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kidney carcinoma
In a clonogenic assay, the MTX-225.28 conjugate was three times more potent in inhibiting the growth of M21 melanoma cells than free MTX, but did not inhibit the growth of kidney carcinoma cells Caki-1, which do not express high-Mr MAA.
      
In contrast, MTX linked to the mAb DAL K29, reacting with kidney carcinoma cells Caki-1, inhibited their growth but did not affect that of melanoma cells.
      
Finally, neutralizing anti-human EPO antibody had no effect on the clonal growth of two kidney carcinoma cell lines, making autocrine growth regulation by hEPO in these lines unlikely.
      
Angio-infarction followed by nephrectomy cannot be recommended for widespread use in patients with primary metastatic kidney carcinoma.
      
Of 39 human kidney carcinoma transplanted to nude mice, four tumor lines were maintained on nude mice by serial transplantation.
      
A kidney carcinoma with features of clear cell renal carcinoma and transitional cell carcinoma: a combined renal cell and transi
      
Presentation of MHC I-restricted self peptides in kidney carcinoma cells
      
The authors describe their experiments in creating Vx2 kidney carcinoma and their method, namely the method of transcapsular kidney punction after laparotomy.
      
We present two cases of IVC variation as an incidental finding in patients studied by means of CT scan for the gradation of kidney carcinoma and pancreatic cancer respectively.
      
Furthermore, induction of human NGFr expression was observed in hybrids derived from NGFr- human kidney epithelial cells and mouse L cells, but not in hybrids derived from human kidney epithelial cells and mouse RAG kidney carcinoma cells.
      
The authors prepare and utilize LAK cells and IL-2 for adoptive immunotherapy of patients with metastatic melanoma and kidney carcinoma.
      
We have observed that the kidney carcinoma cell line 769-P shows a very high level of expression of KIM-1.
      
 

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