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Biochemical and Biophysical Research Communications|February 13, 2001
Characterization of the mouse Cblc/Cbl3 geneF Fiore, V Ollendorff, D Birnbaum
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|February 1, 1994
The GARP gene encodes a new member of the family of leucine-rich repeat-containing proteinsV Ollendorff, T Noguchi, O deLapeyriere, et al.
Progress in Growth Factor Research|January 1, 1994
The human and mouse fibroblast growth factor 6 (FGF6) genes and their products: possible implication in muscle developmentF Coulier, S Pizette, V Ollendorff, et al.
Biochimie|November 1, 1992
Isolation and sequence of the murine Fgf6 cDNAV Ollendorff, O Rosnet, I Marics, et al.
Biochemical and Biophysical Research Communications|June 29, 2000
Skeletal muscle regeneration is not impaired in Fgf6 -/- mutant miceF Fiore, A Sébille, D Birnbaum
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regionsV Ollendorff, P Szepetowski, M G Mattei, et al.
Molecular and Cellular Biology|November 2, 2001
8p12 stem cell myeloproliferative disorder: the FOP-fibroblast growth factor receptor 1 fusion protein of the t(6;8) translocation induces cell survival mediated by mitogen-activated protein kinase and phosphatidylinositol 3-kinase/Akt/mTOR pathwaysG Guasch, V Ollendorff, J P Borg, et al.
The International Journal of Developmental Biology|June 1, 1996
Structure and developmental expression of mouse Garp, a gene encoding a new leucine-rich repeat-containing proteinR Roubin, S Pizette, V Ollendorff, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Characterization of a yeast artificial chromosome from human chromosome band 13q12 containing the FLT1 and FLT3 receptor-type tyrosine kinase genesA Imbert, O Rosnet, S Marchetto, et al.
The Journal of Biological Chemistry|September 10, 1999
Characterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocationV Ollendorff, G Guasch, D Isnardon, et al.
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