Ciliary entry of the kinesin-2 motor KIF17 is regulated by importin-β2 and RanGTP von Dishinger, John F., Kee, Hooi Lynn, Jenkins, Paul M., Fan, Shuling, Hurd, Toby W., Hammond, Jennetta W., Truong, Yen Nhu-Thi, Margolis, Ben, Martens, Jeffrey R., Verhey, Kristen J.

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Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling von Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Yasunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O’Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Omran, Heymut, Lee, Eva Y.-H.P., Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm

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Localization of retinitis pigmentosa 2 to cilia is regulated by Importin β2 von Hurd, Toby W, Fan, Shuling, Margolis, Ben L

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FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair von Zhou, Weibin, Otto, Edgar A, Cluckey, Andrew, Airik, Rannar, Hurd, Toby W, Chaki, Moumita, Diaz, Katrina, Lach, Francis P, Bennett, Geoffrey R, Gee, Heon Yung, Ghosh, Amiya K, Natarajan, Sivakumar, Thongthip, Supawat, Veturi, Uma, Allen, Susan J, Janssen, Sabine, Ramaswami, Gokul, Dixon, Joanne, Burkhalter, Felix, Spoendlin, Martin, Moch, Holger, Mihatsch, Michael J, Verine, Jerome, Reade, Richard, Soliman, Hany, Godin, Michel, Kiss, Denes, Monga, Guido, Mazzucco, Gianna, Amann, Kerstin, Artunc, Ferruh, Newland, Ronald C, Wiech, Thorsten, Zschiedrich, Stefan, Huber, Tobias B, Friedl, Andreas, Slaats, Gisela G, Joles, Jaap A, Goldschmeding, Roel, Washburn, Joseph, Giles, Rachel H, Levy, Shawn, Smogorzewska, Agata, Hildebrandt, Friedhelm

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The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification von Cross, Sally H., Mckie, Lisa, Hurd, Toby W., Riley, Sam, Wills, Jimi, Barnard, Alun R., Young, Fiona, MacLaren, Robert E., Jackson, Ian J.

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Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia von Austin-Tse, Christina, Halbritter, Jan, Zariwala, Maimoona A., Gilberti, Renée M., Gee, Heon Yung, Hellman, Nathan, Pathak, Narendra, Liu, Yan, Panizzi, Jennifer R., Patel-King, Ramila S., Tritschler, Douglas, Bower, Raqual, O’Toole, Eileen, Porath, Jonathan D., Hurd, Toby W., Chaki, Moumita, Diaz, Katrina A., Kohl, Stefan, Lovric, Svjetlana, Hwang, Daw-Yang, Braun, Daniela A., Schueler, Markus, Airik, Rannar, Otto, Edgar A., Leigh, Margaret W., Noone, Peadar G., Carson, Johnny L., Davis, Stephanie D., Pittman, Jessica E., Ferkol, Thomas W., Atkinson, Jeffry J., Olivier, Kenneth N., Sagel, Scott D., Dell, Sharon D., Rosenfeld, Margaret, Milla, Carlos E., Loges, Niki T., Omran, Heymut, Porter, Mary E., King, Stephen M., Knowles, Michael R., Drummond, Iain A., Hildebrandt, Friedhelm

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Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome von Gee, Heon Yung, Ashraf, Shazia, Wan, Xiaoyang, Vega-Warner, Virginia, Esteve-Rudd, Julian, Lovric, Svjetlana, Fang, Humphrey, Hurd, Toby W., Sadowski, Carolin E., Allen, Susan J., Otto, Edgar A., Korkmaz, Emine, Washburn, Joseph, Levy, Shawn, Williams, David S., Bakkaloglu, Sevcan A., Zolotnitskaya, Anna, Ozaltin, Fatih, Zhou, Weibin, Hildebrandt, Friedhelm

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Mechanisms of Nephronophthisis and Related Ciliopathies von Hurd, Toby W., Hildebrandt, Friedhelm

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Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling von Airik, Rannar, Slaats, Gisela G, Guo, Zhi, Weiss, Anna-Carina, Khan, Naheed, Ghosh, Amiya, Hurd, Toby W, Bekker-Jensen, Simon, Schrøder, Jacob M, Elledge, Steve J, Andersen, Jens S, Kispert, Andreas, Castelli, Maddalena, Boletta, Alessandra, Giles, Rachel H, Hildebrandt, Friedhelm

