5 Result(s)

Article

Aux origines de la maladie osseuse de Paget. Un nouveau cas néolithique dans le sud de la France

Parmi les ossements recueillis dans une grotte sépulcrale du sud de la France, nous avons reconnu un cas de maladie de Paget polyostotique. La datation C₁₄, après calibration, donne un âge d’environ 3350 ans avan...

J. -P. Arnautou, J. Blondiaux… in Bulletins et mémoires de la Société d'anth… (2011)

Article

High frequency of β-catenin heterozygous mutations in extra-abdominal fibromatosis: a potential molecular tool for disease management

Fibromatosis comprises distinct clinical entities, including sporadic extra-abdominal fibromatosis, which have a high tendency for recurrence, even after adequate resection. There are no known molecular biomar...

J Dômont, S Salas, L Lacroix, V Brouste, P Saulnier, P Terrier… in British Journal of Cancer (2010)

Article

Prognosis and predictive value of KIT exon 11 deletion in GISTs

KIT exon 11 mutations are observed in 60% of gastrointestinal stromal tumours (GIST). Exon 11 codes for residues Tyr568 and Tyr570, which play a major role in signal transduction and degradation of KIT. Our aim w...

J-B Bachet, I Hostein, A Le Cesne, S Brahimi, A Beauchet… in British Journal of Cancer (2009)

Article

DNA topoisomerase IIα expression and the response to primary chemotherapy in breast cancer

The α isoform of Topoisomerase IIα (Topo IIα) is a proliferation marker as well as a target for several chemotherapeutic agents such as anthracyclines. In vitro studies have demonstrated the relationship between ...

G MacGrogan, P Rudolph, I de Mascarel, L Mauriac, M Durand… in British Journal of Cancer (2003)

Article

Summary of the Standards, Options and Recommendations for the management of patients with carcinoma of unknown primary site (2002)

R Bugat, A Bataillard, T Lesimple, J J Voigt, S Culine… in British Journal of Cancer (2003)