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期刊名:Sarcoma

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ISSN:1357-714X

e-ISSN:1369-1643

IF/分区:0.0/

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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
Mi-Jung Kim,Kyung-Ja Cho,Alberto G Ayala et al. Mi-Jung Kim et al.
Chondrosarcoma (CHS) is a malignant cartilage-forming tumor and usually occurs within the medullary canal of long bones and pelvic bones. Based on the morphologic feature alone, a correct diangosis of CHS may be difficult, Therefore, correl...
Caroline Peyrode,François Gouin,Aurélien Vidal et al. Caroline Peyrode et al.
Our lab developed (99m)Tc-NTP 15-5 radiotracer as targeting proteoglycans (PGs) for the scintigraphic imaging of joint. This paper reports preclinical results of (99m)Tc-NTP 15-5 imaging of an orthotopic model of Swarm rat chondrosarcoma (S...
Thomas Karsten Kilvaer,Andrej Valkov,Sveinung W Sorbye et al. Thomas Karsten Kilvaer et al.
Background. Optimal treatment of nongastrointestinal stromal tumor soft-tissue sarcomas (non-GIST STSs) is resection with wide margins. This study investigates the prognostic impact of the angiogenesis-associated platelet-derived growth fac...
Seth M Pollack,Elizabeth T Loggers,Eve T Rodler et al. Seth M Pollack et al.
Immunotherapy has shown promise in a number of tumor types, but its exact role in sarcoma remains to be defined. Advanced bone and soft tissue sarcomas are challenging diseases to treat with an unmet need for effective systemic therapy. Pre...
Rachel Conyers,Sophie Young,David M Thomas Rachel Conyers
Sarcomas are a group of heterogeneous tumours with varying genetic basis. Cytogenetic abnormalities range from distinct genomic rearrangements such as pathognomonic translocation events and common chromosomal amplification or loss, to more ...
Katia Bifulco,Immacolata Longanesi-Cattani,Maria Teresa Masucci et al. Katia Bifulco et al.
High levels of urokinase receptor (uPAR) in tissue and serum of patients with chondrosarcoma correlate with poor prognosis. First, we analyzed the uPAR levels in tissues and plasma of five patients affected by chondrosarcoma. Interestingly,...
Krithi Rao-Bindal,Eugenie S Kleinerman Krithi Rao-Bindal
The role of genetic mutations in the development of osteosarcoma, such as alterations in p53 and Rb, is well understood. However, the significance of epigenetic mechanisms in the progression of osteosarcoma remains unclear and is increasing...
Silke Brüderlein,Joshua B Sommer,Paul S Meltzer et al. Silke Brüderlein et al.
Immortal tumor cell lines are an important model system for cancer research, however, misidentification and cross-contamination of cell lines are a common problem. Seven chordoma cell lines are reported in the literature, but none has been ...
Lisa E S Crose,Corinne M Linardic Lisa E S Crose
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas of childhood and adolescence. To date, there are no effective treatments that target the genetic abnormalities in RMS, and current treatment options for high-risk groups are ...
Robert Grimer,Nick Athanasou,Craig Gerrand et al. Robert Grimer et al.
These guidelines have been developed in order to provide an overview and a set of broad-based key recommendations for the management of patients with bone sarcomas in the UK. They have taken into consideration the most up-to-date scientific...