5 results for author:"te Brinke H." in Literature citations
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| Functional redundancy of mitochondrial enoyl-CoA isomerases in the oxidation of unsaturated fatty acids. van Weeghel M., te Brinke H., van Lenthe H., Kulik W., Minkler P.E., Stoll M.S., Sass J.O., Janssen U., Stoffel W., Schwab K.O. et al. FASEB J. 26:4316-4326(2012) · Mapped (2) |
| The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1. van Wijk E., van der Zwaag B., Peters T., Zimmermann U., Te Brinke H., Kersten F.F.J., Maerker T., Aller E., Hoefsloot L.H., Cremers C.W.R.J. et al. Hum. Mol. Genet. 15:751-765(2006) · UniProtKB (3) · Mapped (26) |
| Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2. Reiners J., van Wijk E., Maerker T., Zimmermann U., Juergens K., te Brinke H., Overlack N., Roepman R., Knipper M., Kremer H. et al. Hum. Mol. Genet. 14:3933-3943(2005) · UniProtKB (8) |
| USH2A mutation analysis in 70 Dutch families with Usher syndrome type II. Pennings R.J.E., Te Brinke H., Weston M.D., Claassen A., Orten D.J., Weekamp H., Van Aarem A., Huygen P.L.M., Deutman A.F., Hoefsloot L.H. et al. Hum. Mutat. 24:185-185(2004) · UniProtKB (1) |
| Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II. Van Wijk E., Pennings R.J.E., Te Brinke H., Claassen A., Yntema H.G., Hoefsloot L.H., Cremers F.P.M., Cremers C.W.R.J., Kremer H. Am. J. Hum. Genet. 74:738-744(2004) · UniProtKB (1) |