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1 nsistent with that of patients known to have metastatic colon cancer.
2 ithelial and tumor-initiating cells in human metastatic colon cancer.
3 rphisms as independent prognostic markers in metastatic colon cancer.
4 as prognostic marker in female patients with metastatic colon cancer.
5 Gb(3)), this molecule is highly expressed in metastatic colon cancer.
6 pression in cancer-associated fibroblasts in metastatic colon cancer.
7 ceramide analogues in inducing apoptosis in metastatic colon cancer.
8 nsurance, an uninsured man is diagnosed with metastatic colon cancer.
9 s in duration was observed in a patient with metastatic colon cancer.
10 sion of 5-FU and leucovorin for treatment of metastatic colon cancer.
11 ncer, and liver metastasis in a patient with metastatic colon cancer.
12 ated in this manner a molecular karyotype of metastatic colon cancer.
13 quently mutated or deleted in pancreatic and metastatic colon cancers.
14 inor response was observed in a patient with metastatic colon cancer (5 months) at the 480-mg/m(2)-do
15 s into the peripheral blood of patients with metastatic colon cancer and may be associated with incre
16 mbined with oxaliplatin may have efficacy in metastatic colon cancer and may provide the first indica
18 is required for the survival of primary and metastatic colon cancers and that oncogenic K-RAS activa
19 may represent a novel approach for treating metastatic colon cancers by mitigating the development o
20 with MTX displayed significant synergy in a metastatic colon cancer cell line and was effective in a
22 gration of the MUC2 antisense construct into metastatic colon cancer cells (LS LiM6) resulted in an 8
23 Introduction of galectin 3 antisense into metastatic colon cancer cells (LSLiM6, HM7) resulted in
25 ies revealed that overexpression of Drg-1 in metastatic colon cancer cells reduced in vitro invasion
28 Assessment of tissues from a patient with metastatic colon cancer demonstrated a more than threefo
29 broblast cell cultures were established from metastatic colon cancer in liver, liver away from the me
30 ithelial cells also expressed CD133, whereas metastatic colon cancers isolated from liver had distinc
31 put flow cytometric profiling of primary and metastatic colon cancer lines (SW480, SW620, and HCT116)
33 ciated with sex-specific clinical outcome in metastatic colon cancer patients treated with FU-based c
34 f EGFR were analyzed in genomic DNA from 318 metastatic colon cancer patients, 177 males and 141 fema
35 stration of an Ad vector to individuals with metastatic colon cancer resulted in a robust antibody re
37 s of active matriptase in 68% of primary and metastatic colon cancer sections from tissue microarrays
40 ed 318 patients (177 men and 141 women) with metastatic colon cancer treated between 1992 and 2003 at
41 patients with metastatic prostate cancer or metastatic colon cancer were injected s.c. into nude mic
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