van den Hurk JA - Search Results

1

The small GTPase Rab6B, a novel Rab6 subfamily member, is cell-type specifically expressed and localised to the Golgi apparatus.

Opdam FJ, Echard A, Croes HJ, van den Hurk JA, van de Vorstenbosch RA, Ginsel LA, Goud B, Fransen JA. Opdam FJ, et al. Among authors: van den hurk ja. J Cell Sci. 2000 Aug;113 ( Pt 15):2725-35. doi: 10.1242/jcs.113.15.2725. J Cell Sci. 2000. PMID: 10893188

2

Synchronous diversification of Sulawesi's iconic artiodactyls driven by recent geological events.

Frantz LAF, Rudzinski A, Nugraha AMS, Evin A, Burton J, Hulme-Beaman A, Linderholm A, Barnett R, Vega R, Irving-Pease EK, Haile J, Allen R, Leus K, Shephard J, Hillyer M, Gillemot S, van den Hurk J, Ogle S, Atofanei C, Thomas MG, Johansson F, Mustari AH, Williams J, Mohamad K, Damayanti CS, Wiryadi ID, Obbles D, Mona S, Day H, Yasin M, Meker S, McGuire JA, Evans BJ, von Rintelen T, Ho SYW, Searle JB, Kitchener AC, Macdonald AA, Shaw DJ, Hall R, Galbusera P, Larson G. Frantz LAF, et al. Among authors: van den hurk j. Proc Biol Sci. 2018 Apr 11;285(1876):20172566. doi: 10.1098/rspb.2017.2566. Proc Biol Sci. 2018. PMID: 29643207 Free PMC article.

3

L1 retrotransposition can occur early in human embryonic development.

van den Hurk JA, Meij IC, Seleme MC, Kano H, Nikopoulos K, Hoefsloot LH, Sistermans EA, de Wijs IJ, Mukhopadhyay A, Plomp AS, de Jong PT, Kazazian HH, Cremers FP. van den Hurk JA, et al. Hum Mol Genet. 2007 Jul 1;16(13):1587-92. doi: 10.1093/hmg/ddm108. Epub 2007 May 4. Hum Mol Genet. 2007. PMID: 17483097

4

Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.

Renner AB, Kellner U, Cropp E, Preising MN, MacDonald IM, van den Hurk JA, Cremers FP, Foerster MH. Renner AB, et al. Among authors: van den hurk ja. Ophthalmology. 2006 Nov;113(11):2066.e1-10. doi: 10.1016/j.ophtha.2006.05.045. Epub 2006 Aug 28. Ophthalmology. 2006. PMID: 16935340

5

Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes.

Michielse CB, Bhat M, Brady A, Jafrid H, van den Hurk JA, Raashid Y, Brunner HG, van Bokhoven H, Padberg GW. Michielse CB, et al. Among authors: van den hurk ja. Eur J Hum Genet. 2006 Dec;14(12):1306-12. doi: 10.1038/sj.ejhg.5201706. Epub 2006 Aug 16. Eur J Hum Genet. 2006. PMID: 16912702

6

Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.

van den Hurk JA, Rashbass P, Roepman R, Davis J, Voesenek KE, Arends ML, Zonneveld MN, van Roekel MH, Cameron K, Rohrschneider K, Heckenlively JR, Koenekoop RK, Hoyng CB, Cremers FP, den Hollander AI. van den Hurk JA, et al. Mol Vis. 2005 Apr 15;11:263-73. Mol Vis. 2005. PMID: 15851977 Free article.

7

Choroideremia gene product affects trophoblast development and vascularization in mouse extra-embryonic tissues.

Shi W, van den Hurk JA, Alamo-Bethencourt V, Mayer W, Winkens HJ, Ropers HH, Cremers FP, Fundele R. Shi W, et al. Among authors: van den hurk ja. Dev Biol. 2004 Aug 1;272(1):53-65. doi: 10.1016/j.ydbio.2004.04.016. Dev Biol. 2004. PMID: 15242790 Free article.

8

Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon.

van den Hurk JA, van de Pol DJ, Wissinger B, van Driel MA, Hoefsloot LH, de Wijs IJ, van den Born LI, Heckenlively JR, Brunner HG, Zrenner E, Ropers HH, Cremers FP. van den Hurk JA, et al. Hum Genet. 2003 Aug;113(3):268-75. doi: 10.1007/s00439-003-0970-0. Epub 2003 Jun 25. Hum Genet. 2003. PMID: 12827496

9

Molecular genetics of Leber congenital amaurosis.

Cremers FP, van den Hurk JA, den Hollander AI. Cremers FP, et al. Among authors: van den hurk ja. Hum Mol Genet. 2002 May 15;11(10):1169-76. doi: 10.1093/hmg/11.10.1169. Hum Mol Genet. 2002. PMID: 12015276 Review.

10

Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.

van den Hurk JA, Hendriks W, van de Pol DJ, Oerlemans F, Jaissle G, Rüther K, Kohler K, Hartmann J, Zrenner E, van Bokhoven H, Wieringa B, Ropers HH, Cremers FP. van den Hurk JA, et al. Hum Mol Genet. 1997 Jun;6(6):851-8. doi: 10.1093/hmg/6.6.851. Hum Mol Genet. 1997. PMID: 9175730 Free article.

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