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Theo van Veen

Explore the profile of Theo van Veen including associated specialties, affiliations and a list of published articles. Areas
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Articles 23
Citations 733
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Recent Articles
1.
Schijven J, van Veen T, Delmaar C, Kos J, Vermeulen L, Roosien R, et al.
Environ Health Perspect . 2023 Aug; 131(8):87011. PMID: 37589660
Background: SARS-CoV-2 can be effectively transmitted between individuals located in close proximity to each other for extended durations. Aircraft provide such conditions. Although high attack rates during flights were reported,...
2.
Kaur J, Mencl S, Sahaboglu A, Farinelli P, van Veen T, Zrenner E, et al.
PLoS One . 2011 Jul; 6(7):e22181. PMID: 21765948
Retinitis pigmentosa (RP) is a heterogeneous group of inherited neurodegenerative diseases affecting photoreceptors and causing blindness. Many human cases are caused by mutations in the rhodopsin gene. An important question...
3.
Paquet-Durand F, Beck S, Michalakis S, Goldmann T, Huber G, Muhlfriedel R, et al.
Hum Mol Genet . 2010 Dec; 20(5):941-7. PMID: 21149284
The rd1 natural mutant is one of the first and probably the most commonly studied mouse model for retinitis pigmentosa (RP), a severe and frequently blinding human retinal degeneration. In...
4.
Vlachantoni D, Bramall A, Murphy M, Taylor R, Shu X, Tulloch B, et al.
Hum Mol Genet . 2010 Nov; 20(2):322-35. PMID: 21051333
The role of oxidative stress within photoreceptors (PRs) in inherited photoreceptor degeneration (IPD) is unclear. We investigated this question using four IPD mouse models (Pde6b(rd1/rd1), Pde6b(atrd1/atrd1), Rho(-/-) and Prph2(rds/rds)) and...
5.
Paquet-Durand F, Sanges D, McCall J, Silva J, van Veen T, Marigo V, et al.
J Neurochem . 2010 Sep; 115(4):930-40. PMID: 20807308
Photoreceptor degeneration is the hallmark of a group of inherited blinding diseases collectively termed retinitis pigmentosa (RP); a major cause of blindness in humans. RP is at present untreatable and...
6.
Miranda M, Arnal E, Ahuja S, Alvarez-Nolting R, Lopez-Pedrajas R, Ekstrom P, et al.
Free Radic Biol Med . 2009 Oct; 48(2):216-22. PMID: 19854264
We have previously shown that the use of a combination of antioxidants delayed the degeneration process in rd1 mouse retina. In an effort to understand the mechanism of action of...
7.
Bujakowska K, Maubaret C, Chakarova C, Tanimoto N, Beck S, Fahl E, et al.
Invest Ophthalmol Vis Sci . 2009 Jul; 50(12):5927-33. PMID: 19578015
Purpose: Pre-mRNA processing factor 31 (PRPF31) is a ubiquitous protein needed for the assembly of the pre-mRNA splicing machinery. It has been shown that mutations in this gene cause autosomal...
8.
Paquet-Durand F, Hauck S, van Veen T, Ueffing M, Ekstrom P
J Neurochem . 2009 Feb; 108(3):796-810. PMID: 19187097
Photoreceptor degeneration in retinitis pigmentosa is one of the leading causes of hereditary blindness in the developed world. Although causative genetic mutations have been elucidated in many cases, the underlying...
9.
Sancho-Pelluz J, Arango-Gonzalez B, Kustermann S, Romero F, van Veen T, Zrenner E, et al.
Mol Neurobiol . 2008 Nov; 38(3):253-69. PMID: 18982459
Photoreceptor cell death is the major hallmark of a group of human inherited retinal degenerations commonly referred to as retinitis pigmentosa (RP). Although the causative genetic mutations are often known,...
10.
Sancho-Pelluz J, Wunderlich K, Rauch U, Romero F, van Veen T, Limb G, et al.
Invest Ophthalmol Vis Sci . 2008 Jul; 49(12):5602-10. PMID: 18641281
Purpose: Resident microglial cells normally do not express sialoadhesin (Sn; a sialic acid-binding receptor), whereas recruited inflammatory macrophages have been shown to do so. The expression of Sn was examined...