Staying with the Breaks, Dispropriating the Universal: A Response to Eva-Lynn Jagoe von Aiello, Rosa, Annerborn, Erik, Benivolski, Xenia, Chew, May, Cwynar, Sara, Fratila, Stefana, Goldstein, Jesse, Huber, Sandra, Hunter-Young, Nataleah, Kang, Laurie, Kenney, Martha, Lansdowne, Tristram, Lee, Yaniya, Litwack, Michael, McGeough, Ella Dawn, Schaefer, Sandrine, Schneider-Mayerson, Matthew, Wright, Shevaun, Dean, Jodi, Povinelli, Elizabeth A.

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Cell and Molecular Physiology Section of the American Physiological Society in connection with American Journal of Physiology-Cell Physiology von Schaefer, Liliana, Pierre, Sandrine V

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Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1 von Garrelfs, Sander F, Frishberg, Yaacov, Hulton, Sally A, Koren, Michael J, O’Riordan, William D, Cochat, Pierre, Deschênes, Georges, Shasha-Lavsky, Hadas, Saland, Jeffrey M, van’t Hoff, William G, Fuster, Daniel G, Magen, Daniella, Moochhala, Shabbir H, Schalk, Gesa, Simkova, Eva, Groothoff, Jaap W, Sas, David J, Meliambro, Kristin A, Lu, Jiandong, Sweetser, Marianne T, Garg, Pushkal P, Vaishnaw, Akshay K, Gansner, John M, McGregor, Tracy L, Lieske, John C

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Calcium distribution patterns of the aortic valve as a risk factor for the need of permanent pacemaker implantation after transcatheter aortic valve implantation von Fujita, Buntaro, Kütting, Maximilian, Seiffert, Moritz, Scholtz, Smita, Egron, Sandrine, Prashovikj, Emir, Börgermann, Jochen, Schäfer, Timm, Scholtz, Werner, Preuss, Rainer, Gummert, Jan, Steinseifer, Ulrich, Ensminger, Stephan M

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Treacher Collins syndrome: a clinical and molecular study based on a large series of patients von Vincent, Marie, Geneviève, David, Ostertag, Agnès, Marlin, Sandrine, Lacombe, Didier, Martin-Coignard, Dominique, Coubes, Christine, David, Albert, Lyonnet, Stanislas, Vilain, Catheline, Dieux-Coeslier, Anne, Manouvrier, Sylvie, Isidor, Bertrand, Jacquemont, Marie-Line, Julia, Sophie, Layet, Valérie, Naudion, Sophie, Odent, Sylvie, Pasquier, Laurent, Pelras, Sybille, Philip, Nicole, Pierquin, Geneviève, Prieur, Fabienne, Aboussair, Nisrine, Attie-Bitach, Tania, Baujat, Geneviève, Blanchet, Patricia, Blanchet, Catherine, Dollfus, Hélène, Doray, Bérénice, Schaefer, Elise, Edery, Patrick, Giuliano, Fabienne, Goldenberg, Alice, Goizet, Cyril, Guichet, Agnès, Herlin, Christian, Lambert, Laetitia, Leheup, Bruno, Martinovic, Jelena, Mercier, Sandra, Mignot, Cyril, Moutard, Marie-Laure, Perez, Marie-José, Pinson, Lucile, Puechberty, Jacques, Willems, Marjolaine, Randrianaivo, Hanitra, Szaskon, Kateline, Toutain, Annick, Verloes, Alain, Vigneron, Jacqueline, Sanchez, Elodie, Sarda, Pierre, Laplanche, Jean-Louis, Collet, Corinne

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2278 EUROCYS, a European cystinuria registry von Servais, Aude, Capolongo, Giovanna, Tostivint, Isabelle, Lemoine, Sandrine, Ferraro, Pietro Manuel, Decramer, Stephane, Ruggenent, Piero, Capelli, Irene, Engberink, Rik Olde, Schaefer, Franz, Knebelmann, Bertrand, Courbebaisse, Marie

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TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus von Duy, Phan Q, Jux, Bettina, Zhao, Shujuan, Mekbib, Kedous Y, Dennis, Evan, Dong, Weilai, Nelson-Williams, Carol, Mehta, Neel H, Shohfi, John P, Juusola, Jane, Allington, Garrett, Smith, Hannah, Marlin, Sandrine, Belhous, Kahina, Monteleone, Berrin, Schaefer, G Bradley, Pisarska, Margareta D, Vásquez, Jaime, Estrada-Veras, Juvianee I, Keren, Boris, Mignot, Cyril, Flore, Leigh A, Palafoll, Irene V, Alper, Seth L, Lifton, Richard P, Haider, Shozeb, Moreno-De-Luca, Andres, Jin, Sheng Chih, Kolanus, Waldemar, Kahle, Kristopher T

