ライフサイエンスコーパス: soft tissue tumor

1 ;q11.2), which occurs in synovial sarcoma, a soft tissue tumor.

2 ibroblastic tumor (IMT) is a relatively rare soft tissue tumor.

3 ed patients with the aggressive form of this soft-tissue tumor.

4 in this highly aggressive group of bone and soft tissue tumors.

5 rcomas are a heterogeneous group of bone and soft tissue tumors.

6 t metastasis to bone, osteolytic tumors, and soft tissue tumors.

7 ce of GISTs and is rarely expressed in other soft tissue tumors.

8 that is being made in the classification of soft tissue tumors.

9 been found in a significant number of human soft tissue tumors.

10 examination of benign and malignant bond and soft tissue tumors.

11 assess radiation dose to critical organs and soft-tissue tumors.

12 osteolytic bone disease and developed fewer soft-tissue tumors.

13 183 had primary bone tumors; 133 had primary soft-tissue tumors.

14 ypes, with the highest frequency observed in soft tissue tumors (20%), osteosarcomas (16%) and esopha

15 Patients with soft tissue tumors accounted for 20% of the study popula

16 s therapeutics for the treatment of bone and soft tissue tumors along with other neoplasms driven by

17 -specific and applicable to the dosimetry of soft-tissue tumors and normal organs.

18 ronic acid protected Tax+ mice from bone and soft-tissue tumors and prolonged survival.

19 clear, an excess of non-Hodgkin's lymphomas, soft tissue tumors, and, in the case of adolescent girls

20 Because these tumors are rare and benign soft tissue tumors are common, many are initially though

21 readily distinguished from 27 other diverse soft tissue tumors based on their gene expression patter

22 xome and transcriptome sequencing of bone or soft tissue tumor biopsies from a cohort of 150 mCRPC af

23 Bone and soft tissue tumors (BSTT) are relatively poorly understo

24 -FDG PET scans also strongly correlated with soft-tissue tumor burden (P < 0.05).

25 Synovial sarcoma is an aggressive soft tissue tumor characterized by a chromosomal translo

26 Synovial sarcoma is an aggressive soft tissue tumor characterized by a specific chromosoma

27 Soft tissue tumors comprise a vast and heterogeneous gro

28 Data from a prospective soft tissue tumor database was used to analyze clinical

29 anscription factor critical for the bone and soft tissue tumor Ewing sarcoma.

30 leading to ulnar nerve instability and focal soft tissue tumors (fibromas, lipomas, etc).

31 en utilized successfully to treat and ablate soft tissue tumors for over 15 years.

32 s some important recent work in two selected soft tissue tumors-gastrointestinal stromal tumor and in

33 (RMS) is the most commonly occurring type of soft tissue tumor in children.

34 Endothelial cell tumors are the most common soft tissue tumors in infants, yet little is known about

35 Endothelial cell tumors are the most common soft tissue tumors in infants.

36 was performed to evaluate a presumed forearm soft-tissue tumor in a 26-year-old man.

37 c rhabdomyosarcoma (ERMS) is the most common soft-tissue tumor in children.

38 r multiphasic bone scans may localize common soft-tissue tumors in neurofibromatosis.

39 rkers exist, and the cell of origin for many soft tissue tumors is unknown.

40 and, theoretically, separates the gland from soft-tissue tumors lateral to the gland.

41 synthetic DOG1 peptides was assessed on two soft tissue tumor microarrays.

42 ation in Ewing Sarcoma, a malignant bone and soft tissue tumor of children and young adults.

43 Here, we report that SP cells from a soft tissue tumor of enigmatic origin termed undifferent

44 Ossifying fibromyxoid tumor (OFMT) is a soft tissue tumor of unknown lineage.

45 of MDM2 amplification than p53 mutation were soft tissue tumors, testicular germ cell cancers and neu

46 Lipoblastomas are rare soft tissue tumors that occur primarily in young childre

47 Ewing sarcoma is a bone and soft-tissue tumor that depends on the activity of the EW

48 y, at which time the common peripheral nerve soft-tissue tumors that occur in this syndrome (neurofib

49 The majority of soft tissue tumors were first delineated on the basis of

50 omyosarcoma (RMS) is an aggressive childhood soft tissue tumor, which exists in oncoprotein PAX-FOXO1

51 Leiomyosarcoma (LMS) is a soft tissue tumor with a significant degree of morpholog

52 myosarcoma (ARMS) is an aggressive pediatric soft tissue tumor with striated muscle differentiation.

53 The tissue microarrays included 587 soft tissue tumors, with 149 GISTs, including 127 GIST c