Morphogenetic fields within the human dentition: A new, clinically relevant synthesis of an old concept()

gan Townsend, Grant, Harris, Edward F., Lesot, Herve, Clauss, Francois, Brook, Alan
Cyhoeddwyd 2009

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

gan Reibel, Amélie, Manière, Marie-Cécile, Clauss, François, Droz, Dominique, Alembik, Yves, Mornet, Etienne, Bloch-Zupan, Agnès
Cyhoeddwyd 2009

Eruption of Bioengineered Teeth: A New Approach Based on a Polycaprolactone Biomembrane

gan Stutz, Céline, Clauss, François, Huck, Olivier, Schulz, Georg, Benkirane-Jessel, Nadia, Bornert, Fabien, Kuchler-Bopp, Sabine, Strub, Marion
Cyhoeddwyd yn Nanomaterials (Basel) (2021)

Subtle Morphological Changes in the Mandible of Tabby Mice Revealed by Micro-CT Imaging and Elliptical Fourier Quantification

gan Bornert, Fabien, Choquet, Philippe, Gros, Catherine I., Aubertin, Gaelle, Perrin-Schmitt, Fabienne, Clauss, François, Lesot, Hervé, Constantinesco, André, Schmittbuhl, Matthieu
Cyhoeddwyd 2011

Maxillary Bone Regeneration Based on Nanoreservoirs Functionalized ε-Polycaprolactone Biomembranes in a Mouse Model of Jaw Bone Lesion

gan Strub, Marion, Van Bellinghen, Xavier, Fioretti, Florence, Bornert, Fabien, Benkirane-Jessel, Nadia, Idoux-Gillet, Ysia, Kuchler-Bopp, Sabine, Clauss, François
Cyhoeddwyd yn Biomed Res Int (2018)

A New Polycaprolactone-Based Biomembrane Functionalized with BMP-2 and Stem Cells Improves Maxillary Bone Regeneration

gan Stutz, Céline, Strub, Marion, Clauss, François, Huck, Olivier, Schulz, Georg, Gegout, Hervé, Benkirane-Jessel, Nadia, Bornert, Fabien, Kuchler-Bopp, Sabine
Cyhoeddwyd yn Nanomaterials (Basel) (2020)

Periodontal Tissues, Maxillary Jaw Bone, and Tooth Regeneration Approaches: From Animal Models Analyses to Clinical Applications

gan Batool, Fareeha, Strub, Marion, Petit, Catherine, Bugueno, Isaac Maximiliano, Bornert, Fabien, Clauss, François, Huck, Olivier, Kuchler-Bopp, Sabine, Benkirane-Jessel, Nadia
Cyhoeddwyd yn Nanomaterials (Basel) (2018)

Application of Chitosan in Bone and Dental Engineering

gan Aguilar, Alicia, Zein, Naimah, Harmouch, Ezeddine, Hafdi, Brahim, Bornert, Fabien, Offner, Damien, Clauss, François, Fioretti, Florence, Huck, Olivier, Benkirane-Jessel, Nadia, Hua, Guoqiang
Cyhoeddwyd yn Molecules (2019)

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss

gan Morkmued, Supawich, Clauss, François, Schuhbaur, Brigitte, Fraulob, Valérie, Mathieu, Eric, Hemmerlé, Joseph, Clevers, Hans, Koo, Bon-Kyoung, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen
Cyhoeddwyd yn Sci Rep (2020)

Polymer-Based Instructive Scaffolds for Endodontic Regeneration

gan Zein, Naimah, Harmouch, Ezeddine, Lutz, Jean-Christophe, Fernandez De Grado, Gabriel, Kuchler-Bopp, Sabine, Clauss, François, Offner, Damien, Hua, Guoqiang, Benkirane-Jessel, Nadia, Fioretti, Florence
Cyhoeddwyd yn Materials (Basel) (2019)

Temporomandibular joint damage in K/BxN arthritic mice

gan Kuchler-Bopp, Sabine, Mariotte, Alexandre, Strub, Marion, Po, Chrystelle, De Cauwer, Aurore, Schulz, Georg, Van Bellinghen, Xavier, Fioretti, Florence, Clauss, François, Georgel, Philippe, Benkirane-Jessel, Nadia, Bornert, Fabien
Cyhoeddwyd yn Int J Oral Sci (2020)

Temporomandibular Joint Regenerative Medicine

gan Van Bellinghen, Xavier, Idoux-Gillet, Ysia, Pugliano, Marion, Strub, Marion, Bornert, Fabien, Clauss, Francois, Schwinté, Pascale, Keller, Laetitia, Benkirane-Jessel, Nadia, Kuchler-Bopp, Sabine, Lutz, Jean Christophe, Fioretti, Florence
Cyhoeddwyd yn Int J Mol Sci (2018)