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Modulation of Oral Bioavailability and Metabolism for Closely Related Cyclic Hexapeptides von Vorherr, Thomas, Lewis, Ian, Berghausen, Joerg, Desrayaud, Sandrine, Schaefer, Michael

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Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study von White, Helen E., Salmon, Matthew, Albano, Francesco, Andersen, Christina Søs Auður, Balabanov, Stefan, Balatzenko, Gueorgui, Barbany, Gisela, Cayuela, Jean-Michel, Cerveira, Nuno, Cochaux, Pascale, Colomer, Dolors, Coriu, Daniel, Diamond, Joana, Dietz, Christian, Dulucq, Stéphanie, Engvall, Marie, Franke, Georg N., Gineikiene-Valentine, Egle, Gniot, Michal, Gómez-Casares, María Teresa, Gottardi, Enrico, Hayden, Chloe, Hayette, Sandrine, Hedblom, Andreas, Ilea, Anca, Izzo, Barbara, Jiménez-Velasco, Antonio, Jurcek, Tomas, Kairisto, Veli, Langabeer, Stephen E., Lion, Thomas, Meggyesi, Nora, Mešanović, Semir, Mihok, Luboslav, Mitterbauer-Hohendanner, Gerlinde, Moeckel, Sylvia, Naumann, Nicole, Nibourel, Olivier, Oppliger Leibundgut, Elisabeth, Panayiotidis, Panayiotis, Podgornik, Helena, Pott, Christiane, Rapado, Inmaculada, Rose, Susan J., Schäfer, Vivien, Touloumenidou, Tasoula, Veigaard, Christopher, Venniker-Punt, Bianca, Venturi, Claudia, Vigneri, Paolo, Vorkinn, Ingvild, Wilkinson, Elizabeth, Zadro, Renata, Zawada, Magdalena, Zizkova, Hana, Müller, Martin C., Saussele, Susanne, Ernst, Thomas, Machova Polakova, Katerina, Hochhaus, Andreas, Cross, Nicholas C. P.

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Autosomal recessive primary microcephaly due to ASPM mutations: An update von Létard, Pascaline, Drunat, Séverine, Vial, Yoann, Duerinckx, Sarah, Ernault, Anais, Amram, Daniel, Arpin, Stéphanie, Bertoli, Marta, Busa, Tiffany, Ceulemans, Berten, Desir, Julie, Doco‐Fenzy, Martine, Elalaoui, Siham Chafai, Devriendt, Koenraad, Faivre, Laurence, Francannet, Christine, Geneviève, David, Gérard, Marion, Gitiaux, Cyril, Julia, Sophie, Lebon, Sébastien, Lubala, Toni, Mathieu‐Dramard, Michèle, Maurey, Hélène, Metreau, Julia, Nasserereddine, Sanaa, Nizon, Mathilde, Pierquin, Geneviève, Pouvreau, Nathalie, Rivier‐Ringenbach, Clothilde, Rossi, Massimiliano, Schaefer, Elise, Sefiani, Abdelaziz, Sigaudy, Sabine, Sznajer, Yves, Tunca, Yusuf, Guilmin Crepon, Sophie, Alberti, Corinne, Elmaleh‐Bergès, Monique, Benzacken, Brigitte, Wollnick, Bernd, Woods, C. Geoffrey, Rauch, Anita, Abramowicz, Marc, El Ghouzzi, Vincent, Gressens, Pierre, Verloes, Alain, Passemard, Sandrine

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Mitotic figure counts are significantly overestimated in resection specimens of invasive breast carcinomas von Lehr, Hans-Anton, Rochat, Candice, Schaper, Cornelia, Nobile, Antoine, Shanouda, Sherien, Vijgen, Sandrine, Gauthier, Arnaud, Obermann, Ellen, Leuba, Susana, Schmidt, Marcus, C, Curzio Ruegg, Delaloye, Jean-Francois, Simiantonaki, Nectaria, Schaefer, Stephan C

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Amelogenesis imperfecta : Next-generation sequencing sheds light on Witkop's classification von Bloch-Zupan, Agnes, Rey, Tristan, Jimenez-Armijo, Alexandra, Kawczynski, Marzena, Kharouf, Naji, Dure-Molla, Muriel de La, Noirrit, Emmanuelle, Hernandez, Magali, Joseph-Beaudin, Clara, Lopez, Serena, Tardieu, Corinne, Thivichon-Prince, Béatrice, Dostalova, Tatjana, Macek, Jr, Milan, Alloussi, Mustapha El, Qebibo, Leila, Morkmued, Supawich, Pungchanchaikul, Patimaporn, Orellana, Blanca Urzúa, Manière, Marie-Cécile, Gérard, Bénédicte, Bugueno, Isaac Maximiliano, Laugel-Haushalter, Virginie

