Showing results (121-130 of 131) with videos related to
Sort By:
Pageof 14
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|October 3, 2006
Expression of aminopeptidase N/CD13 in human ovarian cancersP Surowiak, M Drag, V Materna, et al.Anticancer Research|May 27, 2004
New silicon compounds as resistance modifiers against multidrug-resistant cancer cellsJ Molnar, I Mucsi, J Nacsa, et al.Journal of the National Cancer Institute|March 10, 1999
Atypical multidrug resistance: breast cancer resistance protein messenger RNA expression in mitoxantrone-selected cell linesD D Ross, W Yang, L V Abruzzo, et al.Zeitschrift Fur Gastroenterologie|January 7, 2006
[Effectiveness of antiviral therapy in patients with chronic hepatitis C treated by private practice gastroenterologists]W P Hofmann, H Bock, C Weber, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degenerationF Krämer, K White, D Pauleikhoff, et al.British Journal of Cancer|August 8, 2006
Multivariate analysis of oestrogen receptor alpha, pS2, metallothionein and CD24 expression in invasive breast cancersP Surowiak, V Materna, B Györffy, et al.Cancer Gene Therapy|April 14, 2009
Adenovirus-based virotherapy enabled by cellular YB-1 expression in vitro and in vivoE Rognoni, M Widmaier, C Haczek, et al.American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.Pageof 14