Unexpected CEP290 mRNA Splicing in a Humanized Knock-In Mouse Model for Leber Congenital Amaurosis

le Garanto, Alejandro, van Beersum, Sylvia E. C., Peters, Theo A., Roepman, Ronald, Cremers, Frans P. M., Collin, Rob W. J.
Foilsithe 2013

Kidney failure in mice lacking the tetraspanin CD151

le Sachs, Norman, Kreft, Maaike, van den Bergh Weerman, Marius A., Beynon, Andy J., Peters, Theo A., Weening, Jan J., Sonnenberg, Arnoud
Foilsithe 2006

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish

le Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.
Foilsithe in Sci Rep (2018)

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish

le Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A., Corral-Serrano, Julio C., Slijkerman, Ralph W. N., van Wijk, Erwin, Collin, Rob W. J.
Foilsithe in PLoS One (2018)

Identification of a Rat Model for Usher Syndrome Type 1B by N-Ethyl-N-nitrosourea Mutagenesis-Driven Forward Genetics

le Smits, Bart M. G., Peters, Theo A., Mul, Joram D., Croes, Huib J., Fransen, Jack A. M., Beynon, Andy J., Guryev, Victor, Plasterk, Ronald H. A., Cuppen, Edwin
Foilsithe 2005

Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal Vasculature

le Karjosukarso, Dyah W., Ali, Zaheer, Peters, Theo A., Zhang, Jia Qi Cheng, Hoogendoorn, Anita D M., Garanto, Alejandro, van Wijk, Erwin, Jensen, Lasse D., Collin, Rob W J.
Foilsithe in Invest Ophthalmol Vis Sci (2020)

The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically

le Kersten, Ferry FJ, van Wijk, Erwin, Hetterschijt, Lisette, Bauβ, Katharina, Peters, Theo A, Aslanyan, Mariam G, van der Zwaag, Bert, Wolfrum, Uwe, Keunen, Jan EE, Roepman, Ronald, Kremer, Hannie
Foilsithe 2012

Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein

le van Wijk, Erwin, Kersten, Ferry F.J., Kartono, Aileen, Mans, Dorus A., Brandwijk, Kim, Letteboer, Stef J.F., Peters, Theo A., Märker, Tina, Yan, Xiumin, Cremers, Cor W.R.J., Cremers, Frans P.M., Wolfrum, Uwe, Roepman, Ronald, Kremer, Hannie
Foilsithe 2009

Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy

le Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Peters, Theo A., Hoyng, Carel B., Kremer, Hannie, Hetterschijt, Lisette, Letteboer, Stef J.F., van Wijk, Erwin, Roepman, Ronald, den Hollander, Anneke I., Cremers, Frans P.M.
Foilsithe 2014

ATP8B1 is essential for maintaining normal hearing

le Stapelbroek, Janneke M., Peters, Theo A., van Beurden, Denis H. A., Curfs, Jo H. A. J., Joosten, Anneke, Beynon, Andy J., van Leeuwen, Bibian M., van der Velden, Lieke M., Bull, Laura, Oude Elferink, Ronald P., van Zanten, Bert A., Klomp, Leo W. J., Houwen, Roderick H. J.
Foilsithe 2009

Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy

le Roosing, Susanne, Rohrschneider, Klaus, Beryozkin, Avigail, Sharon, Dror, Weisschuh, Nicole, Staller, Jennifer, Kohl, Susanne, Zelinger, Lina, Peters, Theo A., Neveling, Kornelia, Strom, Tim M., van den Born, L. Ingeborgh, Hoyng, Carel B., Klaver, Caroline C.W., Roepman, Ronald, Wissinger, Bernd, Banin, Eyal, Cremers, Frans P.M., den Hollander, Anneke I.
Foilsithe 2013

NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish

le Dona, Margo, Bachmann-Gagescu, Ruxandra, Texier, Yves, Toedt, Grischa, Hetterschijt, Lisette, Tonnaer, Edith L., Peters, Theo A., van Beersum, Sylvia E. C., Bergboer, Judith G. M., Horn, Nicola, de Vrieze, Erik, Slijkerman, Ralph W. N., van Reeuwijk, Jeroen, Flik, Gert, Keunen, Jan E., Ueffing, Marius, Gibson, Toby J., Roepman, Ronald, Boldt, Karsten, Kremer, Hannie, van Wijk, Erwin
Foilsithe in PLoS Genet (2015)

Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

le Yariz, Kemal O., Duman, Duygu, Seco, Celia Zazo, Dallman, Julia, Huang, Mingqian, Peters, Theo A., Sirmaci, Asli, Lu, Na, Schraders, Margit, Skromne, Isaac, Oostrik, Jaap, Diaz-Horta, Oscar, Young, Juan I., Tokgoz-Yilmaz, Suna, Konukseven, Ozlem, Shahin, Hashem, Hetterschijt, Lisette, Kanaan, Moien, Oonk, Anne M.M., Edwards, Yvonne J.K., Li, Huawei, Atalay, Semra, Blanton, Susan, DeSmidt, Alexandra A., Liu, Xue-Zhong, Pennings, Ronald J.E., Lu, Zhongmin, Chen, Zheng-Yi, Kremer, Hannie, Tekin, Mustafa
Foilsithe 2012

Flow of energy in the outer retina in darkness and in light

le Linton, Jonathan D., Holzhausen, Lars C., Babai, Norbert, Song, Hongman, Miyagishima, Kiyoharu J., Stearns, George W., Lindsay, Ken, Wei, Junhua, Chertov, Andrei O., Peters, Theo A., Caffe, Romeo, Pluk, Helma, Seeliger, Mathias W., Tanimoto, Naoyuki, Fong, Kimberly, Bolton, Laura, Kuok, Denise L. T., Sweet, Ian R., Bartoletti, Theodore M., Radu, Roxana A., Travis, Gabriel H., Zagotta, Willam N., Townes-Anderson, Ellen, Parker, Ed, Van der Zee, Catharina E. E. M., Sampath, Alapakkam P., Sokolov, Maxim, Thoreson, Wallace B., Hurley, James B.
Foilsithe 2010