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Por Ghadiri, Argang., Habermacher, Andreas., Peters, Theo.
Publicado em 2012

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

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

Kidney failure in mice lacking the tetraspanin CD151

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

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

Por Corral-Serrano, Julio C., Messchaert, Muriël, Dona, Margo, Peters, Theo A., Kamminga, Leonie M., van Wijk, Erwin, Collin, Rob W. J.
Publicado no Sci Rep (2018)

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

Por Messchaert, Muriël, Dona, Margo, Broekman, Sanne, Peters, Theo A., Corral-Serrano, Julio C., Slijkerman, Ralph W. N., van Wijk, Erwin, Collin, Rob W. J.
Publicado no PLoS One (2018)

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

Por 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
Publicado em 2005

Hair Bundles Are Specialized for ATP Delivery via Creatine Kinase

Por Shin, Jung-Bum, Streijger, Femke, Beynon, Andy, Peters, Theo, Gadzalla, Laura, McMillen, Debra, Bystrom, Cory, Van der Zee, Catharina E.E.M, Wallimann, Theo, Gillespie, Peter G.
Publicado em 2007

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

Por 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
Publicado em 2012

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

Por 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
Publicado em 2009

Usherin defects lead to early-onset retinal dysfunction in zebrafish

Por Dona, Margo, Slijkerman, Ralph, Lerner, Kimberly, Broekman, Sanne, Wegner, Jeremy, Howat, Taylor, Peters, Theo, Hetterschijt, Lisette, Boon, Nando, de Vrieze, Erik, Sorusch, Nasrin, Wolfrum, Uwe, Kremer, Hannie, Neuhauss, Stephan, Zang, Jingjing, Kamermans, Maarten, Westerfield, Monte, Phillips, Jennifer, van Wijk, Erwin
Publicado no Exp Eye Res (2018)

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

Por 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.
Publicado em 2014

ATP8B1 is essential for maintaining normal hearing

Por 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.
Publicado em 2009

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

Por 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.
Publicado em 2013

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking

Por Bachmann-Gagescu, Ruxandra, Dona, Margo, Hetterschijt, Lisette, Tonnaer, Edith, Peters, Theo, de Vrieze, Erik, Mans, Dorus A., van Beersum, Sylvia E. C., Phelps, Ian G., Arts, Heleen H., Keunen, Jan E., Ueffing, Marius, Roepman, Ronald, Boldt, Karsten, Doherty, Dan, Moens, Cecilia B., Neuhauss, Stephan C. F., Kremer, Hannie, van Wijk, Erwin
Publicado no PLoS Genet (2015)

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

Por 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
Publicado no PLoS Genet (2015)

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

Por Collin, Rob W.J., Kalay, Ersan, Tariq, Muhammad, Peters, Theo, van der Zwaag, Bert, Venselaar, Hanka, Oostrik, Jaap, Lee, Kwanghyuk, Ahmed, Zubair M., Çaylan, Refik, Li, Yun, Spierenburg, Henk A., Eyupoglu, Erol, Heister, Angelien, Riazuddin, Saima, Bahat, Elif, Ansar, Muhammad, Arslan, Selcuk, Wollnik, Bernd, Brunner, Han G., Cremers, Cor W.R.J., Karaguzel, Ahmet, Ahmad, Wasim, Cremers, Frans P.M., Vriend, Gert, Friedman, Thomas B., Riazuddin, Sheikh, Leal, Suzanne M., Kremer, Hannie
Publicado em 2008

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

Por 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
Publicado em 2012

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

Por 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.
Publicado em 2010

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse

Por Wesdorp, Mieke, Murillo-Cuesta, Silvia, Peters, Theo, Celaya, Adelaida M., Oonk, Anne, Schraders, Margit, Oostrik, Jaap, Gomez-Rosas, Elena, Beynon, Andy J., Hartel, Bas P., Okkersen, Kees, Koenen, Hans J.P.M., Weeda, Jack, Lelieveld, Stefan, Voermans, Nicol C., Joosten, Irma, Hoyng, Carel B., Lichtner, Peter, Kunst, Henricus P.M., Feenstra, Ilse, de Bruijn, Suzanne E., Admiraal, Ronald J.C., Yntema, Helger G., van Wijk, Erwin, del Castillo, Ignacio, Serra, Pau, Varela-Nieto, Isabel, Pennings, Ronald J.E., Kremer, Hannie
Publicado no Am J Hum Genet (2018)