Extensive sequence turnover of the signal peptides of members of the GDF/BMP family: exploring their evolutionary landscape

Por Veitia, Reiner A, Caburet, Sandrine
Publicado em 2009

A genomic basis for the evolution of vertebrate transcription factors containing amino Acid runs.

Por Caburet, Sandrine, Vaiman, Daniel, Veitia, Reiner A
Publicado em 2004

Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments

Por Koszul, Romain, Caburet, Sandrine, Dujon, Bernard, Fischer, Gilles
Publicado em 2004

Compositional biases and polyalanine runs in humans.

Por Cocquet, Julie, De Baere, Elfride, Caburet, Sandrine, Veitia, Reiner A
Publicado em 2003

A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation

Por Caburet, S, Demarez, A, Moumne, L, Fellous, M, De Baere, E, Veitia, R
Publicado em 2004

Human ribosomal RNA gene arrays display a broad range of palindromic structures

Por Caburet, Sandrine, Conti, Chiara, Schurra, Catherine, Lebofsky, Ronald, Edelstein, Stuart J., Bensimon, Aaron
Publicado em 2005

Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes

Por Caburet, Sandrine, Anttonen, Mikko, Todeschini, Anne-Laure, Unkila-Kallio, Leila, Mestivier, Denis, Butzow, Ralf, Veitia, Reiner A
Publicado no BMC Cancer (2015)

Natural and molecular history of prolactinoma: insights from a Prlr (–/–) mouse model

Por Bernard, Valérie, Villa, Chiara, Auguste, Aurélie, Lamothe, Sophie, Guillou, Anne, Martin, Agnès, Caburet, Sandrine, Young, Jacques, Veitia, Reiner A., Binart, Nadine
Publicado no Oncotarget (2017)

Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

Por Benayoun, Bérénice A., Caburet, Sandrine, Dipietromaria, Aurélie, Georges, Adrien, D'Haene, Barbara, Pandaranayaka, P. J. Eswari, L'Hôte, David, Todeschini, Anne-Laure, Krishnaswamy, Sankaran, Fellous, Marc, De Baere, Elfride, Veitia, Reiner A.
Publicado em 2010

Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

Por Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner A., Fellous, Marc
Publicado em 2012

Mutant Cohesin in Premature Ovarian Failure

Por Caburet, Sandrine, Arboleda, Valerie A., Llano, Elena, Overbeek, Paul A., Barbero, Jose Luis, Oka, Kazuhiro, Harrison, Wilbur, Vaiman, Daniel, Ben-Neriah, Ziva, García-Tuñón, Ignacio, Fellous, Marc, Pendás, Alberto M., Veitia, Reiner A., Vilain, Eric
Publicado em 2014

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency

Por Fouquet, Baptiste, Pawlikowska, Patrycja, Caburet, Sandrine, Guigon, Celine, Mäkinen, Marika, Tanner, Laura, Hietala, Marja, Urbanska, Kaja, Bellutti, Laura, Legois, Bérangère, Bessieres, Bettina, Gougeon, Alain, Benachi, Alexandra, Livera, Gabriel, Rosselli, Filippo, Veitia, Reiner A, Misrahi, Micheline
Publicado no eLife (2017)

GermOnline, a cross-species community knowledgebase on germ cell differentiation

Por Wiederkehr, C., Basavaraj, R., Sarrauste de Menthière, C., Hermida, L., Koch, R., Schlecht, U., Amon, A., Brachat, S., Breitenbach, M., Briza, P., Caburet, S., Cherry, M., Davis, R., Deutschbauer, A., Dickinson, H. G., Dumitrescu, T., Fellous, M., Goldman, A., Grootegoed, J. A., Hawley, R., Ishii, R., Jégou, B., Kaufman, R. J., Klein, F., Lamb, N., Maro, B., Nasmyth, K., Nicolas, A., Orr-Weaver, T., Philippsen, P., Pineau, C., Rabitsch, K. P., Reinke, V., Roest, H., Saunders, W., Schröder, M., Schedl, T., Siep, M., Villeneuve, A., Wolgemuth, D. J., Yamamoto, M., Zickler, D., Esposito, R. E., Primig, M.
Publicado em 2004