Willemsen R - Search Results

1

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.

Wong TH, Chiu WZ, Breedveld GJ, Li KW, Verkerk AJ, Hondius D, Hukema RK, Seelaar H, Frick P, Severijnen LA, Lammers GJ, Lebbink JH, van Duinen SG, Kamphorst W, Rozemuller AJ; Netherlands Brain Bank; Bakker EB; International Parkinsonism Genetics Network; Neumann M, Willemsen R, Bonifati V, Smit AB, van Swieten J. Wong TH, et al. Among authors: willemsen r. Brain. 2014 May;137(Pt 5):1361-73. doi: 10.1093/brain/awu067. Epub 2014 Apr 9. Brain. 2014. PMID: 24722252

2

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA. Verheij C, et al. Among authors: willemsen r. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

3

Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.

Rizzu P, Joosse M, Ravid R, Hoogeveen A, Kamphorst W, van Swieten JC, Willemsen R, Heutink P. Rizzu P, et al. Among authors: willemsen r. Hum Mol Genet. 2000 Dec 12;9(20):3075-82. doi: 10.1093/hmg/9.20.3075. Hum Mol Genet. 2000. PMID: 11115852

4

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

Rosso SM, Kamphorst W, de Graaf B, Willemsen R, Ravid R, Niermeijer MF, Spillantini MG, Heutink P, van Swieten JC. Rosso SM, et al. Among authors: willemsen r. Brain. 2001 Oct;124(Pt 10):1948-57. doi: 10.1093/brain/124.10.1948. Brain. 2001. PMID: 11571213 Free article.

5

A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.

Rosso SM, van Herpen E, Deelen W, Kamphorst W, Severijnen LA, Willemsen R, Ravid R, Niermeijer MF, Dooijes D, Smith MJ, Goedert M, Heutink P, van Swieten JC. Rosso SM, et al. Among authors: willemsen r. Ann Neurol. 2002 Mar;51(3):373-6. doi: 10.1002/ana.10140. Ann Neurol. 2002. PMID: 11891833

6

Timing of the absence of FMR1 expression in full mutation chorionic villi.

Willemsen R, Bontekoe CJ, Severijnen LA, Oostra BA. Willemsen R, et al. Hum Genet. 2002 Jun;110(6):601-5. doi: 10.1007/s00439-002-0723-5. Epub 2002 Apr 16. Hum Genet. 2002. PMID: 12107447

7

Transport of fragile X mental retardation protein via granules in neurites of PC12 cells.

De Diego Otero Y, Severijnen LA, van Cappellen G, Schrier M, Oostra B, Willemsen R. De Diego Otero Y, et al. Among authors: willemsen r. Mol Cell Biol. 2002 Dec;22(23):8332-41. doi: 10.1128/MCB.22.23.8332-8341.2002. Mol Cell Biol. 2002. PMID: 12417734 Free PMC article.

8

Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.

van Herpen E, Rosso SM, Serverijnen LA, Yoshida H, Breedveld G, van de Graaf R, Kamphorst W, Ravid R, Willemsen R, Dooijes D, Majoor-Krakauer D, Kros JM, Crowther RA, Goedert M, Heutink P, van Swieten JC. van Herpen E, et al. Among authors: willemsen r. Ann Neurol. 2003 Nov;54(5):573-81. doi: 10.1002/ana.10721. Ann Neurol. 2003. PMID: 14595646

9

Proteomic analysis of exosomes isolated from human malignant pleural effusions.

Bard MP, Hegmans JP, Hemmes A, Luider TM, Willemsen R, Severijnen LA, van Meerbeeck JP, Burgers SA, Hoogsteden HC, Lambrecht BN. Bard MP, et al. Among authors: willemsen r. Am J Respir Cell Mol Biol. 2004 Jul;31(1):114-21. doi: 10.1165/rcmb.2003-0238OC. Epub 2004 Feb 19. Am J Respir Cell Mol Biol. 2004. PMID: 14975938

10

Characterization of Fxr1 in Danio rerio; a simple vertebrate model to study costamere development.

Engels B, van 't Padje S, Blonden L, Severijnen LA, Oostra BA, Willemsen R. Engels B, et al. Among authors: willemsen r. J Exp Biol. 2004 Sep;207(Pt 19):3329-38. doi: 10.1242/jeb.01146. J Exp Biol. 2004. PMID: 15326209 Free article.

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