ZFIN

ZFIN ID: ZDB-MRPHLNO-060127-3

CITATIONS (7 total)

Morpholino Name:	MO3-crx
Morpholino Symbol:	MO3-crx

Heon, E., Kim, G., Qin, S., Garrison, J.E., Tavares, E., Vincent, A., Nuangchamnong, N., Scott, C.A., Slusarski, D.C., Sheffield, V.C. (2016) Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21). Human molecular genetics. 25(11):2283-2294

Scott, C.A., Marsden, A.N., Slusarski, D.C. (2016) Automated, high-throughput, in vivo analysis of visual function using the zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 245(5):605-13

Mei, X., Wu, S., Bassuk, A.G., and Slusarski, D.C. (2013) Mechanisms of prickle 1a function in zebrafish epilepsy and retinal neurogenesis. Disease models & mechanisms. 6(3):679-688

Baye, L.M., Patrinostro, X., Swaminathan, S., Beck, J.S., Zhang, Y., Stone, E.M., Sheffield, V.C., and Slusarski, D.C. (2011) The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindness. Human molecular genetics. 20(8):1467-77

Nishimura, D.Y., Baye, L.M., Perveen, R., Searby, C.C., Avila-Fernandez, A., Pereiro, I., Ayuso, C., Valverde, D., Bishop, P.N., Manson, F.D., Urquhart, J., Stone, E.M., Slusarski, D.C., Black, G.C., and Sheffield, V.C. (2010) Discovery and Functional Analysis of a Retinitis Pigmentosa Gene, C2ORF71. American journal of human genetics. 86(5):686-695

Pretorius, P.R., Baye, L.M., Nishimura, D.Y., Searby, C.C., Bugge, K., Yang, B., Mullins, R.F., Stone, E.M., Sheffield, V.C., and Slusarski, D.C. (2010) Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform. PLoS Genetics. 6(3):e1000884

Yen, H.J., Tayeh, M.K., Mullins, R.F., Stone, E.M., Sheffield, V.C., and Slusarski, D.C. (2006) Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function. Human molecular genetics. 15(5):667-677