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Neoadjuvant Chemoradiotherapy versus Chemotherapy for Gastroesophageal Junction Adenocarcinoma; Which Is the Optimal Treatment Option? von Zandirad, Eric, Teixeira Farinha, Hugo, Barberá-Carbonell, Beatriz, Geinoz, Sandrine, Demartines, Nicolas, Schäfer, Markus, Mantziari, Styliani

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Cerebral dural arteriovenous fistulas in patients with PTEN‐related hamartoma tumor syndrome von Gerasimenko, Anna, Mignot, Cyril, Naggara, Olivier, Coulet, Florence, Ekram, Samar, Heide, Solveig, Sorato, Clarisse, Mazowiecki, Maxime, Perrin, Laurence, Colas, Chrystelle, Cusin, Veronica, Caux, Frédéric, Dardenne, Antoine, El Chehadeh, Salima, Verloes, Alain, Maurey, Hélène, Afenjar, Alexandra, Petit, Florence, Barete, Stéphane, Boespflug‐Tanguy, Odile, Bourrat, Emmanuelle, Capri, Yline, Ciorna, Viorica, Deb, Wallid, Doummar, Diane, Perrier, Alexandre, Guédon, Alexis, Houdart, Emmanuel, Isidor, Bertrand, Jacquemont, Marie‐Line, Buffet, Camille, Mercier, Sandra, Passemard, Sandrine, Riquet, Audrey, Ruaud, Lyse, Schaefer, Elise, Heron, Delphine, Bisdorff, Annouk, Benusiglio, Patrick R.

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Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder von Courraud, Jérémie, Chater-Diehl, Eric, Durand, Benjamin, Vincent, Marie, del Mar Muniz Moreno, Maria, Boujelbene, Imene, Drouot, Nathalie, Genschik, Loréline, Schaefer, Elise, Nizon, Mathilde, Gerard, Bénédicte, Abramowicz, Marc, Cogné, Benjamin, Bronicki, Lucas, Burglen, Lydie, Barth, Magalie, Charles, Perrine, Colin, Estelle, Coubes, Christine, David, Albert, Delobel, Bruno, Demurger, Florence, Passemard, Sandrine, Denommé, Anne-Sophie, Faivre, Laurence, Feger, Claire, Fradin, Mélanie, Francannet, Christine, Genevieve, David, Goldenberg, Alice, Guerrot, Anne-Marie, Isidor, Bertrand, Johannesen, Katrine M., Keren, Boris, Kibæk, Maria, Kuentz, Paul, Mathieu-Dramard, Michèle, Demeer, Bénédicte, Metreau, Julia, Steensbjerre Møller, Rikke, Moutton, Sébastien, Pasquier, Laurent, Pilekær Sørensen, Kristina, Perrin, Laurence, Renaud, Mathilde, Saugier, Pascale, Rio, Marlène, Svane, Joane, Thevenon, Julien, Tran Mau Them, Frédéric, Tronhjem, Cathrine Elisabeth, Vitobello, Antonio, Layet, Valérie, Auvin, Stéphane, Khachnaoui, Khaoula, Birling, Marie-Christine, Drunat, Séverine, Bayat, Allan, Dubourg, Christèle, El Chehadeh, Salima, Fagerberg, Christina, Mignot, Cyril, Guipponi, Michel, Bienvenu, Thierry, Herault, Yann, Thompson, Julie, Willems, Marjolaine, Mandel, Jean-Louis, Weksberg, Rosanna, Piton, Amélie

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Design and Development of a Cyclic Decapeptide Scaffold with Suitable Properties for Bioavailability and Oral Exposure von Fouché, Marianne, Schäfer, Michael, Berghausen, Jörg, Desrayaud, Sandrine, Blatter, Markus, Piéchon, Philippe, Dix, Ina, Martin Garcia, Aimar, Roth, Hans-Jörg

