Rhabdomyosarcoma (RMS) and Ewing sarcoma (ES) are among the most common pediatric sarcomas (Arndt et al., 2012). Despite sarcomas representing a highly heterogeneous group of tumors, ES and alveolar RMS (ARMS) typically share one common genetic characteristic, namely a specific chromosomal translocation (Helman and Meltzer, 2003; Lessnick and Ladanyi, 2012). These translocations generate fusion proteins, which are composed of two transcription factors (TF). Typically, one TF is a developmentally regulated factor that is essential for proper specification of a given lineage and provides the DNA-binding domain, while the partner TF contributes a transactivation domain that drives aberrant expression of target genes. Based on these common gene...
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas in children/adolescents less than ...
Sarcomas are heterogeneous and clinically challenging soft tissue and bone cancers. Although constit...
Ewing's sarcoma is characterized by the presence of fusion oncoproteins involving EWSR1 and an ETS g...
Rhabdomyosarcoma (RMS) and Ewing sarcoma (ES) are among the most common pediatric sarcomas (Arndt et...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The ...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Review on t(11;22)(q24;q12) in rhabdomyosarcomas (RMS), with data on clinics, and the genes involved
AbstractEwing's sarcoma is a rare bone tumor that affects children and adolescents. We have recently...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Sarcomas are a rare subgroup of pediatric cancers comprised of a variety of bone and soft-tissue tum...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Sarcomas are heterogeneous cancers of bone or soft tissue. They occur in children, adolescents, and ...
The childhood sarcomas are malignant tumors with high mortality rates. They are divided into two gen...
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas in children/adolescents less than ...
Sarcomas are heterogeneous and clinically challenging soft tissue and bone cancers. Although constit...
Ewing's sarcoma is characterized by the presence of fusion oncoproteins involving EWSR1 and an ETS g...
Rhabdomyosarcoma (RMS) and Ewing sarcoma (ES) are among the most common pediatric sarcomas (Arndt et...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The ...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Review on t(11;22)(q24;q12) in rhabdomyosarcomas (RMS), with data on clinics, and the genes involved
AbstractEwing's sarcoma is a rare bone tumor that affects children and adolescents. We have recently...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Sarcomas are a rare subgroup of pediatric cancers comprised of a variety of bone and soft-tissue tum...
Despite multimodal treatment, long term outcome for patients with Ewing sarcoma is still poor. The s...
Sarcomas are heterogeneous cancers of bone or soft tissue. They occur in children, adolescents, and ...
The childhood sarcomas are malignant tumors with high mortality rates. They are divided into two gen...
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas in children/adolescents less than ...
Sarcomas are heterogeneous and clinically challenging soft tissue and bone cancers. Although constit...
Ewing's sarcoma is characterized by the presence of fusion oncoproteins involving EWSR1 and an ETS g...