Results 51 to 60 of about 44,634 (268)
The effect of Imp-2 on Ewing sarcoma cancer stem cells: when epigenetics orchestrate tumor growth [PDF]
Ewing's sarcoma family tumors Ewing sarcoma is part of the Ewing's sarcoma family tumors (ESFTs) that includes peripheral primitive neuroectodermal tumor (PNET), extraosseous ewing sarcoma, Askin's tumor and atypical Ewing sarcoma.
BAKARIC, A.
core
The epidemiology of bone cancer in 0 - 39 year olds in northern England, 1981 - 2002 [PDF]
Background: There is a paucity of recent epidemiological data on bone cancers. The aim of this study was to describe incidence and survival patterns for bone cancers diagnosed during 1981 - 2002.Methods: Cases aged 0 - 39 years (236 osteosarcomas, 166 ...
Rachel Eyre +8 more
core +1 more source
Metastatic Ewing Sarcoma carries a poor prognosis, and novel therapeutics to prevent and treat metastatic disease are greatly needed. Recent evidence demonstrates that tumor-associated macrophages in Ewing Sarcoma are associated with more advanced ...
Anthony J Hesketh +8 more
doaj +1 more source
The combination of temozolomide-irinotecan regresses a doxorubicin-resistant patient-derived orthotopic xenograft (PDOX) nude-mouse model of recurrent Ewing's sarcoma with a FUS-ERG fusion and CDKN2A deletion: Direction for third-line patient therapy. [PDF]
The aim of the present study was to determine the usefulness of a patient-derived orthotopic xenograft (PDOX) nude-mouse model of a doxorubicin-resistant metastatic Ewing's sarcoma, with a unique combination of a FUS-ERG fusion and CDKN2A deletion, to ...
Bouvet, Michael +20 more
core +1 more source
Budny Agnieszka, Litak Jakub, Kulesza Bartłomiej, Czyżewski Wojciech, Grochowski Cezary. Ewing`s Sarcoma. Journal of Education, Health and Sport. 2017;7(6):265-272. eISSN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.804631 http://ojs.ukw.edu.pl/index.php/johs/article/view/4534 The journal has had 7 points in Ministry of Science and ...
Agnieszka Budny +4 more
openaire +3 more sources
Ewing sarcoma with renal localization is one of the rarest members of the Ewing sarcoma family with less than 200 cases reported in the Medline database.
Sava Alexandra Daniela +5 more
doaj +1 more source
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with overall long-term survival rates of ∼65-70%. Thus, additional molecular insights and representative models are critical for identifying and evaluating new treatment ...
Kengo Nakahata +10 more
doaj +1 more source
ABSTRACT Introduction The management of extremity soft tissue sarcomas (STS) involving major vessels presents unique challenges, historically leading to amputation. Advances in vascular reconstruction have enabled limb‐sparing surgery (LSS), but outcomes and perioperative risks remain uncertain.
Lucas Monteiro Delgado +9 more
wiley +1 more source
The second European interdisciplinary Ewing sarcoma research summit – A joint effort to deconstructing the multiple layers of a complex disease [PDF]
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The second “European interdisciplinary Ewing sarcoma research summit” assembled a large group of scientific experts in the field to discuss their latest ...
Amatruda, James +5 more
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BCL11B is up-regulated by EWS/FLI and contributes to the transformed phenotype in Ewing sarcoma.
The EWS/FLI translocation product is the causative oncogene in Ewing sarcoma and acts as an aberrant transcription factor. EWS/FLI dysregulates gene expression during tumorigenesis by abnormally activating or repressing genes.
Elizabeth T Wiles +3 more
doaj +1 more source

