Publication: NINL and DZANK1 co-function in vesicle transport and are essential for photoreceptor development in Zebrafish
NINL and DZANK1 co-function in vesicle transport and are essential for photoreceptor development in Zebrafish
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Dona, M., Bachmann-Gagescu, R., Texier, Y., Toedt, G., Hetterschijt, L., Tonnaer, E. L., Peters, T. A., van Beersum, S. E. C., Bergboer, J. G. M., Horn, N., de Vrieze, E., Slijkerman, R. W. N., van Reeuwijk, J., Flik, G., Keunen, J. E., Ueffing, M., Gibson, T. J., Roepman, R., Boldt, K., … van Wijk, E. (2015). NINL and DZANK1 co-function in vesicle transport and are essential for photoreceptor development in Zebrafish. PLoS Genetics, 11(10), e1005574. https://doi.org/10.1371/journal.pgen.1005574
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Ciliopathies are Mendelian disorders caused by dysfunction of cilia, ubiquitous organelles involved in fluid propulsion (motile cilia) or signal transduction (primary cilia). Retinal dystrophy is a common phenotypic characteristic of ciliopathies since photoreceptor outer segments are specialized primary cilia. These ciliary structures heavily rely on intracellular minus-end directed transport of cargo, mediated at least in part by the cytoplasmic dynein 1 motor complex, for their formation, maintenance and function. Ninein-like prote
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Dona, M., Bachmann-Gagescu, R., Texier, Y., Toedt, G., Hetterschijt, L., Tonnaer, E. L., Peters, T. A., van Beersum, S. E. C., Bergboer, J. G. M., Horn, N., de Vrieze, E., Slijkerman, R. W. N., van Reeuwijk, J., Flik, G., Keunen, J. E., Ueffing, M., Gibson, T. J., Roepman, R., Boldt, K., … van Wijk, E. (2015). NINL and DZANK1 co-function in vesicle transport and are essential for photoreceptor development in Zebrafish. PLoS Genetics, 11(10), e1005574. https://doi.org/10.1371/journal.pgen.1005574