A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells
Maerker, Tina, van Wijk, Erwin, Overlack, Nora, Kersten, Ferry F.J., McGee, JoAnn, Goldmann, Tobias, Sehn, Elisabeth, Roepman, Ronald, Walsh, Edward J., Kremer, Hannie, Wolfrum, Uwe
Published in Human molecular genetics (01.01.2008)
Published in Human molecular genetics (01.01.2008)
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Journal Article
Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
Reiners, Jan, Nagel-Wolfrum, Kerstin, Jürgens, Karin, Märker, Tina, Wolfrum, Uwe
Published in Experimental eye research (01.07.2006)
Published in Experimental eye research (01.07.2006)
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Journal Article
Usher syndrome: molecular links of pathogenesis, proteins and pathways
Kremer, Hannie, van Wijk, Erwin, Märker, Tina, Wolfrum, Uwe, Roepman, Ronald
Published in Human molecular genetics (15.10.2006)
Published in Human molecular genetics (15.10.2006)
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Journal Article
Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina
Overlack, Nora, Kilic, Dilek, Bauß, Katharina, Märker, Tina, Kremer, Hannie, van Wijk, Erwin, Wolfrum, Uwe
Published in Biochimica et biophysica acta (01.10.2011)
Published in Biochimica et biophysica acta (01.10.2011)
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Journal Article
Heat Shock Protein 60 as a Mediator of Adipose Tissue Inflammation and Insulin Resistance
MÄRKER, Tina, SELL, Henrike, ECKEL, Jürgen, HABICH, Christiane, ZILLESSEN, Pia, GLÖDE, Anja, KRIEBEL, Jennifer, MARGRIET OUWENS, D, PATTYN, Piet, RUIGE, Johannes, FAMULLA, Susanne, RODEN, Michael
Published in Diabetes (New York, N.Y.) (01.03.2012)
Published in Diabetes (New York, N.Y.) (01.03.2012)
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Journal Article
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
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
Published in Nature genetics (01.07.2007)
Published in Nature genetics (01.07.2007)
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Journal Article
Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis
Bauß, Katharina, Knapp, Barbara, Jores, Pia, Roepman, Ronald, Kremer, Hannie, Wijk, Erwin V, Märker, Tina, Wolfrum, Uwe
Published in Human molecular genetics (01.08.2014)
Published in Human molecular genetics (01.08.2014)
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Journal Article
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
Reiners, Jan, van Wijk, Erwin, Märker, Tina, Zimmermann, Ulrike, Jürgens, Karin, te Brinke, Heleen, Overlack, Nora, Roepman, Ronald, Knipper, Marlies, Kremer, Hannie, Wolfrum, Uwe
Published in Human molecular genetics (15.12.2005)
Published in Human molecular genetics (15.12.2005)
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Journal Article
SANS (USH1G) expression in developing and mature mammalian retina
Overlack, Nora, Maerker, Tina, Latz, Martin, Nagel-Wolfrum, Kerstin, Wolfrum, Uwe
Published in Vision research (Oxford) (01.02.2008)
Published in Vision research (Oxford) (01.02.2008)
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Journal Article
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1
van Wijk, Erwin, van der Zwaag, Bert, Peters, Theo, Zimmermann, Ulrike, te Brinke, Heleen, Kersten, Ferry F.J., Märker, Tina, Aller, Elena, Hoefsloot, Lies H., Cremers, Cor W.R.J., Cremers, Frans P.M., Wolfrum, Uwe, Knipper, Marlies, Roepman, Ronald, Kremer, Hannie
Published in Human molecular genetics (01.03.2006)
Published in Human molecular genetics (01.03.2006)
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Journal Article
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment
Schneider, Eberhard, Märker, Tina, Daser, Angelika, Frey-Mahn, Gabriele, Beyer, Vera, Farcas, Ruxandra, Schneider-Rätzke, Brigitte, Kohlschmidt, Nicolai, Grossmann, Bärbel, Bauss, Katharina, Napiontek, Ulrike, Keilmann, Annerose, Bartsch, Oliver, Zechner, Ulrich, Wolfrum, Uwe, Haaf, Thomas
Published in Human molecular genetics (15.02.2009)
Published in Human molecular genetics (15.02.2009)
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Journal Article
Heat shock protein 60: Evidence for receptor-mediated induction of proinflammatory mediators during adipocyte differentiation
Gülden, Elke, Märker, Tina, Kriebel, Jennifer, Kolb-Bachofen, Victoria, Burkart, Volker, Habich, Christiane
Published in FEBS letters (03.09.2009)
Published in FEBS letters (03.09.2009)
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Journal Article
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein
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
Published in Human molecular genetics (01.01.2009)
Published in Human molecular genetics (01.01.2009)
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Journal Article
MPP1 links the Usher protein network and the Crumbs protein complex in the retina
Gosens, Ilse, van Wijk, Erwin, Kersten, Ferry F.J., Krieger, Elmar, van der Zwaag, Bert, Märker, Tina, Letteboer, Stef J.F., Dusseljee, Simone, Peters, Theo, Spierenburg, Henk A., Punte, Ingrid M., Wolfrum, Uwe, Cremers, Frans P.M., Kremer, Hannie, Roepman, Ronald
Published in Human molecular genetics (15.08.2007)
Published in Human molecular genetics (15.08.2007)
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