ライフサイエンスコーパス: embryonal rhabdomyosarcoma

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1 potential therapeutic targets for high-risk embryonal rhabdomyosarcoma.

2 subgroups of patients with intermediate-risk embryonal rhabdomyosarcoma.

3 on-arrested and proliferative phenotypes for embryonal rhabdomyosarcoma.

4 rom the two major subtypes, ie, alveolar and embryonal rhabdomyosarcoma.

5 ressed at least threefold more myogenin than embryonal rhabdomyosarcomas.

6 unct for distinguishing between alveolar and embryonal rhabdomyosarcomas.

7 In contrast, most embryonal rhabdomyosarcomas (13 of 15) were either negat

8 a secondary tumour (head and neck anaplastic embryonal rhabdomyosarcoma), all patients were alive at

9 activity as single agents in both zebrafish embryonal rhabdomyosarcoma and a human cell line of rhab

10 Although the primary cancer was an embryonal rhabdomyosarcoma and there was a family histor

11 atous testicular germ-cell tumors, in 2 of 5 embryonal rhabdomyosarcomas, and in 1 of 266 epithelial

12 Patients with embryonal rhabdomyosarcoma are generally cured, although

13 nt of lineage (alveolar rhabdomyosarcoma and embryonal rhabdomyosarcoma), are particularly sensitive

14 le node-positive or unresectable (group III) embryonal rhabdomyosarcoma arising at certain favorable

15 The childhood cancer embryonal rhabdomyosarcoma can arise in tissue without s

16 chanisms that prevent MyoD activity in human embryonal rhabdomyosarcoma cells.

17 Introduction of miR-1 and miR-133a into an embryonal rhabdomyosarcoma-derived cell line is cytostat

18 partitioning of tumour-propagating cells in embryonal rhabdomyosarcoma, emergence of clonal dominanc

19 Embryonal rhabdomyosarcoma (ERMS) and alveolar rhabdomyo

20 Embryonal Rhabdomyosarcoma (ERMS) and Undifferentiated P

21 child was diagnosed with ganglioneuroma and embryonal rhabdomyosarcoma (ERMS) at 2 years of age.

22 y resected, or gross residual (orbital only) embryonal rhabdomyosarcoma (ERMS) had 5-year failure-fre

23 Embryonal rhabdomyosarcoma (ERMS) is a common pediatric

24 Embryonal rhabdomyosarcoma (ERMS) is a devastating cance

25 Embryonal rhabdomyosarcoma (ERMS) is an aggressive pedia

26 fusion protein PAX3-FOXO1 or PAX7-FOXO1, and embryonal rhabdomyosarcoma (ERMS), which is genetically

27 port that YAP1 activity is elevated in human embryonal rhabdomyosarcoma (ERMS).

28 n (VA) for patients with subset-one low-risk embryonal rhabdomyosarcoma (ERMS; stage 1/2 group I/II E

29 associated with intermediate- and high-risk embryonal rhabdomyosarcomas (ERMS).

30 Only patients with unresectable embryonal rhabdomyosarcoma (group III) at unfavorable si

31 e a cell of origin for Sonic Hedgehog-driven embryonal rhabdomyosarcoma in an adipocyte-restricted co

32 tiation block in the childhood muscle cancer embryonal rhabdomyosarcoma is often thought to hold prom

33 Assay of PAX3 and PAX7 mRNA expression in embryonal rhabdomyosarcoma, neuroblastoma, Ewing's sarco

34 n IRS-IV for patients with intermediate-risk embryonal rhabdomyosarcoma (P =.02).

35 We propose that embryonal rhabdomyosarcomas result from an early block i

36 he spontaneous development of muscle-derived embryonal rhabdomyosarcoma (RMS) after 1 year of age.

37 ntreated patients with incompletely resected embryonal rhabdomyosarcoma (RMS), undifferentiated sarco

38 5 KIP2 gene in normal human tissues, WTs and embryonal rhabdomyosarcoma (RMS).

39 In contrast, 10 of 11 (91%) embryonal rhabdomyosarcomas showed a methylation pattern

40 One of two embryonal rhabdomyosarcomas that strongly stained for my

41 vival rate (FFSR) was 73%, and patients with embryonal rhabdomyosarcoma treated on IRS-IV fared espec

42 A diagnosis of embryonal rhabdomyosarcoma was made.

43 A KRAS(G12D)-induced zebrafish embryonal rhabdomyosarcoma was then used to assess the t

44 ic variegated aneuploidy, including two with embryonal rhabdomyosarcoma, we identified truncating and

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