Results 171 to 180 of about 18,440 (214)
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Journal of the American Veterinary Medical Association, 1989
Hydrallantois was detected in a pregnant ewe by physical examination and ultrasonographic evaluation. Clinical signs of disease included acute progressive bilateral abdominal distention, anorexia, and recumbency. Right-flank celiotomy and cesarean section were used to alleviate the condition.
A, Milton, B, Welker, P, Modransky
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Hydrallantois was detected in a pregnant ewe by physical examination and ultrasonographic evaluation. Clinical signs of disease included acute progressive bilateral abdominal distention, anorexia, and recumbency. Right-flank celiotomy and cesarean section were used to alleviate the condition.
A, Milton, B, Welker, P, Modransky
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Oral Surgery, Oral Medicine, Oral Pathology, 1971
Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Abstract Ewing's sarcoma, a rare neoplasm that usually occurs in persons under 25 years of age, is considered the most lethal of all bone tumors. Treatment usually consists of radiation therapy. Although the value of prophylactic chemotherapy has not been established, encouraging results have been achieved with the use of Cytoxan at periodic ...
W, Carl +3 more
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Phosphorylation of Ewing's sarcoma protein (EWS) and EWS-Fli1 in response to DNA damage
Biochemical Journal, 2009In Ewing's sarcomas, chromosomal translocations cause the N-terminal domain of the EWS (Ewing's sarcoma protein) to fuse with the DNA-binding domains of the Ets (E26 transformation-specific) family of transcription factors. Here we show that EWS and EWS-Fli1 (Friend leukaemia virus integration 1), the fusion most frequently found in Ewing's sarcomas ...
Klevernic, Iva V. +3 more
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Targeting the EWS–FLI1 transcription factor in Ewing sarcoma
Cancer Chemotherapy and Pharmacology, 2015Preclinical data indicate there is strong synergism of action against Ewing sarcoma in sequential treatment with trabectedin followed by irinotecan and it appears to be related to a selective blockade of the transcription factor EWS-FLI1. This combination was evaluated in Ewing sarcoma patient who was progressing with standard therapies.Trabectedin was
Tancredi, R +8 more
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Clinical Radiology, 1971
A study of 244 histologically proven cases of Ewing's Tumour is presented, illustrating its clinical behaviour and radiological appearances. 170 patients were treated between 1941 and 1964 by radiation, surgery, chemotherapy or combinations of these methods. Nine cases survived for more than 5 years.
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A study of 244 histologically proven cases of Ewing's Tumour is presented, illustrating its clinical behaviour and radiological appearances. 170 patients were treated between 1941 and 1964 by radiation, surgery, chemotherapy or combinations of these methods. Nine cases survived for more than 5 years.
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Oral Surgery, Oral Medicine, Oral Pathology, 1993
A primary Ewing's tumor in the mandible is reported, and the diagnostic imaging features of this lesion are discussed. Modalities used included panoramic and plain films, computed tomography, and 99mTc-MDP scintigraphy.
GURBUZER, B +5 more
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A primary Ewing's tumor in the mandible is reported, and the diagnostic imaging features of this lesion are discussed. Modalities used included panoramic and plain films, computed tomography, and 99mTc-MDP scintigraphy.
GURBUZER, B +5 more
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Journal of the American Veterinary Medical Association, 2023
Mary Jane, Drake +3 more
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Mary Jane, Drake +3 more
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EWS–ETS oncoproteins: The linchpins of Ewing tumors
Gene, 2005Ewing tumors, which comprise Ewing's sarcoma and peripheral primitive neuroectodermal tumors, are highly aggressive and mostly affect children and adolescents. Their molecular signature is a chromosomal translocation leading to the generation of EWS-ETS (or very rarely FUS-ETS) fusion proteins that are capable of transforming cells.
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Abstract: Ewing sarcoma (ES) is the second most common primary musculoskeletal neoplasm in children and adolescents after osteosarcoma with a peak between 10 and 20. Rarely, the tumor develops in newborns or in adults over the age of 30. ES can affect either the appendicular or axial skeleton. Extraosseous ES is less prevalent. Clinical presentation is
Vanhoenacker, Filip M. +3 more
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Vanhoenacker, Filip M. +3 more
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