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1 n aid in the visualization of ovarian cancer micrometastasis.
2 because of the associated increased risk of micrometastasis.
3 be overlooked during SLND as they may harbor micrometastasis.
4 th cisplatin to enhance suppression of liver micrometastasis.
5 ften by just one growth-restricted dangerous micrometastasis.
6 trigel plug angiogenesis, and uveal melanoma micrometastasis.
7 ecurrence of established cancer, and to find micrometastasis.
8 androgen-independent growth, accompanied by micrometastasis.
9 (subsequent outgrowth) of lung experimental micrometastasis.
10 the effect of inhibiting VEGF on tumor cell micrometastasis.
11 nt IFN-alpha 2b results in decreased hepatic micrometastasis and increased survival time through incr
13 owing at various secondary sites to generate micrometastasis and metastatic colonization than control
15 but not parental cells) were capable of lung micrometastasis and of binding exogenously-added hyaluro
16 p120 isoforms, is predictive of renal tumor micrometastasis and systemic progression, following neph
17 ts of cancer progression (local invasion and micrometastasis) and may no longer be required once meta
18 layer or small cluster of cells simulating a micrometastasis, and little effect in a sphere analogous
19 rognosis similar to that associated with SLN micrometastasis, and the number of positive qRT biomarke
20 ualization of intraperitoneal ovarian cancer micrometastasis as small as 100 mum with optimal resolut
21 implanted human PC3-M PCa cells formed lung micrometastasis by 4 weeks in >80% of inbred athymic mic
23 l cancers, perhaps because of more effective micrometastasis eradication and reduced risk of incomple
24 -mediated signaling, LUAD cell survival, and micrometastasis expansion in hyaluronan-rich microenviro
25 atic potential of tumor cells by quantifying micrometastasis formation within the ovarioles of adult
31 for the first time small, apparently dormant micrometastasis in the liver of patients with uveal mela
32 The procedure has improved the diagnosis of micrometastasis in the regional tumor-draining lymph nod
37 ection of high-risk breast cancer, including micrometastasis, is critical in tailoring appropriate an
38 olvement was 7% when the sentinel node had a micrometastasis (< or =2 mm), compared with 55% when the
39 it equally as clear when to perform ALND if micrometastasis (Mi) or isolated tumor cells (ITCs) are
45 be the underlying determinant of spontaneous micrometastasis produced by these cells when compared wi
46 turnover rate, antigen expression level, and micrometastasis size on antibody penetration and retenti
50 or primary tumor outgrowth but that promotes micrometastasis to the lungs at the very earliest stages
51 tients with primary tumors < or = 2.0 cm and micrometastasis to the SLN had remaining axillary lymph
52 ate that PEG tuning can provide control over micrometastasis tracking with high tumor-to-background c
53 010 vs 18 for years 1992-2001, P < .001), LN micrometastasis vs macrometastasis (20 vs 19, P = .005),
56 us 1.0, P = 0.02); however, the incidence of micrometastasis was statistically similar in both HSA an
57 f the ocular tumor and the number of hepatic micrometastasis were compared between the mice inoculate
58 he ocular melanoma and the number of hepatic micrometastasis were decreased and microvessel density w
59 ng patients with melanoma and regional nodal micrometastasis who may benefit from full nodal basin re
60 icellular spheroids are an in vitro model of micrometastasis whose adhesive abilities have not been e
61 capability of CREKA-Tris(Gd-DOTA)3 to detect micrometastasis with MRI in co-registration with high-re
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