Page last updated: 2024-10-25

clofilium and Rhabdoid Tumor

clofilium has been researched along with Rhabdoid Tumor in 1 studies

clofilium: RN given refers to parent cpd; structure

Rhabdoid Tumor: A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chauvin, C1
Leruste, A1
Tauziede-Espariat, A1
Andrianteranagna, M1
Surdez, D1
Lescure, A1
Han, ZY1
Anthony, E1
Richer, W1
Baulande, S1
Bohec, M1
Zaidi, S1
Aynaud, MM1
Maillot, L1
Masliah-Planchon, J1
Cairo, S1
Roman-Roman, S1
Delattre, O1
Del Nery, E1
Bourdeaut, F1

Other Studies

1 other study available for clofilium and Rhabdoid Tumor

ArticleYear
High-Throughput Drug Screening Identifies Pazopanib and Clofilium Tosylate as Promising Treatments for Malignant Rhabdoid Tumors.
    Cell reports, 2017, Nov-14, Volume: 21, Issue:7

    Topics: Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Drug Discovery; Endoplasmic Reticulum Stress; Hi

2017