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期刊名:Sarcoma

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ISSN:1357-714X

e-ISSN:1369-1643

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共收录本刊相关文章索引163条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Heidi M Namløs,Stine H Kresse,Christoph R Müller et al. Heidi M Namløs et al.
Global gene expression analysis was performed on a panel of 23 osteosarcoma samples of primary and metastatic origin using the Applied Biosystems Gene Expression Array System. When comparing the primary tumours with the metastases, we found...
Eivind Smeland,Thomas K Kilvaer,Sveinung Sorbye et al. Eivind Smeland et al.
Background. We aimed to explore the prognostic impact of the hypoxia-induced factors (HIFαs) 1 and 2, the metabolic HIF-regulated glucose transporter GLUT-1, and carbonic anhydrase IX (CAIX) in non-gastrointestinal stromal tumor soft tissu...
Sergey Malchenko,Elisabeth A Seftor,Yuri Nikolsky et al. Sergey Malchenko et al.
Chondrosarcomas are among the most malignant skeletal tumors. Dedifferentiated chondrosarcoma is a highly aggressive subtype of chondrosarcoma, with lung metastases developing within a few months of diagnosis in 90% of patients. In this pap...
Kosei Ando,Kanji Mori,Franck Verrecchia et al. Kosei Ando et al.
Osteosarcoma is the most frequent malignant primary bone tumor characterized by a high potency to form lung metastases which is the main cause of death. Unfortunately, the conventional chemotherapy is not fully effective on osteosarcoma met...
Maurice Balke,Marcel P Henrichs,Georg Gosheger et al. Maurice Balke et al.
Background. We report on 19 cases of giant cell tumor of bone (GCT) affecting the spine or sacrum and evaluate the outcome of different treatment modalities. Methods. Nineteen patients with GCT of the spine (n = 6) or sacrum (n = 13) have b...
Allie H Grossmann,Lester J Layfield,R Lor Randall Allie H Grossmann
Leiomyosarcoma is a malignant smooth muscle neoplasm with a complicated histopathologic classification scheme and marked differences in clinical behavior depending on the anatomic site of origin. Overlapping morphologic features of benign a...
Sam Behjati,B Piku Basu,Rebecca Wallace et al. Sam Behjati et al.
The Ewing sarcoma family of tumors (ESFT) represents an aggressive spectrum of malignant tumour types with common defining histological and cytogenetic features. To evaluate the functional activation of signal transducer and activator of tr...
Simone Fulda Simone Fulda
Resistance of rhabdomyosarcoma to current therapies remains one of the key issues in pediatric oncology. Since the success of most cytotoxic therapies in the treatment of cancer, for example, chemotherapy, depends on intact signaling pathwa...
J Haniball,V P Sumathi,L-G Kindblom et al. J Haniball et al.
Background. This study aimed to investigate prognostic factors for patients with myxoid/round-cell liposarcoma (MRCLS), in particular the significance of the round cell component, and to identify metastatic patterns as well as possibly sugg...
Kurt R Weiss,David J Biau,Rej Bhumbra et al. Kurt R Weiss et al.
Introduction. Ewing's sarcomas (EWSs) of bone and soft tissue are neuroectodermal tumors that affect both axial and appendicular locations. We hypothesized that axial location predicted poor outcome in EWS patients. Materials and Methods. S...