From Google Scholar Alerts
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Glycogen synthase kinase 3β represses MYOGENIN function in alveolar rhabdomyosarcoma.
MG Dionyssiou, S Ehyai, E Avrutin, MK Connor… - Cell death & disease, 2014
MYOGENIN is a member of the muscle regulatory factor family that orchestrates an
obligatory step in myogenesis, the terminal differentiation of skeletal muscle cells. A
paradoxical feature of alveolar rhabdomyosarcoma (ARMS), a prevalent soft tissue ...

Cardiac rhabdomyosarcoma of the left atrium
A Dirican, Y Kucukzeybek, C Erten, I Somali, A Can… - Contemp Oncol (Pozn), 2014
Primary cardiac tumours are quite rare. Only 7 cases were reported in a series of 12,000
autopsies, and its prevalence is less than 0.1%[1]. Malignant tumours account for
approximately 15% of primary cardiac tumours, and sarcomas are the most common [2]. ...

Decitabine facilitates immune recognition of sarcoma cells by upregulating CT antigens, MHC molecules, and ICAM-1
DK Krishnadas, L Bao, F Bai, SC Chencheri, K Lucas - Tumor Biology, 2014
... Received: 17 August 2013 /Accepted: 14 February 2014 © International Society of Oncology
and BioMarkers (ISOBM) 2014 Abstract Rhabdomyosarcoma, osteosarcoma, and Ewing's
sarcoma are the most common types of sarcoma in children. ...

Protective Role of Humanin on Bortezomib-Induced Bone Growth Impairment in Anticancer Treatment
E Eriksson, M Wickström, LS Perup, JI Johnsen… - Journal of the National …, 2014
... malignancies (15–17). Bortezomib is able to suppress cancer cell growth in childhood
malignancies such as leukemias and lymphomas (18), NBL (19,20), MBL (21,22),
rhabdomyosarcoma (11), and Ewing's sarcoma (23). Recent phase ...

Evaluation and Management of Neck Masses in Children.
JD MEIER, JF GRIMMER - American Family Physician, 2014
... urgent evaluation and possible biopsy. Although rare, malignant lesions such as
lymphoma, rhabdomyosarcoma, thyroid carcinoma, and metastatic nasopharyngeal
carcinoma can occur in children. An asymptomatic lesion that ...

The clinical development of p53-reactivating drugs in sarcomas – charting future therapeutic approaches and understanding the clinical molecular toxicology of Nutlins
S Biswas, E Killick, AG Jochemsen, J Lunec - Expert Opinion on Investigational …, 2014
... genetic signature of well-differentiated and dedifferentiated liposarcomas (WDLPS/ DDLPS)
[7] and which almost exclusively arise in adults, but it is also present in a subgroup of
predominantly paediatric sarcomas, such as osteosarcoma [3,8] and rhabdomyosarcoma [3,9, ...

Orbital Alveolar Rhabdomyosarcoma –Unusual Presentation and Dreadful Experience
EDP Verma
Abstract Introduction: Orbital Rhabdomyosarcoma (RMS) is one of the few life-threatening
diseases seen by ophthalmologists and prompt diagnosis and treatment can save the life of
the affected patient. Survival after treatment of RMS has improved from 25% in 1970 to 70 ...

A new bright-field dual-colour chromogenic and silver in situ hybridization method for the detection of FGFR1 gene copy number status
D Boehm, W Vogel, A Franzen, A Schrock, F Bootz… - Virchows Archiv, 2014
... doi:10.1159/000355018 000355018 [pii] 10. Missiaglia E et al (2009) Genomic imbalances in
rhabdomyosarcoma cell lines affect expression of genes frequently altered in primary tumors:
an approach to identify candidate genes involved in tumor development. ...