modulates bile flow and bile salt pool independently from the cystic fibrosis transmembrane regulator (Cftr) in mice.

Bodewes FA, Wouthuyzen-Bakker M, Bijvelds MJ, Havinga R, de Jonge HR, Verkade HJ. Bodewes FA, et al. Among authors: bijvelds mj. Am J Physiol Gastrointest Liver Physiol. 2012 May 1;302(9):G1035-42. doi: 10.1152/ajpgi.00258.2011. Epub 2012 Feb 2. Am J Physiol Gastrointest Liver Physiol. 2012. PMID: 22301109 Free article.

10

Bile acid handling in cystic fibrosis: marked phenotypic differences between mouse models.

Bijvelds MJ, de Jonge HR, Verkade HJ. Bijvelds MJ, et al. Gastroenterology. 2012 Dec;143(6):e19-20; author reply e20. doi: 10.1053/j.gastro.2012.08.052. Epub 2012 Oct 19. Gastroenterology. 2012. PMID: 23085355 No abstract available.

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