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Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11 von Goldenberg, Alice, Riccardi, Florence, Tessier, Aude, Pfundt, Rolph, Busa, Tiffany, Cacciagli, Pierre, Capri, Yline, Coutton, Charles, Delahaye-Duriez, Andree, Frebourg, Thierry, Gatinois, Vincent, Guerrot, Anne-Marie, Genevieve, David, Lecoquierre, Francois, Jacquette, Aurélia, Khau Van Kien, Philippe, Leheup, Bruno, Marlin, Sandrine, Verloes, Alain, Michaud, Vincent, Nadeau, Gwenael, Mignot, Cyril, Parent, Philippe, Rossi, Massimiliano, Toutain, Annick, Schaefer, Elise, Thauvin-Robinet, Christel, Van Maldergem, Lionel, Thevenon, Julien, Satre, Véronique, Perrin, Laurence, Vincent-Delorme, Catherine, Sorlin, Arthur, Missirian, Chantal, Villard, Laurent, Mancini, Julien, Saugier-Veber, Pascale, Philip, Nicole

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Modelling survival: exposure pattern, species sensitivity and uncertainty von Ashauer, Roman, Albert, Carlo, Augustine, Starrlight, Cedergreen, Nina, Charles, Sandrine, Ducrot, Virginie, Focks, Andreas, Gabsi, Faten, Gergs, André, Goussen, Benoit, Jager, Tjalling, Kramer, Nynke I., Nyman, Anna-Maija, Poulsen, Veronique, Reichenberger, Stefan, Schäfer, Ralf B., Van den Brink, Paul J., Veltman, Karin, Vogel, Sören, Zimmer, Elke I., Preuss, Thomas G.

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Sex dependence of postoperative pulmonary complications – A post hoc unmatched and matched analysis of LAS VEGAS von Hollmann, Markus W., Kahn, David, Heyse, Bjorn, Van Limmen, Jurgen, Damster, Sandrine, Juros-Zovko, Marina, Pernar, Selma, Miskovic, Petar, Zilic, Antonio, Frkovic, Vedran, Mirkovic, Ivan, Saric, Jadranka Pavicic, Erceg, Gorjana, Pavicic, Anna Marija, Radocaj, Tomislav, Sehovic, Mirna, Harazim, Hana, Dzurnakova, Paula, Liskova, Katarina, Filipsky, Radek, Abdel-Razek, Ahmed, Sarapuu, Kaili, Mall, Merilin, Treschan, Tanja, Wrigge, Hermann, Simon, Philipp, Reske, Andreas, Andreou, Antonis, Theodoraki, Kassiani, Sidiropoulou, Tatiana, Zafeiropoulou, Foteini, Pourzitaki, Chryssa, Bystritski, Dmitri, Pesce, Caterina Valeria, Marrella, Antonella, De Michele, Michele, Sottosanti, Luigi Giancarlo Vicari, Cinnella, Gilda, Molin, Alexandre, Pellerano, Giulia, Pezzatto, Stefano, Zangrillo, Alberto, Tarzia, Valentina, Delunas, Luigi, Baciarello, Marco, Karbonskiene, Aurika, Tikuisis, Renatas, Borg, Francis Joseph, Hollmann, Markus, Werger, Alice, Wutai, Stanley, Ferreira, Daniel, Amaral, Joana, Cadilha, Susana, Correia, Mariana, Ricardo, Ana, Negoita, Silvius, Popescu, Mihai, Petcu, Ana Maria, Costea, Dan, Korolkov, Oleg, Lugovoy, Alexander, Pejakovic, Jasmina, Mihajlovic, Dunja, Pekle-Golez, Ana, Unzueta, Mari Carmen, Fava, Josep, Perez, Gisela, de Andrés Ibañez, Jose Antonio, Ferrando, Carlos, Rico, Jesus, Sanli, Suat, Yilmaz, Murat, Senturk, Nuzhet Mert, Sivrikoz, Nukhet, Toraman, Fevzi, Senturk, Ozgur, Maral, Jale, Rousseau, Guy, Wayman, Lisa, Deane, Jill, Williams, John, Pulletz, Mark, Brown, Lucy, Goodall, Cait, Kusre, Sandeep, Everett, Lynn, Clements, Deborah, Creagh-Brown, Ben, Franklin, Danielle, Minto, Gary, Calton, Emily, Jackson, Clare, Paddle, Jonathan, Welch, Leanne, Das, Ashok, Algarsamy, Shivarajan, Szewczyk, Margaret, Smith, Thomas, Luzier, Elizabeth

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Wide clinical spectrum in ALG8-CDG: clues from molecular findings suggest an explanation for a milder phenotype in the first-described patient von Vuillaumier-Barrot, Sandrine, Schiff, Manuel, Mattioli, Francesca, Schaefer, Elise, Dupont, Audrey, Dancourt, Julia, Dupré, Thierry, Couvineau, Alain, de Baulny, Hélène Ogier, de Lonlay, Pascale, Seta, Nathalie, Moore, Stuart, Chantret, Isabelle

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