R. Veitia

Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation (2008)

BEYSEN, DIANE, MOUMNE, L, VEITIA, R, PETERS, H, LEROY, BART, De Paepe, Anne, ...

Compositional biases and polyalanine runs in humans (2003)

Cocquet, J, De Baere, E, Caburet, S, Veitia, R

Human proteins containing polyalanine tracts tend to have runs of other amino acids and their open reading frames (ORFs) display a biased codon usage. Their alanine, glycine, proline, and histidine...

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

De Baere, E, Beysen, D, Oley, C, Lorenz, B, Cocquet, J, De Sutter, P, ...

Blepharophimosis syndrome (BPES), an autosomal dominant syndrome in which an eyelid malformation is associated (type I) or not (type II) with premature ovarian failure (POF), has recently been...

Structure, evolution and expression of the FOXL2 transcription unit (2003)

Cocquet, J, De Baere, E, Gareil, M, Pannetier, M, Xia, X, Fellous, M, ...

FOXL2 is a putative transcription factor involved in ovarian development and function. Its mutations in humans are responsible for the blepharophimosis syndrome, characterized by eyelid malformations...

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

Baere, E. De, Beysen, D., Oley, C., Lorenz, B., Cocquet, J., Sutter, P. De, ...

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

De Baere, Elfride, Beysen, Diane, OLEY, C, LORENZ, B, COCQUET, J, De Sutter, Petra, ...

Novel insights in genotype-phenotype correlations in BPES through in-depth FOXL2 mutation analysis (2002)

De Baere, Elfride, Beysen, Diane, OLEY, C, De Sutter, Petra, GARZA, A, JONSRUD, C, ...

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation (2001)

Dixon, M J, Small, K W, Jabs, E W, Leroy, B P, ...

Mutations in FOXL2, a forkhead transcription factor gene, have recently been shown to cause blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) types I and II, a rare genetic disorder. In...

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation (2001)

De Baere, Elfride, DIXON, MJ, SMALL, KW, JABS, EW, Leroy, Ben, DEVRIENDT, K, ...

Spectrum and distribution of FOXL2 gene mutations and variants in BPES, POF and XX male patients: tentative genotype-phenotype correlation (2001)

De Baere, Elfride, DIXON, M, SMALL, K, JABS, E, Leroy, Bart, DEVRIENDT, K, ...

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism (1999)

Hurles, Matthew E., Veitia, R., Arroyo, Eduardo, Armenteros, M., Bertranpetit, J., Perez-Lezaun, A., ...

This is the version as published in the American Journal of Human Genetics by the University Of Chicago Press. Their website is http://www.journals.uchicago.edu/AJHG.home.html

ALGUNAS CARACTERISTICAS DE STICHOLYSINA, UNA NUEVA CITOLISINA DE Stichodactyla helianthus (1995)

Alvarez, C., Morera, Vivian, Besada, Vladimir, Pazos, F, Tejuca, M, Veitia, R, ...

A partir de los estudios de pH se pudo demostrar que la actividad hemolitica de la Sticholysina no depende de manera significativa, de su actividad fosfolipasica. En el presente trabajo se muestran...

ALGUNAS CARACTERISTICAS DE STICHOLYSINA, UNA NUEVA CITOLISINA DE Stichodactyla helianthus (1995)

Alvarez, C., Morera, Vivian, Besada, Vladimir, Pazos, F, Tejuca, M, Veitia, R, ...

A partir de los estudios de pH se pudo demostrar que la actividad hemolitica de la Sticholysina no depende de manera significativa, de su actividad fosfolipasica. En el presente trabajo se muestran...

Algunas caracteristicas de Sticholysina, una nueva Citolisina de Stichodactyla helianthus (1995)

Alvarez, C., Morera, Vivian, Besada, Vladimir, Pazos, F., Tejuca, M., Veitia, R., ...

A partir de los estudios de pH se pudo demostrar que la actividad hemolitica de la Sticholysina no depende de manera significativa, de su actividad fosfolipasica. En el presente trabajo se muestran...

FOXL2 mutation screening in a large panel of POF patients and XX males

De Baere, E, Lemercier, B, Christin-Maitre, S, Durval, D, Messiaen, L, Fellous, M, ...

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

Caburet, S, Demarez, A, Moumne, L, Fellous, M, De Baere, E, Veitia, R

Blepharophimosis syndrome is an autosomal dominant disease characterised by eyelid malformations, associated or not with premature ovarian failure. It is caused by mutations in the FOXL2 gene, which...

Evolution and expression of FOXL2

Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, ...

Tau expression in model adenocarcinomas correlates with docetaxel sensitivity in tumour-bearing mice.

Veitia, R., Bissery, M. C., Martinez, C., Fellous, A.

Docetaxel is a new taxoid with clinical activity in breast and lung cancer. Using docetaxel-sensitive and -refractory mammary and pancreatic murine tumours, as well as human-derived neoplasms, we...

Proteolysis of microtubule associated protein 2 and sensitivity of pancreatic tumours to docetaxel

Veitia, R, David, S, Barbier, P, Vantard, M, Gounon, P, Bissery, M C, ...

We have studied the state of microtubule associated protein 2 (MAP2) in the pancreatic ductal adenocarcinomas P03 and P02 (sensitive and refractory to docetaxel respectively) since they express the...