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rolipram and Neuroectodermal Tumors, Primitive, Peripheral

rolipram has been researched along with Neuroectodermal Tumors, Primitive, Peripheral in 1 studies

Neuroectodermal Tumors, Primitive, Peripheral: A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA.

Research Excerpts

ExcerptRelevanceReference
" Dose-response experiments in clonal density conditions showed IC50 of 5 microM and 1."1.30Phosphodiesterase specific inhibitors control cell growth of a human neuroepithelioma cell line. ( Augusti-Tocco, G; Campagnolo, L; Giorgi, M, 1997)

Research

Studies (1)

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

Authors

AuthorsStudies
Campagnolo, L1
Giorgi, M1
Augusti-Tocco, G1

Other Studies

1 other study available for rolipram and Neuroectodermal Tumors, Primitive, Peripheral

ArticleYear
Phosphodiesterase specific inhibitors control cell growth of a human neuroepithelioma cell line.
    Journal of neuro-oncology, 1997, Volume: 31, Issue:1-2

    Topics: Cell Division; Humans; Neuroectodermal Tumors, Primitive, Peripheral; Phosphodiesterase Inhibitors;

1997