Targeted Apc;Twist Double-Mutant Mice: A New Model of Spontaneous Osteosarcoma That Mimics the Human Disease

gan Entz-Werlé, Natacha, Choquet, Philippe, Neuville, Agnès, Kuchler-Bopp, Sabine, Clauss, François, Danse, Jean-Marc, Simo-Noumbissie, Pauline, Guérin, Eric, Gaub, Marie-Pierre, Freund, Jean-Noel, Boehm, Nelly, Constantinesco, André, Lutz, Patrick, Guenot, Dominique, Perrin-Schmitt, Fabienne
Cyhoeddwyd 2010

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta

gan Huckert, Mathilde, Stoetzel, Corinne, Morkmued, Supawich, Laugel-Haushalter, Virginie, Geoffroy, Véronique, Muller, Jean, Clauss, François, Prasad, Megana K., Obry, Frédéric, Raymond, Jean Louis, Switala, Marzena, Alembik, Yves, Soskin, Sylvie, Mathieu, Eric, Hemmerlé, Joseph, Weickert, Jean-Luc, Dabovic, Branka Brukner, Rifkin, Daniel B., Dheedene, Annelies, Boudin, Eveline, Caluseriu, Oana, Cholette, Marie-Claude, Mcleod, Ross, Antequera, Reynaldo, Gellé, Marie-Paule, Coeuriot, Jean-Louis, Jacquelin, Louis-Frédéric, Bailleul-Forestier, Isabelle, Manière, Marie-Cécile, Van Hul, Wim, Bertola, Debora, Dollé, Pascal, Verloes, Alain, Mortier, Geert, Dollfus, Hélène, Bloch-Zupan, Agnès
Cyhoeddwyd yn Hum Mol Genet (2015)

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

gan Prasad, Megana K, Geoffroy, Véronique, Vicaire, Serge, Jost, Bernard, Dumas, Michael, Le Gras, Stéphanie, Switala, Marzena, Gasse, Barbara, Laugel-Haushalter, Virginie, Paschaki, Marie, Leheup, Bruno, Droz, Dominique, Dalstein, Amelie, Loing, Adeline, Grollemund, Bruno, Muller-Bolla, Michèle, Lopez-Cazaux, Séréna, Minoux, Maryline, Jung, Sophie, Obry, Frédéric, Vogt, Vincent, Davideau, Jean-Luc, Davit-Beal, Tiphaine, Kaiser, Anne-Sophie, Moog, Ute, Richard, Béatrice, Morrier, Jean-Jacques, Duprez, Jean-Pierre, Odent, Sylvie, Bailleul-Forestier, Isabelle, Rousset, Monique Marie, Merametdijan, Laure, Toutain, Annick, Joseph, Clara, Giuliano, Fabienne, Dahlet, Jean-Christophe, Courval, Aymeric, El Alloussi, Mustapha, Laouina, Samir, Soskin, Sylvie, Guffon, Nathalie, Dieux, Anne, Doray, Bérénice, Feierabend, Stephanie, Ginglinger, Emmanuelle, Fournier, Benjamin, de la Dure Molla, Muriel, Alembik, Yves, Tardieu, Corinne, Clauss, François, Berdal, Ariane, Stoetzel, Corinne, Manière, Marie Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès
Cyhoeddwyd yn J Med Genet (2016)

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

gan Jaureguiberry, Graciana, De la Dure-Molla, Muriel, Parry, David, Quentric, Mickael, Himmerkus, Nina, Koike, Toshiyasu, Poulter, James, Klootwijk, Enriko, Robinette, Steven L., Howie, Alexander J., Patel, Vaksha, Figueres, Marie-Lucile, Stanescu, Horia C., Issler, Naomi, Nicholson, Jeremy K., Bockenhauer, Detlef, Laing, Christopher, Walsh, Stephen B., McCredie, David A., Povey, Sue, Asselin, Audrey, Picard, Arnaud, Coulomb, Aurore, Medlar, Alan J., Bailleul-Forestier, Isabelle, Verloes, Alain, Le Caignec, Cedric, Roussey, Gwenaelle, Guiol, Julien, Isidor, Bertrand, Logan, Clare, Shore, Roger, Johnson, Colin, Inglehearn, Christopher, Al-Bahlani, Suhaila, Schmittbuhl, Matthieu, Clauss, François, Huckert, Mathilde, Laugel, Virginie, Ginglinger, Emmanuelle, Pajarola, Sandra, Spartà, Giuseppina, Bartholdi, Deborah, Rauch, Anita, Addor, Marie-Claude, Yamaguti, Paulo M., Safatle, Heloisa P., Acevedo, Ana Carolina, Martelli-Júnior, Hercílio, dos Santos Netos, Pedro E., Coletta, Ricardo D., Gruessel, Sandra, Sandmann, Carolin, Ruehmann, Denise, Langman, Craig B., Scheinman, Steven J., Ozdemir-Ozenen, Didem, Hart, Thomas C., Hart, P. Suzanne, Neugebauer, Ute, Schlatter, Eberhard, Houillier, Pascal, Gahl, William A., Vikkula, Miikka, Bloch-Zupan, Agnès, Bleich, Markus, Kitagawa, Hiroshi, Unwin, Robert J., Mighell, Alan, Berdal, Ariane, Kleta, Robert
Cyhoeddwyd 2013