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Trafficking of Crumbs3 during cytokinesis is crucial for lumen formation von Schlüter, Marc A, Pfarr, Catherine S, Pieczynski, Jay, Whiteman, Eileen L, Hurd, Toby W, Fan, Shuling, Liu, Chia-Jen, Margolis, Ben

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Direct interaction of two polarity complexes implicated in epithelial tight junction assembly von Macara, Ian G, Margolis, Ben, Hurd, Toby W, Gao, Lin, Roh, Michael H

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Ciliary Targeting of Olfactory CNG Channels Requires the CNGB1b Subunit and the Kinesin-2 Motor Protein, KIF17 von Jenkins, Paul M., Hurd, Toby W., Zhang, Lian, McEwen, Dyke P., Brown, R. Lane, Margolis, Ben, Verhey, Kristen J., Martens, Jeffrey R.

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Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies von Gee, Heon Yung, Otto, Edgar A., Hurd, Toby W., Ashraf, Shazia, Chaki, Moumita, Cluckey, Andrew, Vega-Warner, Virginia, Saisawat, Pawaree, Diaz, Katrina A., Fang, Humphrey, Kohl, Stefan, Allen, Susan J., Airik, Rannar, Zhou, Weibin, Ramaswami, Gokul, Janssen, Sabine, Fu, Clementine, Innis, Jamie L., Weber, Stefanie, Vester, Udo, Davis, Erica E., Katsanis, Nicholas, Fathy, Hanan M., Jeck, Nikola, Klaus, Gunther, Nayir, Ahmet, Rahim, Khawla A., Attrach, Ibrahim Al, Hassoun, Ibrahim Al, Ozturk, Savas, Drozdz, Dorota, Helmchen, Udo, O'Toole, John F., Attanasio, Massimo, Lewis, Richard A., Nürnberg, Gudrun, Nürnberg, Peter, Washburn, Joseph, MacDonald, James, Innis, Jeffrey W., Levy, Shawn, Hildebrandt, Friedhelm

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Mutation of the Mg2+ Transporter SLC41A1 Results in a Nephronophthisis-Like Phenotype von HURD, Toby W, OTTO, Edgar A, WEIBIN ZHOU, YAMANE, Tsutomo, MURAKAMI, Satoshi, CARIDI, Gianluca, GHIGGERI, Gianmarco, ABE, Takaaki, HILDEBRANDT, Friedhelm, MISHIMA, Eikan, HEON YUNG GEE, INOUE, Hana, INAZU, Masato, YAMADA, Hideomi, HALBRITTER, Jan, SEKI, George, KONISHI, Masato

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SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling von Airik, Rannar, Schueler, Markus, Airik, Merlin, Cho, Jang, Ulanowicz, Kelsey A, Porath, Jonathan D, Hurd, Toby W, Bekker-Jensen, Simon, Schrøder, Jacob M, Andersen, Jens S, Hildebrandt, Friedhelm

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Polarity Proteins Control Ciliogenesis via Kinesin Motor Interactions von Fan, Shuling, Hurd, Toby W., Liu, Chia-Jen, Straight, Samuel W., Weimbs, Thomas, Hurd, Elizabeth A., Domino, Steven E., Margolis, Ben

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Induction of Ran GTP drives ciliogenesis von Fan, Shuling, Whiteman, Eileen L, Hurd, Toby W, McIntyre, Jeremy C, Dishinger, John F, Liu, Chia Jen, Martens, Jeffrey R, Verhey, Kristen J, Sajjan, Uma, Margolis, Ben

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Deletion of TSPO Causes Dysregulation of Cholesterol Metabolism in Mouse Retina von Farhan, Fahad, Almarhoun, Mohammad, Wong, Aileen, Findlay, Amy S., Bartholomew, Chris, Williams, Mark T. S., Hurd, Toby W., Shu, Xinhua

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Functional analysis of retinitis pigmentosa 2 (RP2) protein reveals variable pathogenic potential of disease-associated missense variants von Patil, Suresh B, Hurd, Toby W, Ghosh, Amiya K, Murga-Zamalloa, Carlos A, Khanna, Hemant

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RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport Proteins von Khanna, Hemant, Hurd, Toby W., Lillo, Concepcion, Shu, Xinhua, Parapuram, Sunil K., He, Shirley, Akimoto, Masayuki, Wright, Alan F., Margolis, Ben, Williams, David S., Swaroop, Anand

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