Results 71 to 80 of about 244,564 (198)
Immuno-stimulation by OX40 ligand transgenic Ewing sarcoma cells
Frontiers in Oncology, 2015 Interleukin-2 (IL-2) transgenic Ewing sarcoma cells can induce tumor specific T and NK cell responses and reduce tumor growth in vivo and in vitro. Nevertheless, the efficiency of this stimulation is not high enough to inhibit tumor growth completely. In
Dajana eReuter +3 more
doaj +1 more source
Deciphering transcriptome complexity via long‐read sequencing
iMeta, EarlyView.Long‐read sequencing is transforming transcriptomics from gene‐level quantification to isoform‐resolved interpretation by directly resolving full‐length transcript structures, transcription in repetitive regions, and linked molecular features. This review provides an end‐to‐end roadmap covering sequencing platforms, library preparation strategies ...
Chuwen Xu +21 more
wiley +1 more source
Journal of Surgical Oncology, EarlyView.ABSTRACT Introduction Sarcomas are rare malignancies that affect both adults and children. Surgical removal with negative histopathological margins is the foundation of sarcoma treatment. Failure to achieve negative margins puts patients at risk of local recurrence (LR). LR rates range between 10% and 30%.
Sumail Bhogal +13 more
wiley +1 more source
EWS/FLI1 target genes and therapeutic opportunities in Ewing sarcoma
Frontiers in Oncology, 2015 Ewing sarcoma family of tumors are aggressive bone malignancies that affect children and young adults. Ewing sarcoma is the second most common primary bone malignancy in pediatric patients.
Florencia eCidre, Javier eAlonso
doaj +1 more source
Acta Marisiensis - Seria Medica, 2023 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
Ewing's Sarcoma in Adults: A Predictive Nomogram and Survival Analysis of a Cohort of 937 Patients
Journal of Surgical Oncology, EarlyView.ABSTRACT Background Ewing sarcoma is a rare malignancy of bone and soft tissue that most commonly affects children, adolescents, and young adults. Although multimodal treatment has improved survival in localised disease, outcomes remain poorer in adults, particularly in those with metastatic disease, larger tumours, or anatomically complex primary ...
Jonathan Gibson +6 more
wiley +1 more source
Cranial Ewing's sarcoma in children
, 2011 Ewing's sarcoma is a highly malignant neoplasm of bones which accounts for the 10% of primary bone malignancies. Primary Ewing's sarcoma of skull vault is very rare and constitutes 1-6% of all Ewing's sarcomas.
Tsiotra, M. +7 more
core +1 more source
Massive Pulmonary Ewing Sarcoma Mimicking Pulmonary Embolism: A Diagnostic Challenge
Indian Journal of Medical and Paediatric OncologyWhile classic Ewing sarcoma targets bone, the extra-skeletal variant develops in soft tissues, with a rare incidence of 0.4 per million. Although the chest wall is a recognized site for extra-skeletal Ewing sarcoma, primary pulmonary Ewing sarcoma is ...
Malak A. Hassan +4 more
doaj +1 more source
Primary Ewing′s sarcoma of occipital bone
Indian Journal of Radiology and Imaging, 2006 Ewing′s sarcoma commonly involves the long bones. Primary Ewing′s sarcoma of the cranium is rare and is difficult to distinguish from other tumors involving the cranium. Radiological features and immuno-histochemistry are helpful in diagnosing this tumor.
RK Kaza, MS Sandhu, V Ojili
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Primary Ewing sarcoma of the adrenal gland: A rare cause of abdominal mass
Radiology Case Reports, 2020 Ewing sarcoma is a malignant tumor that more commonly affects the long bones. Primary Ewing sarcoma of the adrenal gland is a rare diagnosis. We report an unusual case of primary Ewing sarcoma of the adrenal gland in a 34-year-old man who initially ...
Christopher Ibabao, MS +4 more
doaj +1 more source