van Roon MA - Search Results

1

Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD.

Remme CA, Verkerk AO, Nuyens D, van Ginneken AC, van Brunschot S, Belterman CN, Wilders R, van Roon MA, Tan HL, Wilde AA, Carmeliet P, de Bakker JM, Veldkamp MW, Bezzina CR. Remme CA, et al. Among authors: van roon ma. Circulation. 2006 Dec 12;114(24):2584-94. doi: 10.1161/CIRCULATIONAHA.106.653949. Epub 2006 Dec 4. Circulation. 2006. PMID: 17145985

2

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation.

Demolombe S, Lande G, Charpentier F, van Roon MA, van den Hoff MJ, Toumaniantz G, Baro I, Guihard G, Le Berre N, Corbier A, de Bakker J, Opthof T, Wilde A, Moorman AF, Escande D. Demolombe S, et al. Among authors: van roon ma, van den hoff mj. Cardiovasc Res. 2001 May;50(2):314-27. doi: 10.1016/s0008-6363(01)00231-0. Cardiovasc Res. 2001. PMID: 11334835

3

5th Workshop on innovative mouse models, IMM 2009, June 25-26, Leiden, The Netherlands: a meeting report.

van Roon M. van Roon M. Transgenic Res. 2009 Dec;18(6):993-5. doi: 10.1007/s11248-009-9307-7. Epub 2009 Aug 19. Transgenic Res. 2009. PMID: 19690977 Free PMC article. No abstract available.

4

Cardiac expression of Gal4 causes cardiomyopathy in a dose-dependent manner.

Habets PE, Clout DE, Lekanne Deprez RH, van Roon MA, Moorman AF, Christoffels VM. Habets PE, et al. Among authors: van roon ma. J Muscle Res Cell Motil. 2003;24(2-3):205-9. doi: 10.1023/a:1026055612227. J Muscle Res Cell Motil. 2003. PMID: 14609031

5

Generation of mice with a conditional null allele for Tbx2.

Wakker V, Brons JF, Aanhaanen WT, van Roon MA, Moorman AF, Christoffels VM. Wakker V, et al. Among authors: van roon ma. Genesis. 2010 Mar;48(3):195-9. doi: 10.1002/dvg.20596. Genesis. 2010. PMID: 20095052

6

Cooperative action of Tbx2 and Nkx2.5 inhibits ANF expression in the atrioventricular canal: implications for cardiac chamber formation.

Habets PE, Moorman AF, Clout DE, van Roon MA, Lingbeek M, van Lohuizen M, Campione M, Christoffels VM. Habets PE, et al. Among authors: van roon ma. Genes Dev. 2002 May 15;16(10):1234-46. doi: 10.1101/gad.222902. Genes Dev. 2002. PMID: 12023302 Free PMC article.

7

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease.

Smit JJ, Schinkel AH, Oude Elferink RP, Groen AK, Wagenaar E, van Deemter L, Mol CA, Ottenhoff R, van der Lugt NM, van Roon MA, et al. Smit JJ, et al. Among authors: van roon ma, van deemter l, van der lugt nm. Cell. 1993 Nov 5;75(3):451-62. doi: 10.1016/0092-8674(93)90380-9. Cell. 1993. PMID: 8106172

8

Overexpression of arginase I in enterocytes of transgenic mice elicits a selective arginine deficiency and affects skin, muscle, and lymphoid development.

de Jonge WJ, Hallemeesch MM, Kwikkers KL, Ruijter JM, de Gier-de Vries C, van Roon MA, Meijer AJ, Marescau B, de Deyn PP, Deutz NE, Lamers WH. de Jonge WJ, et al. Among authors: van roon ma. Am J Clin Nutr. 2002 Jul;76(1):128-40. doi: 10.1093/ajcn/76.1.128. Am J Clin Nutr. 2002. PMID: 12081826

9

Developmental rescue of an embryonic-lethal mutation in the retinoblastoma gene in chimeric mice.

Maandag EC, van der Valk M, Vlaar M, Feltkamp C, O'Brien J, van Roon M, van der Lugt N, Berns A, te Riele H. Maandag EC, et al. EMBO J. 1994 Sep 15;13(18):4260-8. doi: 10.1002/j.1460-2075.1994.tb06746.x. EMBO J. 1994. PMID: 7925271 Free PMC article.

10

Conditional deletion of TGF-βR1 using Langerin-Cre mice results in Langerhans cell deficiency and reduced contact hypersensitivity.

Zahner SP, Kel JM, Martina CA, Brouwers-Haspels I, van Roon MA, Clausen BE. Zahner SP, et al. Among authors: van roon ma. J Immunol. 2011 Nov 15;187(10):5069-76. doi: 10.4049/jimmunol.1101880. Epub 2011 Oct 12. J Immunol. 2011. PMID: 21998450

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