Molars and incisors: show your microarray IDs

Por Laugel-Haushalter, Virginie, Paschaki, Marie, Thibault-Carpentier, Christelle, Dembelé, Doulaye, Dollé, Pascal, Bloch-Zupan, Agnès
Publicado em 2013

Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects

Por Morkmued, Supawich, Laugel-Haushalter, Virginie, Mathieu, Eric, Schuhbaur, Brigitte, Hemmerlé, Joseph, Dollé, Pascal, Bloch-Zupan, Agnès, Niederreither, Karen
Publicado no Front Physiol (2017)

Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a model

Por Marangoni, Pauline, Charles, Cyril, Tafforeau, Paul, Laugel-Haushalter, Virginie, Joo, Adriane, Bloch-Zupan, Agnès, Klein, Ophir D., Viriot, Laurent
Publicado no Sci Rep (2015)

Enamel and dental anomalies in latent‐transforming growth factor beta‐binding protein 3 mutant mice

Por Morkmued, Supawich, Hemmerle, Joseph, Mathieu, Eric, Laugel‐Haushalter, Virginie, Dabovic, Branka, Rifkin, Daniel B., Dollé, Pascal, Niederreither, Karen, Bloch‐Zupan, Agnès
Publicado no Eur J Oral Sci (2017)

A Novel Mutation in the ROGDI Gene in a Patient with Kohlschütter-Tönz Syndrome

Por Huckert, Mathilde, Mecili, Helen, Laugel-Haushalter, Virginie, Stoetzel, Corinne, Muller, Jean, Flori, Elisabeth, Laugel, Vincent, Manière, Marie-Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès
Publicado no Mol Syndromol (2014)

Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning

Por Laugel-Haushalter, Virginie, Morkmued, Supawich, Stoetzel, Corinne, Geoffroy, Véronique, Muller, Jean, Boland, Anne, Deleuze, Jean-François, Chennen, Kirsley, Pitiphat, Waranuch, Dollfus, Hélène, Niederreither, Karen, Bloch-Zupan, Agnès, Pungchanchaikul, Patimaporn
Publicado no Front Physiol (2018)

A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta

Por Laugel-Haushalter, Virginie, Bär, Séverine, Schaefer, Elise, Stoetzel, Corinne, Geoffroy, Véronique, Alembik, Yves, Kharouf, Naji, Huckert, Mathilde, Hamm, Pauline, Hemmerlé, Joseph, Manière, Marie-Cécile, Friant, Sylvie, Dollfus, Hélène, Bloch-Zupan, Agnès
Publicado no Front Genet (2019)

RSK2 Is a Modulator of Craniofacial Development

Por Laugel-Haushalter, Virginie, Paschaki, Marie, Marangoni, Pauline, Pilgram, Coralie, Langer, Arnaud, Kuntz, Thibaut, Demassue, Julie, Morkmued, Supawich, Choquet, Philippe, Constantinesco, André, Bornert, Fabien, Schmittbuhl, Matthieu, Pannetier, Solange, Viriot, Laurent, Hanauer, André, Dollé, Pascal, Bloch-Zupan, Agnès
Publicado em 2014

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

Por 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
Publicado no Hum Mol Genet (2015)

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

Por 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
Publicado no J Med Genet (2016)