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1 ormation of this disfiguring and endangering childhood tumor.
2 prognostic factor in neuroblastoma, a common childhood tumor.
3 ical teratoid/rhabdoid tumor (AT/RT), a rare childhood tumor.
4 d overexpression of Nmyc1 is associated with childhood tumors.
5 m tumor that accounts for 8-10% of all solid childhood tumors.
6  and other types of adult cancers as well as childhood tumors.
7 romegaly, and an increased susceptibility to childhood tumors.
8 ha(v)beta5 by microvascular endothelium of a childhood tumor and association of their expression with
9 ymphoblastic leukemia (ALL) is the commonest childhood tumor and remains a leading cause of cancer de
10 oblastic leukemia (B-ALL) is the most common childhood tumor and the leading cause of cancer-related
11  caspase 8 (CASP8) has been reported in some childhood tumors and in neuroendocrine lung tumors.
12                    Given the rarity of these childhood tumors and their propensity to present at adva
13    We show that some cell lines derived from childhood tumors are highly sensitive to growth inhibiti
14                                         Most childhood tumors are radiation sensitive, but the side e
15                                         Most childhood tumors are relatively rare and are therefore s
16  Neuroblastoma, the second most common solid childhood tumor, can be a highly invasive and metastatic
17  rhabdomyosarcoma (ARMS) is a muscle-derived childhood tumor characterized by production of oncogenic
18                                              Childhood tumors containing cells that are morphological
19                    Neuroblastoma is a common childhood tumor derived from the peripheral nervous syst
20 Lin28B is activated in neuroblastoma (NB), a childhood tumor in sympathetic ganglia and adrenal medul
21         Neuroblastoma is a frequently lethal childhood tumor in which MYC gene deregulation, commonly
22                           Neuroblastoma is a childhood tumor in which transient therapeutic responses
23                      Risks for obesity after childhood tumors include hypothalamic injury, with inact
24 owth and conveys a predisposition to certain childhood tumors, including Wilms tumor (WT).
25      Lin28B is aberrantly upregulated in the childhood tumor neuroblastoma (NB).
26 xpressed due to genomic amplification in the childhood tumor neuroblastoma.
27 s frequently inactivated in neuroblastoma, a childhood tumor of the peripheral nervous system.
28                  Clear cell sarcoma (CCS), a childhood tumor of the tendons and aponeuroses, is unifo
29 icated in medulloblastomas, common malignant childhood tumors of the cerebellum.
30      Therefore, the radiological features of childhood tumors of the nasopharynx must be well known.
31                      Neuroblastoma (NB) is a childhood tumor that arises from the sympathoadrenal lin
32                 Malignant neuroblastomas are childhood tumors that remain mostly incurable.
33                           Neuroblastoma is a childhood tumor thought to arise through improper differ
34 gents are of great concern in the context of childhood tumors where they can reduce the quality of li
35 s the clinical features are similar to other childhood tumors which affect the nasopharynx and adenoi
36 creasingly being employed to treat malignant childhood tumors with variable results.
37 asingly is being employed to treat malignant childhood tumors, with variable results.
38 creasingly being employed to treat malignant childhood tumors, with variable results.

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