Transition of myosin isozymes during development of human masseter muscle. Persistence of developmental isoforms during postnatal stage
Soussi-Yanicostas, N., Barbet, J. P., Laurent-Winter, C., Barton, P., Butler-Browne, G. S.
Published in Development (Cambridge) (01.02.1990)
Published in Development (Cambridge) (01.02.1990)
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
Soussi-Yanicostas, Nadia, Baverel, Françoise, Dupont, Jean-Michel, Cabrol, Sylvie, Levilliers, Jacqueline, Bouchard, Philippe, Kottler, Marie-Laure, Sanchez-Franco, Franco, Delmaghani, Sedigheh, Petit, Christine, Hardelin, Jean-Pierre, Delpech, Marc, De Paepe, Anne, Carel, Jean-Claude, Compain-Nouaille, Sylvie, Richard, Odile, Young, Jacques, Coimbra, Roney S, Goulet-Salmon, Barbara, Cruaud, Corinne, Le Tessier, Dominique, Vermeulen, Stefan, Delemarre-van de Waal, Henriette, Le Dû, Nathalie, Speleman, Frank, Saura, Robert, Bachelot, Yvan, Dodé, Catherine, Amalfitano, Andrea, Pêcheux, Christophe
Published in Nature genetics (01.04.2003)
Published in Nature genetics (01.04.2003)
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Journal Article
Kallmann syndrome
Hardelin, J P, Soussi-Yanicostas, N, Ardouin, O, Levilliers, J, Petit, C
Published in Advances in oto-rhino-laryngology (2000)
Published in Advances in oto-rhino-laryngology (2000)
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Anosmin-1, Defective in the X-Linked Form of Kallmann Syndrome, Promotes Axonal Branch Formation from Olfactory Bulb Output Neurons
Soussi-Yanicostas, Nadia, de Castro, Fernando, Julliard, A.Karyn, Perfettini, Isabelle, Chédotal, Alain, Petit, Christine
Published in Cell (19.04.2002)
Published in Cell (19.04.2002)
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Journal Article
Evolution of muscle specific proteins in Werdnig-Hoffman's disease
Soussi-Yanicostas, N., Hamida, C.Ben, Bejaoui, K., Hentati, F., Hamida, M.Ben, Butler-Browne, G.S.
Published in Journal of the neurological sciences (01.05.1992)
Published in Journal of the neurological sciences (01.05.1992)
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Journal Article
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
Ben Hamida, C., Soussi-Yanicostas, N., Bejaoui, K., Butler-Browne, G.S., Hentati, F., Ben Hamida, M.
Published in Journal of the neurological sciences (01.05.1994)
Published in Journal of the neurological sciences (01.05.1994)
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Journal Article
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome
Soussi-Yanicostas, N., Ben Hamida, C., Butler-Browne, G.S., Hentati, F., Bejaoui, K., Ben Hamida, M.
Published in Journal of the neurological sciences (01.07.1991)
Published in Journal of the neurological sciences (01.07.1991)
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Journal Article
Anosmin‐1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome‐linked Kallmann syndrome
Hardelin, Jean‐Pierre, Julliard, A. Karyn, Moniot, Brigitte, Soussi‐Yanicostas, Nadia, Verney, Catherine, Schwanzel‐Fukuda, Marlene, Ayer‐Le Lievre, Christiane, Petit, Christine
Published in Developmental dynamics (01.05.1999)
Published in Developmental dynamics (01.05.1999)
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Journal Article
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner
Soussi-Yanicostas, N, Faivre-Sarrailh, C, Hardelin, J P, Levilliers, J, Rougon, G, Petit, C
Published in Journal of cell science (01.10.1998)
Published in Journal of cell science (01.10.1998)
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Journal Article
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system
Soussi-Yanicostas, N, Hardelin, J P, Arroyo-Jimenez, M M, Ardouin, O, Legouis, R, Levilliers, J, Traincard, F, Betton, J M, Cabanié, L, Petit, C
Published in Journal of cell science (01.07.1996)
Published in Journal of cell science (01.07.1996)
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Journal Article
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome
Hardelin, J P, Soussi-Yanicostas, N, Levilliers, J, Kalatzis, V, Abdelhak, S, Cohen-Salmon, M, Petit, C
Published in Advances in nephrology from the Necker Hospital (1998)
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Published in Advances in nephrology from the Necker Hospital (1998)
Journal Article
Anosmin-1 immunoreactivity during embryogenesis in a primitive eutherian mammal
Dellovade, Tammy L, Hardelin, Jean-Pierre, Soussi-Yanicostas, Nadia, Pfaff, Donald W, Schwanzel-Fukuda, Marlene, Petit, Christine
Published in Brain research. Developmental brain research (16.02.2003)
Published in Brain research. Developmental brain research (16.02.2003)
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Journal Article
The human embryonic myosin alkali light chain gene : use of alternative promoters and 3' non-coding regions
ROTTER, M, ZIMMERMAN, K, POUSTKA, A, STARZINSKI-POWITZ, A
Published in Nucleic acids research (11.04.1991)
Published in Nucleic acids research (11.04.1991)
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Journal Article
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy
Ben Hamida, C, Soussi-Yanicostas, N, Butler-Browne, G S, Bejaoui, K, Hentati, F, Ben Hamida, M
Published in Muscle & nerve (01.04.1994)
Published in Muscle & nerve (01.04.1994)
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Approche moléculaire de la pathogénie d'un déficit héréditaire de l'olfaction : le syndrome de Kallmann de Morsier lié au chromosome X: Les maladies génétiques sensorielles
SOUSSI-YANICOSTAS, N, HARDELIN, J.-P, LEVILLIERS, J, ARDOUIN, O, LEGOUIS, R, COHEN-SALMON, M, PETIT, C
Published in Annales de l'Institut Pasteur. Actualités (1995)
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Published in Annales de l'Institut Pasteur. Actualités (1995)
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