Comprendre les anomalies de développement du crâne et de la charnière crâniovertébrale à l’aide de 3 modèles murins FGFR3 von Di Rocco, F, Kaci, N, Mugniery, E, Benoist-Lasselin, C, Litim, N, Munnich, A, Legeai-Mallet, L

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Reexpression of Cartilage-Specific Genes by Dedifferentiated Human Articular Chondrocytes Cultured in Alginate Beads von Bonaventure, J., Kadhom, N., Cohen-Solal, L., Ng, K.H., Bourguignon, J., Lasselin, C., Freisinger, P.

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Cranial and craniovertebral junction anomalies in FGFR3Y367C/+ mice: New insights in normal and pathological skull growth von Di Rocco, F, Kaci, N, Mugniery, E, Benoist-Lasselin, C, Munnich, A, Legeai-Mallet, L

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Impact of activating fibroblast growth factor receptor 3 mutation in endochondral ossification von Mugniery, E, Dacquin, R, Marty, C, Benoist-Lasselin, C, Munnich, A, de Vernejoul, M.-C, Jurdic, P, Geoffroy, V, Legeai-Mallet, L

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ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome von Dagoneau, Nathalie, Benoist-Lasselin, Catherine, Huber, Céline, Faivre, Laurence, Mégarbané, André, Alswaid, Abdulrahman, Dollfus, Hélène, Alembik, Yves, Munnich, Arnold, Legeai-Mallet, Laurence, Cormier-Daire, Valérie

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REDD2 Gene Is Upregulated by Modified LDL or Hypoxia and Mediates Human Macrophage Cell Death von Cuaz-Pérolin, C, Furman, C, Larigauderie, G, Legedz, L, Lasselin, C, Copin, C, Jaye, M, Searfoss, G, Yu, K T, Duverger, N, Nègre-Salvayre, A, Fruchart, J -C, Rouis, M

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Adipophilin Enhances Lipid Accumulation and Prevents Lipid Efflux From THP-1 Macrophages: Potential Role in Atherogenesis von Larigauderie, Guilhem, Furman, Christophe, Jaye, Michael, Lasselin, Catherine, Copin, Corinne, Fruchart, Jean-Charles, Castro, Graciela, Rouis, Mustapha

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Abnormal FGFR 3 Expression in Cartilage of Thanatophoric Dysplasia Fetuses von Delezoide, Anne-Lise, Lasselin-Benoist, Catherine, Legeai-Mallet, Laurence, Brice, Peggy, Senée, Valérie, Yayon, Avner, Munnich, Arnold, Vekemans, Michel, Bonaventure, Jacky

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Defective chondrocyte proliferation and differentiation in osteochondromas of MHE patients von Benoist-Lasselin, Catherine, de Margerie, Emmanuel, Gibbs, Linda, Cormier, Sarah, Silve, Caroline, Nicolas, Gisèle, LeMerrer, Martine, Mallet, Jean-Francois, Munnich, Arnold, Bonaventure, Jacky, Zylberberg, Louise, Legeai-Mallet, Laurence

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Récepteurs des facteurs de croissance fibroblastique et anomalies héréditaires de la croissance osseuse von Bonaventure, J, Rousseau, F, Legeai-Mallet, L, Benoist-Lasselin, C, Merrer, M Le, Munnich, A

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Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia von Legeai-Mallet, Laurence, Benoist-Lasselin, Catherine, Delezoide, Anne-Lise, Munnich, Arnold, Bonaventure, Jacky

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Human immortalized chondrocytes carrying heterozygous FGFR3 mutations: An in vitro model to study chondrodysplasias von Benoist-Lasselin, Catherine, Gibbs, Linda, Heuertz, Solange, Odent, Thierry, Munnich, Arnold, Legeai-Mallet, Laurence

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Mutations in the basic domain and the loop–helix II junction of TWIST abolish DNA binding in Saethre–Chotzen syndrome von El Ghouzzi, Vincent, Legeai-Mallet, Laurence, Benoist-Lasselin, Catherine, Lajeunie, Elisabeth, Renier, Dominique, Munnich, Arnold, Bonaventure, Jacky

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Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome von Bonaventure, J, Lasselin, C, Mellier, J, Cohen-Solal, L, Maroteaux, P

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Linkage study in a large pedigree with Stickler syndrome : exclusion of COL2A1 as the mutant gene von BONAVENTURE, J, PHILIPPE, C, PLESSIS, G, VIGNERON, J, LASSELIN, C, MAROTEAUX, P, GILGENKRANTZ, S

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Influence of shielding blocks on the output of photon beams as a function of energy and type of treatment unit von Van Dam, J., Bridier, A., Lasselin, C., Blanckaert, N., Dutreix, A.

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Overexpression of FGFR3, Stat 1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias von LEGEAI-MALLET, L, BENOIST-LASSELIN, C, MUNNICH, A, BONAVENTURE, J

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Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias von Legeai-Mallet, L, Benoist-Lasselin, C, Munnich, A, Bonaventure, J

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Overexpression of FGFR3, Stat1, Stat5 and p21 Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias von Legeai-Mallet, L, Benoist-Lasselin, C, Munnich, A, Bonaventure, J

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Overexpression of FGFR3, Stat1, Stat5 and p21 super(Cip1) correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias von Legeai-Mallet, L, Benoist-Lasselin, C, Munnich, A, Bonaventure, J

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