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1 ical teratoid/rhabdoid tumor (AT/RT), a rare childhood tumor.
2 ormation of this disfiguring and endangering childhood tumor.
3 prognostic factor in neuroblastoma, a common childhood tumor.
4 ovide a therapeutic strategy for this lethal childhood tumor.
5 d overexpression of Nmyc1 is associated with childhood tumors.
6 m tumor that accounts for 8-10% of all solid childhood tumors.
7  is still unclear what drives progression of childhood tumors.
8  and other types of adult cancers as well as childhood tumors.
9 romegaly, and an increased susceptibility to childhood tumors.
10 veral previously unknown genomic features of childhood tumors.
11 ha(v)beta5 by microvascular endothelium of a childhood tumor and association of their expression with
12 ymphoblastic leukemia (ALL) is the commonest childhood tumor and remains a leading cause of cancer de
13 oblastic leukemia (B-ALL) is the most common childhood tumor and the leading cause of cancer-related
14  caspase 8 (CASP8) has been reported in some childhood tumors and in neuroendocrine lung tumors.
15                    Given the rarity of these childhood tumors and their propensity to present at adva
16    We show that some cell lines derived from childhood tumors are highly sensitive to growth inhibiti
17                                         Most childhood tumors are radiation sensitive, but the side e
18                                         Most childhood tumors are relatively rare and are therefore s
19 l predictive value, but few studies focus on childhood tumors, because of the relatively small diseas
20  Neuroblastoma, the second most common solid childhood tumor, can be a highly invasive and metastatic
21  rhabdomyosarcoma (ARMS) is a muscle-derived childhood tumor characterized by production of oncogenic
22                                              Childhood tumors containing cells that are morphological
23                    Neuroblastoma is a common childhood tumor derived from the peripheral nervous syst
24 tifying global differentiation, we find that childhood tumors exhibit fetal cellular signals, replaci
25                                  As a whole, childhood tumors had more transcriptional diversity than
26                  Whether the same is true of childhood tumors has been unclear.
27 Lin28B is activated in neuroblastoma (NB), a childhood tumor in sympathetic ganglia and adrenal medul
28         Neuroblastoma is a frequently lethal childhood tumor in which MYC gene deregulation, commonly
29                           Neuroblastoma is a childhood tumor in which transient therapeutic responses
30 to match or clarify the diagnosis for 85% of childhood tumors in a prospective cohort.
31                      Risks for obesity after childhood tumors include hypothalamic injury, with inact
32 enomic rearrangements are a hallmark of most childhood tumors, including medulloblastoma, one of the
33 owth and conveys a predisposition to certain childhood tumors, including Wilms tumor (WT).
34      Lin28B is aberrantly upregulated in the childhood tumor neuroblastoma (NB).
35 xpressed due to genomic amplification in the childhood tumor neuroblastoma.
36 insic pontine glioma (DIPG) is an aggressive childhood tumor of the brainstem with currently no curat
37 s frequently inactivated in neuroblastoma, a childhood tumor of the peripheral nervous system.
38                  Clear cell sarcoma (CCS), a childhood tumor of the tendons and aponeuroses, is unifo
39 icated in medulloblastomas, common malignant childhood tumors of the cerebellum.
40      Therefore, the radiological features of childhood tumors of the nasopharynx must be well known.
41 tion therapy to target these pathways in the childhood tumor rhabdomyosarcoma.
42                      Neuroblastoma (NB) is a childhood tumor that arises from the sympathoadrenal lin
43                                              Childhood tumors that occur synchronously in different a
44                 Malignant neuroblastomas are childhood tumors that remain mostly incurable.
45                           Neuroblastoma is a childhood tumor thought to arise through improper differ
46 re, we reconstructed 3D genomes from diverse childhood tumor types and uncovered a global topology in
47 resenting 18 distinct extracranial and brain childhood tumor types.
48 gents are of great concern in the context of childhood tumors where they can reduce the quality of li
49 s the clinical features are similar to other childhood tumors which affect the nasopharynx and adenoi
50                           Neuroblastomas are childhood tumors with frequent fatal relapses after indu
51 creasingly being employed to treat malignant childhood tumors with variable results.
52          Neuroblastoma (NB) is an aggressive childhood tumor, with high-risk cases having a 5-year ov
53 asingly is being employed to treat malignant childhood tumors, with variable results.
54 creasingly being employed to treat malignant childhood tumors, with variable results.