Progesterone Receptor-A and -B Have Opposite Effects on Proinflammatory Gene Expression in Human Myometrial Cells: Implications for Progesterone Actions in Human Pregnancy and Part... von Tan, Huiqing, Yi, Lijuan, Rote, Neal S, Hurd, William W, Mesiano, Sam

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Current diagnosis and treatment of interstitial pregnancy von Moawad, Nash S., MD, Mahajan, Sangeeta T., MD, Moniz, Michelle H., MD, Taylor, Sarah E., MD, Hurd, William W., MD, MSc

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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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Congenital Uterine Malformation by Experts (CUME): better criteria for distinguishing between normal/arcuate and septate uterus? von Ludwin, A., Martins, W. P., Nastri, C. O., Ludwin, I., Coelho Neto, M. A., Leitão, V. M., Acién, M., Alcazar, J. L., Benacerraf, B., Condous, G., De Wilde, R.‐L., Emanuel, M. H., Gibbons, W., Guerriero, S., Hurd, W. W., Levine, D., Lindheim, S., Pellicer, A., Petraglia, F., Saridogan, E.

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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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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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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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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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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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Differential Effects of Pancreatic Cancer-Derived Extracellular Vesicles Driving a Suppressive Environment von Purushothaman, Anurag, Oliva-Ramírez, Jacqueline, Treekitkarnmongkol, Warapen, Sankaran, Deivendran, Hurd, Mark W, Putluri, Nagireddy, Maitra, Anirban, Haymaker, Cara, Sen, Subrata

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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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3D imaging analysis on an organoid-based platform guides personalized treatment in pancreatic ductal adenocarcinoma von Kang, Ya'an, Deng, Jenying, Ling, Jianhua, Li, Xinqun, Chiang, Yi-Ju, Koay, Eugene J, Wang, Huamin, Burks, Jared K, Chiao, Paul J, Hurd, Mark W, Bhutani, Manoop S, Lee, Jeffrey H, Weston, Brian R, Maitra, Anirban, Ikoma, Naruhiko, Tzeng, Ching-Wei D, Lee, Jeffrey E, DePinho, Ronald A, Wolff, Robert A, Pant, Shubham, McAllister, Florencia, Katz, Matthew Hg, Fleming, Jason B, Kim, Michael P

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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy von Otto, Edgar A, Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J, Zhou, Weibin, Airik, Rannar, Hurd, Toby W, Ghosh, Amiya K, Wolf, Matthias T, Hoppe, Bernd, Neuhaus, Thomas J, Bockenhauer, Detlef, Milford, David V, Soliman, Neveen A, Antignac, Corinne, Saunier, Sophie, Johnson, Colin A, Hildebrandt, Friedhelm

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Congenital Uterine Malformation by Experts (CUME): diagnostic criteria for T‐shaped uterus von Ludwin, A., Coelho Neto, M. A., Ludwin, I., Nastri, C. O., Costa, W., Acién, M., Alcazar, J. L., Benacerraf, B., Condous, G., DeCherney, A., De Wilde, R.‐L., Diamond, M. P., Emanuel, M. H., Guerriero, S., Hurd, W., Levine, D., Lindheim, S., Pellicer, A., Petraglia, F., Saridogan, E., Martins, W. P.

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

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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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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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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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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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