Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish von Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A, Corral-Serrano, Julio C, Slijkerman, Ralph W N, van Wijk, Erwin, Collin, Rob W J

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Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss von YARIZ, Kemal O, DUMAN, Duygu, 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, CELIA ZAZO SECO, HUAWEI LI, ATALAY, Semra, BLANTON, Susan, DESMIDT, Alexandra A, LIU, Xue-Zhong, PENNINGS, Ronald J. E, ZHONGMIN LU, CHEN, Zheng-Yi, KREMER, Hannie, TEKIN, Mustafa, DALLMAN, Julia, MINGQIAN HUANG, PETERS, TheoA, SIRMACI, Asli, NA LU, SCHRADERS, Margit, SKROMNE, Isaac

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Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation von Slijkerman, Radulfus WN, Vaché, Christel, Dona, Margo, García-García, Gema, Claustres, Mireille, Hetterschijt, Lisette, Peters, Theo A, Hartel, Bas P, Pennings, Ronald JE, Millan, José M, Aller, Elena, Garanto, Alejandro, Collin, Rob WJ, Kremer, Hannie, Roux, Anne-Françoise, Van Wijk, Erwin

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Kidney failure in mice lacking the tetraspanin CD151 von Sachs, Norman, Kreft, Maaike, van den Bergh Weerman, Marius A, Beynon, Andy J, Peters, Theo A, Weening, Jan J, Sonnenberg, Arnoud

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

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Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis von Garanto, Alejandro, van Beersum, Sylvia E C, Peters, Theo A, Roepman, Ronald, Cremers, Frans P M, Collin, Rob W J

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome von Roepman, Ronald, Arts, Heleen H, Doherty, Dan, van Beersum, Sylvia E C, Parisi, Melissa A, Letteboer, Stef J F, Gorden, Nicholas T, Peters, Theo A, Märker, Tina, Voesenek, Krysta, Kartono, Aileen, Ozyurek, Hamit, Farin, Federico M, Kroes, Hester Y, Wolfrum, Uwe, Brunner, Han G, Cremers, Frans P M, Glass, Ian A, Knoers, Nine V A M

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Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy von Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Boldt, Karsten, de Baere, Elfride, Klaver, Caroline C.W., Coppieters, Frauke, Koolen, David A., Lugtenberg, Dorien, Neveling, Kornelia, van Reeuwijk, Jeroen, Ueffing, Marius, van Beersum, Sylvia E.C., Zonneveld-Vrieling, Marijke N., 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.

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

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ATP8B1 is essential for maintaining normal hearing von 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

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

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

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C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish von Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.

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Neurofilament localization and phosphorylation in the developing inner ear of the rat von Tonnaer, Edith L.G.M., Peters, Theo A., Curfs, Jo H.A.J.

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Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome von Balemans, Monique C M, Kasri, Nael Nadif, Kopanitsa, Maksym V, Afinowi, Nurudeen O, Ramakers, Ger, Peters, Theo A, Beynon, Andy J, Janssen, Sanne M, van Summeren, Rik C J, Eeftens, Jorine M, Eikelenboom, Nathalie, Benevento, Marco, Tachibana, Makoto, Shinkai, Yoichi, Kleefstra, Tjitske, van Bokhoven, Hans, Van der Zee, Catharina E E M

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

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The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/ threonine kinase von COENE, Karlien L. M, MANS, Dorus A, UEFFING, Marius, ROEPMAN, Ronald, BOLDT, Karsten, JOHANNES GLOECKNER, C, REEUWIJK, Jeroen Van, BOLAT, Emine, ROOSING, Susanne, LETTEBOER, Stef J. F, PETERS, Theo A, CREMERS, FransP. M

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Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein network von Kersten, Ferry F J, van Wijk, Erwin, van Reeuwijk, Jeroen, van der Zwaag, Bert, Märker, Tina, Peters, Theo A, Katsanis, Nicholas, Wolfrum, Uwe, Keunen, Jan E E, Roepman, Ronald, Kremer, Hannie

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

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Changes in ultrastructural characteristics of endolymphatic sac ribosome-rich cells of the rat during development von Peters, Theo A, Tonnaer, Edith L.G.M, Kuijpers, Wim, Curfs, Jo H.A.J

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